Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score![]() | Literature evidence |
LYN | 6735 | COSM4993128, | skin | carcinoma | p.D189N | Substitution - Missense | 8:55952043-55952043, | PATHOGENIC | 0.9951 | 25589618 |
LYN | 6735 | COSM4993129, | skin | carcinoma | p.S283F | Substitution - Missense | 8:55966772-55966772, | PATHOGENIC | 0.99384 | 25589618 |
LYN | 6735 | COSM605, | breast | carcinoma | p.D385Y | Substitution - Missense | 8:55998448-55998448, | PATHOGENIC | 0.99169 | 15908952 |
LYN | 6735 | COSM4993127, | skin | carcinoma | p.G2R | Substitution - Missense | 8:55941863-55941863, | PATHOGENIC | 0.97551 | 25589618 |
LYN | 6735 | COSM4419041, | soft_tissue | haemangioblastoma | p.K233K | Substitution - coding silent | 8:55953893-55953893, | PATHOGENIC | 0.82321 | 25589003 |