Primary Site >> Pancreatic Cancer
Gene >> LRP5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294304 |
| Start | 68423510:68423510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3049A>T |
| AA Mutation | p.Ser1017Cys(p.S1017C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294304 |
| Start | 68386346:68386346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1046G>A |
| AA Mutation | p.Arg349Gln(p.R349Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294304 |
| Start | 68403543:68403543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1645T>C |
| AA Mutation | p.Phe549Leu(p.F549L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294304 |
| Start | 68413856:68413856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2671G>A |
| AA Mutation | p.Asp891Asn(p.D891N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000294304 |
| Start | 68438658:68438658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778882996 |
| CDS Mutation | c.4324G>A |
| AA Mutation | p.Gly1442Ser(p.G1442S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000294304 |
| Start | 68423659:68423659(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370274326 |
| CDS Mutation | c.3198C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |