Primary Site >> Liver Cancer
Gene >> ANKRD11
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301030 |
| Start | 89282043:89282043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4499A>C |
| AA Mutation | p.Gln1500Pro(p.Q1500P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301030 |
| Start | 89283870:89283870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2672A>G |
| AA Mutation | p.Asp891Gly(p.D891G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301030 |
| Start | 89284420:89284420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2122A>G |
| AA Mutation | p.Lys708Glu(p.K708E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301030 |
| Start | 89282945:89282945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3597G>T |
| AA Mutation | p.Glu1199Asp(p.E1199D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301030 |
| Start | 89282167:89282167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4375A>G |
| AA Mutation | p.Lys1459Glu(p.K1459E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301030 |
| Start | 89283921:89283921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2621C>T |
| AA Mutation | p.Ala874Val(p.A874V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301030 |
| Start | 89270876:89270876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7747A>T |
| AA Mutation | p.Asn2583Tyr(p.N2583Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301030 |
| Start | 89281571:89281571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4971G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301030 |
| Start | 89283470:89283470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3072A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301030 |
| Start | 89286124:89286124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149525788 |
| CDS Mutation | c.807G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301030 |
| Start | 89288570:89288570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs192798250 |
| CDS Mutation | c.702C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |