The UMD-MSH6 mutations database
Mutation c.2677_2678delCT



     Data for this mutation

Co occurence of MLH1, MSH2, MSH6, MUTYH and APC mutations (Pathogenic mutations, Unclassified variants, Non-pathogenic variation)
Sample IDMSH6MLH1MSH2MUTYHAPC
8_209251060308-961260c.1730G>A (p.Arg577His)----

Complementary data about this mutation
AnalysisResult DateOriginPMID/dbSNP
Clinical phenotypeAmsterdam II+ (20925-10603)27/04/128 (Nancy)
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Co-occurrenceMSH6 : c.1730G>A; p.Arg577His (20925-10603)27/04/128 (Nancy)
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Biological significanceDate Comment
Causal5/06/14---