Primary Site >> Liver Cancer
Gene >> ANK3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280772 |
| Start | 60073262:60073262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7619C>T |
| AA Mutation | p.Thr2540Ile(p.T2540I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280772 |
| Start | 60389453:60389453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373407780 |
| CDS Mutation | c.86G>A |
| AA Mutation | p.Arg29His(p.R29H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280772 |
| Start | 60070956:60070956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9925C>A |
| AA Mutation | p.Pro3309Thr(p.P3309T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280772 |
| Start | 60074189:60074189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6692A>T |
| AA Mutation | p.Asn2231Ile(p.N2231I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280772 |
| Start | 60071790:60071790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9091T>C |
| AA Mutation | p.Tyr3031His(p.Y3031H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280772 |
| Start | 60072674:60072674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8207A>T |
| AA Mutation | p.Glu2736Val(p.E2736V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280772 |
| Start | 60068969:60068969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11912C>T |
| AA Mutation | p.Thr3971Ile(p.T3971I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280772 |
| Start | 60069272:60069272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11609C>A |
| AA Mutation | p.Thr3870Asn(p.T3870N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280772 |
| Start | 60088150:60088150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3537C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280772 |
| Start | 60069700:60069700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11181T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280772 |
| Start | 60196560:60196560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1755A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280772 |
| Start | 60072268:60072268(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754091164 |
| CDS Mutation | c.8613G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280772 |
| Start | 60072979:60072979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7902G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000280772 |
| Start | 60068686:60068686(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.12195delA |
| AA Mutation | p.Lys4065AsnfsTer32(p.K4065Nfs*32) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |