Primary Site >> Liver Cancer
Gene >> ACACB
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338432 |
| Start | 109199541:109199541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2767G>C |
| AA Mutation | p.Ala923Pro(p.A923P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338432 |
| Start | 109199542:109199542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2768C>T |
| AA Mutation | p.Ala923Val(p.A923V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338432 |
| Start | 109176229:109176229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1403A>T |
| AA Mutation | p.Glu468Val(p.E468V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338432 |
| Start | 109223867:109223867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149793040 |
| CDS Mutation | c.3845A>G |
| AA Mutation | p.Tyr1282Cys(p.Y1282C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338432 |
| Start | 109199455:109199455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2681C>T |
| AA Mutation | p.Pro894Leu(p.P894L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338432 |
| Start | 109191908:109191908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2357T>A |
| AA Mutation | p.Met786Lys(p.M786K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338432 |
| Start | 109254312:109254312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6144G>T |
| AA Mutation | p.Met2048Ile(p.M2048I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338432 |
| Start | 109254235:109254235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6067A>G |
| AA Mutation | p.Ile2023Val(p.I2023V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338432 |
| Start | 109179105:109179105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1455A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338432 |
| Start | 109199406:109199406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2632C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338432 |
| Start | 109253059:109253059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759684564 |
| CDS Mutation | c.5946C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |