Primary Site >> Esophagus Cancer
Gene >> DTL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366991 |
| Start | 212068246:212068246(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.736C>T |
| AA Mutation | p.Arg246Cys(p.R246C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366991 |
| Start | 212080703:212080703(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1214C>T |
| AA Mutation | p.Thr405Met(p.T405M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366991 |
| Start | 212101026:212101026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2036G>A |
| AA Mutation | p.Ser679Asn(p.S679N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000366991 |
| Start | 212080652:212080703(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1165_1216delCGCTTGAATAGAGGCTTAGAGGAGAAACCAGGAGGTGATAAACTTTCCACGG |
| AA Mutation | p.Arg389TrpfsTer15(p.R389Wfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |