The UMD-MSH2 mutations database
Mutation c.1079T>A

     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_H339_H339-1_H339-1A	c.1680T>C (p.Asn560Asn)	-	-	-	-

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