NOL10
nucleolar protein 10
Summary
Enables RNA binding activity. Predicted to be involved in maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA). Located in nucleolus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs9287719 | 2:10,710,730 | C/T | downstream gene variant | — |
| rs191584876 | 2:10,712,241 | C/T | — | uncertain significance |
| rs142436125 | 2:10,712,246 | G/A | — | uncertain significance |
| rs139240350 | 2:10,712,252 | C/T | — | uncertain significance |
| rs6748036 | 2:10,717,489 | C/T | intron variant | — |
| rs772961320 | 2:10,729,199 | T/C | — | uncertain significance |
| rs144219590 | 2:10,729,216 | T/C | — | likely benign |
| rs140097585 | 2:10,729,255 | T/C | — | likely benign |
| rs1490784590 | 2:10,729,268 | T/C | — | uncertain significance |
| rs2528957622 | 2:10,729,303 | C/G | — | uncertain significance |
| rs546811374 | 2:10,729,320 | G/A | — | uncertain significance |
| rs756599019 | 2:10,729,358 | T/C | — | uncertain significance |
| rs1373080489 | 2:10,729,364 | C/T | — | uncertain significance |
| rs924654311 | 2:10,729,374 | T/G | — | uncertain significance |
| rs1675278228 | 2:10,729,389 | G/A | — | uncertain significance |
| rs201341163 | 2:10,729,400 | G/T | — | uncertain significance |
| rs749214861 | 2:10,729,712 | G/A | — | uncertain significance |
| rs17390099 | 2:10,729,719 | T/G | — | uncertain significance |
| rs745677386 | 2:10,729,870 | G/A | — | uncertain significance |
| rs2529011158 | 2:10,740,984 | C/T | — | uncertain significance |
| rs368516979 | 2:10,741,017 | C/G | — | uncertain significance |
| rs566429655 | 2:10,743,251 | G/A | — | uncertain significance |
| rs531990647 | 2:10,747,419 | G/A | — | uncertain significance |
| rs746920797 | 2:10,747,431 | C/G | — | uncertain significance |
| rs1676312992 | 2:10,747,437 | C/T | — | uncertain significance |
| rs750546503 | 2:10,784,486 | G/A | — | uncertain significance |
| rs757040218 | 2:10,794,652 | C/T | — | uncertain significance |
| rs766441548 | 2:10,797,942 | C/A | — | uncertain significance |
| rs1679946730 | 2:10,797,953 | G/C | — | uncertain significance |
| rs748647508 | 2:10,799,324 | T/C | — | uncertain significance |
| rs141929424 | 2:10,803,113 | C/T | — | uncertain significance |
| rs1680944642 | 2:10,811,722 | G/A | — | uncertain significance |
| rs778094190 | 2:10,815,931 | A/G | — | uncertain significance |
| rs1681268498 | 2:10,815,935 | A/G | — | uncertain significance |
| rs781044448 | 2:10,815,983 | G/A | — | uncertain significance |
| rs769455861 | 2:10,815,988 | T/G | — | uncertain significance |
| rs2529531855 | 2:10,822,111 | T/C | — | uncertain significance |
| rs780939988 | 2:10,822,114 | T/G | — | uncertain significance |
| rs777464100 | 2:10,822,136 | T/C | — | uncertain significance |
| rs1271716837 | 2:10,822,155 | C/T | — | uncertain significance |
| rs757440327 | 2:10,829,935 | T/C | — | uncertain significance |
| rs1415504177 | 2:10,829,960 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.