Primary Site >> Stomach Cancer
Gene >> SLCO1B1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256958 |
| Start | 21178590:21178590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751041337 |
| CDS Mutation | c.496T>C |
| AA Mutation | p.Ser166Pro(p.S166P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256958 |
| Start | 21239149:21239149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2036T>G |
| AA Mutation | p.Phe679Cys(p.F679C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256958 |
| Start | 21172698:21172698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs555367334 |
| CDS Mutation | c.133G>A |
| AA Mutation | p.Ala45Thr(p.A45T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256958 |
| Start | 21239050:21239050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1937C>T |
| AA Mutation | p.Ala646Val(p.A646V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256958 |
| Start | 21202526:21202526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1171T>C |
| AA Mutation | p.Phe391Leu(p.F391L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256958 |
| Start | 21239148:21239148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2035T>G |
| AA Mutation | p.Phe679Val(p.F679V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256958 |
| Start | 21224763:21224763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1789A>G |
| AA Mutation | p.Thr597Ala(p.T597A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256958 |
| Start | 21217219:21217219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1598A>C |
| AA Mutation | p.Lys533Thr(p.K533T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256958 |
| Start | 21172734:21172734(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139257324 |
| CDS Mutation | c.169C>T |
| AA Mutation | p.Arg57Trp(p.R57W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256958 |
| Start | 21202548:21202548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1193A>C |
| AA Mutation | p.Lys398Thr(p.K398T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256958 |
| Start | 21178709:21178709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.615T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256958 |
| Start | 21172775:21172775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148697674 |
| CDS Mutation | c.210C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000256958 |
| Start | 21224748:21224748(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1777delG |
| AA Mutation | p.Ala593LeufsTer2(p.A593Lfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000256958 |
| Start | 21197078:21197078(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.864delA |
| AA Mutation | p.Glu289LysfsTer23(p.E289Kfs*23) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |