Primary Site >> Liver Cancer
Gene >> KIF14
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200553764:200553764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4571G>C |
| AA Mutation | p.Cys1524Ser(p.C1524S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200553563:200553563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4772T>C |
| AA Mutation | p.Leu1591Ser(p.L1591S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200589265:200589265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3066A>G |
| AA Mutation | p.Ile1022Met(p.I1022M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200593756:200593756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2563T>G |
| AA Mutation | p.Phe855Val(p.F855V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367350 |
| Start | 200617736:200617736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs116130210 |
| CDS Mutation | c.988G>A |
| AA Mutation | p.Ala330Thr(p.A330T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367350 |
| Start | 200581212:200581212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3324T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367350 |
| Start | 200589229:200589229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3102G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367350 |
| Start | 200553635:200553636(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4699_4700delGT |
| AA Mutation | p.Val1567ProfsTer9(p.V1567Pfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367350 |
| Start | 200618003:200618003(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.721delC |
| AA Mutation | p.Gln241ArgfsTer33(p.Q241Rfs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |