Primary Site >> Esophagus Cancer
Gene >> CLDN7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360325 |
| Start | 7262040:7262040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4G>T |
| AA Mutation | p.Ala2Ser(p.A2S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |