Primary Site >> Liver Cancer
Gene >> LATS1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253339 |
| Start | 149680162:149680162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2306A>G |
| AA Mutation | p.Tyr769Cys(p.Y769C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253339 |
| Start | 149676602:149676602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2729T>C |
| AA Mutation | p.Leu910Ser(p.L910S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000253339 |
| Start | 149701857:149701864(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.263_270delTTGCAAAT |
| AA Mutation | p.Phe88Ter(p.F88*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000253339 |
| Start | 149684335:149684335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.754A>T |
| AA Mutation | p.Arg252Ter(p.R252*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | stop_gained;frameshift_variant |
| Transcription ID | ENST00000253339 |
| Start | 149683580:149683581(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1477_1508dupCCTATTCAACAGCCTGTGAAAAGTATGCGTGT |
| AA Mutation | p.Lys505PhefsTer5(p.K505Ffs*5) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000253339 |
| Start | 149679920:149679922(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2546_2548delTCT |
| AA Mutation | p.Leu849_Cys850delinsArg(p.L849_C850delinsR) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |