Primary Site >> Liver Cancer
Gene >> ZFHX3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268489 |
| Start | 72959229:72959229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142256050 |
| CDS Mutation | c.917G>A |
| AA Mutation | p.Arg306Gln(p.R306Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268489 |
| Start | 72794137:72794137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8545G>C |
| AA Mutation | p.Asp2849His(p.D2849H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268489 |
| Start | 72796084:72796084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6598G>A |
| AA Mutation | p.Glu2200Lys(p.E2200K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268489 |
| Start | 72796407:72796407(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6275T>C |
| AA Mutation | p.Met2092Thr(p.M2092T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268489 |
| Start | 72950488:72950488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3197C>G |
| AA Mutation | p.Ala1066Gly(p.A1066G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268489 |
| Start | 72950669:72950669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3016G>C |
| AA Mutation | p.Asp1006His(p.D1006H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268489 |
| Start | 72889838:72889838(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs187631913 |
| CDS Mutation | c.3341G>A |
| AA Mutation | p.Arg1114Gln(p.R1114Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |