Primary Site >> Liver Cancer
Gene >> MLXIP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319080 |
| Start | 122130032:122130032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.830T>C |
| AA Mutation | p.Leu277Pro(p.L277P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319080 |
| Start | 122138910:122138910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2480G>A |
| AA Mutation | p.Arg827Gln(p.R827Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319080 |
| Start | 122141037:122141037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs561027162 |
| CDS Mutation | c.2592G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000319080 |
| Start | 122127941:122127960(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.581_600delACGTAGACGAGCACCGCCGG |
| AA Mutation | p.Asp194AlafsTer39(p.D194Afs*39) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |