Primary Site >> Liver Cancer
Gene >> SALL4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51791968:51791968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.515C>G |
| AA Mutation | p.Ala172Gly(p.A172G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51790778:51790778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1705C>T |
| AA Mutation | p.Leu569Phe(p.L569F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51790197:51790197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2286C>G |
| AA Mutation | p.Asp762Glu(p.D762E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51792097:51792097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.386G>T |
| AA Mutation | p.Ser129Ile(p.S129I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217086 |
| Start | 51791847:51791847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750424449 |
| CDS Mutation | c.636G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000217086 |
| Start | 51791971:51791971(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.512delT |
| AA Mutation | p.Leu171Ter(p.L171*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000217086 |
| Start | 51792138:51792139(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.344dupT |
| AA Mutation | p.Ser116LeufsTer15(p.S116Lfs*15) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |