Primary Site >> Liver Cancer
Gene >> IQGAP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268182 |
| Start | 90500044:90500044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4910A>C |
| AA Mutation | p.Asp1637Ala(p.D1637A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268182 |
| Start | 90433780:90433780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.452G>C |
| AA Mutation | p.Cys151Ser(p.C151S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268182 |
| Start | 90474502:90474502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2593C>T |
| AA Mutation | p.Pro865Ser(p.P865S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268182 |
| Start | 90477709:90477709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3149C>T |
| AA Mutation | p.Thr1050Met(p.T1050M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268182 |
| Start | 90494772:90494772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4688A>G |
| AA Mutation | p.Tyr1563Cys(p.Y1563C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268182 |
| Start | 90443441:90443441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375134287 |
| CDS Mutation | c.876G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |