Primary Site >> Pancreatic Cancer
Gene >> LRRK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298910 |
| Start | 40310497:40310497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777298637 |
| CDS Mutation | c.4384C>T |
| AA Mutation | p.Arg1462Cys(p.R1462C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298910 |
| Start | 40243612:40243612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.769A>G |
| AA Mutation | p.Met257Val(p.M257V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298910 |
| Start | 40299201:40299201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3440A>G |
| AA Mutation | p.Asn1147Ser(p.N1147S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298910 |
| Start | 40304000:40304000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143710836 |
| CDS Mutation | c.3643G>A |
| AA Mutation | p.Ala1215Thr(p.A1215T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298910 |
| Start | 40308478:40308478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3971A>C |
| AA Mutation | p.Gln1324Pro(p.Q1324P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298910 |
| Start | 40310543:40310543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780334763 |
| CDS Mutation | c.4430G>A |
| AA Mutation | p.Arg1477Gln(p.R1477Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000298910 |
| Start | 40351713:40351713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6556A>G |
| AA Mutation | p.Thr2186Ala(p.T2186A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298910 |
| Start | 40259489:40259489(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1428C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000298910 |
| Start | 40283955:40283955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146103273 |
| CDS Mutation | c.2322G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |