Primary Site >> Pancreatic Cancer
Gene >> CGN
| ID | 1 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000271636 |
| Start | 151524677:151524677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1405C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000271636 |
| Start | 151520594:151520594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1045-2A>G |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |