Primary Site >> Stomach Cancer
Gene >> SLC2A9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264784 |
| Start | 9985693:9985693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776127501 |
| CDS Mutation | c.511C>T |
| AA Mutation | p.Arg171Cys(p.R171C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264784 |
| Start | 9941957:9941957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367643471 |
| CDS Mutation | c.770G>A |
| AA Mutation | p.Arg257His(p.R257H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264784 |
| Start | 9908264:9908264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1084G>A |
| AA Mutation | p.Gly362Ser(p.G362S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264784 |
| Start | 9834931:9834931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200305429 |
| CDS Mutation | c.1369G>A |
| AA Mutation | p.Val457Ile(p.V457I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264784 |
| Start | 10021333:10021333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.97C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264784 |
| Start | 9834998:9834998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556085300 |
| CDS Mutation | c.1302G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264784 |
| Start | 10021391:10021391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372879673 |
| CDS Mutation | c.39C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |