TheUMD-MSH2 mutations database
Large rearrangement: c.793_1076del (deletion from exon 5 to 6)

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_15755_15755-001_15755-	-	-	-	-	-
19_15755_15755-003_15755-	-	-	-	-	-
19_15755_15755-004_15755-	-	-	-	-	-
19_5405_5405-002_5405-002	-	-	-	-	-
19_9954_9954-002_9954-002	-	-	-	-	-
19_9954_9954-003_9954-003	-	-	-	-	-
4_9232233933308	-	-	-	-	-
SO_-2722---G02479	-	-	-	-	-
SO_-2722---G05416	-	-	-	-	-

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

Consequences of the mutation at the protein level No data available