| Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
| PDHA2 | 8807 | COSM2989186, | oesophagus | carcinoma | p.Q78E | Substitution - Missense | 4:95840382-95840382, | PATHOGENIC | 0.9759 | 24686850 |
| PDHA2 | 8807 | COSM5047481, | oesophagus | carcinoma | p.C92* | Substitution - Nonsense | 4:95840426-95840426, | NEUTRAL | 0.32807 | 24686850 |
| PDHA2 | 8807 | COSM39464, | central_nervous_system | glioma | p.E307K | Substitution - Missense | 4:95841069-95841069, | NEUTRAL | 0.0443 | 18772396 |