Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
CAD | 1424 | COSM30457, | kidney | carcinoma | p.V1263L | Substitution - Missense | 2:27235245-27235245, | PATHOGENIC | 0.99864 | 20054297 |
CAD | 1424 | COSM1614726, | liver | carcinoma | p.E1006* | Substitution - Nonsense | 2:27233336-27233336, | PATHOGENIC | 0.99858 | Info_not_available |
CAD | 1424 | COSM33070, | large_intestine | carcinoma | p.Y735C | Substitution - Missense | 2:27226879-27226879, | PATHOGENIC | 0.9888 | 16959974 |
CAD | 1424 | COSM249461, | kidney | carcinoma | p.T430M | Substitution - Missense | 2:27224779-27224779, | PATHOGENIC | 0.98758 | 22138691 |
CAD | 1424 | COSM1580640, | haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm | p.P859L | Substitution - Missense | 2:27232155-27232155, | PATHOGENIC | 0.96289 | 23292937 |
CAD | 1424 | COSM1580640, | haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm | p.P859L | Substitution - Missense | 2:27232155-27232155, | PATHOGENIC | 0.96289 | 23292937 |
CAD | 1424 | COSM309822, | lung | carcinoma | p.L881L | Substitution - coding silent | 2:27232222-27232222, | PATHOGENIC | 0.95566 | 22941188 |
CAD | 1424 | COSM33368, | large_intestine | carcinoma | p.R177Q | Substitution - Missense | 2:27222553-27222553, | PATHOGENIC | 0.94907 | 16959974 |
CAD | 1424 | COSM1614725, | liver | carcinoma | p.V783V | Substitution - coding silent | 2:27231529-27231529, | PATHOGENIC | 0.94771 | Info_not_available |
CAD | 1424 | COSM30460, | kidney | carcinoma | p.K358fs*16 | Deletion - Frameshift | 2:27223994-27223997, | Info_not_available | Info_not_available | 20054297 |