Primary Site >> Liver Cancer
Gene >> NEDD4L
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400345 |
| Start | 58366003:58366003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1838A>T |
| AA Mutation | p.Asp613Val(p.D613V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400345 |
| Start | 58165852:58165852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.113T>A |
| AA Mutation | p.Phe38Tyr(p.F38Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400345 |
| Start | 58329110:58329110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.796G>C |
| AA Mutation | p.Gly266Arg(p.G266R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400345 |
| Start | 58366067:58366067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1902A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400345 |
| Start | 58333836:58333836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1009A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400345 |
| Start | 58389102:58389102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375065890 |
| CDS Mutation | c.2565C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |