Primary Site >> Liver Cancer
Gene >> ZNF687
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324048 |
| Start | 151286356:151286356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.65A>G |
| AA Mutation | p.Asp22Gly(p.D22G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324048 |
| Start | 151286464:151286464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762937626 |
| CDS Mutation | c.173C>T |
| AA Mutation | p.Ser58Phe(p.S58F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324048 |
| Start | 151289975:151289975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2932T>A |
| AA Mutation | p.Tyr978Asn(p.Y978N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324048 |
| Start | 151286607:151286607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.316G>T |
| AA Mutation | p.Gly106Trp(p.G106W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324048 |
| Start | 151287914:151287914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1623C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324048 |
| Start | 151287531:151287531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1240C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324048 |
| Start | 151289128:151289128(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2328G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324048 |
| Start | 151286697:151286697(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.407delG |
| AA Mutation | p.Gly136GlufsTer55(p.G136Efs*55) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324048 |
| Start | 151290153:151290154(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2997dupG |
| AA Mutation | p.Arg1000AlafsTer16(p.R1000Afs*16) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324048 |
| Start | 151289520:151289521(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2616dupC |
| AA Mutation | p.Met873HisfsTer32(p.M873Hfs*32) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324048 |
| Start | 151289851:151289852(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs749403447 |
| CDS Mutation | c.2815dupC |
| AA Mutation | p.Arg939ProfsTer36(p.R939Pfs*36) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |