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)
InsertionNM_007294.4(BRCA1):c.71_72insA (p.Cys24Ter)BRCA1Pathogenic174127604241276043AATreviewed by expert panel-
InsertionNM_007294.4(BRCA1):c.67_68insC (p.Glu23fs)BRCA1Pathogenic174127604641276047TTGreviewed by expert panel-
DuplicationNM_007294.4(BRCA1):c.34dup (p.Gln12fs)BRCA1Pathogenic174127607941276080TTGreviewed by expert panel-
DuplicationNM_007294.4(BRCA1):c.20dup (p.Val8fs)BRCA1Pathogenic174127609341276094GGCreviewed by expert panel-
DuplicationNM_000059.4(BRCA2):c.1062dup (p.Val355fs)BRCA2Pathogenic/Likely pathogenic133290667432906675AATcriteria provided, multiple submitters, no conflicts-
DeletionNM_000059.4(BRCA2):c.3767del (p.His1256fs)BRCA2Pathogenic/Likely pathogenic133291225932912259CACcriteria provided, multiple submitters, no conflicts-
InsertionNM_000059.4(BRCA2):c.4624_4625insCG (p.Val1542fs)BRCA2Likely pathogenic133291311532913116AAGCcriteria provided, single submitter-
InsertionNM_000059.4(BRCA2):c.5216_5217insAATA (p.Tyr1739Ter)BRCA2Likely pathogenic133291370632913707TTTAAAcriteria provided, single submitter-
IndelNM_000059.4(BRCA2):c.5803delinsTT (p.Asn1935fs)BRCA2Pathogenic/Likely pathogenic133291429532914295ATTcriteria provided, multiple submitters, no conflicts-
InsertionNM_000059.4(BRCA2):c.6712_6713insGG (p.Asp2238fs)BRCA2Likely pathogenic133291520332915204TTGGcriteria provided, single submitter-