Primary Site >> Liver Cancer
Gene >> ST18
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276480 |
| Start | 52172520:52172520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.341G>A |
| AA Mutation | p.Arg114Lys(p.R114K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276480 |
| Start | 52172377:52172377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.484G>T |
| AA Mutation | p.Asp162Tyr(p.D162Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276480 |
| Start | 52132033:52132033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2591A>T |
| AA Mutation | p.Gln864Leu(p.Q864L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276480 |
| Start | 52137473:52137473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2179C>A |
| AA Mutation | p.Pro727Thr(p.P727T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000276480 |
| Start | 52166867:52166867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200016532 |
| CDS Mutation | c.1189C>T |
| AA Mutation | p.Arg397Trp(p.R397W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000276480 |
| Start | 52171928:52171928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.933T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000276480 |
| Start | 52142980:52142980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2118A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000276480 |
| Start | 52161556:52161556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1413G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |