ACOT1
acyl-CoA thioesterase 1
Summary
Enables fatty acyl-CoA hydrolase activity. Involved in acyl-CoA metabolic process; long-chain fatty acid metabolic process; and very long-chain fatty acid metabolic process. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs778993401 | 14:74,004,171 | G/A | — | uncertain significance |
| rs772023723 | 14:74,004,177 | C/A | — | uncertain significance |
| rs199573594 | 14:74,004,210 | G/A | — | benign |
| rs753756865 | 14:74,004,275 | G/A | — | benign |
| rs779044350 | 14:74,004,293 | C/T | — | likely benign |
| rs747052239 | 14:74,004,324 | G/C | — | uncertain significance |
| rs766196827 | 14:74,004,392 | C/T | — | likely benign |
| rs781438917 | 14:74,004,447 | G/A | — | uncertain significance |
| rs1350360486 | 14:74,004,475 | G/A | — | uncertain significance |
| rs2504302866 | 14:74,004,486 | T/G | — | likely benign |
| rs770534724 | 14:74,004,507 | T/G | — | likely benign |
| rs200381634 | 14:74,004,508 | A/G | — | conflicting classifications of pathogenicity |
| rs756298246 | 14:74,004,568 | T/G | — | uncertain significance |
| rs762704526 | 14:74,008,259 | C/T | — | uncertain significance |
| rs768462704 | 14:74,008,260 | G/A | — | uncertain significance |
| rs2504312532 | 14:74,008,274 | G/C | — | uncertain significance |
| rs778418921 | 14:74,008,344 | C/T | — | uncertain significance |
| rs779634821 | 14:74,009,767 | G/A | — | uncertain significance |
| rs2504316390 | 14:74,009,772 | G/A | — | uncertain significance |
| rs570534939 | 14:74,009,797 | G/A | — | uncertain significance |
| rs776778694 | 14:74,009,815 | T/C | — | uncertain significance |
| rs1889150105 | 14:74,009,847 | G/A | — | uncertain significance |
| rs776416716 | 14:74,009,875 | T/C | — | uncertain significance |
| rs147168294 | 14:74,009,889 | C/T | — | uncertain significance |
| rs148598881 | 14:74,009,917 | T/C | — | benign |
| rs141161609 | 14:74,009,920 | G/C | — | benign |
| rs746882222 | 14:74,009,922 | G/A | — | uncertain significance |
| rs543032833 | 14:74,009,942 | G/C | — | uncertain significance |
| rs370841081 | 14:74,010,076 | A/G | — | uncertain significance |
| rs1193192621 | 14:74,010,108 | T/C | — | uncertain significance |
| rs530324288 | 14:74,010,146 | G/C | — | uncertain significance |
| rs1889173040 | 14:74,010,199 | T/C | — | uncertain significance |
| rs61987131 | 14:74,010,331 | A/G | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.