Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
ICK | 21219 | COSM5576200, | stomach | carcinoma | p.A485S | Substitution - Missense | 6:53011808-53011808, | PATHOGENIC | 0.9961 | 26489445 |
ICK | 21219 | COSM20755, | kidney | carcinoma | p.F115Y | Substitution - Missense | 6:53031079-53031079, | PATHOGENIC | 0.96979 | 20054297 |
ICK | 21219 | COSM20755, | kidney | carcinoma | p.F115Y | Substitution - Missense | 6:53031079-53031079, | PATHOGENIC | 0.96979 | 20054297 |
ICK | 21219 | COSM13330, | central_nervous_system | glioma | p.A185A | Substitution - coding silent | 6:53018438-53018438, | NEUTRAL | 0.0228 | 16618716 |
ICK | 21219 | COSM13330, | central_nervous_system | glioma | p.A185A | Substitution - coding silent | 6:53018438-53018438, | NEUTRAL | 0.0228 | 16618716 |
ICK | 21219 | COSM20460, | large_intestine | carcinoma | p.Y349fs*49 | Deletion - Frameshift | 6:53013770-53013770, | Info_not_available | Info_not_available | Info_not_available |