--- - allele_string: -/CTG assembly_name: GRCh37 colocated_variants: - allele_string: COSMIC_MUTATION end: 124887095 id: COSV105907233 phenotype_or_disease: 1 seq_region_name: 12 somatic: 1 start: 124887096 strand: 1 var_synonyms: COSMIC: - COSM9961721 - allele_string: COSMIC_MUTATION end: 124887095 id: COSV105907316 phenotype_or_disease: 1 seq_region_name: 12 somatic: 1 start: 124887096 strand: 1 var_synonyms: COSMIC: - COSM10008089 - allele_string: COSMIC_MUTATION end: 124887095 id: COSV62292713 phenotype_or_disease: 1 seq_region_name: 12 somatic: 1 start: 124887096 strand: 1 var_synonyms: COSMIC: - COSM1476307 - allele_string: COSMIC_MUTATION end: 124887095 id: COSV62292935 phenotype_or_disease: 1 seq_region_name: 12 somatic: 1 start: 124887096 strand: 1 var_synonyms: COSMIC: - COSM2227124 - allele_string: COSMIC_MUTATION end: 124887095 id: COSV62300054 phenotype_or_disease: 1 seq_region_name: 12 somatic: 1 start: 124887096 strand: 1 var_synonyms: COSMIC: - COSM5970587 - allele_string: COSMIC_MUTATION end: 124887095 id: COSV62304776 phenotype_or_disease: 1 seq_region_name: 12 somatic: 1 start: 124887096 strand: 1 var_synonyms: COSMIC: - COSM2227132 end: 124887095 id: 12:g124887095_124887096insCTG input: 12:g124887095_124887096insCTG most_severe_consequence: inframe_insertion regulatory_feature_consequences: - biotype: enhancer consequence_terms: - regulatory_region_variant impact: MODIFIER regulatory_feature_id: ENSR00001046314 variant_allele: CTG seq_region_name: 12 start: 124887096 strand: 1 transcript_consequences: - amino_acids: -/Q biotype: protein_coding cdna_end: 1961 cdna_start: 1960 cds_end: 1492 cds_start: 1491 codons: -/CAG consequence_terms: - inframe_insertion gene_id: 9612 gene_symbol: NCOR2 gene_symbol_source: EntrezGene given_ref: "-" hgvs_offset: -37 hgvsc: NM_001077261.4:c.1526_1528dup hgvsp: NP_001070729.2:p.Pro510_Met511insAla impact: MODERATE protein_end: 498 protein_start: 497 strand: -1 transcript_id: NM_001077261.4 used_ref: "-" variant_allele: CTG - amino_acids: -/Q biotype: protein_coding cdna_end: 1961 cdna_start: 1960 cds_end: 1492 cds_start: 1491 codons: -/CAG consequence_terms: - inframe_insertion gene_id: 9612 gene_symbol: NCOR2 gene_symbol_source: EntrezGene given_ref: "-" hgvs_offset: -37 hgvsc: NM_001206654.2:c.1526_1528dup hgvsp: NP_001193583.1:p.Pro510_Met511insAla impact: MODERATE protein_end: 498 protein_start: 497 strand: -1 transcript_id: NM_001206654.2 used_ref: "-" variant_allele: CTG - amino_acids: -/Q biotype: protein_coding cdna_end: 1964 cdna_start: 1963 cds_end: 1495 cds_start: 1494 codons: -/CAG consequence_terms: - inframe_insertion gene_id: 9612 gene_symbol: NCOR2 gene_symbol_source: EntrezGene given_ref: "-" hgvs_offset: -37 hgvsc: NM_006312.6:c.1529_1531dup hgvsp: NP_006303.4:p.Pro511_Met512insAla impact: MODERATE protein_end: 499 protein_start: 498 strand: -1 transcript_id: NM_006312.6 used_ref: "-" variant_allele: CTG