Primary Site >> Stomach Cancer
Gene >> OTOR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246081 |
| Start | 16748430:16748430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373345936 |
| CDS Mutation | c.29C>T |
| AA Mutation | p.Pro10Leu(p.P10L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246081 |
| Start | 16748475:16748475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756618856 |
| CDS Mutation | c.74G>A |
| AA Mutation | p.Arg25His(p.R25H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246081 |
| Start | 16748929:16748929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.178G>A |
| AA Mutation | p.Val60Ile(p.V60I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246081 |
| Start | 16748908:16748908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.157C>A |
| AA Mutation | p.Pro53Thr(p.P53T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000246081 |
| Start | 16749974:16749974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.327T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000246081 |
| Start | 16748431:16748431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772958651 |
| CDS Mutation | c.30G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |