NOL4L
nucleolar protein 4 like
Summary
Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs761373270 | 20:31,035,530 | C/T | — | likely benign |
| rs2515615029 | 20:31,035,534 | C/G | — | uncertain significance |
| rs749152465 | 20:31,035,571 | G/A | — | uncertain significance |
| rs2515615282 | 20:31,035,589 | G/A | — | uncertain significance |
| rs373397422 | 20:31,035,600 | C/T | — | uncertain significance |
| rs767851391 | 20:31,040,044 | C/G | — | uncertain significance |
| rs776088625 | 20:31,040,107 | C/T | — | uncertain significance |
| rs760632730 | 20:31,040,131 | T/C | — | uncertain significance |
| rs754915933 | 20:31,040,135 | C/T | — | uncertain significance |
| rs758077558 | 20:31,040,212 | T/G | — | uncertain significance |
| rs1323683881 | 20:31,040,718 | C/T | — | uncertain significance |
| rs768619974 | 20:31,040,799 | G/A | — | uncertain significance |
| rs2515628544 | 20:31,041,175 | G/A | — | uncertain significance |
| rs150489354 | 20:31,041,515 | C/T | — | uncertain significance |
| rs563159052 | 20:31,041,557 | G/T | — | uncertain significance |
| rs375855101 | 20:31,043,943 | T/C | — | uncertain significance |
| rs762102836 | 20:31,043,952 | C/T | — | uncertain significance |
| rs772253099 | 20:31,043,953 | G/A | — | uncertain significance |
| rs753806615 | 20:31,043,966 | G/C | — | uncertain significance |
| rs751748242 | 20:31,043,968 | C/T | — | uncertain significance |
| rs577281862 | 20:31,043,975 | G/A | — | likely benign |
| rs146253793 | 20:31,044,018 | G/A | — | uncertain significance |
| rs530345796 | 20:31,044,021 | G/A | — | uncertain significance |
| rs552787821 | 20:31,044,058 | C/T | — | uncertain significance |
| rs570929204 | 20:31,044,059 | G/A | — | likely benign |
| rs2515636809 | 20:31,044,060 | G/A | — | uncertain significance |
| rs369464443 | 20:31,044,076 | T/C | — | uncertain significance |
| rs565497590 | 20:31,049,031 | G/A | — | — |
| rs4911236 | 20:31,082,056 | G/T | — | — |
| rs293550 | 20:31,082,286 | T/C | — | — |
| rs143458646 | 20:31,085,417 | C/T | intron variant | — |
| rs910889 | 20:31,104,950 | T/C | regulatory region variant | — |
| rs6141743 | 20:31,107,399 | C/A | — | — |
| rs733852 | 20:31,111,094 | G/C | — | — |
| rs1868385 | 20:31,111,293 | C/G | — | — |
| rs3746615 | 20:31,123,592 | A/T | regulatory region variant | — |
| rs6119893 | 20:31,142,813 | G/C | — | — |
| rs4911242 | 20:31,157,394 | A/T | regulatory region variant | — |
| rs6141752 | 20:31,157,912 | C/G | — | — |
| rs911526 | 20:31,165,018 | G/A | regulatory region variant | — |
| rs4911100 | 20:31,166,129 | G/T | — | — |
| rs6119269 | 20:31,167,877 | G/A | upstream gene variant | — |
| rs6057599 | 20:31,168,439 | C/T | upstream gene variant | — |
| rs34627022 | 20:31,170,277 | G/C | — | — |
| rs67696533 | 20:31,173,362 | G/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.