Primary Site >> Stomach Cancer
Gene >> MAEA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303400 |
| Start | 1322394:1322394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.470T>C |
| AA Mutation | p.Ile157Thr(p.I157T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303400 |
| Start | 1332810:1332810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.710G>A |
| AA Mutation | p.Arg237His(p.R237H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303400 |
| Start | 1322385:1322385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.461T>C |
| AA Mutation | p.Leu154Pro(p.L154P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303400 |
| Start | 1338513:1338513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.991G>A |
| AA Mutation | p.Ala331Thr(p.A331T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303400 |
| Start | 1327696:1327696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.649G>A |
| AA Mutation | p.Ala217Thr(p.A217T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000303400 |
| Start | 1312033:1312033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.124C>T |
| AA Mutation | p.Arg42Trp(p.R42W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303400 |
| Start | 1336956:1336956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.861C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000303400 |
| Start | 1315417:1315417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142517889 |
| CDS Mutation | c.273C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |