Primary Site >> Esophagus Cancer
Gene >> ARID1B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350026 |
| Start | 157206383:157206383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5203G>A |
| AA Mutation | p.Glu1735Lys(p.E1735K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350026 |
| Start | 157207356:157207356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6176C>A |
| AA Mutation | p.Pro2059His(p.P2059H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350026 |
| Start | 157203884:157203884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs544895806 |
| CDS Mutation | c.4874G>A |
| AA Mutation | p.Arg1625His(p.R1625H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000350026 |
| Start | 157200839:157200839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4206C>A |
| AA Mutation | p.Asp1402Glu(p.D1402E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350026 |
| Start | 157148763:157148763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2652A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350026 |
| Start | 157203927:157203927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4917G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000350026 |
| Start | 157206181:157206181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766430210 |
| CDS Mutation | c.5001C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000350026 |
| Start | 157201020:157201020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4387C>T |
| AA Mutation | p.Gln1463Ter(p.Q1463*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |