Primary Site >> Esophagus Cancer
Gene >> RET
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43105155:43105155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.829G>C |
| AA Mutation | p.Asp277His(p.D277H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43112898:43112898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1694G>T |
| AA Mutation | p.Cys565Phe(p.C565F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43105038:43105038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.712G>A |
| AA Mutation | p.Glu238Lys(p.E238K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43119682:43119682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2544G>C |
| AA Mutation | p.Met848Ile(p.M848I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355710 |
| Start | 43111377:43111377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1434T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355710 |
| Start | 43120129:43120129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2656C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355710 |
| Start | 43123767:43123767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373693875 |
| CDS Mutation | c.2898C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |