Primary Site >> Liver Cancer
Gene >> INTS1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000404767 |
| Start | 1478480:1478480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4516G>A |
| AA Mutation | p.Glu1506Lys(p.E1506K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000404767 |
| Start | 1485433:1485433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760716820 |
| CDS Mutation | c.3013G>T |
| AA Mutation | p.Asp1005Tyr(p.D1005Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000404767 |
| Start | 1495452:1495452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1813C>A |
| AA Mutation | p.Pro605Thr(p.P605T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000404767 |
| Start | 1477799:1477799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781720568 |
| CDS Mutation | c.4768G>A |
| AA Mutation | p.Glu1590Lys(p.E1590K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000404767 |
| Start | 1471203:1471203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6277A>G |
| AA Mutation | p.Ser2093Gly(p.S2093G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000404767 |
| Start | 1499516:1499516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.801G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000404767 |
| Start | 1474237:1474237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769069843 |
| CDS Mutation | c.5760G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |