TheUMD-MSH2 mutations database
Large rearrangement: c.1760_2210del (deletion from exon 12 to 13)

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_10086_10086-002_10086-	-	-	-	-	-
19_10086_10086-003_10086-	-	-	-	-	-
19_6259_6259-001_6259-001	-	-	-	-	-
19_8813_8813-001_8813-001	-	-	-	-	-
19_8813_8813-003_8813-003	-	-	-	-	-
19_8813_8813-004_8813-004	-	-	-	-	-
19_8813_8813-005_8813-005	-	-	-	-	-
19_8813_8813-006_8813-006	-	-	-	-	-
19_8813_8813-007_8813-007	-	-	-	-	-

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

Consequences of the mutation at the protein level No data available