The UMD-MSH2 mutations database
Mutation c.2228C>G



     Data for this mutation

Co occurence of MLH1, MSH2, MSH6, MUTYH and APC mutations (Pathogenic mutations, Unclassified variants, Non-pathogenic variation)
Sample IDMSH2MLH1MSH6MUTYHAPC
19_L07.4911340117041-----
37_F07.105_11420_93539-----
37_F07.105_6301_60151-----
37_F07.105_7424_70003-----
37_F07.105_9747_83192-----
37_L07.4925097150519-----

Complementary data about this mutation
AnalysisResult DateOriginPMID/dbSNP
Clinical phenotypeAmsterdam I+5/06/1437 (Lille)
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Biological significanceDate Comment
Causal21/02/14---