Primary Site >> Esophagus Cancer
Gene >> HDAC4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345617 |
| Start | 239115241:239115241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202206567 |
| CDS Mutation | c.1588C>T |
| AA Mutation | p.Arg530Cys(p.R530C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345617 |
| Start | 239081104:239081104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2726C>T |
| AA Mutation | p.Ala909Val(p.A909V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345617 |
| Start | 239081144:239081144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2686G>T |
| AA Mutation | p.Gly896Cys(p.G896C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345617 |
| Start | 239053589:239053589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3086G>C |
| AA Mutation | p.Arg1029Pro(p.R1029P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345617 |
| Start | 239095037:239095037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753482334 |
| CDS Mutation | c.2238C>A |
| AA Mutation | p.Phe746Leu(p.F746L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345617 |
| Start | 239054826:239054826(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2996C>A |
| AA Mutation | p.Pro999His(p.P999H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345617 |
| Start | 239115096:239115096(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201187772 |
| CDS Mutation | c.1733C>T |
| AA Mutation | p.Pro578Leu(p.P578L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000345617 |
| Start | 239115134:239115134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141268656 |
| CDS Mutation | c.1695C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |