Primary Site >> Esophagus Cancer
Gene >> TAP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374897 |
| Start | 32829954:32829954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1771G>A |
| AA Mutation | p.Glu591Lys(p.E591K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |