ACY3
aminoacylase 3
Summary
Predicted to enable aminoacylase activity. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs202083681 | 11:67,410,226 | G/A | — | likely benign |
| rs780801563 | 11:67,410,227 | C/A | — | uncertain significance |
| rs2495789836 | 11:67,410,254 | A/G | — | likely benign |
| rs185370494 | 11:67,410,311 | A/T | — | uncertain significance |
| rs1855435303 | 11:67,410,338 | C/T | — | uncertain significance |
| rs773292003 | 11:67,410,350 | C/T | — | uncertain significance |
| rs1855436243 | 11:67,410,373 | A/G | — | uncertain significance |
| rs1414440533 | 11:67,410,403 | T/A | — | uncertain significance |
| rs187434412 | 11:67,410,454 | C/T | upstream gene variant | — |
| rs537647642 | 11:67,412,293 | C/T | — | uncertain significance |
| rs189035817 | 11:67,412,533 | A/G | — | uncertain significance |
| rs756371433 | 11:67,412,565 | C/T | — | uncertain significance |
| rs771683337 | 11:67,412,808 | C/T | — | uncertain significance |
| rs1855493341 | 11:67,412,815 | A/G | — | uncertain significance |
| rs370834010 | 11:67,412,829 | C/G | — | uncertain significance |
| rs76819752 | 11:67,412,839 | C/T | missense variant | — |
| rs201592455 | 11:67,413,177 | A/T | — | uncertain significance |
| rs532661025 | 11:67,413,281 | G/A | — | uncertain significance |
| rs551376834 | 11:67,413,293 | C/T | — | uncertain significance |
| rs2495801814 | 11:67,413,327 | C/T | — | uncertain significance |
| rs201375174 | 11:67,413,341 | T/C | — | uncertain significance |
| rs928996990 | 11:67,414,304 | G/A | — | uncertain significance |
| rs745363368 | 11:67,414,331 | G/A | — | uncertain significance |
| rs773950556 | 11:67,414,353 | G/C | — | uncertain significance |
| rs373688915 | 11:67,414,358 | C/T | — | uncertain significance |
| rs779671699 | 11:67,414,421 | G/A | — | uncertain significance |
| rs1343708838 | 11:67,414,468 | A/G | — | uncertain significance |
| rs755211338 | 11:67,414,477 | C/T | — | uncertain significance |
| rs754555869 | 11:67,414,487 | G/A | — | uncertain significance |
| rs200922233 | 11:67,414,493 | G/A | — | uncertain significance |
| rs2509715 | 11:67,414,591 | G/A | regulatory region variant | — |
| rs7108760 | 11:67,414,647 | A/G | downstream gene variant | — |
| rs2514035 | 11:67,414,828 | T/A | — | — |
| rs115777389 | 11:67,415,163 | C/G | regulatory region variant | — |
| rs2252577 | 11:67,418,037 | T/C | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.