Primary Site >> Stomach Cancer
Gene >> NOX5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000388866 |
| Start | 69038879:69038879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs117880022 |
| CDS Mutation | c.1394G>A |
| AA Mutation | p.Arg465Gln(p.R465Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000388866 |
| Start | 69035407:69035407(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.909A>C |
| AA Mutation | p.Gln303His(p.Q303H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000388866 |
| Start | 69037164:69037164(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373906925 |
| CDS Mutation | c.1325G>A |
| AA Mutation | p.Arg442His(p.R442H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000388866 |
| Start | 69055468:69055468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767570585 |
| CDS Mutation | c.2134C>T |
| AA Mutation | p.Arg712Cys(p.R712C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000388866 |
| Start | 69042747:69042747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140448769 |
| CDS Mutation | c.1589G>A |
| AA Mutation | p.Arg530His(p.R530H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000388866 |
| Start | 69046854:69046854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1680C>A |
| AA Mutation | p.Phe560Leu(p.F560L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000388866 |
| Start | 69035916:69035916(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773013901 |
| CDS Mutation | c.1168C>T |
| AA Mutation | p.Arg390Cys(p.R390C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000388866 |
| Start | 69056575:69056575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2177A>C |
| AA Mutation | p.Lys726Thr(p.K726T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000388866 |
| Start | 69047510:69047510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1790C>T |
| AA Mutation | p.Ala597Val(p.A597V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000388866 |
| Start | 69042694:69042694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1536C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000388866 |
| Start | 69031696:69031696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.504G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000388866 |
| Start | 69047472:69047472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774041090 |
| CDS Mutation | c.1752C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |