Primary Site >> Stomach Cancer
Gene >> MAGEA4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276344 |
| Start | 151924032:151924032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759710688 |
| CDS Mutation | c.368G>A |
| AA Mutation | p.Arg123His(p.R123H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276344 |
| Start | 151924406:151924406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.742A>G |
| AA Mutation | p.Thr248Ala(p.T248A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276344 |
| Start | 151923912:151923912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.248A>G |
| AA Mutation | p.Gln83Arg(p.Q83R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276344 |
| Start | 151924203:151924203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.539T>G |
| AA Mutation | p.Val180Gly(p.V180G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276344 |
| Start | 151924368:151924368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.704G>A |
| AA Mutation | p.Arg235Lys(p.R235K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276344 |
| Start | 151924411:151924411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.747A>C |
| AA Mutation | p.Gln249His(p.Q249H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276344 |
| Start | 151924395:151924395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.731G>T |
| AA Mutation | p.Arg244Met(p.R244M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000276344 |
| Start | 151923967:151923967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.303C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000276344 |
| Start | 151924306:151924306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376198310 |
| CDS Mutation | c.642C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |