Primary Site >> Liver Cancer
Gene >> PI4KA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255882 |
| Start | 20744698:20744698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3386C>T |
| AA Mutation | p.Pro1129Leu(p.P1129L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255882 |
| Start | 20710845:20710845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5937G>A |
| AA Mutation | p.Met1979Ile(p.M1979I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255882 |
| Start | 20712538:20712538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5750A>G |
| AA Mutation | p.Tyr1917Cys(p.Y1917C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255882 |
| Start | 20711446:20711446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5818A>T |
| AA Mutation | p.Ile1940Phe(p.I1940F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255882 |
| Start | 20807401:20807401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1129A>G |
| AA Mutation | p.Met377Val(p.M377V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255882 |
| Start | 20799189:20799189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1908C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255882 |
| Start | 20813493:20813493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146943439 |
| CDS Mutation | c.870C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |