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)
DeletionNM_007294.4(BRCA1):c.3794del (p.Asn1265fs)BRCA1Pathogenic174124375441243754ATAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA1):3913&base_change=del A,ClinGen:CA002444
DeletionNM_007294.4(BRCA1):c.37_40del (p.Asn13fs)BRCA1Pathogenic174127607441276077ACATTAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA1):156&base_change=del AATG,ClinGen:CA002398
DuplicationNM_007294.4(BRCA1):c.3813dup (p.Asn1272Ter)BRCA1Pathogenic174124373441243735TTAreviewed by expert panelClinGen:CA327899
InsertionNM_007294.4(BRCA1):c.3814_3815insT (p.Asn1272fs)BRCA1Pathogenic174124373341243734TTAreviewed by expert panelClinGen:CA002457
single nucleotide variantNM_007294.4(BRCA1):c.3817C>T (p.Gln1273Ter)BRCA1Pathogenic174124373141243731GAreviewed by expert panelClinGen:CA002459
DeletionNM_007294.4(BRCA1):c.3820del (p.Gln1273_Val1274insTer)BRCA1Pathogenic174124372841243728ACAreviewed by expert panelClinGen:CA002462
DuplicationNM_007294.4(BRCA1):c.3820dup (p.Val1274fs)BRCA1Pathogenic174124372741243728AACreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA1):3939&base_change=ins G,ClinGen:CA002461
InsertionNM_007294.4(BRCA1):c.3822_3823insT (p.Ile1275fs)BRCA1Pathogenic174124372541243726TTAcriteria provided, single submitterClinGen:CA002463
IndelNM_007294.4(BRCA1):c.3839_3843delinsAGGC (p.Ser1280_Gln1281delinsTer)BRCA1Pathogenic174124370541243709CTGAGGCCTreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA1):3958&base_change=del CTCAG ins AGGC,ClinGen:CA002470
single nucleotide variantNM_007294.4(BRCA1):c.3841C>T (p.Gln1281Ter)BRCA1Pathogenic174124370741243707GAreviewed by expert panelClinGen:CA002475