The UMD-MSH2 mutations database
Mutation c.IVS8+28A>G (c.1386+28A>G)

Splice site type	Wild type sequence	CV	Mutant type sequence	CV	Variation (%)
Cryptic Donor?	gcagtagtt	62.3 _	gcGgtagtt	72.8 _ *	14.5 %

     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_981610221E090208	-	c.43_46delGTGG (p.Val15X)	-	-	-

Biological significance	Date	Comment
UV	18/03/10	---