The UMD-MSH2 mutations database
Mutation c.IVS9+1G>C (c.1510+1G>C)

Splice site type	Wild type sequence	CV	Mutant type sequence	CV	Variation (%)
Donor	TTGgtaaga	90.9 _	TTGctaaga	64.1 _ *	-29.5 %

     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
7_1247213013E110468	-	-	-	-	-
7_1247214413E120161	-	-	-	-	-
7_1247214414E112057	-	-	-	-	-

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