Primary Site >> Liver Cancer
Gene >> SLCO5A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260126 |
| Start | 69672951:69672951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2465C>T |
| AA Mutation | p.Pro822Leu(p.P822L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260126 |
| Start | 69682260:69682260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1706T>C |
| AA Mutation | p.Val569Ala(p.V569A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260126 |
| Start | 69679562:69679562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1840A>T |
| AA Mutation | p.Thr614Ser(p.T614S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260126 |
| Start | 69679387:69679387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2015T>A |
| AA Mutation | p.Val672Glu(p.V672E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260126 |
| Start | 69679583:69679583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765107213 |
| CDS Mutation | c.1819C>T |
| AA Mutation | p.Arg607Cys(p.R607C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260126 |
| Start | 69832624:69832624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369685189 |
| CDS Mutation | c.50C>T |
| AA Mutation | p.Ala17Val(p.A17V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260126 |
| Start | 69761856:69761856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.927A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260126 |
| Start | 69832482:69832482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.192G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |