Knowledge base for genomic medicine in Japanese
ウィルムス腫瘍
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DuplicationNM_000059.4(BRCA2):c.1813dup (p.Ile605fs)BRCA2Pathogenic133290742832907428GGAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):2034&base_change=ins A,Breast Cancer Information Core (BIC) (BRCA2):2041&base_change=ins A,ClinGen:CA013353
DeletionNM_000059.4(BRCA2):c.1813del (p.Ile605fs)BRCA2Pathogenic133290742132907421GAGreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):2034&base_change=del A,Breast Cancer Information Core (BIC) (BRCA2):2041&base_change=del A,ClinGen:CA013362
single nucleotide variantNM_000059.4(BRCA2):c.1832C>A (p.Ser611Ter)BRCA2Pathogenic133290744732907447CAreviewed by expert panelClinGen:CA013511
single nucleotide variantNM_000059.4(BRCA2):c.1850C>A (p.Ser617Ter)BRCA2Pathogenic133290746532907465CAreviewed by expert panelClinGen:CA013563
single nucleotide variantNM_000059.4(BRCA2):c.1850C>G (p.Ser617Ter)BRCA2Pathogenic133290746532907465CGreviewed by expert panelClinGen:CA013573
DeletionNM_000059.4(BRCA2):c.1929del (p.Arg645fs)BRCA2Pathogenic133291042132910421TGTreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):2157&base_change=del G,ClinGen:CA013940
single nucleotide variantNM_000059.4(BRCA2):c.1970T>A (p.Leu657Ter)BRCA2Pathogenic133291046232910462TAreviewed by expert panelClinGen:CA014065
DeletionNM_000059.4(BRCA2):c.2036del (p.Asn679fs)BRCA2Pathogenic133291052732910527TATreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):2264&base_change=del A,ClinGen:CA014184
DeletionNM_000059.4(BRCA2):c.2092del (p.Leu698fs)BRCA2Pathogenic133291058432910584ACAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):2320&base_change=del C,ClinGen:CA014309
DuplicationNM_000059.4(BRCA2):c.2175dup (p.Val726fs)BRCA2Pathogenic133291066132910662CCAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):2403&base_change=ins A,ClinGen:CA014516