TheUMD-MSH2 mutations database
Large rearrangement: c.1_2634del (deletion from exon 1 to 15)



Data for this mutation


Co occurence of MLH1, MSH2, MSH6, MUTYH and APC mutations (Pathogenic mutations, Unclassified variants, Non-pathogenic variation)
Sample IDMSH2MLH1MSH6MUTYHAPC
37_L06.03-E_4325_44807/44-----
7_-2348---E041267-----
SO_-2348---G01371-----
SO_-2348---G03155-----

Biological significanceDate Comment
Causal21/02/14---



Consequences of the mutation at the protein level

No data available