The UMD-MSH2 mutations database
Mutation c.2016_2135del

     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
41_HNPCC109HNPCC109001	-	-	-	-	-

Complementary data about this mutation

Analysis	Result	Date	Origin	PMID/dbSNP
Clinical phenotype	Amsterdam II + (HNPCC109)	16/12/14	41 (HEGP)	---
MMR function in tumor cells	MSH2-	16/12/14	41 (HEGP)	---

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