Primary Site >> Stomach Cancer
Gene >> GTPBP3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324894 |
| Start | 17339553:17339553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.928G>A |
| AA Mutation | p.Gly310Ser(p.G310S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324894 |
| Start | 17341601:17341601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1377G>T |
| AA Mutation | p.Glu459Asp(p.E459D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324894 |
| Start | 17339559:17339559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.934G>A |
| AA Mutation | p.Gly312Arg(p.G312R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324894 |
| Start | 17338124:17338124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.170C>G |
| AA Mutation | p.Ala57Gly(p.A57G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000324894 |
| Start | 17339436:17339436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.811C>T |
| AA Mutation | p.Arg271Trp(p.R271W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324894 |
| Start | 17339536:17339536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.911C>T |
| AA Mutation | p.Thr304Met(p.T304M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324894 |
| Start | 17338987:17338987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.625G>A |
| AA Mutation | p.Gly209Ser(p.G209S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324894 |
| Start | 17338579:17338579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145625259 |
| CDS Mutation | c.429C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324894 |
| Start | 17338040:17338040(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.90delC |
| AA Mutation | p.Gly31AlafsTer9(p.G31Afs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |