| Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
| EEF2 | 3214 | COSM1612217, | liver | carcinoma | p.L635L | Substitution - coding silent | 19:3977981-3977981, | PATHOGENIC | 0.94874 | Info_not_available |