TheUMD-MSH2 mutations database
Large rearrangement: c.646_1076del (deletion from exon 4 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
20_20-51885188-01---	-	-	-	-	-

Biological significance	Date	Comment
Causal	11/09/15	---

Consequences of the mutation at the protein level No data available