Primary Site >> Pancreatic Cancer
Gene >> VIM
| ID | 1 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000224237 |
| Start | 17234773:17234773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.963A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000224237 |
| Start | 17235378:17235378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1218C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | splice_donor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000224237 |
| Start | 17233681:17233767(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.721_720+2delTTAGTGGAGTGACTTTCGGGGAATGAATGAGGGTAAGGCAGCCCCCACGGTTGGCAGAGCTGACCGTCTGTCTGTTCTTTTTGCAGG |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |