Primary Site >> Liver Cancer
Gene >> MKI67
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128102653:128102653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9187G>A |
| AA Mutation | p.Glu3063Lys(p.E3063K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128105053:128105053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6787G>T |
| AA Mutation | p.Gly2263Trp(p.G2263W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128115757:128115757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.651A>T |
| AA Mutation | p.Glu217Asp(p.E217D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128107382:128107382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4458C>G |
| AA Mutation | p.His1486Gln(p.H1486Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128115791:128115791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.617T>C |
| AA Mutation | p.Ile206Thr(p.I206T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128103583:128103583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8257G>C |
| AA Mutation | p.Asp2753His(p.D2753H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128115201:128115201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1207G>C |
| AA Mutation | p.Ala403Pro(p.A403P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128115597:128115597(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201650569 |
| CDS Mutation | c.811G>A |
| AA Mutation | p.Ala271Thr(p.A271T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368654 |
| Start | 128106526:128106526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5314A>T |
| AA Mutation | p.Arg1772Trp(p.R1772W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368654 |
| Start | 128102930:128102930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371689181 |
| CDS Mutation | c.8910C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |