| Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
| HIST1H2AG | 4737 | COSM5048207, | oesophagus | carcinoma | p.T121S | Substitution - Missense | 6:27133433-27133433, | PATHOGENIC | 0.78303 | 24686850 |
| HIST1H2AG | 4737 | COSM5046747, | oesophagus | carcinoma | p.K120N | Substitution - Missense | 6:27133431-27133431, | Info_not_available | 0.56465 | 24686850 |