The UMD-MSH2 mutations database
Mutation c.478C>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_14319_14319-001_14319-	-	-	-	-	-
19_14319_14319-002_14319-	-	-	-	-	-
41_HNPCC060_HNPCC060001_-	-	-	-	-	-
SO_-4461---G06658	-	-	-	-	-
SO_-4461---G06751	-	-	-	-	-

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