OASL
2'-5'-oligoadenylate synthetase like
Summary
Enables DNA binding activity and double-stranded RNA binding activity. Involved in several processes, including interleukin-27-mediated signaling pathway; negative regulation of viral genome replication; and positive regulation of RIG-I signaling pathway. Located in cytosol; nucleolus; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1169279 | 12:121,455,873 | C/A | — | — |
| rs775974042 | 12:121,458,423 | C/T | — | uncertain significance |
| rs772693625 | 12:121,458,549 | T/C | — | uncertain significance |
| rs759319882 | 12:121,458,597 | C/T | — | uncertain significance |
| rs755698761 | 12:121,458,600 | A/C | — | uncertain significance |
| rs1237961998 | 12:121,458,683 | C/G | — | uncertain significance |
| rs756365167 | 12:121,458,758 | C/T | — | likely benign |
| rs767845941 | 12:121,458,854 | C/T | — | uncertain significance |
| rs145988796 | 12:121,459,280 | C/G | upstream gene variant | — |
| rs7957197 | 12:121,460,686 | T/A | intron variant | — |
| rs757475141 | 12:121,461,804 | A/G | — | uncertain significance |
| rs144968499 | 12:121,461,903 | C/T | — | uncertain significance |
| rs748864742 | 12:121,461,907 | G/A | — | likely benign |
| rs765526981 | 12:121,461,934 | G/C | — | uncertain significance |
| rs371837561 | 12:121,461,939 | G/A | — | uncertain significance |
| rs936821948 | 12:121,465,441 | C/G | — | uncertain significance |
| rs779607362 | 12:121,465,509 | C/T | — | uncertain significance |
| rs140216868 | 12:121,465,539 | C/G | — | uncertain significance |
| rs1012151810 | 12:121,465,577 | T/C | — | uncertain significance |
| rs140478455 | 12:121,468,454 | C/T | intron variant | — |
| rs367594742 | 12:121,469,270 | C/T | — | uncertain significance |
| rs1423552849 | 12:121,469,296 | C/A | — | likely benign |
| rs2500174480 | 12:121,469,364 | C/A | — | uncertain significance |
| rs138760740 | 12:121,469,376 | T/C | — | uncertain significance |
| rs774760823 | 12:121,471,287 | A/G | — | uncertain significance |
| rs140970607 | 12:121,471,314 | C/T | — | likely benign |
| rs61733224 | 12:121,471,325 | G/A | — | likely benign |
| rs779998873 | 12:121,471,326 | A/G | — | uncertain significance |
| rs3213545 | 12:121,471,337 | G/C | synonymous variant | — |
| rs140204273 | 12:121,471,341 | G/T | — | uncertain significance |
| rs757485079 | 12:121,471,368 | A/G | — | uncertain significance |
| rs768970379 | 12:121,471,420 | A/G | — | likely benign |
| rs1592939473 | 12:121,471,936 | G/C | — | — |
| rs1366382657 | 12:121,472,592 | C/G | — | — |
| rs775423659 | 12:121,476,720 | C/T | — | uncertain significance |
| rs10083043 | 12:121,477,359 | G/T | — | — |
| rs2859402 | 12:121,478,277 | A/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.