The UMD-MSH2 mutations database
Mutation c.1705_1706delGA



     Data for this mutation

Co occurence of MLH1, MSH2, MSH6, MUTYH and APC mutations (Pathogenic mutations, Unclassified variants, Non-pathogenic variation)
Sample IDMSH2MLH1MSH6MUTYHAPC
19_1941319413-01519413-015-----
19_1941319413-01619413-016-----
2_02-PKO1372343357215114430-----
31_H1746H1746-1H1746-1A-----
33_TNN 149__02-817-----
41_HNPCC052_HNPCC052001_------
41_HNPCC052_HNPCC052003_------
41_HNPCC052_HNPCC052004_------
41_HNPCC052_HNPCC052005_------
41_HNPCC052_HNPCC052008_------
SO_-2389---G01667-----
SO_-4192---G06229-----

Complementary data about this mutation
AnalysisResult DateOriginPMID/dbSNP
Clinical phenotypeSon of the index case (HEGP) : corticosurrenaloma at the age of 28 (02-PKO13723-43357)1/09/152 (Villejuif)
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MMR function in tumor cellsMSH2-MSH6- (02-PKO13723-43357)1/09/152 (Villejuif)
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Biological significanceDate Comment
Causal21/02/14---