Primary Site >> Esophagus Cancer
Gene >> BGN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331595 |
| Start | 153508396:153508396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368783683 |
| CDS Mutation | c.1058G>A |
| AA Mutation | p.Arg353His(p.R353H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |