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_000059.4(BRCA2):c.4440T>G (p.Tyr1480Ter)BRCA2Pathogenic133291293232912932TGreviewed by expert panelClinGen:CA020187
DeletionNM_000059.4(BRCA2):c.4456_4459del (p.Val1486fs)BRCA2Pathogenic133291294632912949ATAGTAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):4682&base_change=del TAGT,Breast Cancer Information Core (BIC) (BRCA2):4684&base_change=del GTTA,ClinGen:CA020201
DeletionNM_000059.4(BRCA2):c.4471_4474del (p.Leu1491fs)BRCA2Pathogenic133291296232912965TACTGTreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):4699&base_change=del CTGA,ClinGen:CA020226
DuplicationNM_000059.4(BRCA2):c.4480dup (p.Ser1494fs)BRCA2Pathogenic133291296932912970GGAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):4705&base_change=ins A,ClinGen:CA020242
single nucleotide variantNM_000059.4(BRCA2):c.4525C>T (p.Gln1509Ter)BRCA2Pathogenic133291301732913017CTreviewed by expert panelClinGen:CA020321
DeletionNM_000059.4(BRCA2):c.4535del (p.Arg1512fs)BRCA2Pathogenic133291302732913027CGCreviewed by expert panelClinGen:CA020340
DuplicationNM_000059.4(BRCA2):c.4536_4539dup (p.Glu1514Ter)BRCA2Pathogenic133291302732913028GGTGATreviewed by expert panelClinGen:CA020370
DeletionNM_000059.4(BRCA2):c.4544del (p.Lys1515fs)BRCA2Pathogenic133291303332913033GAGreviewed by expert panelClinGen:CA020378
DuplicationNM_000059.4(BRCA2):c.4546dup (p.Ile1516fs)BRCA2Pathogenic133291303732913038GGAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):4773&base_change=ins A,ClinGen:CA020383
DeletionNM_000059.4(BRCA2):c.4551_4554del (p.Lys1517fs)BRCA2Pathogenic133291304132913044CAAAGCreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):4779&base_change=del AGAA,ClinGen:CA020410