Primary Site >> Pancreatic Cancer
Gene >> ADCY10
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367851 |
| Start | 167809752:167809752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4759G>T |
| AA Mutation | p.Gly1587Cys(p.G1587C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367851 |
| Start | 167833092:167833092(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143185037 |
| CDS Mutation | c.3488G>A |
| AA Mutation | p.Arg1163Gln(p.R1163Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367851 |
| Start | 167905019:167905019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.122G>A |
| AA Mutation | p.Gly41Glu(p.G41E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367851 |
| Start | 167905136:167905136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5A>C |
| AA Mutation | p.Asn2Thr(p.N2T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367851 |
| Start | 167893889:167893889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.792C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367851 |
| Start | 167833019:167833019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3561G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000367851 |
| Start | 167901674:167901674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776954739 |
| CDS Mutation | c.424C>T |
| AA Mutation | p.Arg142Ter(p.R142*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |