Primary Site >> Esophagus Cancer
Gene >> CARTPT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296777 |
| Start | 71719396:71719396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.103C>T |
| AA Mutation | p.Pro35Ser(p.P35S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |