Primary Site >> Pancreatic Cancer
Gene >> DSP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7571510:7571510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1829C>G |
| AA Mutation | p.Ser610Cys(p.S610C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7577813:7577813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2912G>T |
| AA Mutation | p.Gly971Val(p.G971V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7579404:7579404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3214T>C |
| AA Mutation | p.Phe1072Leu(p.F1072L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7582792:7582792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5530G>A |
| AA Mutation | p.Glu1844Lys(p.E1844K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7584567:7584567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7305G>T |
| AA Mutation | p.Lys2435Asn(p.K2435N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7585391:7585391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8129C>T |
| AA Mutation | p.Ala2710Val(p.A2710V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7565418:7565418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368051840 |
| CDS Mutation | c.837G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7580399:7580399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4209G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7582726:7582726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5464C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000379802 |
| Start | 7562781:7562781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs111295218 |
| CDS Mutation | c.726+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |