Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score![]() | Literature evidence |
MTMR8 | 16825 | COSM32551, | breast | carcinoma | p.W127R | Substitution - Missense | 23:64354866-64354866, | PATHOGENIC | 0.98885 | 16959974 |
MTMR8 | 16825 | COSM33057, | breast | carcinoma | p.E454K | Substitution - Missense | 23:64328893-64328893, | PATHOGENIC | 0.82554 | 16959974 |
MTMR8 | 16825 | COSM142826, | skin | malignant_melanoma | p.A104T | Substitution - Missense | 23:64356176-64356176, | PATHOGENIC | 0.73623 | 19074898 |
MTMR8 | 16825 | COSM5009885, | large_intestine | carcinoma | p.G574A | Substitution - Missense | 23:64268931-64268931, | NEUTRAL | 0.40782 | 24951259 |
MTMR8 | 16825 | COSM144678, | haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm | p.G574D | Substitution - Missense | 23:64268931-64268931, | NEUTRAL | 0.20899 | 21804550 |
MTMR8 | 16825 | COSM5008093, | large_intestine | carcinoma | p.I690T | Substitution - Missense | 23:64268583-64268583, | NEUTRAL | 0.04793 | 24951259 |
MTMR8 | 16825 | COSM142827, | skin | malignant_melanoma | p.S701F | Substitution - Missense | 23:64268550-64268550, | NEUTRAL | 0.02955 | 19074898 |
MTMR8 | 16825 | COSM5752043, | haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm | p.S458fs*19 | Insertion - Frameshift | 23:64328881-64328882, | Info_not_available | Info_not_available | 26206799 |