Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score![]() | Literature evidence |
TPTE2 | 17299 | COSM2264906, | oesophagus | carcinoma | p.R174W | Substitution - Missense | 13:19451216-19451216, | NEUTRAL | 0.45231 | 24686850 |
TPTE2 | 17299 | COSM5048670, | oesophagus | carcinoma | p.P68H | Substitution - Missense | 13:19473992-19473992, | NEUTRAL | 0.04951 | 24686850 |
TPTE2 | 17299 | COSM316107, | lung | carcinoma | p.S328S | Substitution - coding silent | 13:19432480-19432480, | NEUTRAL | 0.01953 | 22941188 |