ACSM2B
acyl-CoA synthetase medium chain family member 2B
Summary
Enables benzoate-CoA ligase activity. Predicted to be involved in acyl-CoA metabolic process and fatty acid biosynthetic process. Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1476923493 | 16:20,552,048 | G/T | — | uncertain significance |
| rs77922582 | 16:20,554,248 | G/C | synonymous variant | — |
| rs2548899431 | 16:20,554,267 | A/T | — | uncertain significance |
| rs761525079 | 16:20,554,285 | G/T | — | uncertain significance |
| rs753174483 | 16:20,554,484 | C/T | — | uncertain significance |
| rs143500332 | 16:20,554,485 | G/A | — | uncertain significance |
| rs1460808972 | 16:20,554,517 | T/G | — | uncertain significance |
| rs1474594076 | 16:20,554,568 | G/A | — | uncertain significance |
| rs7499271 | 16:20,555,259 | T/A | intron variant | — |
| rs1389964531 | 16:20,556,513 | G/C | — | uncertain significance |
| rs142553905 | 16:20,556,528 | C/T | missense variant | — |
| rs752366107 | 16:20,556,576 | A/G | — | uncertain significance |
| rs2548900616 | 16:20,556,579 | A/T | — | uncertain significance |
| rs7499358 | 16:20,557,634 | A/T | regulatory region variant | — |
| rs146865904 | 16:20,557,741 | G/A | — | uncertain significance |
| rs1240845190 | 16:20,557,769 | T/C | — | uncertain significance |
| rs1391640961 | 16:20,557,777 | G/A | — | uncertain significance |
| rs142106780 | 16:20,559,466 | T/G | — | uncertain significance |
| rs141915122 | 16:20,559,754 | A/G | — | benign |
| rs80135299 | 16:20,559,777 | T/C | — | benign |
| rs35623745 | 16:20,563,544 | T/G | — | benign |
| rs2152138308 | 16:20,565,109 | T/C | — | uncertain significance |
| rs2015390235 | 16:20,565,193 | A/T | — | uncertain significance |
| rs1274329386 | 16:20,565,242 | A/C | — | likely benign |
| rs2548906755 | 16:20,566,734 | C/T | — | uncertain significance |
| rs771105536 | 16:20,566,772 | G/T | — | uncertain significance |
| rs35243287 | 16:20,567,889 | A/C | — | — |
| rs8056693 | 16:20,570,661 | T/A | missense variant | — |
| rs542088831 | 16:20,570,675 | T/C | — | uncertain significance |
| rs765808799 | 16:20,576,010 | T/A | — | uncertain significance |
| rs367698409 | 16:20,576,046 | G/A | — | uncertain significance |
| rs564472730 | 16:20,576,154 | C/T | — | uncertain significance |
| rs59532339 | 16:20,579,672 | A/T | intron variant | — |
| rs142593364 | 16:20,587,568 | C/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.