Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
DSTN | 15750 | COSM33163, | large_intestine | carcinoma | p.G139E | Substitution - Missense | 20:17607064-17607064, | PATHOGENIC | 0.96978 | 16959974 |