Primary Site >> Esophagus Cancer
Gene >> TRIOBP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37713385:37713385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.430G>C |
| AA Mutation | p.Asp144His(p.D144H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37755132:37755132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376340052 |
| CDS Mutation | c.5519G>A |
| AA Mutation | p.Arg1840His(p.R1840H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406386 |
| Start | 37734527:37734527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4191G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406386 |
| Start | 37726330:37726330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377749969 |
| CDS Mutation | c.3774C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000406386 |
| Start | 37734766:37734766(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs778824544 |
| CDS Mutation | c.4436delG |
| AA Mutation | p.Gly1479AlafsTer28(p.G1479Afs*28) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000406386 |
| Start | 37734712:37734712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4376G>A |
| AA Mutation | p.Trp1459Ter(p.W1459*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000406386 |
| Start | 37733297:37733297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3948-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |