Primary Site >> Pancreatic Cancer
Gene >> CHAT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337653 |
| Start | 49625570:49625570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146236256 |
| CDS Mutation | c.850G>A |
| AA Mutation | p.Gly284Ser(p.G284S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337653 |
| Start | 49646634:49646634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1241G>T |
| AA Mutation | p.Ser414Ile(p.S414I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000337653 |
| Start | 49651987:49651987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1615C>A |
| AA Mutation | p.Leu539Ile(p.L539I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337653 |
| Start | 49627706:49627706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145203976 |
| CDS Mutation | c.1032C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000337653 |
| Start | 49619737:49619737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.400C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000337653 |
| Start | 49649635:49649635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371470622 |
| CDS Mutation | c.1510C>T |
| AA Mutation | p.Arg504Ter(p.R504*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |