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.5945dup (p.Ser1982fs)BRCA2Pathogenic133291443632914437AAGreviewed by expert panelClinGen:CA023394
DeletionNM_000059.4(BRCA2):c.5946_5949del (p.Ser1982fs)BRCA2Pathogenic133291443832914441GTGGAGreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):6174&base_change=del TGGA,ClinGen:CA023398
DeletionNM_000059.4(BRCA2):c.5946_5950del (p.Ser1982fs)BRCA2Pathogenic133291443832914442GTGGAAGreviewed by expert panelClinGen:CA023400
DuplicationNM_000059.4(BRCA2):c.5952dup (p.Ser1985fs)BRCA2Pathogenic133291444032914441GGAreviewed by expert panelClinGen:CA023405
DeletionNM_000059.4(BRCA2):c.5954_5955del (p.Ser1985fs)BRCA2Pathogenic133291444532914446ATCAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):6181&base_change=del TC,ClinGen:CA023409
single nucleotide variantNM_000059.4(BRCA2):c.5959C>T (p.Gln1987Ter)BRCA2Pathogenic133291445132914451CTreviewed by expert panelClinGen:CA023417
DuplicationNM_000059.4(BRCA2):c.595_599dup (p.Pro201fs)BRCA2Pathogenic133290071332900714AAGCTACreviewed by expert panelClinGen:CA023481
DeletionNM_000059.4(BRCA2):c.5964_5965del (p.Ser1989fs)BRCA2Pathogenic133291445532914456GTAGreviewed by expert panelClinGen:CA023427
DuplicationNM_000059.4(BRCA2):c.5967dup (p.Asp1990fs)BRCA2Pathogenic133291445832914459CCAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):6195&base_change=ins A,ClinGen:CA023429
DeletionNM_000059.4(BRCA2):c.5968_5969del (p.Asp1990fs)BRCA2Pathogenic133291445932914460CAGCreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):6196&base_change=del GA,ClinGen:CA023431