Primary Site >> Esophagus Cancer
Gene >> DNTT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371174 |
| Start | 96332562:96332562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767993308 |
| CDS Mutation | c.1325G>A |
| AA Mutation | p.Arg442His(p.R442H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |