Primary Site >> Esophagus Cancer
Gene >> PER1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317276 |
| Start | 8141949:8141949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3456G>A |
| AA Mutation | p.Met1152Ile(p.M1152I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317276 |
| Start | 8143526:8143526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771510158 |
| CDS Mutation | c.2812G>A |
| AA Mutation | p.Ala938Thr(p.A938T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317276 |
| Start | 8149578:8149578(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139250084 |
| CDS Mutation | c.737G>A |
| AA Mutation | p.Arg246Gln(p.R246Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317276 |
| Start | 8146414:8146414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377111904 |
| CDS Mutation | c.1996G>A |
| AA Mutation | p.Asp666Asn(p.D666N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317276 |
| Start | 8150050:8150050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.450G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317276 |
| Start | 8142749:8142749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148594937 |
| CDS Mutation | c.3159C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |