Knowledge base for genomic medicine in Japanese
遺伝性乳がん・卵巣がん症候群
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
InsertionNM_000059.4(BRCA2):c.8826_8827insG (p.Gln2943fs)BRCA2Pathogenic133295352532953526TTGreviewed by expert panel-
DuplicationNM_000059.4(BRCA2):c.8982_8985dup (p.Leu2996fs)BRCA2Pathogenic133295391432953915CCAGATreviewed by expert panel-
InsertionNM_000059.4(BRCA2):c.9017_9018insTCTA (p.Arg3007fs)BRCA2Pathogenic133295394832953949AATATCreviewed by expert panel-
InsertionNM_000059.4(BRCA2):c.9096_9097insT (p.Thr3033fs)BRCA2Pathogenic133295402932954030AATreviewed by expert panel-
InsertionNM_000059.4(BRCA2):c.9193_9194insA (p.Phe3065fs)BRCA2Pathogenic133295421932954220TTAreviewed by expert panel-
InsertionNM_000059.4(BRCA2):c.9218_9219insTTTA (p.Ile3075fs)BRCA2Pathogenic133295424332954244GGATTTreviewed by expert panel-
InsertionNM_000059.4(BRCA2):c.9310_9311insTTAT (p.Lys3104fs)BRCA2Pathogenic133296887932968880AATTATreviewed by expert panel-
InsertionNM_000059.4(BRCA2):c.9323_9324insATTA (p.Asp3108fs)BRCA2Pathogenic133296889132968892GGAATTreviewed by expert panel-
DuplicationNM_000059.4(BRCA2):c.9383dup (p.Pro3129fs)BRCA2Pathogenic133296895132968952CCGreviewed by expert panel-
InsertionNM_000059.4(BRCA2):c.9386_9387insCTGATTTGGACCACT (p.Pro3129_Glu3130insTer)BRCA2Pathogenic133296895532968956CCCTGATTTGGACCACTreviewed by expert panel-