Primary Site >> Liver Cancer
Gene >> PDS5B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315596 |
| Start | 32759650:32759650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3332A>G |
| AA Mutation | p.Tyr1111Cys(p.Y1111C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315596 |
| Start | 32764514:32764514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3544A>T |
| AA Mutation | p.Ser1182Cys(p.S1182C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315596 |
| Start | 32658264:32658264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.338A>T |
| AA Mutation | p.Gln113Leu(p.Q113L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315596 |
| Start | 32667824:32667824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.685A>G |
| AA Mutation | p.Ile229Val(p.I229V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315596 |
| Start | 32746072:32746072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2708A>T |
| AA Mutation | p.Gln903Leu(p.Q903L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315596 |
| Start | 32667776:32667776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.637C>G |
| AA Mutation | p.Gln213Glu(p.Q213E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |