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_007294.4(BRCA1):c.1121del (p.Thr374fs)BRCA1Pathogenic174124642741246427TGTreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA1):1240&base_change=del C,ClinGen:CA000751
single nucleotide variantNM_007294.4(BRCA1):c.116G>A (p.Cys39Tyr)BRCA1Pathogenic174126776141267761CTcriteria provided, multiple submitters, no conflictsClinGen:CA000772
single nucleotide variantNM_007294.4(BRCA1):c.116G>T (p.Cys39Phe)BRCA1Pathogenic/Likely pathogenic174126776141267761CAcriteria provided, multiple submitters, no conflictsClinGen:CA000773
DeletionNM_007294.4(BRCA1):c.1175_1215del (p.Leu392fs)BRCA1Pathogenic174124633341246373TTGATTCAGACTCCCCATCATGTGAGTCATCAGAACCTAACATreviewed by expert panelClinGen:CA000778
DeletionNM_007294.4(BRCA1):c.1177_1219del (p.Leu393fs)BRCA1Pathogenic174124632941246371GCATTTGATTCAGACTCCCCATCATGTGAGTCATCAGAACCTAAGreviewed by expert panelClinGen:CA000780
DeletionNM_007294.4(BRCA1):c.1175_1218del (p.Leu392fs)BRCA1Pathogenic174124633041246373CATTTGATTCAGACTCCCCATCATGTGAGTCATCAGAACCTAACACreviewed by expert panelClinGen:CA000781
single nucleotide variantNM_007294.4(BRCA1):c.134+5G>CBRCA1Pathogenic174126773841267738CGcriteria provided, single submitterClinGen:CA000887
InsertionNM_007294.4(BRCA1):c.1340_1341insG (p.His448fs)BRCA1Pathogenic174124620741246208AACreviewed by expert panelClinGen:CA000877
single nucleotide variantNM_007294.4(BRCA1):c.135-1G>TBRCA1Pathogenic174125855141258551CAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA1):254-1&base_change=G to T,ClinGen:CA000895
IndelNM_007294.4(BRCA1):c.1389_1390delinsG (p.Thr464fs)BRCA1Pathogenic174124615841246159TTCreviewed by expert panelClinGen:CA000927,Breast Cancer Information Core (BIC) (BRCA1):1508&base_change=del AA ins G