The UMD-MSH2 mutations database
Mutation c.1255C>T



     Data for this mutation

Co occurence of MLH1, MSH2, MSH6, MUTYH and APC mutations (Pathogenic mutations, Unclassified variants, Non-pathogenic variation)
Sample IDMSH2MLH1MSH6MUTYHAPC
2_02-OCN716231198212065435-----
7_-1011C010121-----

Complementary data about this mutation
AnalysisResult DateOriginPMID/dbSNP
MMR function in tumor cellsMSH2-MSH6- (02-OCN7162-31198)1/07/142 (Villejuif)
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Clinical phenotypeAmsterdam II+ (02-OCN7162)1/07/142 (Villejuif)
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Biological significanceDate Comment
Causal21/02/14---