Primary Site >> Esophagus Cancer
Gene >> MYBL2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217026 |
| Start | 43682803:43682803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.196G>A |
| AA Mutation | p.Asp66Asn(p.D66N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |