Primary Site >> Stomach Cancer
Gene >> ZHX1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297857 |
| Start | 123255364:123255364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369013427 |
| CDS Mutation | c.583C>T |
| AA Mutation | p.Arg195Trp(p.R195W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297857 |
| Start | 123253780:123253780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2167T>C |
| AA Mutation | p.Tyr723His(p.Y723H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297857 |
| Start | 123253350:123253350(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780185709 |
| CDS Mutation | c.2597G>A |
| AA Mutation | p.Arg866Gln(p.R866Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297857 |
| Start | 123255081:123255081(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.866A>G |
| AA Mutation | p.Tyr289Cys(p.Y289C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297857 |
| Start | 123254403:123254403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1544C>T |
| AA Mutation | p.Thr515Ile(p.T515I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297857 |
| Start | 123255294:123255294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372444054 |
| CDS Mutation | c.653G>A |
| AA Mutation | p.Arg218His(p.R218H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297857 |
| Start | 123255363:123255363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746535667 |
| CDS Mutation | c.584G>A |
| AA Mutation | p.Arg195Gln(p.R195Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297857 |
| Start | 123254769:123254769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1178A>G |
| AA Mutation | p.Gln393Arg(p.Q393R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297857 |
| Start | 123255332:123255332(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750741810 |
| CDS Mutation | c.615C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297857 |
| Start | 123253477:123253477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2470A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000297857 |
| Start | 123253819:123253819(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2128delG |
| AA Mutation | p.Asp710ThrfsTer11(p.D710Tfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000297857 |
| Start | 123253363:123253363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2584C>T |
| AA Mutation | p.Arg862Ter(p.R862*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |