Primary Site >> Pancreatic Cancer
Gene >> PLXNA2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208217549:208217549(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771808559 |
| CDS Mutation | c.374G>A |
| AA Mutation | p.Arg125His(p.R125H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208103166:208103166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1588T>C |
| AA Mutation | p.Trp530Arg(p.W530R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208044526:208044526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3856G>A |
| AA Mutation | p.Ala1286Thr(p.A1286T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208051278:208051278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3139G>A |
| AA Mutation | p.Glu1047Lys(p.E1047K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208084418:208084418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374437126 |
| CDS Mutation | c.2260C>T |
| AA Mutation | p.Arg754Cys(p.R754C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208092851:208092851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2032C>T |
| AA Mutation | p.Arg678Cys(p.R678C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367033 |
| Start | 208217387:208217387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.536A>T |
| AA Mutation | p.Asp179Val(p.D179V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367033 |
| Start | 208039684:208039684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs188406573 |
| CDS Mutation | c.4437C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |