ACSS3
acyl-CoA synthetase short chain family member 3
Summary
Enables propionate-CoA ligase activity. Predicted to be involved in ketone body biosynthetic process. Located in mitochondrial matrix. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs775472956 | 12:81,471,982 | G/T | — | uncertain significance |
| rs1287024355 | 12:81,471,999 | C/T | — | uncertain significance |
| rs777662872 | 12:81,472,068 | G/A | — | uncertain significance |
| rs150343298 | 12:81,472,071 | A/G | — | likely benign |
| rs1217783472 | 12:81,472,138 | C/T | — | uncertain significance |
| rs7138951 | 12:81,475,633 | G/A | regulatory region variant | — |
| rs1340163383 | 12:81,503,353 | T/G | — | uncertain significance |
| rs749183389 | 12:81,503,370 | A/G | — | uncertain significance |
| rs760956945 | 12:81,503,403 | G/A | — | uncertain significance |
| rs770014944 | 12:81,503,433 | C/G | — | uncertain significance |
| rs4240723 | 12:81,510,452 | G/A | intron variant | — |
| rs527576451 | 12:81,528,602 | A/G | — | uncertain significance |
| rs773886334 | 12:81,528,629 | G/A | — | uncertain significance |
| rs2540864509 | 12:81,528,644 | A/T | — | uncertain significance |
| rs1258810302 | 12:81,528,664 | C/T | — | uncertain significance |
| rs773759730 | 12:81,528,724 | A/G | — | uncertain significance |
| rs2540873814 | 12:81,532,916 | G/A | — | uncertain significance |
| rs2540873905 | 12:81,532,953 | G/A | — | uncertain significance |
| rs779094916 | 12:81,532,967 | G/A | — | likely benign |
| rs774052791 | 12:81,533,019 | T/C | — | uncertain significance |
| rs931582721 | 12:81,533,031 | A/G | — | uncertain significance |
| rs147777981 | 12:81,536,890 | C/A | — | uncertain significance |
| rs768536849 | 12:81,536,910 | C/T | — | uncertain significance |
| rs759930604 | 12:81,536,955 | G/A | — | uncertain significance |
| rs756175673 | 12:81,536,981 | C/G | — | uncertain significance |
| rs10492002 | 12:81,544,536 | C/T | intron variant | — |
| rs201300759 | 12:81,545,645 | G/A | — | uncertain significance |
| rs754885673 | 12:81,545,650 | G/A | — | uncertain significance |
| rs1382940657 | 12:81,545,671 | A/G | — | uncertain significance |
| rs753607600 | 12:81,545,820 | A/C | — | uncertain significance |
| rs762839597 | 12:81,568,666 | A/G | — | uncertain significance |
| rs2540946732 | 12:81,568,676 | A/C | — | uncertain significance |
| rs35166008 | 12:81,571,248 | G/A | — | — |
| rs140203359 | 12:81,590,456 | A/T | intron variant | — |
| rs1205588965 | 12:81,593,128 | C/T | — | uncertain significance |
| rs765641114 | 12:81,593,172 | T/G | — | uncertain significance |
| rs963896786 | 12:81,593,188 | T/C | — | uncertain significance |
| rs2540991380 | 12:81,593,197 | C/T | — | uncertain significance |
| rs12826108 | 12:81,603,369 | G/A | intron variant | — |
| rs769283301 | 12:81,613,810 | A/G | — | uncertain significance |
| rs776830004 | 12:81,613,813 | T/G | — | uncertain significance |
| rs763027564 | 12:81,627,239 | G/A | — | uncertain significance |
| rs766522710 | 12:81,647,116 | T/A | — | uncertain significance |
| rs2034212645 | 12:81,647,153 | A/G | — | uncertain significance |
| rs370167638 | 12:81,647,307 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.