Knowledge base for genomic medicine in Japanese
リンチ症候群
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
single nucleotide variantNM_000249.4(MLH1):c.497T>A (p.Leu166Ter)MLH1Pathogenic33705034837050348TAreviewed by expert panelClinGen:CA010700
DeletionNM_000249.4(MLH1):c.497del (p.Ala165_Leu166insTer)MLH1Pathogenic33705034637050346CTCreviewed by expert panelClinGen:CA010691
DeletionNM_000249.4(MLH1):c.502_503del (p.Asn168fs)MLH1Pathogenic33705034937050350TAATreviewed by expert panelClinGen:CA010715
DuplicationNM_000249.4(MLH1):c.503dup (p.Asn168fs)MLH1Pathogenic33705034837050349TTAreviewed by expert panelClinGen:CA010732
DeletionNM_000249.4(MLH1):c.513del (p.Glu172fs)MLH1Pathogenic33705036337050363GAGreviewed by expert panelClinGen:CA010758
InsertionNM_000249.4(MLH1):c.524_525insGA (p.Ile176fs)MLH1Pathogenic33705037437050375AAAGreviewed by expert panelClinGen:CA010767
DeletionNM_000249.4(MLH1):c.52del (p.Arg18fs)MLH1Pathogenic33703508937035089ACAreviewed by expert panelClinGen:CA010785
IndelNM_000249.4(MLH1):c.531_532delinsAT (p.Glu178Ter)MLH1Pathogenic33705038237050383GGATreviewed by expert panelClinGen:CA010794
IndelNM_000249.4(MLH1):c.531_532delinsCT (p.Leu177_Glu178delinsPheTer)MLH1Pathogenic33705038237050383GGCTreviewed by expert panelClinGen:CA010802
single nucleotide variantNM_000249.4(MLH1):c.544A>G (p.Arg182Gly)MLH1Pathogenic33705039537050395AGreviewed by expert panelClinGen:CA010872,UniProtKB:P40692#VAR_012909