ACOT4
acyl-CoA thioesterase 4
Summary
Enables fatty acyl-CoA hydrolase activity and succinyl-CoA hydrolase activity. Involved in carboxylic acid metabolic process and succinyl-CoA metabolic process. Located in peroxisome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs573072624 | 14:74,058,711 | C/G | — | uncertain significance |
| rs753858819 | 14:74,058,716 | C/T | — | uncertain significance |
| rs558779035 | 14:74,058,740 | T/C | — | uncertain significance |
| rs768474591 | 14:74,058,805 | G/A | — | uncertain significance |
| rs1890162695 | 14:74,058,856 | G/A | — | uncertain significance |
| rs771558009 | 14:74,058,857 | C/T | — | uncertain significance |
| rs1890163485 | 14:74,058,871 | G/T | — | uncertain significance |
| rs777258608 | 14:74,058,950 | G/C | — | uncertain significance |
| rs898624506 | 14:74,058,982 | G/A | — | uncertain significance |
| rs752291573 | 14:74,059,025 | G/A | — | uncertain significance |
| rs749212684 | 14:74,059,069 | C/G | — | uncertain significance |
| rs532468724 | 14:74,059,115 | C/G | — | uncertain significance |
| rs11159028 | 14:74,059,450 | G/T | — | — |
| rs773778839 | 14:74,060,444 | A/T | — | uncertain significance |
| rs1445340640 | 14:74,060,489 | C/T | — | uncertain significance |
| rs139322329 | 14:74,060,502 | C/T | — | uncertain significance |
| rs35724886 | 14:74,060,508 | C/A | — | benign |
| rs35909515 | 14:74,060,572 | C/G | — | uncertain significance |
| rs372772376 | 14:74,060,586 | G/A | — | uncertain significance |
| rs2504404194 | 14:74,061,796 | C/G | — | uncertain significance |
| rs766566347 | 14:74,061,817 | C/T | — | uncertain significance |
| rs557692176 | 14:74,061,856 | A/G | — | uncertain significance |
| rs1890225373 | 14:74,061,871 | G/T | — | uncertain significance |
| rs1270933636 | 14:74,061,981 | A/T | — | uncertain significance |
| rs368078748 | 14:74,061,990 | G/A | — | uncertain significance |
| rs140243085 | 14:74,062,000 | A/G | — | likely benign |
| rs2049857750 | 14:74,062,060 | G/C | — | uncertain significance |
| rs763254912 | 14:74,062,072 | A/G | — | uncertain significance |
| rs146020227 | 14:74,062,207 | C/G | — | uncertain significance |
| rs745754725 | 14:74,062,239 | A/G | — | uncertain significance |
| rs374310894 | 14:74,062,259 | G/C | — | uncertain significance |
| rs751168912 | 14:74,062,305 | T/G | — | uncertain significance |
| rs757062870 | 14:74,062,306 | T/C | — | uncertain significance |
| rs779441148 | 14:74,062,329 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.