TheUMD-MSH2 mutations database
Large rearrangement: c.1077_1386del (deletion from exon 7 to 8)

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_13096_13096-001_13096-	-	-	-	-	-
4_11149_27666_3817	-	-	-	-	-

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

Consequences of the mutation at the protein level No data available