Primary Site >> Pancreatic Cancer
Gene >> LAMB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49128800:49128800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs544982873 |
| CDS Mutation | c.1751G>A |
| AA Mutation | p.Arg584His(p.R584H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49122271:49122271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772743970 |
| CDS Mutation | c.4673C>T |
| AA Mutation | p.Ala1558Val(p.A1558V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49125116:49125116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs536235346 |
| CDS Mutation | c.2774G>A |
| AA Mutation | p.Arg925Gln(p.R925Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305544 |
| Start | 49129611:49129611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756925281 |
| CDS Mutation | c.1511G>A |
| AA Mutation | p.Arg504His(p.R504H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000305544 |
| Start | 49131442:49131442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.649G>A |
| AA Mutation | p.Val217Ile(p.V217I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305544 |
| Start | 49131547:49131547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.636C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |