Primary Site >> Esophagus Cancer
Gene >> CHEK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328354 |
| Start | 28696962:28696962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1034A>T |
| AA Mutation | p.His345Leu(p.H345L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |