The UMD-MSH2 mutations database
Mutation c.IVS9-41G>C (c.1511-41G>C)

     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_L12.043-E_19166_127617	-	-	-	-	-

Complementary data about this mutation

Analysis	Result	Date	Origin	PMID/dbSNP
Clinical phenotype	Sporadic colorectal cancer < 50 years old	7/07/14	37 (Lille)	---

Biological significance	Date	Comment
UV	28/04/14	---