Primary Site >> Esophagus Cancer
Gene >> BCL9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234739 |
| Start | 147614454:147614454(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.398C>T |
| AA Mutation | p.Ser133Phe(p.S133F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234739 |
| Start | 147619974:147619974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1819C>G |
| AA Mutation | p.Pro607Ala(p.P607A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234739 |
| Start | 147624422:147624422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782211226 |
| CDS Mutation | c.3744G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234739 |
| Start | 147619670:147619670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782720985 |
| CDS Mutation | c.1515C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234739 |
| Start | 147619727:147619727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1572A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234739 |
| Start | 147624062:147624062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782462964 |
| CDS Mutation | c.3384G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000234739 |
| Start | 147613076:147613088(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.256_268delAAGAATGGGGCTG |
| AA Mutation | p.Lys86GlufsTer42(p.K86Efs*42) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |