Primary Site >> Esophagus Cancer
Gene >> CTGF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367976 |
| Start | 131950409:131950409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.424C>A |
| AA Mutation | p.Arg142Ser(p.R142S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |