Primary Site >> Liver Cancer
Gene >> LAMB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222399 |
| Start | 107964679:107964679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139348334 |
| CDS Mutation | c.1571C>T |
| AA Mutation | p.Ala524Val(p.A524V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222399 |
| Start | 107994900:107994900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.410T>G |
| AA Mutation | p.Ile137Arg(p.I137R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222399 |
| Start | 107929170:107929170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772591661 |
| CDS Mutation | c.4781T>C |
| AA Mutation | p.Met1594Thr(p.M1594T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222399 |
| Start | 107940342:107940342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3408C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000222399 |
| Start | 107962959:107962959(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1803delT |
| AA Mutation | p.Ile601MetfsTer13(p.I601Mfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000222399 |
| Start | 107975689:107975689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768323491 |
| CDS Mutation | c.1189C>T |
| AA Mutation | p.Arg397Ter(p.R397*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000222399 |
| Start | 107961655:107961656(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1878dupA |
| AA Mutation | p.Ala627SerfsTer19(p.A627Sfs*19) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000222399 |
| Start | 107937195:107937239(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3800_3844delTAGAAGTGAAATTATCTGACACAACTTCCCAAAGCAACAGCACAG |
| AA Mutation | p.Val1267_Thr1281del(p.V1267_T1281del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |