| Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
| PDCD10 | 8761 | COSM94947, | lung | carcinoma | p.R35P | Substitution - Missense | 3:167704888-167704888, | PATHOGENIC | 0.97937 | 20668451 |
| PDCD10 | 8761 | COSM40445, | central_nervous_system | glioma | p.K132K | Substitution - coding silent | 3:167687693-167687693, | PATHOGENIC | 0.90539 | 18772396 |
| PDCD10 | 8761 | COSM1617176, | liver | carcinoma | p.T77T | Substitution - coding silent | 3:167697046-167697046, | NEUTRAL | 0.11937 | Info_not_available |
| PDCD10 | 8761 | COSM314035, | lung | carcinoma | p.S71fs*18 | Deletion - Frameshift | 3:167697066-167697066, | Info_not_available | Info_not_available | 22941188 |