Primary Site >> Stomach Cancer
Gene >> ACKR3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272928 |
| Start | 236581360:236581360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.895G>A |
| AA Mutation | p.Val299Ile(p.V299I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272928 |
| Start | 236580691:236580691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.226G>T |
| AA Mutation | p.Gly76Cys(p.G76C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272928 |
| Start | 236581237:236581237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.772G>A |
| AA Mutation | p.Val258Met(p.V258M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272928 |
| Start | 236581055:236581055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776743438 |
| CDS Mutation | c.590G>A |
| AA Mutation | p.Arg197Gln(p.R197Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272928 |
| Start | 236580988:236580988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147358005 |
| CDS Mutation | c.523G>A |
| AA Mutation | p.Val175Met(p.V175M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272928 |
| Start | 236581150:236581150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200775693 |
| CDS Mutation | c.685G>A |
| AA Mutation | p.Ala229Thr(p.A229T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000272928 |
| Start | 236580813:236580813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs528077974 |
| CDS Mutation | c.348G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000272928 |
| Start | 236580546:236580546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767699327 |
| CDS Mutation | c.81C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000272928 |
| Start | 236581254:236581254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.789C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000272928 |
| Start | 236580663:236580663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.198C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000272928 |
| Start | 236580804:236580804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762709549 |
| CDS Mutation | c.339C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000272928 |
| Start | 236581032:236581032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139490851 |
| CDS Mutation | c.567G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000272928 |
| Start | 236580603:236580603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375172239 |
| CDS Mutation | c.138G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |