The UMD-MSH2 mutations database
Mutation c.IVS9-1G>A (c.1511-1G>A)

Splice site type	Wild type sequence	CV	Mutant type sequence	CV	Variation (%)
Acceptor	ttgattatcaagGC	79 _	ttgattatcaaaGC	50.1 _ *	-36.6 %

     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
4_H01H03_---_515	-	-	-	-	-

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