| Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
| NFATC2 | 7776 | COSM1615727, | liver | carcinoma | p.? | Unknown | 20:51391455-51391455, | PATHOGENIC | 0.73607 | Info_not_available |
| NFATC2 | 7776 | COSM313208, | lung | carcinoma | p.L33L | Substitution - coding silent | 20:51542401-51542401, | NEUTRAL | 0.41097 | 22941188 |