| Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
| OCLN | 8104 | COSM5989704, | haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm | p.Q41E | Substitution - Missense | 5:69509211-69509211, | PATHOGENIC | 0.99234 | 26648538 |
| OCLN | 8104 | COSM5989705, | haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm | p.R66L | Substitution - Missense | 5:69509287-69509287, | PATHOGENIC | 0.95459 | 26648538 |
| OCLN | 8104 | COSM5989725, | haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm | p.V160I | Substitution - Missense | 5:69509568-69509568, | PATHOGENIC | 0.85595 | 26648538 |
| OCLN | 8104 | COSM3072302, | haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm | p.V308M | Substitution - Missense | 5:69534724-69534724, | NEUTRAL | 0.09046 | 26648538 |