Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score![]() | Literature evidence |
ENOPH1 | 24599 | COSM304868, | large_intestine | carcinoma | p.R143K | Substitution - Missense | 4:82454760-82454760, | PATHOGENIC | 0.97378 | 21892161 |