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)
IndelNM_007294.4(BRCA1):c.2392_2393delinsA (p.Pro798fs)BRCA1Pathogenic174124515541245156GGTcriteria provided, single submitterClinGen:CA658656696
DeletionNM_007294.4(BRCA1):c.3083del (p.Arg1028fs)BRCA1Pathogenic174124446541244465ACAcriteria provided, single submitterClinGen:CA626221301
single nucleotide variantNM_007294.4(BRCA1):c.1154G>A (p.Trp385Ter)BRCA1Pathogenic174124639441246394CTcriteria provided, multiple submitters, no conflictsClinGen:CA10599747
DeletionNM_007294.4(BRCA1):c.3870_3877del (p.Lys1290fs)BRCA1Pathogenic174124367141243678GCAGAACATGcriteria provided, single submitterClinGen:CA658656674
DeletionNM_007294.4(BRCA1):c.998_1010del (p.Thr333fs)BRCA1Pathogenic174124653841246550TTCTGTGCTGGGAGTcriteria provided, single submitterClinGen:CA658656801
DeletionNM_007294.4(BRCA1):c.799del (p.Ser267fs)BRCA1Pathogenic174124674941246749GAGcriteria provided, single submitterClinGen:CA658656633
IndelNM_007294.4(BRCA1):c.1929_1930delinsA (p.Ser643fs)BRCA1Pathogenic174124561841245619AATcriteria provided, multiple submitters, no conflictsClinGen:CA658656743
DeletionNM_007294.4(BRCA1):c.1676del (p.Gly559fs)BRCA1Pathogenic174124587241245872ACAcriteria provided, multiple submitters, no conflictsClinGen:CA658656759
IndelNM_007294.4(BRCA1):c.288_292delinsAACCTGT (p.Asp96fs)BRCA1Pathogenic174125689441256898CTGTGACAGGTTcriteria provided, multiple submitters, no conflictsClinGen:CA658656667
DeletionNM_007294.4(BRCA1):c.83del (p.Leu28fs)BRCA1Pathogenic174126779441267794CACcriteria provided, multiple submitters, no conflictsClinGen:CA658656690