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)
DeletionNM_000059.4(BRCA2):c.2259del (p.Gln754fs)BRCA2Pathogenic133291074932910749CTCreviewed by expert panelClinGen:CA014791
single nucleotide variantNM_000059.4(BRCA2):c.227C>G (p.Ser76Ter)BRCA2Pathogenic133289337332893373CGreviewed by expert panelClinGen:CA014851
DeletionNM_000059.4(BRCA2):c.2287del (p.His763fs)BRCA2Pathogenic133291077932910779TCTreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):2515&base_change=del C,ClinGen:CA014881
single nucleotide variantNM_000059.4(BRCA2):c.2372C>A (p.Ser791Ter)BRCA2Pathogenic133291086432910864CAreviewed by expert panelClinGen:CA015065
single nucleotide variantNM_000059.4(BRCA2):c.2376C>A (p.Tyr792Ter)BRCA2Pathogenic133291086832910868CAreviewed by expert panelClinGen:CA015072
DeletionNM_000059.4(BRCA2):c.2402_2412del (p.Asn801fs)BRCA2Pathogenic133291089332910903TAACAATTATGATreviewed by expert panelClinGen:CA015136
DeletionNM_000059.4(BRCA2):c.2435del (p.Asn812fs)BRCA2Pathogenic133291092332910923CACreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):2663&base_change=del A,ClinGen:CA015250
DuplicationNM_000059.4(BRCA2):c.2435dup (p.Asn812fs)BRCA2Pathogenic133291092232910923CCAreviewed by expert panelClinGen:CA015248
DeletionNM_000059.4(BRCA2):c.2442del (p.Met815fs)BRCA2Pathogenic133291093232910932TCTreviewed by expert panelClinGen:CA015283
DeletionNM_000059.4(BRCA2):c.2446del (p.Glu816fs)BRCA2Pathogenic133291093732910937TGTreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):2674&base_change=del G,ClinGen:CA015301