Primary Site >> Liver Cancer
Gene >> EXOC7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335146 |
| Start | 76087686:76087686(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1550A>T |
| AA Mutation | p.Gln517Leu(p.Q517L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335146 |
| Start | 76091193:76091193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.851A>T |
| AA Mutation | p.Gln284Leu(p.Q284L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335146 |
| Start | 76097869:76097869(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.567G>T |
| AA Mutation | p.Glu189Asp(p.E189D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335146 |
| Start | 76088091:76088091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1484A>G |
| AA Mutation | p.Lys495Arg(p.K495R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335146 |
| Start | 76089212:76089212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1163A>T |
| AA Mutation | p.Glu388Val(p.E388V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000335146 |
| Start | 76089283:76089283(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1092C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |