Primary Site >> Esophagus Cancer
Gene >> NCOR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124350656:124350656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373295499 |
| CDS Mutation | c.3775C>T |
| AA Mutation | p.Arg1259Trp(p.R1259W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124342003:124342003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772634427 |
| CDS Mutation | c.5008A>G |
| AA Mutation | p.Ile1670Val(p.I1670V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124336839:124336839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757979246 |
| CDS Mutation | c.6029C>T |
| AA Mutation | p.Ala2010Val(p.A2010V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124343095:124343095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4846C>T |
| AA Mutation | p.Arg1616Trp(p.R1616W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124347850:124347850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4047C>A |
| AA Mutation | p.His1349Gln(p.H1349Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124333182:124333182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6703C>G |
| AA Mutation | p.Arg2235Gly(p.R2235G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405201 |
| Start | 124335569:124335569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6179G>T |
| AA Mutation | p.Ser2060Ile(p.S2060I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405201 |
| Start | 124378307:124378307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2097G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405201 |
| Start | 124344757:124344757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs551690182 |
| CDS Mutation | c.4554G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405201 |
| Start | 124335210:124335210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747314164 |
| CDS Mutation | c.6336G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405201 |
| Start | 124362199:124362199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374201637 |
| CDS Mutation | c.3027C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |