Primary Site >> Stomach Cancer
Gene >> DRAM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258534 |
| Start | 101901359:101901359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.268C>T |
| AA Mutation | p.Pro90Ser(p.P90S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258534 |
| Start | 101908219:101908219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751719297 |
| CDS Mutation | c.376G>A |
| AA Mutation | p.Ala126Thr(p.A126T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258534 |
| Start | 101901321:101901321(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.230T>C |
| AA Mutation | p.Ile77Thr(p.I77T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258534 |
| Start | 101908258:101908258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.415C>A |
| AA Mutation | p.Leu139Ile(p.L139I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258534 |
| Start | 101908246:101908246(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748500198 |
| CDS Mutation | c.403G>A |
| AA Mutation | p.Val135Met(p.V135M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258534 |
| Start | 101920162:101920162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.633T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258534 |
| Start | 101908212:101908212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs528322922 |
| CDS Mutation | c.369C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |