| Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
| CORO1B | 2253 | COSM32982, | large_intestine | carcinoma | p.V411M | Substitution - Missense | 11:67438784-67438784, | NEUTRAL | 0.12244 | 16959974 |