The UMD-MSH2 mutations database
Mutation c.1147C>T



     Data for this mutation

Co occurence of MLH1, MSH2, MSH6, MUTYH and APC mutations (Pathogenic mutations, Unclassified variants, Non-pathogenic variation)
Sample IDMSH2MLH1MSH6MUTYHAPC
20_20-1509_1509-01_4835-----
31_H1501_H1501-1_H1501-1A-----
37_L08.083_10291_86892-----
37_L08.083_6673_72114-----
37_L08.083_9598_81966-----
37_L08.083_9599_81967-----
37_L08.083_9602_81968-----
37_L97.01_256_187-----
37_L97.01_710_1322-----
4_SE1302304474420-----
5_2010264_P0042590_AAE217-----
5_2011298P0047493AAH410-----
7_34791660E03393c.IVS1+9C>G (c.211+9C>G)c.655A>G (p.Ile219Val)---
SO_-2150---G00931-----
SO_-4662---G06988-----
SO_-4773---G07176-----

Complementary data about this mutation
AnalysisResult DateOriginPMID/dbSNP
MMR function in tumor cellsMSI-H (SE1302-30447)17/03/154 (Lyon)
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Biological significanceDate Comment
Causal21/02/14---