HNRNPUL2
heterogeneous nuclear ribonucleoprotein U like 2
Summary
Enables RNA binding activity. Predicted to be involved in alternative mRNA splicing, via spliceosome. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs894464 | 11:62,482,267 | T/C | upstream gene variant | — |
| rs2539200839 | 11:62,482,820 | T/G | — | uncertain significance |
| rs746364943 | 11:62,482,829 | T/G | — | uncertain significance |
| rs200712527 | 11:62,482,979 | T/C | — | uncertain significance |
| rs755246 | 11:62,483,386 | C/A | — | uncertain significance |
| rs747224169 | 11:62,483,397 | C/T | — | uncertain significance |
| rs2539202972 | 11:62,484,487 | T/A | — | uncertain significance |
| rs374233501 | 11:62,484,583 | G/A | — | uncertain significance |
| rs371223625 | 11:62,484,591 | T/C | — | likely benign |
| rs2083666924 | 11:62,484,638 | A/G | — | uncertain significance |
| rs530696789 | 11:62,487,528 | C/T | — | uncertain significance |
| rs2119996 | 11:62,488,806 | C/G | — | uncertain significance |
| rs559974309 | 11:62,489,327 | C/T | — | uncertain significance |
| rs757103660 | 11:62,489,342 | C/T | — | uncertain significance |
| rs143617458 | 11:62,489,579 | T/C | — | likely benign |
| rs200099583 | 11:62,489,629 | A/G | — | uncertain significance |
| rs371263471 | 11:62,489,674 | G/A | — | uncertain significance |
| rs757364046 | 11:62,489,758 | C/T | — | uncertain significance |
| rs2539209366 | 11:62,490,173 | A/C | — | uncertain significance |
| rs377641267 | 11:62,490,297 | G/A | — | uncertain significance |
| rs572214914 | 11:62,491,076 | C/T | — | uncertain significance |
| rs758282858 | 11:62,491,100 | T/C | — | uncertain significance |
| rs1590900583 | 11:62,491,795 | G/T | — | uncertain significance |
| rs2539212059 | 11:62,491,802 | C/T | — | uncertain significance |
| rs367701849 | 11:62,491,822 | A/T | — | uncertain significance |
| rs200203108 | 11:62,491,908 | C/T | — | likely benign |
| rs1255444026 | 11:62,494,162 | T/C | — | uncertain significance |
| rs745511216 | 11:62,494,219 | C/T | — | uncertain significance |
| rs375115329 | 11:62,494,221 | G/A | — | likely benign |
| rs773423915 | 11:62,494,244 | C/T | — | conflicting classifications of pathogenicity |
| rs755780740 | 11:62,494,286 | C/T | — | uncertain significance |
| rs749156018 | 11:62,494,289 | G/A | — | uncertain significance |
| rs771954062 | 11:62,494,366 | G/A | — | uncertain significance |
| rs1178739948 | 11:62,494,396 | T/C | — | uncertain significance |
| rs763589221 | 11:62,494,406 | C/A | — | likely pathogenic |
| rs760325484 | 11:62,494,417 | G/A | — | uncertain significance |
| rs376882579 | 11:62,494,434 | G/A | — | likely benign |
| rs1049823117 | 11:62,494,441 | G/A | — | uncertain significance |
| rs1456665906 | 11:62,494,447 | G/C | — | uncertain significance |
| rs965932522 | 11:62,494,472 | G/A | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.