Primary Site >> Liver Cancer
Gene >> KIF20B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371728 |
| Start | 89760614:89760614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4769A>T |
| AA Mutation | p.Glu1590Val(p.E1590V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371728 |
| Start | 89762719:89762719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4873A>G |
| AA Mutation | p.Ile1625Val(p.I1625V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371728 |
| Start | 89715135:89715135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.893A>G |
| AA Mutation | p.Lys298Arg(p.K298R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371728 |
| Start | 89760627:89760627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4782T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371728 |
| Start | 89709428:89709428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.318A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371728 |
| Start | 89738285:89738285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764171222 |
| CDS Mutation | c.3444G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371728 |
| Start | 89717451:89717452(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1081_1082delCA |
| AA Mutation | p.Gln361AspfsTer2(p.Q361Dfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |