The UMD-MSH2 mutations database
Mutation c.IVS8+1G>T (c.1386+1G>T)

Splice site type	Wild type sequence	CV	Mutant type sequence	CV	Variation (%)
Donor	CAGgtatgc	89 _	CAGttatgc	62.2 _ *	-30.1 %

     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_10236_10236-001_10236-	-	-	-	-	-
4_C01034_---_723	-	-	-	-	-
6_603006_200404613_S6762	-	-	-	-	-
7_-652---E050210	-	-	-	-	-
7_-6523323E050210	-	-	-	-	-
SO_-652---G01561	-	-	-	-	-
SO_-652---G04404	-	-	-	-	-

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