| Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
| VIM | 12692 | COSM33155, | large_intestine | carcinoma | p.E187* | Substitution - Nonsense | 10:17229981-17229981, | PATHOGENIC | 0.96805 | 16959974 |