| Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
| MAP3K7 | 6859 | COSM98927, | stomach | carcinoma | p.G317C | Substitution - Missense | 6:90550468-90550468, | PATHOGENIC | 0.99414 | 21097718 |
| MAP3K7 | 6859 | COSM4992786, | skin | carcinoma | p.F496L | Substitution - Missense | 6:90518520-90518520, | PATHOGENIC | 0.9912 | 25589618 |
| MAP3K7 | 6859 | COSM95717, | lung | carcinoma | p.? | Unknown | 6:90553587-90553587, | PATHOGENIC | 0.99098 | 20668451 |
| MAP3K7 | 6859 | COSM34217, | salivary_gland | carcinoma | p.R83C | Substitution - Missense | 6:90568608-90568608, | PATHOGENIC | 0.9878 | Info_not_available |
| MAP3K7 | 6859 | COSM34217, | salivary_gland | carcinoma | p.R83C | Substitution - Missense | 6:90568608-90568608, | PATHOGENIC | 0.9878 | 23778141 |
| MAP3K7 | 6859 | COSM94667, | lung | carcinoma | p.N463S | Substitution - Missense | 6:90519313-90519313, | PATHOGENIC | 0.98168 | 20668451 |
| MAP3K7 | 6859 | COSM4992789, | skin | carcinoma | p.R372C | Substitution - Missense | 6:90547354-90547354, | PATHOGENIC | 0.98079 | 25589618 |
| MAP3K7 | 6859 | COSM4700407, | skin | carcinoma | p.S14delS | Deletion - In frame | 6:90586849-90586851, | Info_not_available | Info_not_available | 25589618 |