TheUMD-MSH2 mutations database
Large rearrangement: c.1387_1661dup ()

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_12156_12156-001_12156-	-	-	-	-	-
19_12156_12156-002_12156-	-	-	-	-	-
19_12156_12156-004_12156-	-	-	-	-	-
19_12172_12172-001_12172-	-	-	-	-	-
19_4264_4264-001_4264-001	-	-	-	-	-
19_7722_7722-001_7722-001	-	-	-	-	-
19_7722_7722-002_7722-002	-	-	-	-	-
4_H95H006_---_125	-	-	-	-	-

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

Consequences of the mutation at the protein level No data available