Primary Site >> Liver Cancer
Gene >> CYP2C8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371270 |
| Start | 95067221:95067221(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.468G>C |
| AA Mutation | p.Leu156Phe(p.L156F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000371270 |
| Start | 95043077:95043077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.962C>G |
| AA Mutation | p.Ala321Gly(p.A321G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371270 |
| Start | 95037168:95037168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1433C>G |
| AA Mutation | p.Ser478Cys(p.S478C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371270 |
| Start | 95037212:95037212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1389T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371270 |
| Start | 95039009:95039009(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs774216153 |
| CDS Mutation | c.1179delC |
| AA Mutation | p.Val394CysfsTer20(p.V394Cfs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371270 |
| Start | 95042967:95042968(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1053_1071dupAGTGCACGAGATCCAGAGA |
| AA Mutation | p.Tyr358SerfsTer9(p.Y358Sfs*9) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |