The UMD-MSH2 mutations database
Mutation c.862C>T

     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
17_140106218871001---	-	-	c.IVS7-51del17 (c.3647-51del17)	-	-

Biological significance	Date	Comment
Causal	24/06/15	---