Primary Site >> Liver Cancer
Gene >> SOX30
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265007 |
| Start | 157638379:157638379(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1731T>A |
| AA Mutation | p.Ser577Arg(p.S577R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265007 |
| Start | 157626473:157626473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758531533 |
| CDS Mutation | c.2129C>T |
| AA Mutation | p.Pro710Leu(p.P710L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265007 |
| Start | 157638680:157638680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1430A>T |
| AA Mutation | p.Gln477Leu(p.Q477L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265007 |
| Start | 157638275:157638275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1835T>C |
| AA Mutation | p.Phe612Ser(p.F612S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265007 |
| Start | 157626718:157626718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1884A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265007 |
| Start | 157651725:157651725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs577314769 |
| CDS Mutation | c.354C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |