Primary Site >> Liver Cancer
Gene >> APBA2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000558259 |
| Start | 29113999:29113999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2161T>A |
| AA Mutation | p.Ser721Thr(p.S721T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000558259 |
| Start | 29054294:29054294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143649138 |
| CDS Mutation | c.410C>T |
| AA Mutation | p.Ala137Val(p.A137V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000558259 |
| Start | 29054627:29054627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.743C>T |
| AA Mutation | p.Ala248Val(p.A248V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000558259 |
| Start | 29113943:29113943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2105A>G |
| AA Mutation | p.Glu702Gly(p.E702G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000558259 |
| Start | 29053994:29053994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746831479 |
| CDS Mutation | c.110C>T |
| AA Mutation | p.Pro37Leu(p.P37L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000558259 |
| Start | 29106762:29106762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1860C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000558259 |
| Start | 29054067:29054067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.183G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000558259 |
| Start | 29113909:29113909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765311604 |
| CDS Mutation | c.2071C>T |
| AA Mutation | p.Arg691Ter(p.R691*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |