Primary Site >> Esophagus Cancer
Gene >> CCNB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288207 |
| Start | 59116790:59116790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778475417 |
| CDS Mutation | c.698T>C |
| AA Mutation | p.Phe233Ser(p.F233S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |