Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
NT5M | 15769 | COSM3717205, | liver | carcinoma | p.R226W | Substitution - Missense | 17:17346936-17346936, | PATHOGENIC | 0.95506 | Info_not_available |