Knowledge base for genomic medicine in Japanese
ロイス・ディーツ症候群
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
IndelNM_005902.4(SMAD3):c.275_281delinsC (p.Trp92_Trp94delinsSer)SMAD3Pathogenic/Likely pathogenic156745730167457307GGCGATGCcriteria provided, multiple submitters, no conflictsClinGen:CA320096
single nucleotide variantNM_005902.4(SMAD3):c.277C>T (p.Arg93Ter)SMAD3Pathogenic/Likely pathogenic156745730367457303CTcriteria provided, multiple submitters, no conflictsClinGen:CA062085
single nucleotide variantNM_005902.4(SMAD3):c.401-6G>ASMAD3Pathogenic/Likely pathogenic156745758567457585GAcriteria provided, multiple submitters, no conflicts-
DeletionNM_005902.4(SMAD3):c.455del (p.Pro152fs)SMAD3Pathogenic156745764067457640TCTcriteria provided, multiple submitters, no conflictsClinGen:CA320725
DeletionNM_005902.4(SMAD3):c.483del (p.Glu162fs)SMAD3Pathogenic156745767067457670TCTcriteria provided, single submitterClinGen:CA323716
DuplicationNM_005902.4(SMAD3):c.492dup (p.Asn165Ter)SMAD3Pathogenic156745768167457682CCTcriteria provided, single submitter-
single nucleotide variantNM_005902.4(SMAD3):c.733G>A (p.Gly245Arg)SMAD3Pathogenic/Likely pathogenic156747365367473653GAcriteria provided, multiple submitters, no conflictsClinGen:CA323714
single nucleotide variantNM_005902.4(SMAD3):c.772G>C (p.Asp258His)SMAD3Likely pathogenic156747369267473692GCcriteria provided, multiple submitters, no conflictsClinGen:CA325318
single nucleotide variantNM_005902.4(SMAD3):c.787C>G (p.Pro263Ala)SMAD3Pathogenic156747370767473707CGcriteria provided, single submitterClinGen:CA321192
single nucleotide variantNM_005902.4(SMAD3):c.803G>A (p.Arg268His)SMAD3Pathogenic/Likely pathogenic156747372367473723GAcriteria provided, multiple submitters, no conflictsClinGen:CA321807