Primary Site >> Stomach Cancer
Gene >> KHSRP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398148 |
| Start | 6417757:6417757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1063C>T |
| AA Mutation | p.Arg355Trp(p.R355W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398148 |
| Start | 6418511:6418511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.851G>A |
| AA Mutation | p.Arg284His(p.R284H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398148 |
| Start | 6415384:6415384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1962G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398148 |
| Start | 6417044:6417044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1125C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398148 |
| Start | 6416493:6416493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769685889 |
| CDS Mutation | c.1485C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398148 |
| Start | 6422383:6422383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.303T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |