The UMD-MSH2 mutations database
Mutation c.2191delG



     Data for this mutation

Co occurence of MLH1, MSH2, MSH6, MUTYH and APC mutations (Pathogenic mutations, Unclassified variants, Non-pathogenic variation)
Sample IDMSH2MLH1MSH6MUTYHAPC
19_2438224382-00124382-001-----
38_18_A1_633-----
38_18_A2_1574-----
38_18_A3_1576-----
38_18_A4_1882-----
SO_-3204---G03430-----
SO_-3204---G05177-----
SO_-3204---G05986-----

Complementary data about this mutation
AnalysisResult DateOriginPMID/dbSNP
Clinical phenotypeAmsterdam + (24382)5/08/1419 (Rouen)
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MMR function in tumor cellsMSS/ MLH1+MSH2-/+MSH6-/+PMS2+ (24382-001) 5/08/1419 (Rouen)
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Biological significanceDate Comment
Causal21/02/14---