The UMD-MSH2 mutations database
Mutation
c.IVS5+2T>G (c.942+2T>G)
| Splice site type | Wild type sequence | CV | Mutant type sequence | CV | Variation (%) |
| Donor | CAGgtaaaa | | CAGggaaaa | | -31.4 % |
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 |
|---|
| 37_L98.01_2285_23660 | - | - | - | - | - |
| 37_L98.01_2405_25726 | - | - | - | - | - |
| 37_L98.01_253_185 | - | - | - | - | - |
| 37_L98.01_2680_29090 | - | - | - | - | - |
| 37_L98.01_292_242 | - | - | - | - | - |
| 37_L98.01_641_633 | - | - | - | - | - |
| SO_-2111---G00817 | - | - | - | - | - |
| Biological significance | Date | Comment | | Causal | 21/02/14 | --- |
