ACSM1
acyl-CoA synthetase medium chain family member 1
Summary
Enables benzoate-CoA ligase activity; decanoate-CoA ligase activity; and long-chain fatty acid-CoA ligase activity. Predicted to be involved in acyl-CoA metabolic process and fatty acid biosynthetic process. Located in mitochondrial matrix. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201624784 | 16:20,634,833 | C/T | — | uncertain significance |
| rs142695037 | 16:20,634,851 | A/G | — | uncertain significance |
| rs2548933563 | 16:20,634,878 | T/C | — | uncertain significance |
| rs1343474136 | 16:20,635,434 | T/C | — | likely benign |
| rs532894700 | 16:20,635,477 | T/A | — | uncertain significance |
| rs144174326 | 16:20,635,510 | G/A | — | uncertain significance |
| rs2548941683 | 16:20,638,514 | G/A | — | uncertain significance |
| rs148084363 | 16:20,638,592 | T/C | — | uncertain significance |
| rs61739414 | 16:20,648,076 | G/T | — | likely benign |
| rs2548965317 | 16:20,648,077 | A/G | — | uncertain significance |
| rs147224925 | 16:20,648,089 | C/T | — | likely benign |
| rs369778926 | 16:20,648,098 | T/C | — | uncertain significance |
| rs1421080382 | 16:20,648,135 | G/A | — | uncertain significance |
| rs776711775 | 16:20,648,763 | C/A | — | uncertain significance |
| rs2548969021 | 16:20,648,767 | T/G | — | uncertain significance |
| rs578181180 | 16:20,651,790 | G/A | — | uncertain significance |
| rs2548976881 | 16:20,651,838 | T/A | — | uncertain significance |
| rs1217023946 | 16:20,651,854 | G/A | — | uncertain significance |
| rs1348555240 | 16:20,651,856 | A/G | — | uncertain significance |
| rs774706434 | 16:20,651,892 | G/A | — | uncertain significance |
| rs163234 | 16:20,652,023 | T/C | intron variant | — |
| rs377430734 | 16:20,673,168 | A/C | — | uncertain significance |
| rs145195826 | 16:20,673,171 | G/T | — | uncertain significance |
| rs151222 | 16:20,674,492 | G/A | — | — |
| rs433598 | 16:20,680,206 | C/T | intron variant | — |
| rs2549042757 | 16:20,681,189 | A/G | — | uncertain significance |
| rs1002938429 | 16:20,681,232 | A/T | — | uncertain significance |
| rs374312430 | 16:20,681,280 | C/T | — | uncertain significance |
| rs61742591 | 16:20,681,288 | T/C | — | benign |
| rs771763513 | 16:20,681,293 | G/C | — | uncertain significance |
| rs143859924 | 16:20,693,586 | C/T | — | likely benign |
| rs148646745 | 16:20,693,590 | C/T | — | uncertain significance |
| rs970780421 | 16:20,693,618 | G/T | — | uncertain significance |
| rs2079463066 | 16:20,693,651 | G/C | — | uncertain significance |
| rs376043595 | 16:20,693,695 | A/G | — | likely benign |
| rs200574024 | 16:20,693,743 | T/A | — | uncertain significance |
| rs145701758 | 16:20,696,628 | C/T | — | uncertain significance |
| rs369139443 | 16:20,696,631 | C/T | — | uncertain significance |
| rs201269386 | 16:20,696,673 | T/G | — | uncertain significance |
| rs116005516 | 16:20,702,310 | A/T | — | benign |
| rs1482527607 | 16:20,702,333 | C/G | — | uncertain significance |
| rs147062129 | 16:20,702,422 | C/T | — | likely benign |
| rs768403860 | 16:20,702,440 | G/A | — | uncertain significance |
| rs143613381 | 16:20,702,492 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.