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

Splice site type	Wild type sequence	CV	Mutant type sequence	CV	Variation (%)
Donor	CAGgtaagc	97.8 _	CAGataagc	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
19_6206_6206-001_6206-001	-	-	-	-	-
19_6206_6206-002_6206-002	-	-	-	-	-
19_6206_6206-003_6206-003	-	-	-	-	-
19_6206_6206-004_6206-004	-	-	-	-	-
19_6206_6206-005_6206-005	-	-	-	-	-
19_6206_6206-006_6206-006	-	-	-	-	-
19_6206_6206-008_6206-008	-	-	-	-	-
19_6206_6206-010_6206-010	-	-	-	-	-
19_6206_6206-011_6206-011	-	-	-	-	-
19_6206_6206-013_6206-013	-	-	-	-	-
19_6206_6206-014_6206-014	-	-	-	-	-
19_6206_6206-015_6206-015	-	-	-	-	-
19_6206_6206-019_6206-019	-	-	-	-	-
19_6206_6206-020_6206-020	-	-	-	-	-
19_6206_6206-023_6206-023	-	-	-	-	-
19_6206_6206-027_6206-027	-	-	-	-	-
19_6206_6206-029_6206-029	-	-	-	-	-
19_6206_6206-033_6206-033	-	-	-	-	-
SO_-4828---G07256	-	-	-	-	-

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