Primary Site >> Liver Cancer
Gene >> CKAP5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529230 |
| Start | 46750405:46750405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5573A>G |
| AA Mutation | p.Lys1858Arg(p.K1858R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529230 |
| Start | 46795641:46795641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1603A>G |
| AA Mutation | p.Ile535Val(p.I535V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529230 |
| Start | 46797842:46797842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1301A>T |
| AA Mutation | p.Lys434Met(p.K434M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529230 |
| Start | 46783299:46783299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2224G>A |
| AA Mutation | p.Ala742Thr(p.A742T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000529230 |
| Start | 46795623:46795623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1621G>A |
| AA Mutation | p.Gly541Arg(p.G541R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000529230 |
| Start | 46744082:46744083(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs765113582 |
| CDS Mutation | c.6037_6039dupTCC |
| AA Mutation | p.Ser2013dup(p.S2013dup) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |