The UMD-MSH2 mutations database
Mutation c.1165C>T

     Data for this mutation

Co occurence of MLH1, MSH2, MSH6, MUTYH and APC mutations (Pathogenic mutations, Unclassified variants, Non-pathogenic variation)

Sample ID	MSH2	MLH1	MSH6	MUTYH	APC
19_10498_10498-001_10498-	-	-	-	-	-
19_L98.0315118109330	-	-	-	-	-
2_02-ACT109634795213078412	-	-	-	-	-
2_02-ACT1096_11520_11520	-	-	-	-	-
2_02-DDM4505_23242_23242	-	-	-	-	-
33_TNN 150__02-863	-	-	-	-	-
37_L08.046_6829_64758	-	-	-	-	-
37_L08.046_8723_77415	-	-	-	-	-
37_L08.046_8725_77475	-	-	-	-	-
37_L08.046_9236_---	-	-	-	-	-
37_L08.046_9237_---	-	-	-	-	-
37_L98.03_1021_4887	-	-	-	-	-
37_L98.03_257_194	-	-	-	-	-
38_589_---_1561	-	-	-	-	-
SO_-1065---G00275	-	-	-	-	-
SO_-1065---G00793	-	-	-	-	-
SO_-1065---G00797	-	-	-	-	-
SO_-2564---G02124	-	-	-	-	-
SO_-2564---G03228	-	-	-	-	-
SO_-3699---G09022	-	-	-	-	-
SO_-36993088G09022	-	-	-	-	-
SO_-3952---G05452	-	-	-	-	-

Biological significance	Date	Comment
Causal	21/02/14	---