Primary Site >> Stomach Cancer
Gene >> TBX1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329705 |
| Start | 19764992:19764992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.719G>A |
| AA Mutation | p.Arg240His(p.R240H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329705 |
| Start | 19779397:19779397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs207477905 |
| CDS Mutation | c.1187G>A |
| AA Mutation | p.Arg396His(p.R396H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329705 |
| Start | 19779368:19779368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1158C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329705 |
| Start | 19765068:19765068(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763559631 |
| CDS Mutation | c.795C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329705 |
| Start | 19764999:19764999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201412495 |
| CDS Mutation | c.726C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329705 |
| Start | 19761170:19761170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755146299 |
| CDS Mutation | c.300G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |