| Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
| TBC1D4 | 19165 | COSM1949189, | oesophagus | carcinoma | p.? | Unknown | 13:75309941-75309941, | PATHOGENIC | 0.99227 | 24686850 |
| TBC1D4 | 19165 | COSM5049488, | oesophagus | carcinoma | p.C885R | Substitution - Missense | 13:75306412-75306412, | PATHOGENIC | 0.99039 | 24686850 |
| TBC1D4 | 19165 | COSM40678, | central_nervous_system | glioma | p.A1223T | Substitution - Missense | 13:75287022-75287022, | PATHOGENIC | 0.9756 | 18772396 |
| TBC1D4 | 19165 | COSM315805, | lung | carcinoma | p.R1103G | Substitution - Missense | 13:75294863-75294863, | PATHOGENIC | 0.91799 | 22941188 |