Primary Site >> Liver Cancer
Gene >> CYP2E1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252945 |
| Start | 133538956:133538956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759928543 |
| CDS Mutation | c.1474C>T |
| AA Mutation | p.Arg492Cys(p.R492C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252945 |
| Start | 133527460:133527460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.65T>C |
| AA Mutation | p.Met22Thr(p.M22T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000252945 |
| Start | 133527422:133527445(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.38_61delGGGCGGCCTTCCTCCTGCTGGTGT |
| AA Mutation | p.Trp13_Val20del(p.W13_V20del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | start_lost |
| Transcription ID | ENST00000252945 |
| Start | 133527396:133527396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1A>G |
| AA Mutation | p.Met1?(p.M1?) |
| Mutation Classification | Translation_Start_Site |
| Feature Type | Transcript |