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)
DeletionNM_000059.4(BRCA2):c.2961del (p.Asn987fs)BRCA2Pathogenic133291145332911453ATAreviewed by expert panelClinGen:CA10586508
single nucleotide variantNM_000059.4(BRCA2):c.3016G>T (p.Gly1006Ter)BRCA2Pathogenic133291150832911508GTreviewed by expert panelClinGen:CA10586509
single nucleotide variantNM_000059.4(BRCA2):c.3046G>T (p.Glu1016Ter)BRCA2Pathogenic133291153832911538GTreviewed by expert panelClinGen:CA6940656
DeletionNM_000059.4(BRCA2):c.3175del (p.Lys1058_Leu1059insTer)BRCA2Pathogenic133291166732911667ACAreviewed by expert panelClinGen:CA10586510
DeletionNM_000059.4(BRCA2):c.3293del (p.Asn1098fs)BRCA2Pathogenic133291178432911784TATreviewed by expert panelClinGen:CA017716
DeletionNM_000059.4(BRCA2):c.3295del (p.Ser1099fs)BRCA2Pathogenic133291178632911786ATAreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):3522&base_change=del T,ClinGen:CA017723
DuplicationNM_000059.4(BRCA2):c.3455dup (p.Leu1152fs)BRCA2Pathogenic133291194532911946CCTreviewed by expert panelBreast Cancer Information Core (BIC) (BRCA2):3681&base_change=ins T,ClinGen:CA018080
DuplicationNM_000059.4(BRCA2):c.3593dup (p.Asn1198fs)BRCA2Pathogenic133291208032912081GGAreviewed by expert panelClinGen:CA280072
DeletionNM_000059.4(BRCA2):c.3599del (p.Cys1200fs)BRCA2Pathogenic133291209132912091TGTreviewed by expert panelClinGen:CA10586511
DeletionNM_000059.4(BRCA2):c.3639_3652del (p.Val1214fs)BRCA2Pathogenic133291213132912144AAGTGGGGTTTAGGGAreviewed by expert panelClinGen:CA10586512