Primary Site >> Liver Cancer
Gene >> SALL3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000537592 |
| Start | 78997080:78997080(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3661A>T |
| AA Mutation | p.Asn1221Tyr(p.N1221Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000537592 |
| Start | 78993069:78993069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1078A>G |
| AA Mutation | p.Ser360Gly(p.S360G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000537592 |
| Start | 78994132:78994132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2141G>T |
| AA Mutation | p.Arg714Leu(p.R714L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000537592 |
| Start | 78997118:78997118(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3699C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000537592 |
| Start | 78994127:78994127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2136C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000537592 |
| Start | 78993827:78993827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1836C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000537592 |
| Start | 78993074:78993074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377646222 |
| CDS Mutation | c.1083G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000537592 |
| Start | 78995362:78995362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3371C>A |
| AA Mutation | p.Ser1124Ter(p.S1124*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |