The UMD-MSH2 mutations database
Mutation c.1783_1787delCTCAA

     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_-4493---G06670	-	-	-	-	-
SO_-4493---G07858	-	-	-	-	-
SO_-5389---G08264	-	-	-	-	-

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