ACAD10
acyl-CoA dehydrogenase family member 10
Summary
This gene encodes a member of the acyl-CoA dehydrogenase family of enzymes (ACADs), which participate in the beta-oxidation of fatty acids in mitochondria. The encoded enzyme contains a hydrolase domain at the N-terminal portion, a serine/threonine protein kinase catlytic domain in the central region, and a conserved ACAD domain at the C-terminus. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Nov 2008]
Known Variants80 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs659964 | 12:112,130,199 | G/C | intron variant | — |
| rs753877638 | 12:112,130,514 | A/G | missense variant | — |
| rs771861294 | 12:112,130,544 | C/T | — | likely benign |
| rs146873324 | 12:112,130,545 | G/A | — | uncertain significance |
| rs1329653451 | 12:112,130,575 | T/G | — | uncertain significance |
| rs374462831 | 12:112,130,595 | C/T | — | uncertain significance |
| rs150310415 | 12:112,130,659 | T/G | — | uncertain significance |
| rs184504568 | 12:112,133,665 | A/G | intron variant | — |
| rs76592670 | 12:112,134,085 | G/A | intron variant | — |
| rs2542234102 | 12:112,140,031 | A/G | — | uncertain significance |
| rs2542234136 | 12:112,140,049 | T/C | — | uncertain significance |
| rs138927383 | 12:112,140,068 | C/T | — | uncertain significance |
| rs11066008 | 12:112,140,669 | A/G | intron variant | — |
| rs766583324 | 12:112,143,641 | C/T | — | uncertain significance |
| rs2542241009 | 12:112,143,700 | A/C | — | uncertain significance |
| rs374287121 | 12:112,143,705 | T/A | — | uncertain significance |
| rs200380265 | 12:112,143,720 | G/A | — | uncertain significance |
| rs56750693 | 12:112,144,586 | A/T | intron variant | — |
| rs577434576 | 12:112,145,090 | G/A | — | — |
| rs2542250758 | 12:112,150,348 | G/A | — | uncertain significance |
| rs150051004 | 12:112,150,365 | G/T | — | uncertain significance |
| rs1888718808 | 12:112,150,420 | T/C | — | uncertain significance |
| rs847888 | 12:112,151,742 | C/T | — | — |
| rs376407610 | 12:112,153,625 | G/A | — | uncertain significance |
| rs747866176 | 12:112,153,654 | G/A | — | uncertain significance |
| rs772975056 | 12:112,153,663 | A/C | — | uncertain significance |
| rs750824318 | 12:112,153,693 | C/T | — | uncertain significance |
| rs2542265580 | 12:112,159,515 | A/G | — | uncertain significance |
| rs190517550 | 12:112,165,276 | C/T | intron variant | — |
| rs373192095 | 12:112,165,825 | C/T | — | uncertain significance |
| rs542306618 | 12:112,165,903 | G/A | — | uncertain significance |
| rs748687718 | 12:112,167,616 | A/G | — | uncertain significance |
| rs575221081 | 12:112,167,624 | C/T | — | uncertain significance |
| rs750115811 | 12:112,167,685 | T/C | — | uncertain significance |
| rs771935027 | 12:112,167,720 | C/G | — | uncertain significance |
| rs375729084 | 12:112,167,723 | C/T | — | uncertain significance |
| rs368642732 | 12:112,167,724 | G/A | — | likely benign |
| rs36046440 | 12:112,167,753 | G/A | — | likely benign |
| rs753056489 | 12:112,167,756 | T/A | — | uncertain significance |
| rs11066015 | 12:112,168,009 | G/A | intron variant | — |
| rs747954484 | 12:112,171,773 | G/A | — | uncertain significance |
| rs1274383922 | 12:112,171,806 | C/A | — | uncertain significance |
| rs199529402 | 12:112,171,830 | T/C | — | uncertain significance |
| rs2542285585 | 12:112,171,852 | C/G | — | uncertain significance |
| rs746643943 | 12:112,174,694 | A/G | — | uncertain significance |
| rs766204833 | 12:112,182,491 | G/A | — | uncertain significance |
| rs372475122 | 12:112,182,509 | G/A | — | uncertain significance |
| rs377499155 | 12:112,182,521 | G/A | — | uncertain significance |
| rs112401787 | 12:112,182,612 | A/T | — | likely benign |
| rs2542301237 | 12:112,182,641 | A/G | — | uncertain significance |
| rs980566161 | 12:112,182,737 | C/T | — | uncertain significance |
| rs756084470 | 12:112,182,738 | G/C | — | uncertain significance |
| rs374399374 | 12:112,184,005 | G/C | — | uncertain significance |
| rs144218728 | 12:112,184,027 | T/C | — | uncertain significance |
| rs767230315 | 12:112,184,069 | C/A | — | uncertain significance |
| rs2542304453 | 12:112,184,072 | C/T | — | uncertain significance |
| rs190926321 | 12:112,184,928 | C/T | — | uncertain significance |
| rs1361711864 | 12:112,184,961 | C/T | — | uncertain significance |
| rs765259177 | 12:112,184,962 | G/A | — | likely benign |
| rs367661194 | 12:112,186,175 | A/G | — | uncertain significance |
| rs141914437 | 12:112,186,189 | C/T | — | uncertain significance |
| rs150643910 | 12:112,186,253 | C/T | — | uncertain significance |
| rs1469335376 | 12:112,187,009 | C/T | — | uncertain significance |
| rs138044386 | 12:112,187,025 | A/G | — | uncertain significance |
| rs763081398 | 12:112,187,049 | G/T | — | uncertain significance |
| rs751290561 | 12:112,187,061 | C/T | — | uncertain significance |
| rs145484987 | 12:112,187,138 | A/G | — | uncertain significance |
| rs7295396 | 12:112,189,880 | G/T | upstream gene variant | — |
| rs6490294 | 12:112,190,438 | C/G | — | — |
| rs143391323 | 12:112,191,580 | A/C | — | uncertain significance |
| rs770585998 | 12:112,191,585 | C/T | — | uncertain significance |
| rs1212960676 | 12:112,191,622 | C/A | — | uncertain significance |
| rs775118172 | 12:112,191,691 | C/T | — | uncertain significance |
| rs143276470 | 12:112,191,718 | A/C | — | uncertain significance |
| rs757552774 | 12:112,193,508 | G/T | — | uncertain significance |
| rs747732996 | 12:112,193,527 | G/A | — | uncertain significance |
| rs748666716 | 12:112,194,170 | C/T | — | uncertain significance |
| rs1297470622 | 12:112,194,240 | C/T | — | uncertain significance |
| rs768575444 | 12:112,194,270 | G/A | — | uncertain significance |
| rs737280 | 12:112,194,976 | T/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.