Primary Site >> Pancreatic Cancer
Gene >> CDC73
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367435 |
| Start | 193135442:193135442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.359G>A |
| AA Mutation | p.Arg120Gln(p.R120Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367435 |
| Start | 193141908:193141908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.571G>A |
| AA Mutation | p.Ala191Thr(p.A191T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367435 |
| Start | 193147961:193147961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.824C>T |
| AA Mutation | p.Pro275Leu(p.P275L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367435 |
| Start | 193141893:193141893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.556A>G |
| AA Mutation | p.Lys186Glu(p.K186E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | splice_acceptor_variant;coding_sequence_variant |
| Transcription ID | ENST00000367435 |
| Start | 193203793:193203819(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.973_999delGAGGGTGCATCTGCCCGGAAGACTCAG |
| AA Mutation | p.Glu325_Gln333del(p.X325_splice) |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |