Primary Site >> Liver Cancer
Gene >> IQGAP3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361170 |
| Start | 156534110:156534110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3772G>C |
| AA Mutation | p.Glu1258Gln(p.E1258Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361170 |
| Start | 156526589:156526589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4793A>T |
| AA Mutation | p.Gln1598Leu(p.Q1598L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361170 |
| Start | 156528922:156528922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4565A>G |
| AA Mutation | p.Asp1522Gly(p.D1522G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361170 |
| Start | 156548170:156548170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2207A>T |
| AA Mutation | p.Gln736Leu(p.Q736L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361170 |
| Start | 156552090:156552090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1454T>C |
| AA Mutation | p.Phe485Ser(p.F485S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361170 |
| Start | 156550307:156550307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1779C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |