Primary Site >> Esophagus Cancer
Gene >> VILL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283713 |
| Start | 37999368:37999368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1111G>T |
| AA Mutation | p.Gly371Cys(p.G371C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |