Knowledge base for genomic medicine in Japanese
若年性ポリポーシス症候群
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DuplicationNM_005359.6(SMAD4):c.1407_1410dup (p.Gly471fs)SMAD4Pathogenic184860310448603105AATCCCcriteria provided, single submitterClinGen:CA658799052
DeletionNM_005359.6(SMAD4):c.1409del (p.Pro470fs)SMAD4Pathogenic184860310648603106TCTcriteria provided, single submitterClinGen:CA658799053
single nucleotide variantNM_005359.6(SMAD4):c.454+2T>CSMAD4Likely pathogenic184857569648575696TCcriteria provided, single submitterClinGen:CA402459644
DeletionNM_005359.6(SMAD4):c.955+1delSMAD4Likely pathogenic184858628648586286TGTcriteria provided, single submitterClinGen:CA658799061
DuplicationNM_004329.3(BMPR1A):c.40dup (p.Tyr14fs)BMPR1APathogenic/Likely pathogenic108863581488635815CCTcriteria provided, multiple submitters, no conflicts-
IndelNM_004329.3(BMPR1A):c.987_992delinsTGTA (p.Arg329fs)BMPR1APathogenic108867904788679052AGCCCTTGTAcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_005359.6(SMAD4):c.1308+2T>CSMAD4Pathogenic184859355948593559TCcriteria provided, single submitter-
single nucleotide variantNM_005359.6(SMAD4):c.1523G>A (p.Gly508Asp)SMAD4Likely pathogenic184860470148604701GAcriteria provided, single submitter-
DeletionNM_004329.3(BMPR1A):c.-547_-268+1delBMPR1APathogenic108851639588516675CGGCGGCCGCTGCAGAGATTGGAATCCGCCTGCCGGGCTTGGCGAAGGAGAAGGGAGGAGGCAGGAGCGAGGAGGGAGGAGGGCCAAGGGCGGGCAGGAAGGCTTAGGCTCGGCGCGTCCGTCCGCGCGCGGCGAAGATCGCACGGCCCGATCGAGGGGCGACCGGGTCGGGGCCGCTGCACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTTCGCCCCGGCGGCTCGCCGCGCCCACCCGCTCCGCGCCGAGGGCTGGAGGATGCGTTCCCTGGGGTCCGCcriteria provided, single submitter-
DeletionNM_004329.3(BMPR1A):c.133_134del (p.Glu45fs)BMPR1APathogenic108864988388649884CAGCcriteria provided, single submitter-