The UMD-MSH2 mutations database
Mutation c.792delG

     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
31_H1289H1289-1H1289-1A	-	-	-	-	-

Biological significance	Date	Comment
Causal	16/12/14	---