Primary Site >> Stomach Cancer
Gene >> OSR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297565 |
| Start | 98949266:98949266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.314T>A |
| AA Mutation | p.Val105Asp(p.V105D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297565 |
| Start | 98949476:98949476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.524A>C |
| AA Mutation | p.Lys175Thr(p.K175T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297565 |
| Start | 98949265:98949265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372847306 |
| CDS Mutation | c.313G>A |
| AA Mutation | p.Val105Ile(p.V105I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297565 |
| Start | 98949193:98949193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.241G>A |
| AA Mutation | p.Ala81Thr(p.A81T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297565 |
| Start | 98949432:98949432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.480T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297565 |
| Start | 98949318:98949318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs564255670 |
| CDS Mutation | c.366G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |