Primary Site >> Liver Cancer
Gene >> DSP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7576308:7576308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2645A>G |
| AA Mutation | p.Glu882Gly(p.E882G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7580786:7580786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4596G>T |
| AA Mutation | p.Glu1532Asp(p.E1532D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7581423:7581423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5233A>G |
| AA Mutation | p.Lys1745Glu(p.K1745E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7585159:7585159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7897A>G |
| AA Mutation | p.Ile2633Val(p.I2633V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7583194:7583194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770077556 |
| CDS Mutation | c.5932A>G |
| AA Mutation | p.Met1978Val(p.M1978V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379802 |
| Start | 7579864:7579864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3674C>G |
| AA Mutation | p.Ser1225Cys(p.S1225C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7571472:7571472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1791A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7580615:7580615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4425C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7579865:7579865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3675C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7585248:7585248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7986C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7585224:7585224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767539050 |
| CDS Mutation | c.7962G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379802 |
| Start | 7583577:7583577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6315A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000379802 |
| Start | 7568440:7568440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1270G>T |
| AA Mutation | p.Glu424Ter(p.E424*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |