Primary Site >> Esophagus Cancer
Gene >> HDAC9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000432645 |
| Start | 18767121:18767121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2171A>C |
| AA Mutation | p.Lys724Thr(p.K724T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000432645 |
| Start | 18634713:18634713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.874T>C |
| AA Mutation | p.Ser292Pro(p.S292P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000432645 |
| Start | 18648568:18648568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1343G>A |
| AA Mutation | p.Arg448Gln(p.R448Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000432645 |
| Start | 18666420:18666420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1666G>A |
| AA Mutation | p.Glu556Lys(p.E556K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000432645 |
| Start | 18634722:18634722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.883C>T |
| AA Mutation | p.Pro295Ser(p.P295S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000432645 |
| Start | 18634729:18634729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.890C>T |
| AA Mutation | p.Thr297Ile(p.T297I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000441542 |
| Start | 18975844:18975844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3061A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000432645 |
| Start | 18749082:18749082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758672820 |
| CDS Mutation | c.1978C>T |
| AA Mutation | p.Arg660Ter(p.R660*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000432645 |
| Start | 18749103:18749103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1999C>T |
| AA Mutation | p.Arg667Ter(p.R667*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |