| Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
| TRIP6 | 12311 | COSM40717, | central_nervous_system | glioma | p.L468F | Substitution - Missense | 7:100873274-100873274, | PATHOGENIC | 0.98809 | 18772396 |
| TRIP6 | 12311 | COSM316186, | lung | carcinoma | p.T341T | Substitution - coding silent | 7:100871566-100871566, | NEUTRAL | 0.18934 | 22941188 |