TheUMD-MSH2 mutations database
Large rearrangement: c.943_1076del (deletion from exon 6 to 6)

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_9503_9503-001_9503-001	-	-	-	-	-
19_L11.08317342118900	-	-	-	-	-
37_L06.42_4457_46178	-	-	-	-	-
37_L06.42_6374_60673	-	-	-	-	-
37_L11.08323573144643	-	-	-	-	-
37_L11.083_17342_126383	-	-	-	-	-
37_L11.083_20239_131455	-	-	-	-	-
37_L11.083_20239_131465	-	-	-	-	-
37_L14.209-E29715166399	-	-	-	-	-
SO_-4079---G06841	-	-	-	-	-

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

Consequences of the mutation at the protein level No data available