The UMD-MSH2 mutations database
Mutation c.IVS11+1G>T (c.1759+1G>T)

Splice site type	Wild type sequence	CV	Mutant type sequence	CV	Variation (%)
Donor	CAGgtaaac	85.7 _	CAGttaaac	58.8 _ *	-31.3 %

     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_-5532---G08604	-	-	-	-	-

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