Primary Site >> Stomach Cancer
Gene >> ABCB6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265316 |
| Start | 219210264:219210264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753788507 |
| CDS Mutation | c.2386G>A |
| AA Mutation | p.Val796Ile(p.V796I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265316 |
| Start | 219210261:219210261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201123852 |
| CDS Mutation | c.2389A>G |
| AA Mutation | p.Ile797Val(p.I797V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265316 |
| Start | 219211014:219211014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757264353 |
| CDS Mutation | c.2063G>A |
| AA Mutation | p.Arg688His(p.R688H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265316 |
| Start | 219213639:219213639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1606T>C |
| AA Mutation | p.Tyr536His(p.Y536H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265316 |
| Start | 219213855:219213855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs532805022 |
| CDS Mutation | c.1549G>A |
| AA Mutation | p.Ala517Thr(p.A517T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265316 |
| Start | 219218353:219218353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.321A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265316 |
| Start | 219210804:219210804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145427690 |
| CDS Mutation | c.2163C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265316 |
| Start | 219216032:219216032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752219177 |
| CDS Mutation | c.1119G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265316 |
| Start | 219216381:219216381(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs777439793 |
| CDS Mutation | c.953delG |
| AA Mutation | p.Gly318ValfsTer9(p.G318Vfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |