Primary Site >> Stomach Cancer
Gene >> RRH
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317735 |
| Start | 109835433:109835433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.365A>G |
| AA Mutation | p.Asp122Gly(p.D122G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317735 |
| Start | 109833284:109833284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.252C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317735 |
| Start | 109835422:109835422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373432160 |
| CDS Mutation | c.354C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317735 |
| Start | 109836086:109836086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.477T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317735 |
| Start | 109835461:109835461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762940459 |
| CDS Mutation | c.393C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000317735 |
| Start | 109835385:109835385(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs780263253 |
| CDS Mutation | c.324delT |
| AA Mutation | p.Phe108LeufsTer18(p.F108Lfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |