Primary Site >> Esophagus Cancer
Gene >> AKT3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263826 |
| Start | 243512417:243512417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1261C>A |
| AA Mutation | p.Pro421Thr(p.P421T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263826 |
| Start | 243637719:243637719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.453G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | splice_acceptor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000263826 |
| Start | 243512421:243512454(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1252-28_1257delATAAAACTCTTTTTCTTTCTTTTTACAGCTTGTA |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |