Primary Site >> Stomach Cancer
Gene >> HOXA9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343483 |
| Start | 27165184:27165184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.274G>A |
| AA Mutation | p.Val92Met(p.V92M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343483 |
| Start | 27165105:27165105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.353C>T |
| AA Mutation | p.Ala118Val(p.A118V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343483 |
| Start | 27163762:27163762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.660A>T |
| AA Mutation | p.Glu220Asp(p.E220D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343483 |
| Start | 27165375:27165375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.83G>A |
| AA Mutation | p.Gly28Asp(p.G28D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343483 |
| Start | 27165059:27165059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.399A>C |
| AA Mutation | p.Lys133Asn(p.K133N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343483 |
| Start | 27163718:27163718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777202871 |
| CDS Mutation | c.704G>A |
| AA Mutation | p.Arg235His(p.R235H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |