Primary Site >> Liver Cancer
Gene >> TBC1D9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442267 |
| Start | 140668955:140668955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769634349 |
| CDS Mutation | c.1550C>T |
| AA Mutation | p.Pro517Leu(p.P517L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442267 |
| Start | 140622821:140622821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3175C>T |
| AA Mutation | p.Leu1059Phe(p.L1059F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442267 |
| Start | 140622655:140622655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199802386 |
| CDS Mutation | c.3341C>T |
| AA Mutation | p.Pro1114Leu(p.P1114L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000442267 |
| Start | 140679615:140679615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.589G>A |
| AA Mutation | p.Ala197Thr(p.A197T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000442267 |
| Start | 140622282:140622282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3714C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000442267 |
| Start | 140634003:140634003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2691A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |