| Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
| EPM2A | 3413 | COSM1645528, | large_intestine | carcinoma | p.A275V | Substitution - Missense | 6:145627588-145627588, | PATHOGENIC | 0.98996 | 23700467 |