| Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
| NT5E | 8021 | COSM40400, | central_nervous_system | glioma | p.G261E | Substitution - Missense | 6:85485265-85485265, | PATHOGENIC | 0.99011 | 18772396 |
| NT5E | 8021 | COSM313378, | lung | carcinoma | p.T246T | Substitution - coding silent | 6:85471412-85471412, | NEUTRAL | 0.07861 | 22941188 |