Primary Site >> Esophagus Cancer
Gene >> RICTOR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357387 |
| Start | 38945505:38945505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4619T>A |
| AA Mutation | p.Ile1540Lys(p.I1540K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357387 |
| Start | 38950333:38950333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3515C>T |
| AA Mutation | p.Thr1172Ile(p.T1172I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357387 |
| Start | 38990987:38990987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.545G>T |
| AA Mutation | p.Arg182Ile(p.R182I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357387 |
| Start | 38944919:38944919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4783T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000357387 |
| Start | 38942858:38942858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5027T>G |
| AA Mutation | p.Leu1676Ter(p.L1676*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000357387 |
| Start | 38953010:38953011(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2871dupA |
| AA Mutation | p.Gln958ThrfsTer3(p.Q958Tfs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |