TheUMD-MSH2 mutations database
Large rearrangement: c.1_792del (deletion from exon 1 to 4)

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_4347_4347-001_4347-001	-	-	-	-	-
19_4347_4347-002_4347-002	-	-	-	-	-
19_4347_4347-003_4347-003	-	-	-	-	-
19_9069_9069-001_9069-001	-	-	-	-	-
4_C97060_---_116	-	-	-	-	-
4_H-JCS0411_17947_1136	-	-	-	-	-

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

Consequences of the mutation at the protein level No data available