Primary Site >> Esophagus Cancer
Gene >> FHL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000345434 |
| Start | 136209261:136209261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.707G>A |
| AA Mutation | p.Arg236Lys(p.R236K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |