Primary Site >> Pancreatic Cancer
Gene >> HDAC9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000432645 |
| Start | 18590426:18590426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.346G>A |
| AA Mutation | p.Glu116Lys(p.E116K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000432645 |
| Start | 18647887:18647887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1129A>G |
| AA Mutation | p.Ser377Gly(p.S377G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000432645 |
| Start | 18762266:18762266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2144G>T |
| AA Mutation | p.Arg715Met(p.R715M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000432645 |
| Start | 18585383:18585383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763335887 |
| CDS Mutation | c.125G>A |
| AA Mutation | p.Arg42His(p.R42H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000432645 |
| Start | 18749116:18749116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2012C>A |
| AA Mutation | p.Thr671Asn(p.T671N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000432645 |
| Start | 18591607:18591607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778746610 |
| CDS Mutation | c.498T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |