Primary Site >> Stomach Cancer
Gene >> HOXA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343060 |
| Start | 27094589:27094589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.859C>T |
| AA Mutation | p.Arg287Cys(p.R287C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343060 |
| Start | 27095393:27095393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.520G>T |
| AA Mutation | p.Ala174Ser(p.A174S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343060 |
| Start | 27095822:27095822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762135120 |
| CDS Mutation | c.91G>A |
| AA Mutation | p.Asp31Asn(p.D31N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343060 |
| Start | 27095767:27095767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.146G>A |
| AA Mutation | p.Gly49Asp(p.G49D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343060 |
| Start | 27094751:27094751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.697C>T |
| AA Mutation | p.Arg233Cys(p.R233C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343060 |
| Start | 27094679:27094679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749684801 |
| CDS Mutation | c.769G>A |
| AA Mutation | p.Ala257Thr(p.A257T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |