Primary Site >> Liver Cancer
Gene >> SMG1
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000446231 |
| Start | 18829755:18829755(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9134G>T |
| AA Mutation | p.Gly3045Val(p.G3045V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000446231 |
| Start | 18876381:18876381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1633G>T |
| AA Mutation | p.Ala545Ser(p.A545S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000446231 |
| Start | 18876360:18876360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1654G>A |
| AA Mutation | p.Val552Met(p.V552M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000446231 |
| Start | 18850297:18850297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5223C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000446231 |
| Start | 18835092:18835092(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8130G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000446231 |
| Start | 18842308:18842308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754045372 |
| CDS Mutation | c.6366T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |