Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
PTPRF | 9670 | COSM4605137, | upper_aerodigestive_tract | carcinoma | p.D1098A | Substitution - Missense | 1:43605347-43605347, | PATHOGENIC | 0.99717 | 25056374 |
PTPRF | 9670 | COSM4605137, | upper_aerodigestive_tract | carcinoma | p.D1098A | Substitution - Missense | 1:43605347-43605347, | PATHOGENIC | 0.99717 | 25056374 |
PTPRF | 9670 | COSM6848004, | pleura | mesothelioma | p.Y1405C | Substitution - Missense | 1:43617754-43617754, | PATHOGENIC | 0.99551 | 26928227 |
PTPRF | 9670 | COSM6848006, | pleura | mesothelioma | p.P1292L | Substitution - Missense | 1:43609400-43609400, | PATHOGENIC | 0.99515 | 26928227 |
PTPRF | 9670 | COSM1581562, | haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm | p.V1636M | Substitution - Missense | 1:43619547-43619547, | PATHOGENIC | 0.95976 | 23292937 |
PTPRF | 9670 | COSM4604924, | upper_aerodigestive_tract | carcinoma | p.I889M | Substitution - Missense | 1:43603819-43603819, | PATHOGENIC | 0.95749 | 25056374 |
PTPRF | 9670 | COSM40517, | central_nervous_system | glioma | p.W683* | Substitution - Nonsense | 1:43597983-43597983, | PATHOGENIC | 0.91029 | 18772396 |
PTPRF | 9670 | COSM4605451, | upper_aerodigestive_tract | carcinoma | p.E1571E | Substitution - coding silent | 1:43619354-43619354, | PATHOGENIC | 0.88233 | 25056374 |
PTPRF | 9670 | COSM27006, | kidney | renal_cell_carcinoma | p.R1182H | Substitution - Missense | 1:43606301-43606301, | NEUTRAL | 0.35891 | 20054297 |
PTPRF | 9670 | COSM6848138, | pleura | mesothelioma | p.F1493L | Substitution - Missense | 1:43618737-43618737, | NEUTRAL | 0.18301 | 26928227 |
PTPRF | 9670 | COSM5025257, | breast | carcinoma | p.V638I | Substitution - Missense | 1:43597846-43597846, | NEUTRAL | 0.08608 | 22722193 |