Primary Site >> Liver Cancer
Gene >> UGGT2
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000376747 |
| Start | 95989973:95989973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.931G>A |
| AA Mutation | p.Asp311Asn(p.D311N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376747 |
| Start | 95947080:95947080(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1634C>T |
| AA Mutation | p.Ala545Val(p.A545V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376747 |
| Start | 95927223:95927223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2091A>G |
| AA Mutation | p.Ile697Met(p.I697M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376747 |
| Start | 95947040:95947040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1674A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376747 |
| Start | 95902878:95902878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2478T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376747 |
| Start | 95927331:95927331(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773423460 |
| CDS Mutation | c.1983A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |