TheUMD-MSH2 mutations database
Large rearrangement: c.367_1759del (deletion from exon 3 to 11)

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_7084_7084-001_7084-001	-	-	-	-	-
SO_-5497---G08513	-	-	-	-	-

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

Consequences of the mutation at the protein level No data available