Primary Site >> Stomach Cancer
Gene >> TAX1BP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396319 |
| Start | 27785484:27785484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.847T>C |
| AA Mutation | p.Tyr283His(p.Y283H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396319 |
| Start | 27792067:27792067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748509003 |
| CDS Mutation | c.1100G>A |
| AA Mutation | p.Arg367Gln(p.R367Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396319 |
| Start | 27792087:27792087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1120G>A |
| AA Mutation | p.Ala374Thr(p.A374T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396319 |
| Start | 27800086:27800086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1760A>G |
| AA Mutation | p.Tyr587Cys(p.Y587C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396319 |
| Start | 27793127:27793127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1325T>G |
| AA Mutation | p.Leu442Arg(p.L442R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396319 |
| Start | 27765884:27765884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.316A>G |
| AA Mutation | p.Thr106Ala(p.T106A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396319 |
| Start | 27816376:27816376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1792G>A |
| AA Mutation | p.Ala598Thr(p.A598T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396319 |
| Start | 27785408:27785408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.771C>A |
| AA Mutation | p.Asp257Glu(p.D257E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396319 |
| Start | 27793074:27793074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1272T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396319 |
| Start | 27785300:27785300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139970643 |
| CDS Mutation | c.750C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |