Primary Site >> Esophagus Cancer
Gene >> TNFRSF12A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326577 |
| Start | 3021774:3021774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.338C>T |
| AA Mutation | p.Pro113Leu(p.P113L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |