[{"polyphen":null,"id":"COSV56247013","allele":"COSMIC_MUTATION","start":201,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":201},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":455,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":455,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56118079"},{"sift":null,"clinical_significance":[],"end":367,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":367,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56100061"},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":258,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":258,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV56085407","polyphen":null},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":597,"codons":"","polyphen":null,"id":"COSV56136756","start":597,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"start":113,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV56184190","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":113,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"allele":"COSMIC_MUTATION","start":220,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV99969002","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":220,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"allele":"COSMIC_MUTATION","start":602,"Parent":"ENST00000288602","residues":"","id":"COSV56096821","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":602,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"codons":"","clinical_significance":[],"sift":null,"end":259,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":259,"id":"COSV99970584","polyphen":null},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":516,"codons":"","polyphen":null,"id":"COSV99962884","allele":"COSMIC_MUTATION","start":516,"Parent":"ENST00000288602","residues":""},{"end":469,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":470,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56252767"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":109,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56065601","polyphen":null,"residues":"","Parent":"ENST00000288602","start":109,"allele":"COSMIC_MUTATION"},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":354,"polyphen":null,"id":"COSV56434661","clinical_significance":[],"codons":"","sift":null,"end":354,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"allele":"COSMIC_MUTATION","start":433,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56102963","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":433,"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":312,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":312,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV99953770","polyphen":null},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":612,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56120140","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":612},{"codons":"","clinical_significance":[],"sift":null,"end":719,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":719,"polyphen":null,"id":"COSV56237864"},{"residues":"","Parent":"ENST00000288602","start":327,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56236256","clinical_significance":[],"end":327,"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"splice_region_variant","minor_allele_frequency":null},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":297,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":297,"Parent":"ENST00000288602","residues":"","id":"COSV99973777","polyphen":null},{"clinical_significance":[],"sift":null,"end":594,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":594,"polyphen":null,"id":"COSV56061673"},{"start":748,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV99973774","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":748,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"Parent":"ENST00000288602","residues":"","start":667,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV104608265","sift":null,"clinical_significance":[],"end":667,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"id":"COSV56075762","polyphen":null,"allele":"COSMIC_MUTATION","start":600,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":600,"codons":""},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":590,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":590,"residues":"","Parent":"ENST00000288602","id":"COSV56295665","polyphen":null},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"end":461,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV105170771","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":461},{"start":277,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56106845","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":277,"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"Parent":"ENST00000288602","residues":"","start":582,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56246338","clinical_significance":[],"codons":"","sift":null,"end":582,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":619,"codons":"","id":"COSV56197744","polyphen":null,"allele":"COSMIC_MUTATION","start":619,"residues":"","Parent":"ENST00000288602"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":125,"polyphen":null,"id":"COSV56440723","start":125,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":639,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56322075","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":639},{"polyphen":null,"id":"COSV56070593","residues":"","Parent":"ENST00000288602","start":466,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"end":466,"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"end":526,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":526,"id":"COSV56115047","polyphen":null},{"id":"COSV56444575","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":476,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"end":476,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"allele":"COSMIC_MUTATION","start":735,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV104608664","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":735,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"id":"COSV56394786","polyphen":null,"Parent":"ENST00000288602","residues":"","start":762,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":762,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":490,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":485,"Parent":"ENST00000288602","residues":"","id":"COSV104608678","polyphen":null},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":115,"codons":"","id":"COSV56248402","polyphen":null,"start":115,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":365,"codons":"","id":"COSV56279123","polyphen":null,"allele":"COSMIC_MUTATION","start":365,"Parent":"ENST00000288602","residues":""},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":333,"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":333,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV105858614"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":376,"codons":"","polyphen":null,"id":"COSV106391720","allele":"COSMIC_MUTATION","start":376,"residues":"","Parent":"ENST00000288602"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":694,"sift":null,"codons":"","polyphen":null,"id":"COSV99973522","start":694,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":307,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":307,"Parent":"ENST00000288602","residues":"","id":"COSV106389639","polyphen":null},{"polyphen":null,"id":"COSV56074780","start":401,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":401},{"sift":null,"clinical_significance":[],"codons":"","end":590,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":590,"id":"COSV56455727","polyphen":null},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":542,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56223027","residues":"","Parent":"ENST00000288602","start":542,"allele":"COSMIC_MUTATION"},{"clinical_significance":[],"sift":null,"codons":"","end":600,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":600,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56059110"},{"allele":"COSMIC_MUTATION","start":609,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56169989","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":609,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":444,"id":"COSV56200294","polyphen":null,"allele":"COSMIC_MUTATION","start":444,"Parent":"ENST00000288602","residues":""},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":581,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"splice_region_variant","allele":"COSMIC_MUTATION","start":581,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56077649"},{"id":"COSV56409921","polyphen":null,"start":442,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":442,"codons":""},{"start":581,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56062673","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":581,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"type":"splice_region_variant","translation":"ENSP00000288602"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"end":156,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV56191659","polyphen":null,"residues":"","Parent":"ENST00000288602","start":156,"allele":"COSMIC_MUTATION"},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":226,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":226,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56102976"},{"end":606,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":606,"allele":"COSMIC_MUTATION","id":"COSV56199545","polyphen":null},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":209,"sift":null,"codons":"","id":"COSV106088490","polyphen":null,"start":209,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"id":"COSV56192935","polyphen":null,"start":119,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":119,"codons":""},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":306,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":306,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV105173114"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"end":618,"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","polyphen":null,"id":"COSV56079632","Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":618},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":594,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56082626","Parent":"ENST00000288602","residues":"","start":594,"allele":"COSMIC_MUTATION"},{"start":173,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV56379486","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":173,"sift":null,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"id":"COSV105857546","polyphen":null,"start":657,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":657,"codons":""},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"end":469,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56061424","Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":469},{"clinical_significance":[],"sift":null,"end":449,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":449,"allele":"COSMIC_MUTATION","id":"COSV56201486","polyphen":null},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":305,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56067967","Parent":"ENST00000288602","residues":"","start":305,"allele":"COSMIC_MUTATION"},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":594,"id":"COSV56284149","polyphen":null,"clinical_significance":[],"end":594,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"end":252,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":252,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV105171645"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":347,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56374850","Parent":"ENST00000288602","residues":"","start":347,"allele":"COSMIC_MUTATION"},{"allele":"COSMIC_MUTATION","start":462,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56275998","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":462,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"polyphen":null,"id":"COSV56260838","start":121,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":121},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":56,"codons":"","polyphen":null,"id":"COSV56274574","allele":"COSMIC_MUTATION","start":56,"residues":"","Parent":"ENST00000288602"},{"polyphen":null,"id":"COSV56077148","residues":"","Parent":"ENST00000288602","start":537,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":537,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":751,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV99961532","polyphen":null,"Parent":"ENST00000288602","residues":"","start":751,"allele":"COSMIC_MUTATION"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":220,"clinical_significance":[],"sift":null,"codons":"","id":"COSV99951740","polyphen":null,"start":220,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"id":"COSV56177152","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":586,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":586,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":304,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":304,"residues":"","Parent":"ENST00000288602","id":"COSV56070568","polyphen":null},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":610,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56340223","Parent":"ENST00000288602","residues":"","start":610,"allele":"COSMIC_MUTATION"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":337,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":337,"residues":"","Parent":"ENST00000288602","id":"COSV56253371","polyphen":null},{"polyphen":null,"id":"COSV56137680","start":91,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":91},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":434,"codons":"","id":"COSV105858867","polyphen":null,"allele":"COSMIC_MUTATION","start":434,"residues":"","Parent":"ENST00000288602"},{"clinical_significance":[],"sift":null,"end":132,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":132,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV104608302"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":599,"clinical_significance":[],"sift":null,"codons":"","polyphen":null,"id":"COSV99072650","start":600,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":53,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":53,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56418665"},{"allele":"COSMIC_MUTATION","start":57,"Parent":"ENST00000288602","residues":"","id":"COSV56172195","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":57,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"allele":"COSMIC_MUTATION","start":318,"residues":"","Parent":"ENST00000288602","id":"COSV99958451","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"codons":"","end":318,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":490,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV56171538","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":490},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"end":601,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV56058494","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":601},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":468,"clinical_significance":[],"sift":null,"codons":"","id":"COSV56159875","polyphen":null,"start":468,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":603,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56150898","Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":603},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":494,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56137493","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":494},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":8,"id":"COSV56221055","polyphen":null,"codons":"","clinical_significance":[],"sift":null,"end":8,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":363,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":363,"residues":"","Parent":"ENST00000288602","id":"COSV56082279","polyphen":null},{"start":375,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56435393","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":375,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":705,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":705,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV99951202"},{"polyphen":null,"id":"COSV56439801","start":331,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":331},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":82,"clinical_significance":[],"sift":null,"codons":"","polyphen":null,"id":"COSV99967266","start":82,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"allele":"COSMIC_MUTATION","start":475,"Parent":"ENST00000288602","residues":"","id":"COSV56447448","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":475,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":464,"codons":"","polyphen":null,"id":"COSV106054686","start":464,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"id":"COSV56074234","polyphen":null,"Parent":"ENST00000288602","residues":"","start":152,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":152,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"codons":"","end":765,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":765,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV56411324","polyphen":null},{"clinical_significance":[],"sift":null,"codons":"","end":491,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":487,"id":"COSV56176207","polyphen":null},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":13,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","polyphen":null,"id":"COSV56109509","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":13},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":65,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56193990","Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":65},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":246,"polyphen":null,"id":"COSV105858879","start":246,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":682,"clinical_significance":[],"sift":null,"codons":"","id":"COSV56314445","polyphen":null,"start":682,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"residues":"","Parent":"ENST00000288602","start":497,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56188926","end":497,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"residues":"","Parent":"ENST00000288602","start":191,"allele":"COSMIC_MUTATION","id":"COSV56115140","polyphen":null,"clinical_significance":[],"end":191,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"allele":"COSMIC_MUTATION","start":759,"residues":"","Parent":"ENST00000288602","id":"COSV56130709","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":759,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":531,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","polyphen":null,"id":"COSV56111992","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":531},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":438,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"type":"splice_region_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":438,"Parent":"ENST00000288602","residues":"","id":"COSV99961523","polyphen":null},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"end":162,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56190013","Parent":"ENST00000288602","residues":"","start":162,"allele":"COSMIC_MUTATION"},{"Parent":"ENST00000288602","residues":"","start":262,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56330121","sift":null,"clinical_significance":[],"end":262,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"polyphen":null,"id":"COSV56250212","start":725,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":725,"codons":""},{"Parent":"ENST00000288602","residues":"","start":607,"allele":"COSMIC_MUTATION","id":"COSV105170773","polyphen":null,"sift":null,"clinical_significance":[],"codons":"","end":607,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":597,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":597,"Parent":"ENST00000288602","residues":"","id":"COSV56070905","polyphen":null},{"polyphen":null,"id":"COSV56155642","start":428,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":428},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":688,"id":"COSV56137378","polyphen":null,"start":688,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"polyphen":null,"id":"COSV56415377","start":600,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":604,"codons":""},{"sift":null,"clinical_significance":[],"end":380,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"splice_region_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":380,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56174024"},{"polyphen":null,"id":"COSV56070557","start":469,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":469,"codons":""},{"polyphen":null,"id":"COSV56079647","residues":"","Parent":"ENST00000288602","start":616,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":616,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":583,"id":"COSV56339676","polyphen":null,"start":583,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"polyphen":null,"id":"COSV56257859","start":247,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":247,"codons":""},{"Parent":"ENST00000288602","residues":"","start":315,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56149960","sift":null,"clinical_significance":[],"end":315,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"allele":"COSMIC_MUTATION","start":349,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56403954","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":349,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"id":"COSV56065695","polyphen":null,"allele":"COSMIC_MUTATION","start":594,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":594,"clinical_significance":[],"sift":null,"codons":""},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":695,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56171407","Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":695},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":568,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56241933","Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":568},{"id":"COSV56379787","polyphen":null,"allele":"COSMIC_MUTATION","start":33,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":33,"codons":""},{"polyphen":null,"id":"COSV99963414","start":608,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":608,"codons":""},{"id":"COSV105171531","polyphen":null,"start":490,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":495,"sift":null,"codons":""},{"clinical_significance":[],"codons":"","sift":null,"end":95,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":95,"polyphen":null,"id":"COSV56306760"},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":308,"polyphen":null,"id":"COSV56137583","codons":"","clinical_significance":[],"sift":null,"end":308,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"Parent":"ENST00000288602","residues":"","start":5,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56290185","clinical_significance":[],"sift":null,"end":5,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":189,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":189,"Parent":"ENST00000288602","residues":"","id":"COSV56122767","polyphen":null},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":198,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":198,"Parent":"ENST00000288602","residues":"","id":"COSV56101977","polyphen":null},{"start":30,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV105172727","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":30,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"polyphen":null,"id":"COSV56066607","allele":"COSMIC_MUTATION","start":600,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":600},{"id":"COSV56422344","polyphen":null,"residues":"","Parent":"ENST00000288602","start":666,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":666,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"end":693,"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56137363","polyphen":null,"residues":"","Parent":"ENST00000288602","start":693,"allele":"COSMIC_MUTATION"},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":345,"id":"COSV99967475","polyphen":null,"clinical_significance":[],"end":345,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":341,"id":"COSV99960167","polyphen":null,"clinical_significance":[],"sift":null,"codons":"","end":341,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"clinical_significance":[],"sift":null,"end":60,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":60,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56263276"},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":136,"id":"COSV56430469","polyphen":null,"clinical_significance":[],"sift":null,"end":136,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"polyphen":null,"id":"COSV56343015","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":114,"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"end":114,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"polyphen":null,"id":"COSV56075245","allele":"COSMIC_MUTATION","start":249,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":249,"codons":""},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":604,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56278169","polyphen":null,"Parent":"ENST00000288602","residues":"","start":604,"allele":"COSMIC_MUTATION"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":126,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":126,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56149568","polyphen":null},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":555,"polyphen":null,"id":"COSV56137428","start":555,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":463,"id":"COSV104386541","polyphen":null,"clinical_significance":[],"codons":"","sift":null,"end":463,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"residues":"","Parent":"ENST00000288602","start":609,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56391154","clinical_significance":[],"sift":null,"codons":"","end":609,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":764,"polyphen":null,"id":"COSV104608474","allele":"COSMIC_MUTATION","start":764,"Parent":"ENST00000288602","residues":""},{"polyphen":null,"id":"COSV56335065","allele":"COSMIC_MUTATION","start":69,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":69,"codons":""},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":637,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":637,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56199103"},{"clinical_significance":[],"sift":null,"end":563,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":563,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56070053"},{"end":467,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":467,"allele":"COSMIC_MUTATION","id":"COSV56106484","polyphen":null},{"polyphen":null,"id":"COSV56159745","start":305,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"codons":"","end":305},{"clinical_significance":[],"sift":null,"end":258,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":258,"id":"COSV104608687","polyphen":null},{"id":"COSV56427077","polyphen":null,"residues":"","Parent":"ENST00000288602","start":537,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"end":537,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"allele":"COSMIC_MUTATION","start":33,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56189976","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":33,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":656,"codons":"","id":"COSV105172742","polyphen":null,"start":656,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"polyphen":null,"id":"COSV99965014","allele":"COSMIC_MUTATION","start":251,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":251},{"sift":null,"clinical_significance":[],"codons":"","end":233,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":233,"id":"COSV99972530","polyphen":null},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"end":318,"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","polyphen":null,"id":"COSV56233689","Parent":"ENST00000288602","residues":"","start":318,"allele":"COSMIC_MUTATION"},{"sift":null,"clinical_significance":[],"end":600,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":600,"polyphen":null,"id":"COSV56109586"},{"id":"COSV56371236","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":274,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":274,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":0,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"splice_donor_variant","start":546,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56432083"},{"id":"COSV56136773","polyphen":null,"allele":"COSMIC_MUTATION","start":597,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":597},{"clinical_significance":[],"sift":null,"codons":"","end":63,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":63,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV106088452"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":301,"codons":"","id":"COSV56361500","polyphen":null,"start":301,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"polyphen":null,"id":"COSV56136867","allele":"COSMIC_MUTATION","start":192,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":192},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":452,"id":"COSV105171701","polyphen":null,"allele":"COSMIC_MUTATION","start":452,"Parent":"ENST00000288602","residues":""},{"residues":"","Parent":"ENST00000288602","start":91,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV105172677","end":91,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":171,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":171,"Parent":"ENST00000288602","residues":"","id":"COSV56254296","polyphen":null},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":600,"id":"COSV106088313","polyphen":null,"sift":null,"clinical_significance":[],"end":605,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"id":"COSV56374957","polyphen":null,"allele":"COSMIC_MUTATION","start":243,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":243,"codons":""},{"polyphen":null,"id":"COSV56107641","residues":"","Parent":"ENST00000288602","start":584,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":584,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"clinical_significance":[],"sift":null,"codons":"","end":600,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":600,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56076564"},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":336,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":336,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV105858698"},{"start":413,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV99072600","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":413,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"sift":null,"clinical_significance":[],"end":568,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":568,"allele":"COSMIC_MUTATION","id":"COSV56372516","polyphen":null},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":153,"polyphen":null,"id":"COSV56437940","clinical_significance":[],"codons":"","sift":null,"end":153,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"end":251,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":251,"polyphen":null,"id":"COSV105171886"},{"start":469,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56065622","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":469,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"start":633,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56423164","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":633,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":357,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","polyphen":null,"id":"COSV56241262","Parent":"ENST00000288602","residues":"","start":357,"allele":"COSMIC_MUTATION"},{"start":755,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV56213655","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":755,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"start":487,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56274667","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":487,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":762,"codons":"","id":"COSV56368837","polyphen":null,"allele":"COSMIC_MUTATION","start":762,"Parent":"ENST00000288602","residues":""},{"id":"COSV56294995","polyphen":null,"allele":"COSMIC_MUTATION","start":48,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"codons":"","end":48},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":598,"polyphen":null,"id":"COSV56116052","allele":"COSMIC_MUTATION","start":598,"residues":"","Parent":"ENST00000288602"},{"end":363,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":363,"polyphen":null,"id":"COSV56188572"},{"id":"COSV99968300","polyphen":null,"allele":"COSMIC_MUTATION","start":235,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":235},{"start":506,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56288942","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":506,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"splice_region_variant"},{"id":"COSV99949554","polyphen":null,"allele":"COSMIC_MUTATION","start":446,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":446,"codons":""},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":676,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56062521","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":676},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"codons":"","end":80,"minor_allele_frequency":null,"type":"splice_region_variant","translation":"ENSP00000288602","start":80,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV99071388","polyphen":null},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":339,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":339,"residues":"","Parent":"ENST00000288602","id":"COSV99949406","polyphen":null},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":159,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":159,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV99956954","polyphen":null},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":598,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56147430","Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":598},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":456,"sift":null,"codons":"","polyphen":null,"id":"COSV56145696","allele":"COSMIC_MUTATION","start":456,"residues":"","Parent":"ENST00000288602"},{"id":"COSV56181274","polyphen":null,"start":599,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":599},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":590,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":590,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV56237053","polyphen":null},{"id":"COSV56115685","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":599,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"end":600,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"allele":"COSMIC_MUTATION","start":699,"residues":"","Parent":"ENST00000288602","id":"COSV56062499","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":699,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"polyphen":null,"id":"COSV56263217","residues":"","Parent":"ENST00000288602","start":283,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":283,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"clinical_significance":[],"sift":null,"codons":"","end":662,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":662,"polyphen":null,"id":"COSV99967415"},{"polyphen":null,"id":"COSV56060749","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":598,"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":598,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":584,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56096161","Parent":"ENST00000288602","residues":"","start":584,"allele":"COSMIC_MUTATION"},{"end":727,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":727,"allele":"COSMIC_MUTATION","id":"COSV104608661","polyphen":null},{"clinical_significance":[],"end":145,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":144,"allele":"COSMIC_MUTATION","id":"COSV104608300","polyphen":null},{"codons":"","clinical_significance":[],"sift":null,"end":169,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"splice_acceptor_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":0,"polyphen":null,"id":"COSV99959679"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":443,"polyphen":null,"id":"COSV105172854","allele":"COSMIC_MUTATION","start":443,"residues":"","Parent":"ENST00000288602"},{"id":"COSV56361810","polyphen":null,"allele":"COSMIC_MUTATION","start":285,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":284,"clinical_significance":[],"sift":null,"codons":""},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":597,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56072463","polyphen":null,"residues":"","Parent":"ENST00000288602","start":597,"allele":"COSMIC_MUTATION"},{"sift":null,"clinical_significance":[],"codons":"","end":394,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"splice_region_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":394,"allele":"COSMIC_MUTATION","id":"COSV56111105","polyphen":null},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":468,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":468,"Parent":"ENST00000288602","residues":"","id":"COSV56193137","polyphen":null},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":597,"id":"COSV56128388","polyphen":null,"start":597,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"clinical_significance":[],"end":601,"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":601,"allele":"COSMIC_MUTATION","id":"COSV56070869","polyphen":null},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":594,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":594,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56195504"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"end":574,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","polyphen":null,"id":"COSV56187614","Parent":"ENST00000288602","residues":"","start":574,"allele":"COSMIC_MUTATION"},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":487,"id":"COSV56226915","polyphen":null,"clinical_significance":[],"sift":null,"end":487,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"residues":"","Parent":"ENST00000288602","start":598,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56215781","sift":null,"clinical_significance":[],"codons":"","end":598,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"polyphen":null,"id":"COSV56306747","Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":159,"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"end":159,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"end":482,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":483,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV105172699"},{"polyphen":null,"id":"COSV56325777","Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":326,"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":326,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":618,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":618,"Parent":"ENST00000288602","residues":"","id":"COSV56057024","polyphen":null},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":594,"clinical_significance":[],"sift":null,"codons":"","polyphen":null,"id":"COSV56066597","start":593,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"codons":"","end":694,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":694,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56347975"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":677,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56246364","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":677},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":695,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":695,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56062510"},{"polyphen":null,"id":"COSV56374840","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":347,"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"end":347,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":416,"id":"COSV99072644","polyphen":null,"allele":"COSMIC_MUTATION","start":416,"residues":"","Parent":"ENST00000288602"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"end":190,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV56137627","polyphen":null,"Parent":"ENST00000288602","residues":"","start":190,"allele":"COSMIC_MUTATION"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"end":518,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV99972062","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":518},{"start":359,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56160296","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":359,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":447,"polyphen":null,"id":"COSV104386540","allele":"COSMIC_MUTATION","start":447,"residues":"","Parent":"ENST00000288602"},{"codons":"","clinical_significance":[],"sift":null,"end":294,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":294,"polyphen":null,"id":"COSV56101984"},{"clinical_significance":[],"codons":"","sift":null,"end":603,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":603,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56377255"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":600,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56202764","polyphen":null,"residues":"","Parent":"ENST00000288602","start":599,"allele":"COSMIC_MUTATION"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":456,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","polyphen":null,"id":"COSV105173220","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":456},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"end":454,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56176826","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":454},{"polyphen":null,"id":"COSV56365133","residues":"","Parent":"ENST00000288602","start":727,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":727,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"Parent":"ENST00000288602","residues":"","start":600,"allele":"COSMIC_MUTATION","id":"COSV56057713","polyphen":null,"clinical_significance":[],"end":600,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"id":"COSV56196423","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":588,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"end":588,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"start":657,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56347987","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":657,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"id":"COSV56100024","polyphen":null,"allele":"COSMIC_MUTATION","start":486,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":490},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":404,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":404,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV99961861","polyphen":null},{"sift":null,"clinical_significance":[],"codons":"","end":178,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":178,"allele":"COSMIC_MUTATION","id":"COSV56105105","polyphen":null},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":604,"polyphen":null,"id":"COSV99958531","start":600,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"codons":"","end":360,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":360,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56205306"},{"polyphen":null,"id":"COSV56187359","allele":"COSMIC_MUTATION","start":593,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":593,"clinical_significance":[],"sift":null,"codons":""},{"id":"COSV56201590","polyphen":null,"Parent":"ENST00000288602","residues":"","start":553,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"end":553,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"polyphen":null,"id":"COSV56124012","residues":"","Parent":"ENST00000288602","start":600,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"end":600,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"start":204,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56348198","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":204,"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"sift":null,"clinical_significance":[],"end":604,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":604,"polyphen":null,"id":"COSV56131868"},{"id":"COSV56089960","polyphen":null,"start":309,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":309},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":762,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":762,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV104386407"},{"id":"COSV56224199","polyphen":null,"allele":"COSMIC_MUTATION","start":594,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":594},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":727,"codons":"","polyphen":null,"id":"COSV56395544","allele":"COSMIC_MUTATION","start":727,"residues":"","Parent":"ENST00000288602"},{"id":"COSV56201191","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":599,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":598,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"splice_acceptor_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":581,"sift":null,"codons":"","polyphen":null,"id":"COSV56366344","start":0,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"id":"COSV56077202","polyphen":null,"start":323,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":323,"sift":null,"codons":""},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":583,"polyphen":null,"id":"COSV56071556","sift":null,"clinical_significance":[],"end":583,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"polyphen":null,"id":"COSV56074247","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":599,"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":600,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":613,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV99971490","polyphen":null,"Parent":"ENST00000288602","residues":"","start":613,"allele":"COSMIC_MUTATION"},{"polyphen":null,"id":"COSV56137385","start":678,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":678,"clinical_significance":[],"sift":null,"codons":""},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":600,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":600,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56288520"},{"allele":"COSMIC_MUTATION","start":732,"Parent":"ENST00000288602","residues":"","id":"COSV56090401","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":732,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"end":153,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56070060","residues":"","Parent":"ENST00000288602","start":153,"allele":"COSMIC_MUTATION"},{"start":492,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56065611","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":492,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"polyphen":null,"id":"COSV56344549","allele":"COSMIC_MUTATION","start":605,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":605},{"id":"COSV56360406","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":322,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":322,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"clinical_significance":[],"codons":"","sift":null,"end":367,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":367,"allele":"COSMIC_MUTATION","id":"COSV56448507","polyphen":null},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":492,"polyphen":null,"id":"COSV56194068","start":487,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":146,"sift":null,"codons":"","polyphen":null,"id":"COSV56375054","start":146,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"polyphen":null,"id":"COSV56137514","start":451,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":451,"clinical_significance":[],"sift":null,"codons":""},{"codons":"","clinical_significance":[],"sift":null,"end":326,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":326,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56234618"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":574,"polyphen":null,"id":"COSV56111969","allele":"COSMIC_MUTATION","start":574,"residues":"","Parent":"ENST00000288602"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":206,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV99967310","polyphen":null,"residues":"","Parent":"ENST00000288602","start":206,"allele":"COSMIC_MUTATION"},{"id":"COSV105172066","polyphen":null,"allele":"COSMIC_MUTATION","start":178,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":178,"clinical_significance":[],"sift":null,"codons":""},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"codons":"","end":277,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":277,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56099777"},{"id":"COSV56224489","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":726,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":726,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":464,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56066746","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":464},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":569,"codons":"","id":"COSV104608744","polyphen":null,"allele":"COSMIC_MUTATION","start":569,"residues":"","Parent":"ENST00000288602"},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":587,"id":"COSV56423294","polyphen":null,"end":587,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"allele":"COSMIC_MUTATION","start":604,"Parent":"ENST00000288602","residues":"","id":"COSV104608727","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":604,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"id":"COSV56236813","polyphen":null,"allele":"COSMIC_MUTATION","start":483,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":483,"clinical_significance":[],"sift":null,"codons":""},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"end":183,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56243281","residues":"","Parent":"ENST00000288602","start":183,"allele":"COSMIC_MUTATION"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":551,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV56137441","polyphen":null,"Parent":"ENST00000288602","residues":"","start":551,"allele":"COSMIC_MUTATION"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"end":606,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56137862","polyphen":null,"Parent":"ENST00000288602","residues":"","start":606,"allele":"COSMIC_MUTATION"},{"clinical_significance":[],"codons":"","sift":null,"end":698,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":698,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56328531"},{"start":747,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56411766","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":747,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"id":"COSV56089486","polyphen":null,"Parent":"ENST00000288602","residues":"","start":514,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"end":514,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":601,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56255469","residues":"","Parent":"ENST00000288602","start":601,"allele":"COSMIC_MUTATION"},{"polyphen":null,"id":"COSV56078028","start":471,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":471},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":499,"codons":"","polyphen":null,"id":"COSV56417995","start":499,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"clinical_significance":[],"end":29,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":29,"allele":"COSMIC_MUTATION","id":"COSV105858085","polyphen":null},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":469,"id":"COSV99968297","polyphen":null,"clinical_significance":[],"sift":null,"end":469,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":339,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":339,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56122576","polyphen":null},{"id":"COSV56119548","polyphen":null,"allele":"COSMIC_MUTATION","start":205,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":205},{"id":"COSV56097427","polyphen":null,"start":615,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":615,"codons":""},{"start":648,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56130252","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":648,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"end":131,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV56110443","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":131},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":421,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":421,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56355997"},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":614,"id":"COSV56255456","polyphen":null,"clinical_significance":[],"sift":null,"codons":"","end":614,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":298,"id":"COSV56355049","polyphen":null,"end":298,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"minor_allele_frequency":null,"type":"splice_region_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":439,"sift":null,"codons":"","id":"COSV56447415","polyphen":null,"allele":"COSMIC_MUTATION","start":439,"residues":"","Parent":"ENST00000288602"},{"sift":null,"clinical_significance":[],"codons":"","end":358,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":358,"polyphen":null,"id":"COSV56393801"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":281,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56215804","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":281},{"start":473,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV104608473","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":473,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"end":148,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":148,"allele":"COSMIC_MUTATION","id":"COSV56149592","polyphen":null},{"clinical_significance":[],"sift":null,"codons":"","end":194,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":194,"id":"COSV56395264","polyphen":null},{"polyphen":null,"id":"COSV56289992","Parent":"ENST00000288602","residues":"","start":241,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"end":241,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"allele":"COSMIC_MUTATION","start":211,"residues":"","Parent":"ENST00000288602","id":"COSV56099340","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":211,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":129,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":129,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56191665"},{"start":612,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56164013","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":612,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"clinical_significance":[],"sift":null,"codons":"","end":471,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":471,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56391019"},{"polyphen":null,"id":"COSV56192919","start":0,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"splice_acceptor_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":238,"clinical_significance":[],"sift":null,"codons":""},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":636,"codons":"","polyphen":null,"id":"COSV56376383","start":636,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":233,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV56065632","polyphen":null,"residues":"","Parent":"ENST00000288602","start":233,"allele":"COSMIC_MUTATION"},{"polyphen":null,"id":"COSV56110431","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":712,"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"end":712,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"clinical_significance":[],"codons":"","sift":null,"end":734,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":734,"polyphen":null,"id":"COSV99954797"},{"polyphen":null,"id":"COSV56099318","start":345,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":345},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"splice_region_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":238,"clinical_significance":[],"sift":null,"codons":"","polyphen":null,"id":"COSV99972161","start":238,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"clinical_significance":[],"end":671,"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":671,"polyphen":null,"id":"COSV99072596"},{"id":"COSV56139540","polyphen":null,"Parent":"ENST00000288602","residues":"","start":606,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":606,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"allele":"COSMIC_MUTATION","start":485,"Parent":"ENST00000288602","residues":"","id":"COSV56396779","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":485,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"allele":"COSMIC_MUTATION","start":401,"Parent":"ENST00000288602","residues":"","id":"COSV56248932","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":401,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"id":"COSV56236935","polyphen":null,"allele":"COSMIC_MUTATION","start":599,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":604},{"Parent":"ENST00000288602","residues":"","start":606,"allele":"COSMIC_MUTATION","id":"COSV56227340","polyphen":null,"clinical_significance":[],"sift":null,"codons":"","end":606,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"clinical_significance":[],"end":210,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":210,"polyphen":null,"id":"COSV99962917"},{"id":"COSV56254248","polyphen":null,"residues":"","Parent":"ENST00000288602","start":576,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":576,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":260,"id":"COSV56260454","polyphen":null,"end":260,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"codons":"","clinical_significance":[],"sift":null,"end":189,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":189,"polyphen":null,"id":"COSV104386598"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":741,"sift":null,"codons":"","polyphen":null,"id":"COSV56319179","start":741,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"sift":null,"clinical_significance":[],"end":241,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":241,"allele":"COSMIC_MUTATION","id":"COSV56289708","polyphen":null},{"residues":"","Parent":"ENST00000288602","start":421,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56417842","sift":null,"clinical_significance":[],"codons":"","end":421,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"allele":"COSMIC_MUTATION","start":384,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV99072649","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":384,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":464,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV56361117","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":464},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":22,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV99071386","polyphen":null,"Parent":"ENST00000288602","residues":"","start":22,"allele":"COSMIC_MUTATION"},{"polyphen":null,"id":"COSV56059334","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":407,"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":407,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"allele":"COSMIC_MUTATION","start":703,"residues":"","Parent":"ENST00000288602","id":"COSV56263580","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"codons":"","end":703,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"polyphen":null,"id":"COSV56065204","start":600,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":600,"codons":""},{"id":"COSV56386604","polyphen":null,"Parent":"ENST00000288602","residues":"","start":64,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":64,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"id":"COSV99953768","polyphen":null,"allele":"COSMIC_MUTATION","start":388,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":388},{"clinical_significance":[],"sift":null,"end":27,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":27,"allele":"COSMIC_MUTATION","id":"COSV56150881","polyphen":null},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":466,"id":"COSV56059390","polyphen":null,"end":466,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":603,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":599,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56079950"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"end":595,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","polyphen":null,"id":"COSV56088678","Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":595},{"clinical_significance":[],"codons":"","sift":null,"end":624,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":624,"allele":"COSMIC_MUTATION","id":"COSV99969410","polyphen":null},{"end":201,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":201,"polyphen":null,"id":"COSV56411666"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":606,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56070824","polyphen":null,"Parent":"ENST00000288602","residues":"","start":606,"allele":"COSMIC_MUTATION"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":601,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":601,"Parent":"ENST00000288602","residues":"","id":"COSV56115928","polyphen":null},{"polyphen":null,"id":"COSV99949417","Parent":"ENST00000288602","residues":"","start":80,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"splice_region_variant","minor_allele_frequency":null,"clinical_significance":[],"end":80,"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"polyphen":null,"id":"COSV56112042","start":595,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"codons":"","end":595},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":450,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":450,"Parent":"ENST00000288602","residues":"","id":"COSV56248893","polyphen":null},{"id":"COSV56140830","polyphen":null,"start":394,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":394},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":215,"id":"COSV56374974","polyphen":null,"clinical_significance":[],"sift":null,"codons":"","end":215,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":247,"id":"COSV56165267","polyphen":null,"allele":"COSMIC_MUTATION","start":247,"Parent":"ENST00000288602","residues":""},{"polyphen":null,"id":"COSV56254057","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":469,"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"end":469,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":284,"polyphen":null,"id":"COSV56270985","clinical_significance":[],"sift":null,"codons":"","end":284,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"residues":"","Parent":"ENST00000288602","start":462,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56383150","clinical_significance":[],"end":462,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":585,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56197266","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":585},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"end":725,"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","polyphen":null,"id":"COSV99962741","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":725},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":459,"codons":"","id":"COSV56291128","polyphen":null,"start":459,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"clinical_significance":[],"end":15,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":14,"polyphen":null,"id":"COSV105171669"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"codons":"","end":89,"polyphen":null,"id":"COSV56147956","start":89,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"end":596,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":596,"allele":"COSMIC_MUTATION","id":"COSV56066561","polyphen":null},{"clinical_significance":[],"end":352,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":352,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56106900"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"codons":"","end":444,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":444,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56257334"},{"id":"COSV56137567","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":337,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":337,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"allele":"COSMIC_MUTATION","start":540,"Parent":"ENST00000288602","residues":"","id":"COSV56158918","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":540,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":598,"sift":null,"codons":"","id":"COSV56245019","polyphen":null,"allele":"COSMIC_MUTATION","start":598,"Parent":"ENST00000288602","residues":""},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":260,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV104608297","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":260},{"Parent":"ENST00000288602","residues":"","start":485,"allele":"COSMIC_MUTATION","id":"COSV56173975","polyphen":null,"sift":null,"clinical_significance":[],"codons":"","end":485,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":449,"id":"COSV56058533","polyphen":null,"start":449,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":239,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":239,"Parent":"ENST00000288602","residues":"","id":"COSV56448519","polyphen":null},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":599,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56338165","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":599},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":549,"id":"COSV99972740","polyphen":null,"codons":"","clinical_significance":[],"sift":null,"end":549,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":442,"polyphen":null,"id":"COSV56166828","allele":"COSMIC_MUTATION","start":442,"residues":"","Parent":"ENST00000288602"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":571,"sift":null,"codons":"","id":"COSV56192299","polyphen":null,"start":571,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"id":"COSV56068050","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":389,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":389,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"residues":"","Parent":"ENST00000288602","start":348,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56403182","sift":null,"clinical_significance":[],"codons":"","end":348,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"start":620,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56214981","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":620,"codons":"","minor_allele_frequency":null,"type":"splice_region_variant","translation":"ENSP00000288602"},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":636,"id":"COSV56065703","polyphen":null,"end":636,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"start":686,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56074924","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":686,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":79,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV105858412","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":79},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":118,"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":118,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV104608304"},{"allele":"COSMIC_MUTATION","start":497,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV99955482","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":497,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"residues":"","Parent":"ENST00000288602","start":543,"allele":"COSMIC_MUTATION","id":"COSV56374781","polyphen":null,"codons":"","clinical_significance":[],"sift":null,"end":543,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":469,"id":"COSV56190051","polyphen":null,"clinical_significance":[],"sift":null,"end":469,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"polyphen":null,"id":"COSV56137505","residues":"","Parent":"ENST00000288602","start":487,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":487,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":428,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56113934","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":428},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":423,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56075230","polyphen":null,"Parent":"ENST00000288602","residues":"","start":423,"allele":"COSMIC_MUTATION"},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":674,"id":"COSV56262874","polyphen":null,"end":674,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":758,"codons":"","polyphen":null,"id":"COSV56342959","start":758,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"allele":"COSMIC_MUTATION","start":521,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV105857957","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":521,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":459,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":459,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56167110","polyphen":null},{"id":"COSV56226275","polyphen":null,"allele":"COSMIC_MUTATION","start":671,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":671},{"clinical_significance":[],"end":413,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":413,"polyphen":null,"id":"COSV56374814"},{"Parent":"ENST00000288602","residues":"","start":106,"allele":"COSMIC_MUTATION","id":"COSV56137673","polyphen":null,"clinical_significance":[],"sift":null,"end":106,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":288,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"splice_region_variant","start":288,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV105857796"},{"polyphen":null,"id":"COSV56374746","Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":614,"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":614,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":600,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56056643","Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":600},{"id":"COSV99956568","polyphen":null,"allele":"COSMIC_MUTATION","start":517,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":517,"sift":null,"codons":""},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":33,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56444587","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":26},{"start":685,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV99972155","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"codons":"","end":685,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":209,"id":"COSV105858285","polyphen":null,"start":209,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":258,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":258,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56290004","polyphen":null},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":591,"polyphen":null,"id":"COSV56060253","start":591,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":561,"id":"COSV105858906","polyphen":null,"allele":"COSMIC_MUTATION","start":561,"Parent":"ENST00000288602","residues":""},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":179,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":179,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56323935"},{"polyphen":null,"id":"COSV56082285","residues":"","Parent":"ENST00000288602","start":591,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":591,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":587,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":587,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56443879"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"end":443,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV56167259","polyphen":null,"Parent":"ENST00000288602","residues":"","start":443,"allele":"COSMIC_MUTATION"},{"polyphen":null,"id":"COSV99972156","start":267,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":267,"codons":""},{"start":334,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56192974","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"codons":"","end":334,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":732,"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":732,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56253634"},{"clinical_significance":[],"end":604,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":604,"allele":"COSMIC_MUTATION","id":"COSV56348386","polyphen":null},{"clinical_significance":[],"sift":null,"end":25,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":25,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56189992"},{"polyphen":null,"id":"COSV56236773","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":484,"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":486,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"Parent":"ENST00000288602","residues":"","start":10,"allele":"COSMIC_MUTATION","id":"COSV56330293","polyphen":null,"clinical_significance":[],"codons":"","sift":null,"end":10,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":469,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":469,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56077154"},{"id":"COSV56070652","polyphen":null,"Parent":"ENST00000288602","residues":"","start":534,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":534,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"id":"COSV56137419","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":575,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"end":575,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"id":"COSV99952510","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":635,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":635,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"id":"COSV56250103","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":464,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":464,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"polyphen":null,"id":"COSV56374830","start":351,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":351,"codons":""},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":462,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56176801","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":462},{"id":"COSV104608136","polyphen":null,"allele":"COSMIC_MUTATION","start":26,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":33},{"residues":"","Parent":"ENST00000288602","start":502,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56196320","sift":null,"clinical_significance":[],"end":502,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"residues":"","Parent":"ENST00000288602","start":579,"allele":"COSMIC_MUTATION","id":"COSV105858814","polyphen":null,"clinical_significance":[],"end":579,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"end":422,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","polyphen":null,"id":"COSV56238174","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":422},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":549,"sift":null,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":549,"Parent":"ENST00000288602","residues":"","id":"COSV56250201","polyphen":null},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":682,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV56096882","polyphen":null,"residues":"","Parent":"ENST00000288602","start":682,"allele":"COSMIC_MUTATION"},{"residues":"","Parent":"ENST00000288602","start":183,"allele":"COSMIC_MUTATION","id":"COSV56110289","polyphen":null,"clinical_significance":[],"sift":null,"codons":"","end":183,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"id":"COSV99958793","polyphen":null,"allele":"COSMIC_MUTATION","start":347,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":347,"codons":""},{"allele":"COSMIC_MUTATION","start":202,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56348043","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":202,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"residues":"","Parent":"ENST00000288602","start":252,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56387915","clinical_significance":[],"end":252,"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"polyphen":null,"id":"COSV56190001","start":485,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"codons":"","end":485},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":341,"polyphen":null,"id":"COSV56275932","codons":"","clinical_significance":[],"sift":null,"end":341,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"id":"COSV104608303","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":123,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":123,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":606,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56257815","polyphen":null,"residues":"","Parent":"ENST00000288602","start":606,"allele":"COSMIC_MUTATION"},{"polyphen":null,"id":"COSV56293156","start":600,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":600},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":602,"id":"COSV56100040","polyphen":null,"start":601,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"codons":"","end":332,"id":"COSV56137994","polyphen":null,"allele":"COSMIC_MUTATION","start":332,"Parent":"ENST00000288602","residues":""},{"residues":"","Parent":"ENST00000288602","start":567,"allele":"COSMIC_MUTATION","id":"COSV56395313","polyphen":null,"sift":null,"clinical_significance":[],"end":567,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"id":"COSV56166636","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":11,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"end":11,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":360,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV56136786","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":360},{"clinical_significance":[],"end":305,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":305,"id":"COSV99971893","polyphen":null},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":503,"sift":null,"codons":"","id":"COSV56169313","polyphen":null,"allele":"COSMIC_MUTATION","start":503,"Parent":"ENST00000288602","residues":""},{"id":"COSV56188945","polyphen":null,"allele":"COSMIC_MUTATION","start":211,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":211},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":636,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":636,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56115473","polyphen":null},{"id":"COSV56369926","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":451,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":451,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":450,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56113691","Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":450},{"polyphen":null,"id":"COSV56082352","residues":"","Parent":"ENST00000288602","start":469,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":469,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":469,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56190329","Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":469},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":601,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","polyphen":null,"id":"COSV56060025","Parent":"ENST00000288602","residues":"","start":600,"allele":"COSMIC_MUTATION"},{"Parent":"ENST00000288602","residues":"","start":420,"allele":"COSMIC_MUTATION","id":"COSV56072532","polyphen":null,"clinical_significance":[],"codons":"","sift":null,"end":420,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"type":"splice_region_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"end":581,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV56106422","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":581},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":561,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56065456","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":561},{"start":31,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56215005","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":31,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"allele":"COSMIC_MUTATION","start":397,"Parent":"ENST00000288602","residues":"","id":"COSV99967256","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":397,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":599,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":599,"residues":"","Parent":"ENST00000288602","id":"COSV56211012","polyphen":null},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":447,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV104386543","polyphen":null,"residues":"","Parent":"ENST00000288602","start":447,"allele":"COSMIC_MUTATION"},{"id":"COSV56081983","polyphen":null,"start":257,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":257,"sift":null,"codons":""},{"sift":null,"clinical_significance":[],"codons":"","end":602,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":600,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56114037"},{"polyphen":null,"id":"COSV56107175","start":600,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":600,"clinical_significance":[],"sift":null,"codons":""},{"id":"COSV56058419","polyphen":null,"Parent":"ENST00000288602","residues":"","start":600,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":600,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"id":"COSV56423110","polyphen":null,"residues":"","Parent":"ENST00000288602","start":300,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":300,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"polyphen":null,"id":"COSV56132418","start":453,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":453},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":550,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":550,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV99961805"},{"polyphen":null,"id":"COSV56137482","start":502,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":502,"sift":null,"codons":""},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":558,"polyphen":null,"id":"COSV56150818","allele":"COSMIC_MUTATION","start":558,"Parent":"ENST00000288602","residues":""},{"id":"COSV56165940","polyphen":null,"allele":"COSMIC_MUTATION","start":598,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":597},{"polyphen":null,"id":"COSV56366526","start":585,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"codons":"","end":585},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":522,"clinical_significance":[],"sift":null,"codons":"","id":"COSV56361480","polyphen":null,"start":522,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":697,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":697,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV56181171","polyphen":null},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":601,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","polyphen":null,"id":"COSV56193778","Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":601},{"allele":"COSMIC_MUTATION","start":447,"Parent":"ENST00000288602","residues":"","id":"COSV56455091","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":447,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"translation":"ENSP00000288602","type":"splice_region_variant","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":439,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56325035","Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":439},{"clinical_significance":[],"codons":"","sift":null,"end":466,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":466,"id":"COSV56099462","polyphen":null},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":202,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":202,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV105858964","polyphen":null},{"codons":"","clinical_significance":[],"sift":null,"end":595,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":595,"id":"COSV56127790","polyphen":null},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":599,"polyphen":null,"id":"COSV56219385","allele":"COSMIC_MUTATION","start":598,"residues":"","Parent":"ENST00000288602"},{"allele":"COSMIC_MUTATION","start":149,"Parent":"ENST00000288602","residues":"","id":"COSV56375039","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":149,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"allele":"COSMIC_MUTATION","start":648,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV99971055","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":648,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":141,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":141,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56314507"},{"start":238,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56137604","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":238,"codons":"","minor_allele_frequency":null,"type":"splice_region_variant","translation":"ENSP00000288602"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":680,"codons":"","id":"COSV56091284","polyphen":null,"allele":"COSMIC_MUTATION","start":680,"residues":"","Parent":"ENST00000288602"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":485,"codons":"","polyphen":null,"id":"COSV99956290","start":485,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"polyphen":null,"id":"COSV56428819","residues":"","Parent":"ENST00000288602","start":509,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":509,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"polyphen":null,"id":"COSV56115059","Parent":"ENST00000288602","residues":"","start":323,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"end":323,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"polyphen":null,"id":"COSV56263207","allele":"COSMIC_MUTATION","start":306,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":306,"clinical_significance":[],"sift":null,"codons":""},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":262,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV56374895","polyphen":null,"residues":"","Parent":"ENST00000288602","start":262,"allele":"COSMIC_MUTATION"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"end":589,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV56065727","polyphen":null,"Parent":"ENST00000288602","residues":"","start":589,"allele":"COSMIC_MUTATION"},{"polyphen":null,"id":"COSV56074952","allele":"COSMIC_MUTATION","start":401,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":401},{"id":"COSV56058093","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":601,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":601,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":50,"polyphen":null,"id":"COSV56420292","end":50,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"polyphen":null,"id":"COSV56075378","start":464,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":464,"clinical_significance":[],"sift":null,"codons":""},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":105,"codons":"","polyphen":null,"id":"COSV56246406","start":105,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"allele":"COSMIC_MUTATION","start":605,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56420875","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":605,"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"id":"COSV56067953","polyphen":null,"residues":"","Parent":"ENST00000288602","start":472,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":472,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"polyphen":null,"id":"COSV99971391","residues":"","Parent":"ENST00000288602","start":663,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":663,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"codons":"","end":564,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":564,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56074945","polyphen":null},{"clinical_significance":[],"sift":null,"end":362,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":362,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56339604"},{"id":"COSV56132320","polyphen":null,"allele":"COSMIC_MUTATION","start":485,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":490},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":26,"polyphen":null,"id":"COSV56062586","start":26,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":600,"polyphen":null,"id":"COSV56228237","allele":"COSMIC_MUTATION","start":600,"Parent":"ENST00000288602","residues":""},{"start":487,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV56274656","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":487,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"id":"COSV56185391","polyphen":null,"Parent":"ENST00000288602","residues":"","start":210,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":210,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"allele":"COSMIC_MUTATION","start":465,"Parent":"ENST00000288602","residues":"","id":"COSV56406529","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":465,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"start":581,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56110832","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":581,"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"splice_region_variant"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"codons":"","end":600,"id":"COSV56080151","polyphen":null,"start":600,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":106,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV99967302","polyphen":null,"Parent":"ENST00000288602","residues":"","start":106,"allele":"COSMIC_MUTATION"},{"id":"COSV56111870","polyphen":null,"Parent":"ENST00000288602","residues":"","start":301,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":301,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":272,"polyphen":null,"id":"COSV56118843","clinical_significance":[],"end":272,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"codons":"","clinical_significance":[],"sift":null,"end":347,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":347,"id":"COSV56059226","polyphen":null},{"start":577,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56314323","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":577,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":539,"id":"COSV56386321","polyphen":null,"clinical_significance":[],"sift":null,"end":539,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":519,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV56348002","polyphen":null,"residues":"","Parent":"ENST00000288602","start":519,"allele":"COSMIC_MUTATION"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"end":594,"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","polyphen":null,"id":"COSV56283955","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":594},{"polyphen":null,"id":"COSV56137657","allele":"COSMIC_MUTATION","start":118,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":118,"sift":null,"codons":""},{"allele":"COSMIC_MUTATION","start":518,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56254809","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":518,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"allele":"COSMIC_MUTATION","start":611,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56281627","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":611,"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":403,"id":"COSV56263190","polyphen":null,"codons":"","clinical_significance":[],"sift":null,"end":403,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":30,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV105858696","polyphen":null,"Parent":"ENST00000288602","residues":"","start":27,"allele":"COSMIC_MUTATION"},{"residues":"","Parent":"ENST00000288602","start":140,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV104608301","clinical_significance":[],"sift":null,"codons":"","end":140,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":611,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV99971492","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":611},{"clinical_significance":[],"sift":null,"end":596,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":596,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56105584"},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":607,"id":"COSV56295657","polyphen":null,"clinical_significance":[],"codons":"","sift":null,"end":607,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"id":"COSV99970169","polyphen":null,"allele":"COSMIC_MUTATION","start":609,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":609,"sift":null,"codons":""},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":718,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":718,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56117857"},{"end":181,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":181,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56366102"},{"codons":"","clinical_significance":[],"sift":null,"end":317,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":317,"id":"COSV99947768","polyphen":null},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"codons":"","end":600,"id":"COSV56152883","polyphen":null,"allele":"COSMIC_MUTATION","start":600,"Parent":"ENST00000288602","residues":""},{"id":"COSV99971431","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":233,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":232,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":731,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":731,"residues":"","Parent":"ENST00000288602","id":"COSV56121693","polyphen":null},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":525,"id":"COSV56324597","polyphen":null,"start":525,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"start":574,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56187605","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":574,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":331,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV56374864","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":331},{"polyphen":null,"id":"COSV56166818","start":459,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":459,"clinical_significance":[],"sift":null,"codons":""},{"clinical_significance":[],"sift":null,"end":203,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"splice_region_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":203,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56243201"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":759,"polyphen":null,"id":"COSV104608734","start":759,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":444,"polyphen":null,"id":"COSV105858813","codons":"","clinical_significance":[],"sift":null,"end":444,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"sift":null,"clinical_significance":[],"codons":"","end":255,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":255,"id":"COSV56374919","polyphen":null},{"id":"COSV56260864","polyphen":null,"Parent":"ENST00000288602","residues":"","start":345,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":345,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"polyphen":null,"id":"COSV56364152","Parent":"ENST00000288602","residues":"","start":637,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":637,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"residues":"","Parent":"ENST00000288602","start":404,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56309815","sift":null,"clinical_significance":[],"codons":"","end":404,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"id":"COSV56057324","polyphen":null,"start":601,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"codons":"","end":601},{"polyphen":null,"id":"COSV99958201","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":735,"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":735,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":509,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":509,"Parent":"ENST00000288602","residues":"","id":"COSV56181083","polyphen":null},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":756,"id":"COSV105170772","polyphen":null,"clinical_significance":[],"codons":"","sift":null,"end":756,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"polyphen":null,"id":"COSV56257298","start":207,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":207,"codons":""},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":460,"polyphen":null,"id":"COSV56166809","end":460,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":588,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":588,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56079131"},{"start":104,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV56391510","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"codons":"","end":104,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"polyphen":null,"id":"COSV56058907","allele":"COSMIC_MUTATION","start":643,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":643,"codons":""},{"allele":"COSMIC_MUTATION","start":244,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56374942","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":244,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"end":587,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV56079146","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":587},{"polyphen":null,"id":"COSV104608296","Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":275,"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":275,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"allele":"COSMIC_MUTATION","start":67,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV99964281","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":67,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":639,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56184953","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":639},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":603,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56183050","Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":603},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":719,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":719,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV105858286"},{"id":"COSV105858829","polyphen":null,"start":506,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"splice_region_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":506,"sift":null,"codons":""},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":605,"id":"COSV56276601","polyphen":null,"sift":null,"clinical_significance":[],"codons":"","end":605,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":409,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV104608176","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":409},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":388,"sift":null,"codons":"","polyphen":null,"id":"COSV56189259","allele":"COSMIC_MUTATION","start":389,"residues":"","Parent":"ENST00000288602"},{"type":"splice_region_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":581,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56286119","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":581},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":465,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":465,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56073908"},{"residues":"","Parent":"ENST00000288602","start":349,"allele":"COSMIC_MUTATION","id":"COSV105173329","polyphen":null,"clinical_significance":[],"end":349,"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"allele":"COSMIC_MUTATION","start":245,"Parent":"ENST00000288602","residues":"","id":"COSV56223754","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":245,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":499,"codons":"","polyphen":null,"id":"COSV56065660","start":499,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":302,"polyphen":null,"id":"COSV56366337","end":302,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"polyphen":null,"id":"COSV56192306","allele":"COSMIC_MUTATION","start":393,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"splice_region_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"codons":"","end":393},{"id":"COSV56260660","polyphen":null,"allele":"COSMIC_MUTATION","start":606,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":606,"codons":""},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"end":472,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56161001","polyphen":null,"Parent":"ENST00000288602","residues":"","start":472,"allele":"COSMIC_MUTATION"},{"start":102,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56130562","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":102,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"sift":null,"clinical_significance":[],"end":401,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":401,"polyphen":null,"id":"COSV56266824"},{"translation":"ENSP00000288602","type":"splice_region_variant","minor_allele_frequency":null,"clinical_significance":[],"end":506,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV105858982","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":506},{"Parent":"ENST00000288602","residues":"","start":595,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56413121","clinical_significance":[],"sift":null,"end":595,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"polyphen":null,"id":"COSV56262847","residues":"","Parent":"ENST00000288602","start":192,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":192,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"start":151,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56193956","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":151,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":748,"clinical_significance":[],"sift":null,"codons":"","polyphen":null,"id":"COSV105170691","start":748,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"codons":"","clinical_significance":[],"sift":null,"end":147,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":147,"id":"COSV104608299","polyphen":null},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":469,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV99953015","polyphen":null,"Parent":"ENST00000288602","residues":"","start":469,"allele":"COSMIC_MUTATION"},{"id":"COSV56115216","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":601,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":601,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"polyphen":null,"id":"COSV56135729","start":354,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":354,"sift":null,"codons":""},{"id":"COSV56136742","polyphen":null,"start":708,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":708,"codons":""},{"id":"COSV56440267","polyphen":null,"allele":"COSMIC_MUTATION","start":572,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":572},{"start":599,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56329839","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":601,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"polyphen":null,"id":"COSV56190066","start":385,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":385,"sift":null,"codons":""},{"clinical_significance":[],"codons":"","sift":null,"end":582,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":582,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56157363"},{"allele":"COSMIC_MUTATION","start":456,"residues":"","Parent":"ENST00000288602","id":"COSV56442791","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":456,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"clinical_significance":[],"sift":null,"end":79,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":79,"polyphen":null,"id":"COSV56375067"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"codons":"","end":382,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":382,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56068266"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":31,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":28,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56189982","polyphen":null},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":468,"id":"COSV56447994","polyphen":null,"start":468,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"id":"COSV56168555","polyphen":null,"allele":"COSMIC_MUTATION","start":608,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":608},{"allele":"COSMIC_MUTATION","start":26,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV104607589","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":26,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":570,"polyphen":null,"id":"COSV56069442","allele":"COSMIC_MUTATION","start":570,"residues":"","Parent":"ENST00000288602"},{"allele":"COSMIC_MUTATION","start":684,"residues":"","Parent":"ENST00000288602","id":"COSV106392138","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":684,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"id":"COSV56189238","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":760,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"end":760,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"codons":"","clinical_significance":[],"sift":null,"end":592,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":592,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56243488"},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":711,"id":"COSV104608490","polyphen":null,"end":711,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"residues":"","Parent":"ENST00000288602","start":141,"allele":"COSMIC_MUTATION","id":"COSV56188894","polyphen":null,"sift":null,"clinical_significance":[],"end":141,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":105,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV105173147","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":105},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":187,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56323231","polyphen":null,"residues":"","Parent":"ENST00000288602","start":187,"allele":"COSMIC_MUTATION"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":554,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56430604","polyphen":null,"residues":"","Parent":"ENST00000288602","start":554,"allele":"COSMIC_MUTATION"},{"Parent":"ENST00000288602","residues":"","start":504,"allele":"COSMIC_MUTATION","id":"COSV56431267","polyphen":null,"sift":null,"clinical_significance":[],"codons":"","end":504,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"codons":"","end":185,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":185,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56395553"},{"residues":"","Parent":"ENST00000288602","start":715,"allele":"COSMIC_MUTATION","id":"COSV56257785","polyphen":null,"clinical_significance":[],"codons":"","sift":null,"end":715,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":597,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56225332","Parent":"ENST00000288602","residues":"","start":597,"allele":"COSMIC_MUTATION"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":594,"sift":null,"codons":"","polyphen":null,"id":"COSV56184663","allele":"COSMIC_MUTATION","start":594,"Parent":"ENST00000288602","residues":""},{"polyphen":null,"id":"COSV105858448","start":545,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":545,"clinical_significance":[],"sift":null,"codons":""},{"Parent":"ENST00000288602","residues":"","start":45,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56146506","clinical_significance":[],"sift":null,"end":45,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":751,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV105170703","polyphen":null,"residues":"","Parent":"ENST00000288602","start":751,"allele":"COSMIC_MUTATION"},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":26,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":26,"residues":"","Parent":"ENST00000288602","id":"COSV99950738","polyphen":null},{"polyphen":null,"id":"COSV56243423","residues":"","Parent":"ENST00000288602","start":463,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":463,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"id":"COSV56205912","polyphen":null,"Parent":"ENST00000288602","residues":"","start":146,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":146,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"sift":null,"clinical_significance":[],"end":116,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":116,"polyphen":null,"id":"COSV56375453"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":360,"polyphen":null,"id":"COSV56209848","allele":"COSMIC_MUTATION","start":360,"residues":"","Parent":"ENST00000288602"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":50,"polyphen":null,"id":"COSV56137706","start":50,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":666,"codons":"","polyphen":null,"id":"COSV56439271","start":666,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"id":"COSV56070411","polyphen":null,"allele":"COSMIC_MUTATION","start":476,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":476,"sift":null,"codons":""},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":600,"id":"COSV56059623","polyphen":null,"start":600,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"clinical_significance":[],"end":194,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":194,"polyphen":null,"id":"COSV56386592"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":461,"polyphen":null,"id":"COSV104607983","allele":"COSMIC_MUTATION","start":461,"Parent":"ENST00000288602","residues":""},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":469,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":469,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56062352"},{"Parent":"ENST00000288602","residues":"","start":446,"allele":"COSMIC_MUTATION","id":"COSV56105766","polyphen":null,"clinical_significance":[],"codons":"","sift":null,"end":446,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"clinical_significance":[],"codons":"","sift":null,"end":489,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":489,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56245013"},{"polyphen":null,"id":"COSV56115488","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":586,"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"end":586,"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"id":"COSV56075312","polyphen":null,"allele":"COSMIC_MUTATION","start":629,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":629},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":733,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV99970586","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":733},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":112,"id":"COSV99968304","polyphen":null,"end":112,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":385,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":385,"Parent":"ENST00000288602","residues":"","id":"COSV56122422","polyphen":null},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":602,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":602,"Parent":"ENST00000288602","residues":"","id":"COSV56254987","polyphen":null},{"end":87,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":87,"allele":"COSMIC_MUTATION","id":"COSV105171109","polyphen":null},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":647,"id":"COSV56427776","polyphen":null,"allele":"COSMIC_MUTATION","start":647,"Parent":"ENST00000288602","residues":""},{"start":309,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV105170701","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":309,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":466,"codons":"","id":"COSV56064038","polyphen":null,"start":466,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"id":"COSV56151324","polyphen":null,"Parent":"ENST00000288602","residues":"","start":587,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":587,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":535,"polyphen":null,"id":"COSV104608668","allele":"COSMIC_MUTATION","start":535,"residues":"","Parent":"ENST00000288602"},{"residues":"","Parent":"ENST00000288602","start":505,"allele":"COSMIC_MUTATION","id":"COSV56178243","polyphen":null,"sift":null,"clinical_significance":[],"codons":"","end":505,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"polyphen":null,"id":"COSV56214602","Parent":"ENST00000288602","residues":"","start":535,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":535,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":122,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV105858717","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":122},{"allele":"COSMIC_MUTATION","start":175,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56137637","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":175,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"start":606,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56128534","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":606,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"allele":"COSMIC_MUTATION","start":40,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56387977","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":40,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"id":"COSV56438362","polyphen":null,"start":599,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":599,"codons":""},{"clinical_significance":[],"sift":null,"end":334,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":334,"allele":"COSMIC_MUTATION","id":"COSV56323690","polyphen":null},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":653,"polyphen":null,"id":"COSV56304756","start":653,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":317,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":317,"Parent":"ENST00000288602","residues":"","id":"COSV105173313","polyphen":null},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":650,"codons":"","polyphen":null,"id":"COSV56347995","start":650,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"allele":"COSMIC_MUTATION","start":690,"Parent":"ENST00000288602","residues":"","id":"COSV104608326","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":690,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"polyphen":null,"id":"COSV56347469","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":262,"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":262,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":479,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"type":"splice_region_variant","translation":"ENSP00000288602","start":479,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV56158457","polyphen":null},{"codons":"","clinical_significance":[],"sift":null,"end":160,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":160,"allele":"COSMIC_MUTATION","id":"COSV105171331","polyphen":null},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":441,"polyphen":null,"id":"COSV56304767","end":441,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":600,"polyphen":null,"id":"COSV56085831","codons":"","clinical_significance":[],"sift":null,"end":600,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"residues":"","Parent":"ENST00000288602","start":122,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56234635","clinical_significance":[],"sift":null,"codons":"","end":122,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"sift":null,"clinical_significance":[],"end":471,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":471,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56171549"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":663,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV105858747","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":663},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":604,"polyphen":null,"id":"COSV56168139","allele":"COSMIC_MUTATION","start":603,"residues":"","Parent":"ENST00000288602"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":406,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":406,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56205095"},{"id":"COSV56086959","polyphen":null,"Parent":"ENST00000288602","residues":"","start":599,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":598,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":259,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","polyphen":null,"id":"COSV56374905","residues":"","Parent":"ENST00000288602","start":259,"allele":"COSMIC_MUTATION"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":341,"clinical_significance":[],"sift":null,"codons":"","id":"COSV99948025","polyphen":null,"allele":"COSMIC_MUTATION","start":341,"Parent":"ENST00000288602","residues":""},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":470,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":470,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56391627"},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":428,"polyphen":null,"id":"COSV56386580","clinical_significance":[],"codons":"","sift":null,"end":428,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":49,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":49,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56317673"},{"residues":"","Parent":"ENST00000288602","start":657,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56057768","clinical_significance":[],"end":657,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":591,"id":"COSV56137410","polyphen":null,"start":591,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"Parent":"ENST00000288602","residues":"","start":251,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV104608298","clinical_significance":[],"codons":"","sift":null,"end":251,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"id":"COSV56236238","polyphen":null,"residues":"","Parent":"ENST00000288602","start":758,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":758,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":157,"id":"COSV56099175","polyphen":null,"sift":null,"clinical_significance":[],"codons":"","end":157,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"start":139,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV99953485","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":139,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"allele":"COSMIC_MUTATION","start":310,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56243293","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"codons":"","end":310,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":567,"polyphen":null,"id":"COSV99971861","start":567,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":659,"id":"COSV56374725","polyphen":null,"clinical_significance":[],"codons":"","sift":null,"end":659,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"codons":"","end":629,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":629,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV105858687"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":594,"clinical_significance":[],"sift":null,"codons":"","id":"COSV56106240","polyphen":null,"allele":"COSMIC_MUTATION","start":594,"residues":"","Parent":"ENST00000288602"},{"start":168,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV56391954","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":168,"sift":null,"codons":"","minor_allele_frequency":null,"type":"splice_region_variant","translation":"ENSP00000288602"},{"Parent":"ENST00000288602","residues":"","start":146,"allele":"COSMIC_MUTATION","id":"COSV56273855","polyphen":null,"codons":"","clinical_significance":[],"sift":null,"end":146,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"id":"COSV56113235","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":590,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":590,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":72,"id":"COSV56107149","polyphen":null,"start":72,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"clinical_significance":[],"end":653,"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":653,"id":"COSV56357563","polyphen":null},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":240,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":240,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56379477"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":695,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":695,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56125554"},{"polyphen":null,"id":"COSV56136502","start":661,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":661,"clinical_significance":[],"sift":null,"codons":""},{"Parent":"ENST00000288602","residues":"","start":451,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56323521","clinical_significance":[],"sift":null,"codons":"","end":451,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"id":"COSV56290852","polyphen":null,"start":117,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":117,"clinical_significance":[],"sift":null,"codons":""},{"polyphen":null,"id":"COSV56082407","start":586,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":586,"codons":""},{"polyphen":null,"id":"COSV56062769","start":440,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":440,"codons":""},{"residues":"","Parent":"ENST00000288602","start":595,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56255479","clinical_significance":[],"end":595,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"clinical_significance":[],"end":80,"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"splice_region_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":80,"allele":"COSMIC_MUTATION","id":"COSV99949422","polyphen":null},{"allele":"COSMIC_MUTATION","start":609,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56059256","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":609,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"id":"COSV56309189","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":529,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"end":529,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":762,"polyphen":null,"id":"COSV56115442","clinical_significance":[],"sift":null,"codons":"","end":762,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":469,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":469,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56351006"},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":617,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":617,"Parent":"ENST00000288602","residues":"","id":"COSV56229675","polyphen":null},{"sift":null,"clinical_significance":[],"end":605,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":600,"allele":"COSMIC_MUTATION","id":"COSV56332633","polyphen":null},{"id":"COSV56309785","polyphen":null,"Parent":"ENST00000288602","residues":"","start":740,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":740,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":30,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56332603","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":30},{"clinical_significance":[],"sift":null,"end":134,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":134,"polyphen":null,"id":"COSV56150849"},{"clinical_significance":[],"sift":null,"end":352,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":352,"polyphen":null,"id":"COSV56096805"},{"residues":"","Parent":"ENST00000288602","start":581,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56058108","sift":null,"clinical_significance":[],"codons":"","end":581,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"splice_region_variant","minor_allele_frequency":null},{"clinical_significance":[],"end":469,"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":469,"polyphen":null,"id":"COSV56075573"},{"polyphen":null,"id":"COSV105172388","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":244,"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"end":244,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"residues":"","Parent":"ENST00000288602","start":339,"allele":"COSMIC_MUTATION","id":"COSV105173167","polyphen":null,"sift":null,"clinical_significance":[],"end":339,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"start":356,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56434649","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":356,"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"start":756,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV104608067","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":756,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":444,"polyphen":null,"id":"COSV56083156","start":444,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"polyphen":null,"id":"COSV56289075","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":482,"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":482,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"start":375,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV56416185","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":375,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":715,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV106088260","residues":"","Parent":"ENST00000288602","start":715,"allele":"COSMIC_MUTATION"},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":271,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":271,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV106391384"},{"allele":"COSMIC_MUTATION","start":616,"Parent":"ENST00000288602","residues":"","id":"COSV105170823","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":616,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"residues":"","Parent":"ENST00000288602","start":448,"allele":"COSMIC_MUTATION","id":"COSV105171688","polyphen":null,"codons":"","clinical_significance":[],"sift":null,"end":448,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"id":"COSV56137455","polyphen":null,"start":514,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"codons":"","end":514},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":271,"sift":null,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":271,"Parent":"ENST00000288602","residues":"","id":"COSV56101990","polyphen":null},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":195,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":195,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV106391385","polyphen":null},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":609,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":609,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56210974"},{"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":312,"polyphen":null,"id":"COSV56353154","sift":null,"clinical_significance":[],"end":312,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":605,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":605,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56156684"},{"allele":"COSMIC_MUTATION","start":598,"residues":"","Parent":"ENST00000288602","id":"COSV56070835","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":598,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"polyphen":null,"id":"COSV56128555","allele":"COSMIC_MUTATION","start":593,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":593,"clinical_significance":[],"sift":null,"codons":""},{"polyphen":null,"id":"COSV99968302","residues":"","Parent":"ENST00000288602","start":234,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":234,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"Parent":"ENST00000288602","residues":"","start":231,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56160263","sift":null,"clinical_significance":[],"end":231,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"start":720,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV99954088","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":720,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"clinical_significance":[],"end":731,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":731,"id":"COSV56058484","polyphen":null},{"Parent":"ENST00000288602","residues":"","start":455,"allele":"COSMIC_MUTATION","id":"COSV56085682","polyphen":null,"codons":"","clinical_significance":[],"sift":null,"end":455,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"codons":"","end":501,"id":"COSV56390795","polyphen":null,"allele":"COSMIC_MUTATION","start":501,"Parent":"ENST00000288602","residues":""},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":711,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":711,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV104386632","polyphen":null},{"start":178,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56374030","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":178,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"sift":null,"clinical_significance":[],"codons":"","end":435,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":435,"polyphen":null,"id":"COSV99958462"},{"end":460,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":460,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV106088481"},{"polyphen":null,"id":"COSV56215763","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":741,"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":741,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"id":"COSV105858988","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":165,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":165,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":516,"id":"COSV105171244","polyphen":null,"allele":"COSMIC_MUTATION","start":516,"residues":"","Parent":"ENST00000288602"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"end":184,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV56144127","polyphen":null,"Parent":"ENST00000288602","residues":"","start":184,"allele":"COSMIC_MUTATION"},{"id":"COSV56142617","polyphen":null,"allele":"COSMIC_MUTATION","start":450,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":450,"codons":""},{"clinical_significance":[],"end":300,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":300,"allele":"COSMIC_MUTATION","id":"COSV56350619","polyphen":null},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":755,"sift":null,"codons":"","id":"COSV56334241","polyphen":null,"start":755,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":419,"clinical_significance":[],"sift":null,"codons":"","id":"COSV56227205","polyphen":null,"start":419,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"allele":"COSMIC_MUTATION","start":588,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56366517","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":588,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"id":"COSV99950150","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":36,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":36,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"start":674,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56281170","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":674,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"polyphen":null,"id":"COSV56131542","Parent":"ENST00000288602","residues":"","start":726,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":726,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"start":480,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56082148","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":480,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"clinical_significance":[],"sift":null,"end":596,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":596,"allele":"COSMIC_MUTATION","id":"COSV99951808","polyphen":null},{"residues":"","Parent":"ENST00000288602","start":598,"allele":"COSMIC_MUTATION","id":"COSV56203004","polyphen":null,"clinical_significance":[],"sift":null,"end":598,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":389,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":389,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV99964505"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"end":159,"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV99962981","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":159},{"residues":"","Parent":"ENST00000288602","start":529,"allele":"COSMIC_MUTATION","id":"COSV56091310","polyphen":null,"sift":null,"clinical_significance":[],"end":529,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"polyphen":null,"id":"COSV56155003","start":600,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":601,"clinical_significance":[],"sift":null,"codons":""},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"codons":"","end":679,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":679,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56357054"},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":457,"polyphen":null,"id":"COSV56401862","end":457,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"polyphen":null,"id":"COSV104608198","residues":"","Parent":"ENST00000288602","start":706,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":706,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":457,"polyphen":null,"id":"COSV56246347","allele":"COSMIC_MUTATION","start":457,"Parent":"ENST00000288602","residues":""},{"id":"COSV56374795","polyphen":null,"residues":"","Parent":"ENST00000288602","start":509,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":509,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":616,"codons":"","polyphen":null,"id":"COSV56147745","allele":"COSMIC_MUTATION","start":616,"residues":"","Parent":"ENST00000288602"},{"end":626,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":626,"allele":"COSMIC_MUTATION","id":"COSV99969506","polyphen":null},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":460,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":460,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56258682","polyphen":null},{"id":"COSV56068636","polyphen":null,"start":592,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":592,"sift":null,"codons":""},{"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":252,"sift":null,"codons":"","id":"COSV56374933","polyphen":null,"allele":"COSMIC_MUTATION","start":252,"Parent":"ENST00000288602","residues":""},{"polyphen":null,"id":"COSV106391386","residues":"","Parent":"ENST00000288602","start":102,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"end":102,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"end":450,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV56254258","polyphen":null,"residues":"","Parent":"ENST00000288602","start":450,"allele":"COSMIC_MUTATION"},{"codons":"","clinical_significance":[],"sift":null,"end":599,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","start":599,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56072224"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":401,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56378642","Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":401},{"start":456,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56176814","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":456,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"id":"COSV56267029","polyphen":null,"Parent":"ENST00000288602","residues":"","start":343,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"end":343,"clinical_significance":[],"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"start":612,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56187002","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"codons":"","end":612,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"polyphen":null,"id":"COSV56131972","start":584,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":584,"codons":""},{"polyphen":null,"id":"COSV99967384","residues":"","Parent":"ENST00000288602","start":671,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":671,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":298,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","polyphen":null,"id":"COSV56343001","Parent":"ENST00000288602","residues":"","start":298,"allele":"COSMIC_MUTATION"},{"Parent":"ENST00000288602","residues":"","start":136,"allele":"COSMIC_MUTATION","id":"COSV105173333","polyphen":null,"clinical_significance":[],"sift":null,"codons":"","end":136,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":320,"sift":null,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":320,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV56074414","polyphen":null},{"start":321,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56263368","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":321,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":613,"polyphen":null,"id":"COSV99954692","allele":"COSMIC_MUTATION","start":613,"Parent":"ENST00000288602","residues":""},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":254,"sift":null,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":254,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV56197563","polyphen":null},{"id":"COSV56375375","polyphen":null,"Parent":"ENST00000288602","residues":"","start":539,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":539,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"Parent":"ENST00000288602","residues":"","start":678,"allele":"COSMIC_MUTATION","id":"COSV56066936","polyphen":null,"clinical_significance":[],"sift":null,"codons":"","end":678,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"codons":"","end":102,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56297891","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":102},{"sift":null,"clinical_significance":[],"codons":"","end":279,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":279,"polyphen":null,"id":"COSV99972989"},{"sift":null,"clinical_significance":[],"end":674,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":674,"id":"COSV56196432","polyphen":null},{"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":596,"polyphen":null,"id":"COSV99954791","end":596,"clinical_significance":[],"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"id":"COSV99955506","polyphen":null,"start":566,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"splice_region_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":566},{"start":105,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV56149826","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":105,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"clinical_significance":[],"sift":null,"codons":"","end":104,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":104,"id":"COSV56160271","polyphen":null},{"clinical_significance":[],"sift":null,"codons":"","end":142,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","start":142,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV105857881"},{"id":"COSV56316158","polyphen":null,"Parent":"ENST00000288602","residues":"","start":596,"allele":"COSMIC_MUTATION","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":596,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"end":82,"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","polyphen":null,"id":"COSV105170748","Parent":"ENST00000288602","residues":"","start":82,"allele":"COSMIC_MUTATION"},{"start":499,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV56188916","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":499,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":236,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":236,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56233714"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":633,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":633,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV105857734"},{"id":"COSV105858896","polyphen":null,"allele":"COSMIC_MUTATION","start":548,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":548},{"allele":"COSMIC_MUTATION","start":610,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56418290","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":610,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"start":11,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV56439841","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":11,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"allele":"COSMIC_MUTATION","start":531,"Parent":"ENST00000288602","residues":"","id":"COSV56398551","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":531,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":465,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":465,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV105171128"},{"start":708,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","id":"COSV105171434","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":708,"sift":null,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"start":478,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56071145","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":478,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"splice_region_variant"},{"id":"COSV105173132","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":3,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":3,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":400,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56137529","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":400},{"allele":"COSMIC_MUTATION","start":638,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV106088334","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"end":638,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"allele":"COSMIC_MUTATION","start":364,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56360210","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":364,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":515,"polyphen":null,"id":"COSV56071137","start":515,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"clinical_significance":[],"sift":null,"end":614,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":614,"id":"COSV56062937","polyphen":null},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":480,"codons":"","polyphen":null,"id":"COSV106088461","start":480,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602"},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":64,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":64,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56237815"},{"clinical_significance":[],"sift":null,"end":749,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":749,"id":"COSV106088496","polyphen":null},{"allele":"COSMIC_MUTATION","start":387,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56137554","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":387,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"Parent":"ENST00000288602","residues":"","start":518,"allele":"COSMIC_MUTATION","id":"COSV104608102","polyphen":null,"clinical_significance":[],"codons":"","sift":null,"end":518,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":116,"sift":null,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":116,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV99972158"},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":75,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","polyphen":null,"id":"COSV56162864","residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":75},{"allele":"COSMIC_MUTATION","start":604,"Parent":"ENST00000288602","residues":"","id":"COSV56199774","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":604,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"codons":"","end":386,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","start":386,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56096869"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"end":590,"codons":"","polyphen":null,"id":"COSV99957259","start":590,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"allele":"COSMIC_MUTATION","start":584,"residues":"","Parent":"ENST00000288602","id":"COSV56361615","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":584,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"polyphen":null,"id":"COSV56163967","start":725,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"end":725,"sift":null,"codons":""},{"polyphen":null,"id":"COSV56106863","Parent":"ENST00000288602","residues":"","start":8,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"clinical_significance":[],"codons":"","sift":null,"end":8,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation"},{"residues":"","Parent":"ENST00000288602","start":437,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV99072590","clinical_significance":[],"end":437,"sift":null,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":466,"codons":"","polyphen":null,"id":"COSV56057462","start":466,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"start":122,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV56150865","polyphen":null,"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"codons":"","end":122,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"polyphen":null,"id":"COSV56440733","start":486,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","end":489,"clinical_significance":[],"sift":null,"codons":""},{"id":"COSV56366111","polyphen":null,"start":178,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","codons":"","clinical_significance":[],"sift":null,"end":178},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"end":412,"sift":null,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":412,"residues":"","Parent":"ENST00000288602","id":"COSV56444600","polyphen":null},{"allele":"COSMIC_MUTATION","start":600,"residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56071501","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","sift":null,"clinical_significance":[],"codons":"","end":605,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"polyphen":null,"id":"COSV56128015","start":594,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":593,"codons":""},{"polyphen":null,"id":"COSV99969005","allele":"COSMIC_MUTATION","start":185,"Parent":"ENST00000288602","residues":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"codons":"","sift":null,"end":185},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"codons":"","end":257,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","allele":"COSMIC_MUTATION","start":257,"residues":"","Parent":"ENST00000288602","id":"COSV56057804","polyphen":null},{"id":"COSV56268820","polyphen":null,"Parent":"ENST00000288602","residues":"","allele":"COSMIC_MUTATION","start":205,"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"codons":"","clinical_significance":[],"sift":null,"end":205,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"end":599,"codons":"","polyphen":null,"id":"COSV56167356","start":599,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":""},{"translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"end":75,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","polyphen":null,"id":"COSV56379503","Parent":"ENST00000288602","residues":"","start":75,"allele":"COSMIC_MUTATION"},{"seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","clinical_significance":[],"sift":null,"end":316,"codons":"","minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","allele":"COSMIC_MUTATION","start":316,"Parent":"ENST00000288602","residues":"","polyphen":null,"id":"COSV56170698"},{"id":"COSV56185580","polyphen":null,"allele":"COSMIC_MUTATION","start":596,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","sift":null,"clinical_significance":[],"codons":"","end":596},{"allele":"COSMIC_MUTATION","start":424,"Parent":"ENST00000288602","residues":"","id":"COSV56374807","polyphen":null,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":424,"minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602"},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"sift":null,"codons":"","end":282,"polyphen":null,"id":"COSV56379465","allele":"COSMIC_MUTATION","start":282,"residues":"","Parent":"ENST00000288602"},{"polyphen":null,"id":"COSV56221048","Parent":"ENST00000288602","residues":"","start":506,"allele":"COSMIC_MUTATION","translation":"ENSP00000288602","type":"splice_region_variant","minor_allele_frequency":null,"clinical_significance":[],"end":506,"sift":null,"codons":"","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602"},{"id":"COSV56269245","polyphen":null,"allele":"COSMIC_MUTATION","start":367,"residues":"","Parent":"ENST00000288602","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","clinical_significance":[],"codons":"","sift":null,"end":367},{"start":459,"allele":"COSMIC_MUTATION","residues":"","Parent":"ENST00000288602","polyphen":null,"id":"COSV56064794","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":459,"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant"},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"sift":null,"clinical_significance":[],"codons":"","end":588,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","id":"COSV56374757","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":588},{"minor_allele_frequency":null,"translation":"ENSP00000288602","type":"coding_sequence_variant","feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","codons":"","clinical_significance":[],"sift":null,"end":719,"polyphen":null,"id":"COSV99973571","allele":"COSMIC_MUTATION","start":719,"Parent":"ENST00000288602","residues":""},{"type":"coding_sequence_variant","translation":"ENSP00000288602","minor_allele_frequency":null,"clinical_significance":[],"sift":null,"end":632,"codons":"","seq_region_name":"ENSP00000288602","feature_type":"somatic_transcript_variation","id":"COSV56242974","polyphen":null,"residues":"","Parent":"ENST00000288602","allele":"COSMIC_MUTATION","start":632},{"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","end":597,"clinical_significance":[],"sift":null,"codons":"","minor_allele_frequency":null,"type":"coding_sequence_variant","translation":"ENSP00000288602","start":597,"allele":"COSMIC_MUTATION","Parent":"ENST00000288602","residues":"","id":"COSV56121113","polyphen":null},{"Parent":"ENST00000288602","residues":"","start":471,"allele":"COSMIC_MUTATION","polyphen":null,"id":"COSV56229839","codons":"","clinical_significance":[],"sift":null,"end":471,"feature_type":"somatic_transcript_variation","seq_region_name":"ENSP00000288602","translation":"ENSP00000288602","type":"coding_sequence_variant","minor_allele_frequency":null}]