Primary Site >> Stomach Cancer
Gene >> TMPO
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266732 |
| Start | 98534085:98534085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369379490 |
| CDS Mutation | c.1828C>T |
| AA Mutation | p.Arg610Cys(p.R610C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266732 |
| Start | 98534032:98534032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1775C>A |
| AA Mutation | p.Ala592Asp(p.A592D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266732 |
| Start | 98533044:98533044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.787G>T |
| AA Mutation | p.Gly263Cys(p.G263C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266732 |
| Start | 98533620:98533620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763388598 |
| CDS Mutation | c.1363G>A |
| AA Mutation | p.Glu455Lys(p.E455K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266732 |
| Start | 98533294:98533294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs561767716 |
| CDS Mutation | c.1037A>G |
| AA Mutation | p.His346Arg(p.H346R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266732 |
| Start | 98534205:98534205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772424658 |
| CDS Mutation | c.1948C>T |
| AA Mutation | p.Arg650Cys(p.R650C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266732 |
| Start | 98516030:98516030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.163G>A |
| AA Mutation | p.Ala55Thr(p.A55T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266732 |
| Start | 98533129:98533129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.872G>A |
| AA Mutation | p.Ser291Asn(p.S291N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000556029 |
| Start | 98544290:98544290(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.724C>T |
| AA Mutation | p.Pro242Ser(p.P242S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000266732 |
| Start | 98533619:98533619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371731646 |
| CDS Mutation | c.1362C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000266732 |
| Start | 98527987:98527987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370093524 |
| CDS Mutation | c.381C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000266732 |
| Start | 98534336:98534336(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2079A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000266732 |
| Start | 98533781:98533781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1524A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000266732 |
| Start | 98533013:98533013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.756T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000266732 |
| Start | 98527894:98527894(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs774744805 |
| CDS Mutation | c.295delA |
| AA Mutation | p.Thr99LeufsTer12(p.T99Lfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |