Primary Site >> Stomach Cancer
Gene >> GNAO1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262493 |
| Start | 56192267:56192267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.32C>T |
| AA Mutation | p.Ala11Val(p.A11V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000262493 |
| Start | 56276071:56276071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.302A>G |
| AA Mutation | p.Lys101Arg(p.K101R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262493 |
| Start | 56328709:56328709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.382A>G |
| AA Mutation | p.Met128Val(p.M128V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262493 |
| Start | 56328741:56328741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141057479 |
| CDS Mutation | c.414A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262493 |
| Start | 56328726:56328726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556058539 |
| CDS Mutation | c.399C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262493 |
| Start | 56351434:56351434(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.774G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |