The UMD-MSH2 mutations database
Mutation c.1435_1436delAG

     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_-4822---G07233	c.965G>A (p.Gly322Asp)	-	-	-	-

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