Primary Site >> Liver Cancer
Gene >> NCOA6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359003 |
| Start | 34741265:34741265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4991C>A |
| AA Mutation | p.Ser1664Tyr(p.S1664Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359003 |
| Start | 34740554:34740554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5702C>G |
| AA Mutation | p.Ala1901Gly(p.A1901G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359003 |
| Start | 34757492:34757492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1256A>T |
| AA Mutation | p.Gln419Leu(p.Q419L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359003 |
| Start | 34782241:34782241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.115A>G |
| AA Mutation | p.Ser39Gly(p.S39G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359003 |
| Start | 34741484:34741484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4772C>T |
| AA Mutation | p.Pro1591Leu(p.P1591L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359003 |
| Start | 34749552:34749552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147990465 |
| CDS Mutation | c.2643G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |