Primary Site >> Liver Cancer
Gene >> PXDN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1665018:1665018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772042816 |
| CDS Mutation | c.1348G>A |
| AA Mutation | p.Val450Met(p.V450M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1638874:1638874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4178A>G |
| AA Mutation | p.Gln1393Arg(p.Q1393R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1649607:1649607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374347969 |
| CDS Mutation | c.2173G>A |
| AA Mutation | p.Ala725Thr(p.A725T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648575:1648575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3205G>T |
| AA Mutation | p.Ala1069Ser(p.A1069S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1663735:1663735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1437C>A |
| AA Mutation | p.His479Gln(p.H479Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1649552:1649552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758592134 |
| CDS Mutation | c.2228C>T |
| AA Mutation | p.Thr743Met(p.T743M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1634285:1634285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4359T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1664986:1664986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs191647762 |
| CDS Mutation | c.1380G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |