Knowledge base for genomic medicine in Japanese
家族性膵がん
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
single nucleotide variantNM_007294.4(BRCA1):c.1729G>T (p.Glu577Ter)BRCA1Pathogenic174124581941245819CAreviewed by expert panelClinGen:CA001133
DeletionNM_007294.4(BRCA1):c.1729_1730del (p.Glu577fs)BRCA1Pathogenic174124581841245819TTCTreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA1):1848&base_change=del GA,ClinGen:CA001132
single nucleotide variantNM_007294.4(BRCA1):c.1741A>T (p.Lys581Ter)BRCA1Pathogenic174124580741245807TAreviewed by expert panelClinGen:CA001139
single nucleotide variantNM_007294.4(BRCA1):c.1747A>T (p.Lys583Ter)BRCA1Pathogenic174124580141245801TAreviewed by expert panelClinGen:CA001145
DeletionNM_007294.4(BRCA1):c.1757del (p.Pro586fs)BRCA1Pathogenic174124579141245791AGAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA1):1876&base_change=del C,ClinGen:CA001148
DeletionNM_007294.4(BRCA1):c.1772del (p.Ile591fs)BRCA1Pathogenic174124577641245776TATreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA1):1891&base_change=del T,ClinGen:CA001152
single nucleotide variantNM_007294.4(BRCA1):c.1789G>T (p.Glu597Ter)BRCA1Pathogenic174124575941245759CAreviewed by expert panelClinGen:CA001161
single nucleotide variantNM_007294.4(BRCA1):c.178C>T (p.Gln60Ter)BRCA1Pathogenic174125850741258507GAreviewed by expert panelClinGen:CA001162
single nucleotide variantNM_007294.4(BRCA1):c.1793T>A (p.Leu598Ter)BRCA1Pathogenic174124575541245755ATreviewed by expert panelClinGen:CA001163
single nucleotide variantNM_007294.4(BRCA1):c.1793T>G (p.Leu598Ter)BRCA1Pathogenic174124575541245755ACreviewed by expert panelClinGen:CA001164