Knowledge base for genomic medicine in Japanese
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腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
IndelNM_007294.4(BRCA1):c.5209_5248delinsTC (p.Arg1737fs)BRCA1Pathogenic174120909841209137TTGGACCTTGGTGGTTTCTTCCATTGACCACATCTCCTCTGAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA1):5328&base_change=del 40 ins TC,ClinGen:CA003359
DeletionNM_007294.4(BRCA1):c.520del (p.Gln174fs)BRCA1Pathogenic174125181941251819TGTreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA1):639&base_change=del C,ClinGen:CA003362
single nucleotide variantNM_007294.4(BRCA1):c.5212G>A (p.Gly1738Arg)BRCA1Pathogenic174120913441209134CTreviewed by expert panelBRCA1-HCI:BRCA1_00043,ClinGen:CA003363,UniProtKB:P38398#VAR_063907
single nucleotide variantNM_007294.4(BRCA1):c.5213G>A (p.Gly1738Glu)BRCA1Pathogenic/Likely pathogenic174120913341209133CTcriteria provided, multiple submitters, no conflictsClinGen:CA003365
single nucleotide variantNM_007294.4(BRCA1):c.5215G>T (p.Asp1739Tyr)BRCA1Likely pathogenic174120913141209131CAcriteria provided, multiple submitters, no conflictsClinGen:CA003366
single nucleotide variantNM_007294.4(BRCA1):c.5216A>G (p.Asp1739Gly)BRCA1Likely pathogenic174120913041209130TCcriteria provided, multiple submitters, no conflictsClinGen:CA003367,UniProtKB:P38398#VAR_070507
single nucleotide variantNM_007294.4(BRCA1):c.5216A>T (p.Asp1739Val)BRCA1Pathogenic/Likely pathogenic174120913041209130TAcriteria provided, multiple submitters, no conflictsClinGen:CA003368,UniProtKB:P38398#VAR_070508
single nucleotide variantNM_007294.4(BRCA1):c.5217T>G (p.Asp1739Glu)BRCA1Likely pathogenic174120912941209129ACcriteria provided, single submitterClinGen:CA003370
DeletionNM_007294.4(BRCA1):c.5229_5230del (p.Arg1744fs)BRCA1Pathogenic174120911641209117CTTCreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA1):5348&base_change=del AA,ClinGen:CA003372
DeletionNM_007294.4(BRCA1):c.5230del (p.Arg1744fs)BRCA1Pathogenic174120911641209116CTCreviewed by expert panelClinGen:CA003374