Primary Site >> Liver Cancer
Gene >> CELSR1
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000262738 |
| Start | 46377062:46377062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533045376 |
| CDS Mutation | c.7583C>T |
| AA Mutation | p.Pro2528Leu(p.P2528L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262738 |
| Start | 46433400:46433400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4604A>G |
| AA Mutation | p.Tyr1535Cys(p.Y1535C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262738 |
| Start | 46380903:46380903(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7141A>G |
| AA Mutation | p.Ser2381Gly(p.S2381G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262738 |
| Start | 46433469:46433469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs573686247 |
| CDS Mutation | c.4535C>T |
| AA Mutation | p.Thr1512Met(p.T1512M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262738 |
| Start | 46398543:46398543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5507G>T |
| AA Mutation | p.Gly1836Val(p.G1836V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262738 |
| Start | 46535423:46535423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1748C>A |
| AA Mutation | p.Pro583His(p.P583H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262738 |
| Start | 46534941:46534941(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2230A>G |
| AA Mutation | p.Ile744Val(p.I744V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262738 |
| Start | 46396726:46396726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5722G>T |
| AA Mutation | p.Val1908Leu(p.V1908L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262738 |
| Start | 46396661:46396661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752880984 |
| CDS Mutation | c.5787G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262738 |
| Start | 46386451:46386451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147425309 |
| CDS Mutation | c.6690C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262738 |
| Start | 46463930:46463930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201238170 |
| CDS Mutation | c.3960C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262738 |
| Start | 46534999:46534999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2172C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |