TheUMD-MSH2 mutations database
Large rearrangement: c.806_807ins13 ()

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
17_121541212576001---	-	-	-	-	-

Biological significance	Date	Comment
Causal	5/08/15	---

Consequences of the mutation at the protein level No data available