The UMD-MSH2 mutations database
Mutation c.1069G>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
SO_-2597---G02192	-	-	-	-	-
SO_-2597---G02670	-	-	-	-	-

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