Primary Site >> Esophagus Cancer
Gene >> WRN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298139 |
| Start | 31124608:31124608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2717G>C |
| AA Mutation | p.Ser906Thr(p.S906T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298139 |
| Start | 31064926:31064926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.367G>A |
| AA Mutation | p.Gly123Arg(p.G123R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298139 |
| Start | 31154727:31154727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3791C>G |
| AA Mutation | p.Ser1264Cys(p.S1264C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298139 |
| Start | 31064418:31064418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374898432 |
| CDS Mutation | c.339C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298139 |
| Start | 31088912:31088912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757279675 |
| CDS Mutation | c.1599T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298139 |
| Start | 31120350:31120350(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2556T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |