Primary Site >> Liver Cancer
Gene >> LAMC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258341 |
| Start | 183137751:183137751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4397A>G |
| AA Mutation | p.Lys1466Arg(p.K1466R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258341 |
| Start | 183133494:183133494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3793G>T |
| AA Mutation | p.Val1265Leu(p.V1265L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258341 |
| Start | 183124808:183124808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769260014 |
| CDS Mutation | c.2579A>G |
| AA Mutation | p.Tyr860Cys(p.Y860C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258341 |
| Start | 183142632:183142632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4672G>A |
| AA Mutation | p.Val1558Met(p.V1558M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258341 |
| Start | 183132454:183132454(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3621G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258341 |
| Start | 183116794:183116794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781326806 |
| CDS Mutation | c.1455A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |