Primary Site >> Stomach Cancer
Gene >> TFRC
| ID | 1 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360110 |
| Start | 196065540:196065540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1101C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360110 |
| Start | 196062914:196062914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1344T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360110 |
| Start | 196065528:196065528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1113G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360110 |
| Start | 196060204:196060204(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747811597 |
| CDS Mutation | c.1512G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360110 |
| Start | 196073989:196073989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.375T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360110 |
| Start | 196071465:196071465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769020607 |
| CDS Mutation | c.618C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |