Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score![]() | Literature evidence |
CTNND1 | 2515 | COSM5049191, | oesophagus | carcinoma | p.L41V | Substitution - Missense | 11:57791599-57791599, | PATHOGENIC | 0.97607 | 24686850 |
CTNND1 | 2515 | COSM24302, | breast | carcinoma | p.L85L | Substitution - coding silent | 11:57794069-57794069, | PATHOGENIC | 0.92334 | 17932254 |
CTNND1 | 2515 | COSM24303, | breast | carcinoma | p.P361T | Substitution - Missense | 11:57801857-57801857, | NEUTRAL | 0.17932 | 17932254 |
CTNND1 | 2515 | COSM1166626, | haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm | p.E138fs*11 | Insertion - Frameshift | 11:57795719-57795720, | Info_not_available | Info_not_available | 22976956 |