TheUMD-MSH2 mutations database
Large rearrangement: c.1387_1661del (deletion from exon 9 to 10)



Data for this mutation


Co occurence of MLH1, MSH2, MSH6, MUTYH and APC mutations (Pathogenic mutations, Unclassified variants, Non-pathogenic variation)
Sample IDMSH2MLH1MSH6MUTYHAPC
19_12963_12963-001_12963------
19_12963_12963-002_12963------
19_13092_13092-001_13092------
19_13092_13092-002_13092------
19_13527_13527-001_13527------
19_13527_13527-002_13527------
19_13530_13530-001_13530------
19_7540_7540-001_7540-001-----
19_7540_7540-002_7540-002-----
19_9505_9505-001_9505-001-----
2_02-ACT1835_15167_15167-----
2_02-ACT1835_16563_16563-----
4_Di1104_27060_3675-----
SO_-2706---G02406-----
SO_-4691---G07081c.1602T>A (p.Arg534Arg)----

Biological significanceDate Comment
Causal21/02/14---



Consequences of the mutation at the protein level

No data available