The UMD-MSH2 mutations database
Mutation c.1777C>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
41_HNPCC080_HNPCC080002_-	-	-	-	-	-
SO_-5060---G00020	-	-	-	-	-
SO_-5060---G07712	c.1666T>C (p.Leu556Leu)	-	-	-	-
SO_-5060---G08852	-	-	-	-	-
SO_-50603673G00020	-	-	-	-	-

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