Primary Site >> Esophagus Cancer
Gene >> VANGL2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368061 |
| Start | 160420521:160420521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.911G>A |
| AA Mutation | p.Gly304Asp(p.G304D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368061 |
| Start | 160419572:160419572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.763G>T |
| AA Mutation | p.Asp255Tyr(p.D255Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368061 |
| Start | 160419077:160419077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149889263 |
| CDS Mutation | c.268C>T |
| AA Mutation | p.Arg90Cys(p.R90C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368061 |
| Start | 160419165:160419165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.356C>G |
| AA Mutation | p.Ser119Cys(p.S119C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368061 |
| Start | 160425204:160425204(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760566236 |
| CDS Mutation | c.1392C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368061 |
| Start | 160419436:160419436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.627G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368061 |
| Start | 160424277:160424277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756021386 |
| CDS Mutation | c.1299G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |