Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
CSE1L | 2431 | COSM32993, | large_intestine | carcinoma | p.C842F | Substitution - Missense | 20:49094217-49094217, | PATHOGENIC | 0.99365 | 16959974 |