--- - allele_string: A/G assembly_name: GRCh37 colocated_variants: - allele_string: HGMD_MUTATION end: 29586086 id: CM111457 phenotype_or_disease: 1 seq_region_name: 17 start: 29586086 strand: 1 - allele_string: HGMD_MUTATION end: 29586086 id: CM1211612 phenotype_or_disease: 1 seq_region_name: 17 start: 29586086 strand: 1 - allele_string: COSMIC_MUTATION end: 29586086 id: COSV106061720 phenotype_or_disease: 1 seq_region_name: 17 somatic: 1 start: 29586086 strand: 1 var_synonyms: COSMIC: - COSM10073601 - allele_string: A/C/G clin_sig: - pathogenic clin_sig_allele: C:pathogenic;G:pathogenic end: 29586086 id: rs878853893 phenotype_or_disease: 1 pubmed: - 21354044 - 22807134 - 23913538 - 21520333 - 9219684 - 29952103 - 27322474 - 24789688 seq_region_name: 17 start: 29586086 strand: 1 var_synonyms: ClinVar: - RCV000699721 - VCV000577061 - RCV001766524 - RCV001557248 - RCV002318966 - RCV000229110 - VCV000237563 end: 29586086 id: NF1:p.K1457E input: NF1:p.K1457E most_severe_consequence: missense_variant seq_region_name: 17 start: 29586086 strand: 1 transcript_consequences: - amino_acids: K/E biotype: protein_coding cdna_end: 4689 cdna_start: 4689 cds_end: 4306 cds_start: 4306 codons: Aaa/Gaa consequence_terms: - missense_variant gene_id: ENSG00000196712 gene_symbol: NF1 gene_symbol_source: HGNC hgnc_id: 7765 impact: MODERATE polyphen_prediction: probably_damaging polyphen_score: '0.969' protein_end: 1436 protein_start: 1436 sift_prediction: deleterious sift_score: 0 strand: 1 transcript_id: ENST00000356175 variant_allele: G - amino_acids: K/E biotype: protein_coding cdna_end: 4752 cdna_start: 4752 cds_end: 4369 cds_start: 4369 codons: Aaa/Gaa consequence_terms: - missense_variant gene_id: ENSG00000196712 gene_symbol: NF1 gene_symbol_source: HGNC hgnc_id: 7765 impact: MODERATE polyphen_prediction: probably_damaging polyphen_score: '0.997' protein_end: 1457 protein_start: 1457 sift_prediction: deleterious sift_score: 0 strand: 1 transcript_id: ENST00000358273 variant_allele: G - amino_acids: K/E biotype: protein_coding cdna_end: 3304 cdna_start: 3304 cds_end: 3304 cds_start: 3304 codons: Aaa/Gaa consequence_terms: - missense_variant flags: - cds_start_NF gene_id: ENSG00000196712 gene_symbol: NF1 gene_symbol_source: HGNC hgnc_id: 7765 impact: MODERATE polyphen_prediction: possibly_damaging polyphen_score: '0.894' protein_end: 1102 protein_start: 1102 sift_prediction: deleterious sift_score: 0 strand: 1 transcript_id: ENST00000456735 variant_allele: G - biotype: nonsense_mediated_decay cdna_end: 885 cdna_start: 885 consequence_terms: - 3_prime_UTR_variant - NMD_transcript_variant flags: - cds_start_NF gene_id: ENSG00000196712 gene_symbol: NF1 gene_symbol_source: HGNC hgnc_id: 7765 impact: MODIFIER strand: 1 transcript_id: ENST00000466819 variant_allele: G - biotype: nonsense_mediated_decay cdna_end: 822 cdna_start: 822 consequence_terms: - 3_prime_UTR_variant - NMD_transcript_variant flags: - cds_start_NF gene_id: ENSG00000196712 gene_symbol: NF1 gene_symbol_source: HGNC hgnc_id: 7765 impact: MODIFIER strand: 1 transcript_id: ENST00000479614 variant_allele: G - biotype: retained_intron cdna_end: 2842 cdna_start: 2842 consequence_terms: - non_coding_transcript_exon_variant gene_id: ENSG00000196712 gene_symbol: NF1 gene_symbol_source: HGNC hgnc_id: 7765 impact: MODIFIER strand: 1 transcript_id: ENST00000493220 variant_allele: G - biotype: nonsense_mediated_decay consequence_terms: - downstream_gene_variant distance: 4776 flags: - cds_start_NF gene_id: ENSG00000196712 gene_symbol: NF1 gene_symbol_source: HGNC hgnc_id: 7765 impact: MODIFIER strand: 1 transcript_id: ENST00000495910 variant_allele: G - amino_acids: K/E biotype: nonsense_mediated_decay cdna_end: 4408 cdna_start: 4408 cds_end: 4408 cds_start: 4408 codons: Aaa/Gaa consequence_terms: - missense_variant - NMD_transcript_variant flags: - cds_start_NF gene_id: ENSG00000196712 gene_symbol: NF1 gene_symbol_source: HGNC hgnc_id: 7765 impact: MODERATE polyphen_prediction: possibly_damaging polyphen_score: '0.714' protein_end: 1470 protein_start: 1470 sift_prediction: deleterious sift_score: 0 strand: 1 transcript_id: ENST00000579081 variant_allele: G