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.823G>T (p.Glu275Ter)DICER1Pathogenic149559299795592997CAcriteria provided, single submitterClinGen:CA390887630
DeletionNM_177438.3(DICER1):c.1137del (p.Lys379fs)DICER1Pathogenic149559077295590772GTGcriteria provided, single submitterClinGen:CA658656455
DeletionNM_177438.3(DICER1):c.535del (p.Ala180fs)DICER1Pathogenic149559643395596433AGAcriteria provided, multiple submitters, no conflictsClinGen:CA658658270
DuplicationNM_177438.3(DICER1):c.1029dup (p.Phe344fs)DICER1Pathogenic/Likely pathogenic149559087995590880AATcriteria provided, multiple submitters, no conflictsClinGen:CA658656456
DeletionNM_177438.3(DICER1):c.5479del (p.Leu1827fs)DICER1Pathogenic149555758895557588AGAreviewed by expert panelClinGen:CA658656432
DeletionNM_177438.3(DICER1):c.1694del (p.Asp565fs)DICER1Pathogenic149558284895582848ATAcriteria provided, single submitterClinGen:CA658656449
DeletionNM_177438.3(DICER1):c.1417del (p.Tyr473fs)DICER1Pathogenic149558405195584051TATcriteria provided, single submitterClinGen:CA658656452
DuplicationNM_177438.3(DICER1):c.2245_2248dup (p.Pro750fs)DICER1Pathogenic149557766195577662GGGGTAcriteria provided, multiple submitters, no conflictsClinGen:CA658656439
single nucleotide variantNM_177438.3(DICER1):c.4638C>A (p.Tyr1546Ter)DICER1Pathogenic149556261995562619GTcriteria provided, multiple submitters, no conflictsClinGen:CA390867638
DeletionNM_177438.3(DICER1):c.1234del (p.Trp412fs)DICER1Pathogenic149559067595590675CACcriteria provided, multiple submitters, no conflictsClinGen:CA658656454