Primary Site >> Esophagus Cancer
Gene >> GSN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373818 |
| Start | 121329289:121329289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2092G>C |
| AA Mutation | p.Val698Leu(p.V698L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |