The UMD-MSH2 mutations database
Mutation c.388_389delCA

     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
37_L99.0726511155780	-	-	-	-	-
37_L99.0726528155797	-	-	-	-	-
37_L99.078798151707	-	-	-	-	-

Biological significance	Date	Comment
Causal	22/06/15	---