Primary Site >> Liver Cancer
Gene >> PGR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325455 |
| Start | 101129049:101129049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.22G>T |
| AA Mutation | p.Gly8Cys(p.G8C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325455 |
| Start | 101062548:101062548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2111A>G |
| AA Mutation | p.Asp704Gly(p.D704G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325455 |
| Start | 101126036:101126036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1760G>C |
| AA Mutation | p.Cys587Ser(p.C587S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325455 |
| Start | 101051562:101051562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149186732 |
| CDS Mutation | c.2219G>A |
| AA Mutation | p.Arg740Gln(p.R740Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325455 |
| Start | 101128561:101128561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.510C>G |
| AA Mutation | p.Cys170Trp(p.C170W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000325455 |
| Start | 101128115:101128115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.956G>A |
| AA Mutation | p.Arg319His(p.R319H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325455 |
| Start | 101127952:101127952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1119G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325455 |
| Start | 101128318:101128318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.753A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000325455 |
| Start | 101128267:101128267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs186653307 |
| CDS Mutation | c.804C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |