Primary Site >> Esophagus Cancer
Gene >> SPHKAP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392056 |
| Start | 228019749:228019749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1105G>A |
| AA Mutation | p.Gly369Arg(p.G369R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392056 |
| Start | 228018632:228018632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755469563 |
| CDS Mutation | c.2222C>T |
| AA Mutation | p.Thr741Ile(p.T741I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392056 |
| Start | 228017724:228017724(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3130G>T |
| AA Mutation | p.Ala1044Ser(p.A1044S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392056 |
| Start | 228132049:228132049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.69A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392056 |
| Start | 228018283:228018283(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533054194 |
| CDS Mutation | c.2571C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392056 |
| Start | 228018616:228018616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2238G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392056 |
| Start | 227995532:227995532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4611C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392056 |
| Start | 227993587:227993587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs528902743 |
| CDS Mutation | c.4668C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |