Primary Site >> Pancreatic Cancer
Gene >> LRP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243077 |
| Start | 57193667:57193667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7786G>A |
| AA Mutation | p.Asp2596Asn(p.D2596N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243077 |
| Start | 57145326:57145326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.677G>T |
| AA Mutation | p.Ser226Ile(p.S226I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000243077 |
| Start | 57165805:57165805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs532661685 |
| CDS Mutation | c.2531C>T |
| AA Mutation | p.Ala844Val(p.A844V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243077 |
| Start | 57185158:57185158(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6416G>A |
| AA Mutation | p.Gly2139Asp(p.G2139D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243077 |
| Start | 57193610:57193610(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7729C>T |
| AA Mutation | p.Arg2577Cys(p.R2577C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243077 |
| Start | 57193931:57193931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367968116 |
| CDS Mutation | c.7837C>T |
| AA Mutation | p.Arg2613Trp(p.R2613W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243077 |
| Start | 57197031:57197031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8942C>T |
| AA Mutation | p.Ala2981Val(p.A2981V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243077 |
| Start | 57212496:57212496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13576G>A |
| AA Mutation | p.Glu4526Lys(p.E4526K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243077 |
| Start | 57179547:57179547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199662511 |
| CDS Mutation | c.4957G>A |
| AA Mutation | p.Val1653Ile(p.V1653I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243077 |
| Start | 57185175:57185175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6433A>G |
| AA Mutation | p.Ile2145Val(p.I2145V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243077 |
| Start | 57195062:57195062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8269G>A |
| AA Mutation | p.Asp2757Asn(p.D2757N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243077 |
| Start | 57200464:57200464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10037G>A |
| AA Mutation | p.Cys3346Tyr(p.C3346Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243077 |
| Start | 57183506:57183506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs560161034 |
| CDS Mutation | c.5790C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243077 |
| Start | 57184110:57184110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5955C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243077 |
| Start | 57193252:57193252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752406364 |
| CDS Mutation | c.7632C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243077 |
| Start | 57194493:57194493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs545868364 |
| CDS Mutation | c.8058C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |