| Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
| PTPRN | 9676 | COSM1614394, | liver | carcinoma | p.E680K | Substitution - Missense | 2:219297283-219297283, | PATHOGENIC | 0.97783 | Info_not_available |
| PTPRN | 9676 | COSM142782, | skin | malignant_melanoma | p.Q143* | Substitution - Nonsense | 2:219302788-219302788, | PATHOGENIC | 0.96559 | 19074898 |
| PTPRN | 9676 | COSM142784, | skin | malignant_melanoma | p.G262E | Substitution - Missense | 2:219302346-219302346, | PATHOGENIC | 0.88813 | 19074898 |
| PTPRN | 9676 | COSM142783, | skin | malignant_melanoma | p.E202K | Substitution - Missense | 2:219302611-219302611, | PATHOGENIC | 0.87449 | 19074898 |
| PTPRN | 9676 | COSM142786, | skin | malignant_melanoma | p.G731E | Substitution - Missense | 2:219297029-219297029, | NEUTRAL | 0.16715 | 19074898 |
| PTPRN | 9676 | COSM142781, | skin | malignant_melanoma | p.R122P | Substitution - Missense | 2:219303747-219303747, | NEUTRAL | 0.02469 | 19074898 |
| PTPRN | 9676 | COSM142785, | skin | malignant_melanoma | p.S429F | Substitution - Missense | 2:219300135-219300135, | NEUTRAL | 0.01574 | 19074898 |
| PTPRN | 9676 | COSM308699, | lung | carcinoma | p.T866fs*35 | Insertion - Frameshift | 2:219295053-219295054, | Info_not_available | Info_not_available | 22941188 |
| PTPRN | 9676 | COSM142779, COSM142780, | skin | malignant_melanoma | p.G65R, p.P121S | Substitution - Missense | 2:219303751-219303751, 2:219307531-219307531, | Info_not_available | 0.56365, .59499 | 19074898 |