RPRD2
regulation of nuclear pre-mRNA domain containing 2
Summary
Predicted to enable RNA polymerase II complex binding activity. Predicted to be involved in mRNA 3'-end processing. Part of transcription preinitiation complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants81 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs587738237 | 1:150,336,603 | C/T | — | — |
| rs782300740 | 1:150,337,227 | T/G | — | uncertain significance |
| rs781865386 | 1:150,337,255 | C/T | — | uncertain significance |
| rs1553876932 | 1:150,337,369 | A/G | — | uncertain significance |
| rs146432752 | 1:150,343,426 | A/T | intron variant | — |
| rs112860617 | 1:150,346,093 | G/A | regulatory region variant | — |
| rs149711341 | 1:150,348,530 | A/G | intron variant | — |
| rs1694369 | 1:150,351,101 | A/T | — | — |
| rs74322702 | 1:150,356,929 | T/G | — | — |
| rs11580960 | 1:150,360,849 | C/T | — | — |
| rs142691903 | 1:150,361,733 | C/T | intron variant | — |
| rs72696859 | 1:150,369,895 | A/G | intron variant | — |
| rs12032387 | 1:150,370,742 | G/T | — | — |
| rs587662030 | 1:150,370,846 | G/A | — | — |
| rs11807952 | 1:150,374,447 | T/A | — | — |
| rs184026046 | 1:150,389,534 | A/G | intron variant | — |
| rs587594426 | 1:150,403,360 | G/A | — | — |
| rs12117104 | 1:150,404,669 | G/A | — | — |
| rs72696880 | 1:150,407,596 | G/A | intron variant | — |
| rs587690766 | 1:150,410,281 | C/G | — | — |
| rs140068986 | 1:150,416,744 | A/G | — | benign |
| rs201468730 | 1:150,416,763 | C/T | — | uncertain significance |
| rs2525955357 | 1:150,418,746 | A/C | — | uncertain significance |
| rs782733101 | 1:150,418,779 | G/C | — | uncertain significance |
| rs371243212 | 1:150,418,804 | C/T | — | uncertain significance |
| rs188066772 | 1:150,419,864 | G/A | intron variant | — |
| rs187799739 | 1:150,425,376 | C/A | intron variant | — |
| rs372494231 | 1:150,432,578 | C/A | — | uncertain significance |
| rs781926538 | 1:150,432,601 | A/G | — | uncertain significance |
| rs1553898504 | 1:150,432,628 | T/C | — | uncertain significance |
| rs1553898506 | 1:150,432,629 | G/A | — | uncertain significance |
| rs1553899512 | 1:150,437,087 | C/T | — | uncertain significance |
| rs199825347 | 1:150,437,095 | A/C | — | uncertain significance |
| rs1383054525 | 1:150,437,125 | T/C | — | uncertain significance |
| rs6685125 | 1:150,440,734 | G/A | intron variant | — |
| rs140447820 | 1:150,441,542 | T/G | intron variant | — |
| rs35699789 | 1:150,442,100 | G/T | intron variant | — |
| rs767748023 | 1:150,443,118 | C/G | — | uncertain significance |
| rs200740470 | 1:150,443,553 | G/A | — | uncertain significance |
| rs749008059 | 1:150,443,573 | A/G | — | likely benign |
| rs201498425 | 1:150,443,600 | C/T | — | uncertain significance |
| rs1421836807 | 1:150,443,601 | G/A | — | uncertain significance |
| rs776288719 | 1:150,443,610 | G/A | — | uncertain significance |
| rs763082982 | 1:150,443,675 | T/C | — | uncertain significance |
| rs200404582 | 1:150,443,707 | C/T | — | likely benign |
| rs2526162320 | 1:150,443,726 | A/G | — | uncertain significance |
| rs375366241 | 1:150,443,763 | G/A | — | uncertain significance |
| rs2526165710 | 1:150,443,990 | T/A | — | uncertain significance |
| rs748567967 | 1:150,444,138 | G/A | — | uncertain significance |
| rs762129901 | 1:150,444,164 | G/T | — | uncertain significance |
| rs753717700 | 1:150,444,204 | G/A | — | uncertain significance |
| rs1178696426 | 1:150,444,290 | A/G | — | uncertain significance |
| rs181198755 | 1:150,444,432 | C/T | — | uncertain significance |
| rs376874270 | 1:150,444,573 | C/G | — | uncertain significance |
| rs747729183 | 1:150,444,575 | G/A | — | likely benign |
| rs2526171434 | 1:150,444,582 | A/G | — | uncertain significance |
| rs757842151 | 1:150,444,671 | G/T | — | uncertain significance |
| rs761932812 | 1:150,444,842 | A/G | — | uncertain significance |
| rs377151090 | 1:150,444,868 | G/C | — | uncertain significance |
| rs941565195 | 1:150,444,870 | C/T | — | uncertain significance |
| rs2526174580 | 1:150,444,918 | C/T | — | uncertain significance |
| rs1570809846 | 1:150,444,931 | A/G | — | likely benign |
| rs1399285670 | 1:150,444,933 | G/A | — | uncertain significance |
| rs2526175902 | 1:150,445,024 | A/T | — | uncertain significance |
| rs201108869 | 1:150,445,058 | C/T | — | uncertain significance |
| rs778094347 | 1:150,445,131 | C/T | — | uncertain significance |
| rs772500605 | 1:150,445,175 | G/A | — | uncertain significance |
| rs758512438 | 1:150,445,308 | C/G | — | uncertain significance |
| rs770483785 | 1:150,445,472 | G/A | — | uncertain significance |
| rs1570811548 | 1:150,445,475 | G/T | — | uncertain significance |
| rs587593556 | 1:150,445,488 | G/A | — | uncertain significance |
| rs1161500884 | 1:150,445,511 | A/G | — | uncertain significance |
| rs376890502 | 1:150,445,575 | G/A | — | uncertain significance |
| rs752662984 | 1:150,445,616 | C/G | — | uncertain significance |
| rs369152525 | 1:150,445,617 | C/G | — | uncertain significance |
| rs746732932 | 1:150,445,637 | G/C | — | uncertain significance |
| rs1199094915 | 1:150,445,659 | T/G | — | uncertain significance |
| rs373510243 | 1:150,445,677 | G/A | — | uncertain significance |
| rs757825715 | 1:150,445,694 | A/G | — | uncertain significance |
| rs375980931 | 1:150,445,768 | G/A | — | likely benign |
| rs12141218 | 1:150,448,707 | T/C | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.