TheUMD-MSH2 mutations database
Large rearrangement: c.1_942del (deletion from exon 1 to 5)



Data for this mutation


Co occurence of MLH1, MSH2, MSH6, MUTYH and APC mutations (Pathogenic mutations, Unclassified variants, Non-pathogenic variation)
Sample IDMSH2MLH1MSH6MUTYHAPC
19_10681_10681-001_10681------
19_10681_10681-003_10681------
19_10681_10681-005_10681------
19_15309_15309-001_15309------
19_9498_9498-001_9498-001-----
19_9498_9498-005_9498-005-----
19_9498_9498-006_9498-006-----
19_9498_9498-007_9498-007-----
19_9498_9498-008_9498-008-----
4_C04286_18251_1379-----
SO_-3923---G05459-----
SO_-3923---G05503-----

Biological significanceDate Comment
Causal21/02/14---



Consequences of the mutation at the protein level

No data available