ACOT2
acyl-CoA thioesterase 2
Summary
This gene encodes a member of the acyl-CoA thioesterase protein family, and is one of four acyl-CoA hydrolase genes located in a cluster on chromosome 14. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs61987136 | 14:74,033,495 | C/T | upstream gene variant | — |
| rs878858402 | 14:74,035,966 | C/G | — | uncertain significance |
| rs1889656837 | 14:74,035,969 | C/T | — | uncertain significance |
| rs1259019694 | 14:74,035,985 | T/G | — | uncertain significance |
| rs144085606 | 14:74,036,007 | G/T | — | uncertain significance |
| rs756249281 | 14:74,036,162 | G/A | — | uncertain significance |
| rs1166814140 | 14:74,036,186 | T/G | — | uncertain significance |
| rs774249499 | 14:74,036,207 | T/C | — | uncertain significance |
| rs903243723 | 14:74,036,276 | A/G | — | uncertain significance |
| rs748967871 | 14:74,036,309 | T/G | — | uncertain significance |
| rs1319964482 | 14:74,036,341 | A/C | — | uncertain significance |
| rs759855280 | 14:74,036,342 | G/T | — | uncertain significance |
| rs368768538 | 14:74,036,372 | T/C | — | uncertain significance |
| rs777587916 | 14:74,036,376 | G/C | — | uncertain significance |
| rs538571976 | 14:74,036,391 | G/T | — | uncertain significance |
| rs1233701235 | 14:74,036,398 | T/G | — | uncertain significance |
| rs774727898 | 14:74,036,417 | G/T | — | uncertain significance |
| rs1175609687 | 14:74,036,483 | G/A | — | uncertain significance |
| rs1369828214 | 14:74,036,495 | A/C | — | uncertain significance |
| rs2504357151 | 14:74,036,522 | C/T | — | uncertain significance |
| rs751364371 | 14:74,036,525 | C/G | — | uncertain significance |
| rs61987137 | 14:74,036,613 | G/T | regulatory region variant | — |
| rs113425878 | 14:74,037,440 | C/G | downstream gene variant | — |
| rs141751909 | 14:74,040,127 | G/A | — | uncertain significance |
| rs374330873 | 14:74,040,139 | G/A | — | uncertain significance |
| rs138474239 | 14:74,040,154 | C/T | — | uncertain significance |
| rs371120372 | 14:74,040,206 | A/G | — | uncertain significance |
| rs144456444 | 14:74,040,247 | C/A | — | uncertain significance |
| rs202093592 | 14:74,040,268 | A/G | — | likely benign |
| rs566644923 | 14:74,041,625 | G/A | — | uncertain significance |
| rs1333630308 | 14:74,041,630 | G/A | — | uncertain significance |
| rs748050270 | 14:74,041,733 | T/C | — | uncertain significance |
| rs149033118 | 14:74,041,748 | A/G | — | benign |
| rs1163124312 | 14:74,041,771 | C/G | — | uncertain significance |
| rs1217059874 | 14:74,041,934 | A/G | — | uncertain significance |
| rs769994894 | 14:74,041,986 | T/A | — | uncertain significance |
| rs2504374227 | 14:74,042,052 | C/A | — | uncertain significance |
| rs774809147 | 14:74,042,057 | T/C | — | uncertain significance |
| rs752481307 | 14:74,042,090 | G/T | — | uncertain significance |
| rs763937556 | 14:74,042,099 | T/C | — | uncertain significance |
| rs1349990656 | 14:74,042,119 | G/A | — | uncertain significance |
| rs781429892 | 14:74,042,120 | C/T | — | uncertain significance |
| rs373287260 | 14:74,042,128 | A/G | — | uncertain significance |
| rs748658805 | 14:74,042,152 | C/G | — | uncertain significance |
| rs767552068 | 14:74,042,188 | C/T | — | uncertain significance |
| rs779958740 | 14:74,042,191 | G/A | — | likely benign |
| rs2504374714 | 14:74,042,200 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.