U2SURP
U2 snRNP associated SURP domain containing
Summary
Enables RNA binding activity. Predicted to be involved in RNA processing. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs758588508 | 3:142,720,486 | C/T | — | uncertain significance |
| rs749860940 | 3:142,720,498 | C/G | — | uncertain significance |
| rs11915462 | 3:142,722,911 | A/C | — | — |
| rs756994177 | 3:142,731,110 | G/A | — | uncertain significance |
| rs372782950 | 3:142,731,130 | C/T | — | uncertain significance |
| rs2472703253 | 3:142,735,158 | T/A | — | uncertain significance |
| rs760272213 | 3:142,735,745 | T/A | — | uncertain significance |
| rs570938056 | 3:142,740,332 | C/T | — | uncertain significance |
| rs748442364 | 3:142,741,700 | A/T | — | uncertain significance |
| rs2472718320 | 3:142,741,702 | G/T | — | uncertain significance |
| rs374471161 | 3:142,741,875 | C/T | — | uncertain significance |
| rs145720949 | 3:142,746,021 | A/T | synonymous variant | — |
| rs570551610 | 3:142,747,350 | C/T | — | uncertain significance |
| rs6808689 | 3:142,749,819 | A/G | intron variant | — |
| rs77794774 | 3:142,752,157 | A/T | — | benign |
| rs763535711 | 3:142,753,768 | A/G | — | uncertain significance |
| rs2472744642 | 3:142,754,849 | C/T | — | uncertain significance |
| rs370077868 | 3:142,756,112 | C/T | — | uncertain significance |
| rs1158591589 | 3:142,762,049 | G/A | — | uncertain significance |
| rs2472759020 | 3:142,762,083 | A/C | — | uncertain significance |
| rs13088265 | 3:142,762,510 | A/T | — | — |
| rs9877128 | 3:142,762,910 | C/T | intron variant | — |
| rs6440132 | 3:142,764,236 | A/T | intron variant | — |
| rs59236208 | 3:142,765,897 | C/T | — | — |
| rs6440133 | 3:142,766,744 | C/G | — | — |
| rs2472778910 | 3:142,769,829 | A/G | — | uncertain significance |
| rs1279695263 | 3:142,769,835 | C/A | — | uncertain significance |
| rs779112330 | 3:142,769,836 | C/T | — | uncertain significance |
| rs1391024897 | 3:142,773,807 | C/G | — | uncertain significance |
| rs2472790143 | 3:142,775,205 | A/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.