IFI44L
interferon induced protein 44 like
Summary
Predicted to be involved in immune response. Predicted to act upstream of or within cellular response to virus. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs375524121 | 1:79,093,614 | C/T | — | uncertain significance |
| rs748219494 | 1:79,093,656 | T/A | — | uncertain significance |
| rs372310725 | 1:79,093,661 | A/T | — | uncertain significance |
| rs143352734 | 1:79,093,698 | A/C | — | uncertain significance |
| rs41292964 | 1:79,093,699 | T/C | — | likely benign |
| rs372837467 | 1:79,093,707 | G/A | — | uncertain significance |
| rs765587785 | 1:79,093,722 | T/C | — | uncertain significance |
| rs149202070 | 1:79,093,737 | G/A | — | likely benign |
| rs780100161 | 1:79,093,773 | A/G | — | uncertain significance |
| rs143077503 | 1:79,093,776 | A/G | — | likely benign |
| rs2523334554 | 1:79,093,917 | A/G | — | uncertain significance |
| rs273258 | 1:79,094,042 | C/T | — | benign |
| rs141849276 | 1:79,094,043 | G/A | — | uncertain significance |
| rs368426493 | 1:79,094,075 | G/C | — | uncertain significance |
| rs1333973 | 1:79,094,081 | T/A | splice region variant | — |
| rs1449108356 | 1:79,094,659 | A/G | — | uncertain significance |
| rs761700063 | 1:79,095,395 | A/G | — | likely benign |
| rs753372312 | 1:79,095,427 | G/C | — | uncertain significance |
| rs1434616567 | 1:79,101,077 | T/G | — | uncertain significance |
| rs139875914 | 1:79,101,115 | G/A | — | uncertain significance |
| rs138987531 | 1:79,101,116 | G/T | — | uncertain significance |
| rs115901054 | 1:79,101,171 | T/A | — | risk factor |
| rs61729831 | 1:79,102,727 | G/A | — | benign |
| rs779446092 | 1:79,102,772 | C/G | — | uncertain significance |
| rs374146000 | 1:79,102,793 | G/C | — | uncertain significance |
| rs773410100 | 1:79,102,798 | G/A | — | uncertain significance |
| rs376331794 | 1:79,102,845 | G/A | — | uncertain significance |
| rs1557690775 | 1:79,106,738 | G/A | — | likely benign |
| rs142635614 | 1:79,106,745 | G/A | — | uncertain significance |
| rs1002531253 | 1:79,106,748 | G/A | — | uncertain significance |
| rs771809041 | 1:79,106,804 | C/T | — | uncertain significance |
| rs762172392 | 1:79,107,133 | A/G | — | uncertain significance |
| rs955407884 | 1:79,107,153 | A/G | — | uncertain significance |
| rs753970944 | 1:79,107,154 | T/C | — | uncertain significance |
| rs758261571 | 1:79,107,168 | A/T | — | uncertain significance |
| rs373251848 | 1:79,107,250 | G/A | — | uncertain significance |
| rs750831210 | 1:79,107,252 | G/T | — | uncertain significance |
| rs754061177 | 1:79,107,271 | A/G | — | uncertain significance |
| rs34615115 | 1:79,107,287 | G/A | — | benign |
| rs1459018734 | 1:79,107,458 | A/G | — | uncertain significance |
| rs201287365 | 1:79,107,475 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.