Primary Site >> Pancreatic Cancer
Gene >> LAMA4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112175316:112175316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1354G>A |
| AA Mutation | p.Glu452Lys(p.E452K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112119226:112119226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4751C>T |
| AA Mutation | p.Ala1584Val(p.A1584V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230538 |
| Start | 112133377:112133377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3668T>C |
| AA Mutation | p.Val1223Ala(p.V1223A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230538 |
| Start | 112158815:112158815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1734C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230538 |
| Start | 112187528:112187528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs17073495 |
| CDS Mutation | c.888C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000230538 |
| Start | 112155576:112155576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782089100 |
| CDS Mutation | c.1948C>T |
| AA Mutation | p.Arg650Ter(p.R650*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |