Primary Site >> Esophagus Cancer
Gene >> ECT2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392692 |
| Start | 172755558:172755558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.286A>C |
| AA Mutation | p.Lys96Gln(p.K96Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |