Primary Site >> Pancreatic Cancer
Gene >> PLXNB3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361971 |
| Start | 153770541:153770541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782461403 |
| CDS Mutation | c.1909G>A |
| AA Mutation | p.Val637Met(p.V637M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361971 |
| Start | 153767081:153767081(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.254C>T |
| AA Mutation | p.Ala85Val(p.A85V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361971 |
| Start | 153767160:153767160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.333G>T |
| AA Mutation | p.Gln111His(p.Q111H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361971 |
| Start | 153771901:153771901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2555C>T |
| AA Mutation | p.Ala852Val(p.A852V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361971 |
| Start | 153773352:153773352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373016226 |
| CDS Mutation | c.3029G>A |
| AA Mutation | p.Arg1010His(p.R1010H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361971 |
| Start | 153767457:153767457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.630G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |