The UMD-MSH2 mutations database
Mutation c.IVS3+1G>C (c.645+1G>C)

Splice site type	Wild type sequence	CV	Mutant type sequence	CV	Variation (%)
Donor	CAGgtaagc	97.8 _	CAGctaagc	71 _ *	-27.4 %

     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
17_F06014_9307906_5694	-	-	-	-	-

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