Primary Site >> Esophagus Cancer
Gene >> NFIC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000443272 |
| Start | 3381986:3381986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.305C>T |
| AA Mutation | p.Pro102Leu(p.P102L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |