ACOT12
acyl-CoA thioesterase 12
Summary
Enables identical protein binding activity. Predicted to be involved in acetyl-CoA metabolic process. Located in cytosol; intercellular bridge; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs779809926 | 5:80,626,220 | G/A | — | likely benign |
| rs536125060 | 5:80,626,286 | A/G | — | uncertain significance |
| rs768684275 | 5:80,626,350 | T/A | — | uncertain significance |
| rs1758796105 | 5:80,626,683 | T/C | — | uncertain significance |
| rs146713585 | 5:80,626,695 | T/G | — | uncertain significance |
| rs1480986367 | 5:80,626,703 | G/A | — | uncertain significance |
| rs147089882 | 5:80,628,302 | T/C | — | uncertain significance |
| rs1248848793 | 5:80,628,311 | T/C | — | likely benign |
| rs372168909 | 5:80,628,317 | C/T | — | uncertain significance |
| rs1758861571 | 5:80,628,342 | T/C | — | uncertain significance |
| rs143972820 | 5:80,628,348 | T/G | — | uncertain significance |
| rs543485003 | 5:80,628,363 | T/C | — | likely benign |
| rs755024401 | 5:80,628,375 | T/C | — | uncertain significance |
| rs1309677454 | 5:80,628,390 | C/T | — | uncertain significance |
| rs557482905 | 5:80,629,499 | C/T | — | — |
| rs564306951 | 5:80,631,636 | G/A | — | uncertain significance |
| rs150497513 | 5:80,638,502 | T/C | — | likely benign |
| rs371159125 | 5:80,640,015 | C/T | — | uncertain significance |
| rs781742839 | 5:80,640,021 | C/A | — | uncertain significance |
| rs199564842 | 5:80,640,798 | C/T | — | uncertain significance |
| rs777679257 | 5:80,640,804 | C/G | — | uncertain significance |
| rs200358101 | 5:80,640,811 | C/T | — | uncertain significance |
| rs368741983 | 5:80,640,813 | G/C | — | uncertain significance |
| rs1759334764 | 5:80,640,855 | T/G | — | uncertain significance |
| rs1252335365 | 5:80,641,764 | G/A | — | uncertain significance |
| rs777311789 | 5:80,641,767 | C/T | — | uncertain significance |
| rs770465905 | 5:80,641,771 | G/A | — | uncertain significance |
| rs1331125689 | 5:80,641,785 | T/A | — | uncertain significance |
| rs2530762521 | 5:80,643,608 | G/T | — | uncertain significance |
| rs999084466 | 5:80,643,618 | C/G | — | uncertain significance |
| rs201855173 | 5:80,643,671 | G/T | — | uncertain significance |
| rs1457856551 | 5:80,643,678 | G/C | — | uncertain significance |
| rs2530763071 | 5:80,643,696 | G/C | — | uncertain significance |
| rs7729671 | 5:80,648,695 | G/A | intron variant | — |
| rs4703516 | 5:80,654,966 | T/C | — | — |
| rs753320206 | 5:80,655,733 | C/T | — | uncertain significance |
| rs138552293 | 5:80,655,741 | C/T | — | likely benign |
| rs552586784 | 5:80,655,790 | C/T | — | uncertain significance |
| rs201904509 | 5:80,659,624 | G/A | — | uncertain significance |
| rs2530801496 | 5:80,659,630 | C/G | — | uncertain significance |
| rs2530801619 | 5:80,659,659 | A/C | — | uncertain significance |
| rs1759994252 | 5:80,659,687 | G/T | — | uncertain significance |
| rs1266140313 | 5:80,667,573 | A/G | — | uncertain significance |
| rs766787273 | 5:80,667,591 | C/T | — | uncertain significance |
| rs899255702 | 5:80,681,637 | G/A | — | uncertain significance |
| rs145695462 | 5:80,684,679 | C/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.