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.1144G>T (p.Glu382Ter)DICER1Pathogenic149559076595590765CAcriteria provided, multiple submitters, no conflictsClinGen:CA10586462
single nucleotide variantNM_177438.3(DICER1):c.996C>A (p.Tyr332Ter)DICER1Pathogenic149559091395590913GTcriteria provided, single submitterClinGen:CA10586463
DeletionNM_177438.3(DICER1):c.878_881del (p.Arg293fs)DICER1Pathogenic149559293995592942ATCTCAreviewed by expert panelClinGen:CA10586464
single nucleotide variantNM_177438.3(DICER1):c.745C>T (p.Gln249Ter)DICER1Pathogenic149559307595593075GAcriteria provided, multiple submitters, no conflictsClinGen:CA10586465
IndelNM_177438.3(DICER1):c.735-1_741delinsADICER1Pathogenic/Likely pathogenic149559307995593086AGTATACCTcriteria provided, multiple submitters, no conflictsClinGen:CA10586466
single nucleotide variantNM_177438.3(DICER1):c.629T>G (p.Leu210Ter)DICER1Pathogenic149559591495595914ACcriteria provided, multiple submitters, no conflictsClinGen:CA10586467
IndelNM_177438.3(DICER1):c.2243_2244delinsAA (p.Cys748Ter)DICER1Pathogenic149557766695577667GCTTcriteria provided, multiple submitters, no conflictsClinGen:CA10586468
InsertionNM_177438.3(DICER1):c.2243_2244insACTA (p.Cys748Ter)DICER1Pathogenic149557766695577667GGTAGTcriteria provided, multiple submitters, no conflictsClinGen:CA10586469
single nucleotide variantNM_177438.3(DICER1):c.2651-2A>GDICER1Pathogenic149557410095574100TCcriteria provided, multiple submitters, no conflictsClinGen:CA16614229
DeletionNM_177438.3(DICER1):c.1767del (p.Lys589fs)DICER1Pathogenic149558214495582144ACAcriteria provided, single submitterClinGen:CA16614256