Primary Site >> Liver Cancer
Gene >> PIWIL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000245255 |
| Start | 130357530:130357530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1642A>G |
| AA Mutation | p.Lys548Glu(p.K548E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000245255 |
| Start | 130343067:130343067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.156G>C |
| AA Mutation | p.Gln52His(p.Q52H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000245255 |
| Start | 130348145:130348145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.696T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000245255 |
| Start | 130349862:130349862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.939C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000245255 |
| Start | 130345841:130345841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752244660 |
| CDS Mutation | c.279A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000245255 |
| Start | 130354609:130354609(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1122delG |
| AA Mutation | p.Thr375HisfsTer18(p.T375Hfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |