Primary Site >> Pancreatic Cancer
Gene >> LRP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169236018:169236018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763963014 |
| CDS Mutation | c.4742G>A |
| AA Mutation | p.Arg1581Gln(p.R1581Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263816 |
| Start | 169181587:169181587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137983840 |
| CDS Mutation | c.10030G>A |
| AA Mutation | p.Ala3344Thr(p.A3344T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263816 |
| Start | 169213856:169213856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs569277988 |
| CDS Mutation | c.5841C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263816 |
| Start | 169170645:169170645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760822204 |
| CDS Mutation | c.11286C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263816 |
| Start | 169320871:169320871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779076036 |
| CDS Mutation | c.93G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263816 |
| Start | 169206064:169206064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773316402 |
| CDS Mutation | c.7515C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |