Primary Site >> Esophagus Cancer
Gene >> GHRL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335542 |
| Start | 10290141:10290141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs540101934 |
| CDS Mutation | c.40G>A |
| AA Mutation | p.Gly14Ser(p.G14S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |