Knowledge base for genomic medicine in Japanese
DICER1症候群
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
single nucleotide variantNM_177438.3(DICER1):c.2350G>T (p.Glu784Ter)DICER1Pathogenic149557474795574747CAcriteria provided, single submitterClinGen:CA390882234
single nucleotide variantNM_177438.3(DICER1):c.2256+1G>ADICER1Pathogenic149557765395577653CTcriteria provided, single submitterClinGen:CA390882460
DuplicationNM_177438.3(DICER1):c.2181_2187dup (p.Asp730delinsPheAlaTer)DICER1Pathogenic149557772295577723CCATGCAAAcriteria provided, single submitterClinGen:CA645369632
single nucleotide variantNM_177438.3(DICER1):c.2041-2A>GDICER1Likely pathogenic149557858695578586TCcriteria provided, single submitterClinGen:CA390883150
single nucleotide variantNM_177438.3(DICER1):c.2040+1G>ADICER1Pathogenic149557942895579428CTcriteria provided, multiple submitters, no conflictsClinGen:CA390883156
single nucleotide variantNM_177438.3(DICER1):c.1907+1G>ADICER1Pathogenic149558200395582003CTreviewed by expert panelClinGen:CA390883876
DeletionNM_177438.3(DICER1):c.1839del (p.Tyr614fs)DICER1Pathogenic149558207295582072ATAcriteria provided, multiple submitters, no conflictsClinGen:CA645369629
DeletionNM_177438.3(DICER1):c.1749_1753del (p.Glu583fs)DICER1Pathogenic149558279095582794CCTTTTCcriteria provided, single submitterClinGen:CA645369621
DuplicationNM_177438.3(DICER1):c.1732dup (p.Thr578fs)DICER1Pathogenic149558280995582810GGTcriteria provided, single submitterClinGen:CA645369623
DuplicationNM_177438.3(DICER1):c.1462dup (p.Gln488fs)DICER1Pathogenic149558400595584006TTGcriteria provided, single submitterClinGen:CA645369631