Primary Site >> Liver Cancer
Gene >> TGFBRAP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258449 |
| Start | 105298522:105298522(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.872A>C |
| AA Mutation | p.Gln291Pro(p.Q291P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258449 |
| Start | 105307958:105307958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.344G>T |
| AA Mutation | p.Arg115Leu(p.R115L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258449 |
| Start | 105269628:105269628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2050C>T |
| AA Mutation | p.His684Tyr(p.H684Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258449 |
| Start | 105307791:105307791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.511C>G |
| AA Mutation | p.Leu171Val(p.L171V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258449 |
| Start | 105275623:105275623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1602C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258449 |
| Start | 105273628:105273628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1728A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258449 |
| Start | 105269440:105269440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763610405 |
| CDS Mutation | c.2238C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |