The UMD-MSH2 mutations database
Mutation c.IVS9-29T>C (c.1511-29T>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
19_2459224592-00124592-001	c.IVS6+5G>T (c.1076+5G>T)	-	-	-	-
7_1105411593E092360	-	-	-	-	-
7_43353969E050622	c.IVS1+9C>G (c.211+9C>G) c.IVS9-9A>T (c.1511-9A>T) c.IVS10+12G>A (c.1661+12G>A) c.IVS12-6T>C (c.2006-6T>C)	-	-	-	-

Complementary data about this mutation

Analysis	Result	Date	Origin	PMID/dbSNP
Clinical phenotype	Sporadic colon cancer at the age of 32 (24592-001)	17/04/15	19 (Rouen)	---
Co-occurrence	MSH2 : c.1076+5G>T (24592-001)	17/04/15	19 (Rouen)	---

Biological significance	Date	Comment
UV	5/06/07	---