Primary Site >> Liver Cancer
Gene >> ACACA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616317 |
| Start | 37263759:37263759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747343847 |
| CDS Mutation | c.1255C>T |
| AA Mutation | p.Arg419Cys(p.R419C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616317 |
| Start | 37257812:37257812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1717A>G |
| AA Mutation | p.Asn573Asp(p.N573D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616317 |
| Start | 37258324:37258324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1550A>T |
| AA Mutation | p.Tyr517Phe(p.Y517F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000616317 |
| Start | 37181305:37181305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4828A>G |
| AA Mutation | p.Ile1610Val(p.I1610V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616317 |
| Start | 37274220:37274220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.981T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000616317 |
| Start | 37188286:37188286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4767G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000616317 |
| Start | 37097899:37097905(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.6645_6651delTTACCAT |
| AA Mutation | p.Tyr2216ArgfsTer2(p.Y2216Rfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000616317 |
| Start | 37129412:37129412(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5897delA |
| AA Mutation | p.Lys1966ArgfsTer10(p.K1966Rfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |