Primary Site >> Pancreatic Cancer
Gene >> NRP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360409 |
| Start | 205725951:205725951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771278601 |
| CDS Mutation | c.859C>T |
| AA Mutation | p.Arg287Trp(p.R287W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360409 |
| Start | 205743307:205743307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756167318 |
| CDS Mutation | c.1396C>T |
| AA Mutation | p.Arg466Cys(p.R466C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360409 |
| Start | 205794802:205794802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2540C>A |
| AA Mutation | p.Ser847Tyr(p.S847Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360409 |
| Start | 205794910:205794910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2648G>A |
| AA Mutation | p.Cys883Tyr(p.C883Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360409 |
| Start | 205727920:205727920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764138566 |
| CDS Mutation | c.1020G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000360409 |
| Start | 205745838:205745838(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1734G>A |
| AA Mutation | p.Trp578Ter(p.W578*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |