| Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
| ACLY | 115 | COSM39766, | central_nervous_system | glioma | p.S525A | Substitution - Missense | 17:41893061-41893061, | PATHOGENIC | 0.9947 | 18772396 |
| ACLY | 115 | COSM3717363, | liver | carcinoma | p.A1000V | Substitution - Missense | 17:41869526-41869526, | PATHOGENIC | 0.96964 | Info_not_available |
| ACLY | 115 | COSM5028298, | breast | carcinoma | p.F197F | Substitution - coding silent | 17:41909014-41909014, | PATHOGENIC | 0.93564 | 22722193 |
| ACLY | 115 | COSM1610253, | liver | carcinoma | p.A1000S | Substitution - Missense | 17:41869527-41869527, | PATHOGENIC | 0.86505 | Info_not_available |