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_007294.4(BRCA1):c.4603G>T (p.Glu1535Ter)BRCA1Pathogenic174122642041226420CAreviewed by expert panelClinGen:CA002924
single nucleotide variantNM_007294.4(BRCA1):c.4609C>T (p.Gln1537Ter)BRCA1Pathogenic174122641441226414GAreviewed by expert panelClinGen:CA002926
InsertionNM_007294.4(BRCA1):c.4611_4612insG (p.Gln1538fs)BRCA1Pathogenic174122641141226412GGCreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA1):4730&base_change=ins G,ClinGen:CA002927
single nucleotide variantNM_007294.4(BRCA1):c.4612C>T (p.Gln1538Ter)BRCA1Pathogenic174122641141226411GAreviewed by expert panelClinGen:CA002928
single nucleotide variantNM_007294.4(BRCA1):c.4618G>T (p.Glu1540Ter)BRCA1Pathogenic174122640541226405CAreviewed by expert panelClinGen:CA002930
single nucleotide variantNM_007294.4(BRCA1):c.4621G>T (p.Glu1541Ter)BRCA1Pathogenic174122640241226402CAreviewed by expert panelClinGen:CA002931
DeletionNM_007294.4(BRCA1):c.4625_4626del (p.Ser1542fs)BRCA1Pathogenic174122639741226398CAGCreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA1):4744&base_change=del CT,ClinGen:CA002932
single nucleotide variantNM_007294.4(BRCA1):c.463C>T (p.Gln155Ter)BRCA1Pathogenic174125187641251876GAreviewed by expert panelClinGen:CA002941
DeletionNM_007294.4(BRCA1):c.4646_4665del (p.Glu1549fs)BRCA1Pathogenic174122635841226377GCCTTGGCAAGTAAGATGTTTGreviewed by expert panel-
DeletionNM_007294.4(BRCA1):c.4655_4658del (p.Tyr1552fs)BRCA1Pathogenic174122636541226368CAAGTCreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA1):4774&base_change=del ACTT,ClinGen:CA002950