Primary Site >> Pancreatic Cancer
Gene >> ADCY3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260600 |
| Start | 24820090:24820090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3277C>A |
| AA Mutation | p.Leu1093Ile(p.L1093I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260600 |
| Start | 24827942:24827942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369803323 |
| CDS Mutation | c.2392G>A |
| AA Mutation | p.Val798Ile(p.V798I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260600 |
| Start | 24872629:24872629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.766C>A |
| AA Mutation | p.Leu256Met(p.L256M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260600 |
| Start | 24918512:24918512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.476T>C |
| AA Mutation | p.Phe159Ser(p.F159S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260600 |
| Start | 24918836:24918836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.152G>A |
| AA Mutation | p.Arg51His(p.R51H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260600 |
| Start | 24823220:24823220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2872G>A |
| AA Mutation | p.Asp958Asn(p.D958N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260600 |
| Start | 24828132:24828132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2202C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260600 |
| Start | 24820079:24820079(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762117912 |
| CDS Mutation | c.3288C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260600 |
| Start | 24823323:24823323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2769A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |