TheUMD-MSH2 mutations database
Large rearrangement: c.1387_2805del (deletion from exon 9 to 16)



Data for this mutation


Co occurence of MLH1, MSH2, MSH6, MUTYH and APC mutations (Pathogenic mutations, Unclassified variants, Non-pathogenic variation)
Sample IDMSH2MLH1MSH6MUTYHAPC
19_8237_8237-001_8237-001-----
19_8237_8237-003_8237-003-----
19_9639_9639-001_9639-001-----
19_9639_9639-002_9639-002-----
4_9348_23748_2969-----
4_C99101_18096_914-----
4_T04157_18211_1226-----

Biological significanceDate Comment
Causal21/02/14---



Consequences of the mutation at the protein level

No data available