| Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
| PTPN4 | 9656 | COSM304466, | large_intestine | carcinoma | p.T405M | Substitution - Missense | 2:119934817-119934817, | PATHOGENIC | 0.87738 | 21892161 |