Primary Site >> Pancreatic Cancer
Gene >> NOLC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000605788 |
| Start | 102161022:102161022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1670G>A |
| AA Mutation | p.Gly557Glu(p.G557E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000605788 |
| Start | 102161638:102161638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1824T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000605788 |
| Start | 102161023:102161024(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1674_1675insAAACAATGTCTACAACATCATAAAACAAA |
| AA Mutation | p.Ala559LysfsTer28(p.A559Kfs*28) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |