HIVEP3

HIVEP zinc finger 3

Summary

This gene encodes a member of the human immunodeficiency virus type 1 enhancer-binding protein family. Members of this protein family contain multiple zinc finger and acid-rich (ZAS) domains and serine-threonine rich regions. This protein acts as a transcription factor and is able to regulate nuclear factor kappaB-mediated transcription by binding the kappaB motif in target genes. This protein also binds the recombination signal sequence that flanks the V, D, and J regions of immunoglobulin and T-cell receptors. Alternate splicing results in both coding and non-coding transcript variants. [provided by RefSeq, Sep 2011]

Known Variants109 total

rsidPosition (GRCh37)AllelesClassClinVar
rs740715591:41,976,132G/C—benign
rs726690051:41,976,217A/G—benign
rs1996960521:41,976,252C/T—likely benign
rs2003238281:41,976,310C/T—benign
rs124065241:41,976,320G/A—benign
rs94390431:41,976,328T/C—benign
rs5593611611:41,976,329C/T—likely benign
rs589304361:41,976,330G/A—benign
rs1408392221:41,976,345C/T—benign
rs2001385111:41,976,375C/T—benign
rs5548448741:41,976,392C/T—likely benign
rs749433371:41,976,422G/T—likely benign
rs2000265651:41,976,455G/A—likely benign
rs1426955721:41,976,497G/A—likely benign
rs118094231:41,976,529C/T—benign
rs602325661:41,976,575A/G—benign
rs1416792881:41,976,584G/A—likely benign
rs1477497271:41,976,621C/T—benign
rs1447590961:41,976,652C/T—likely benign
rs1379183171:41,976,665G/A—benign
rs1140448011:41,976,720C/T—benign
rs14855380641:41,976,917A/G—likely benign
rs1485813121:41,976,928C/T—benign
rs1150490221:41,976,943G/A—benign
rs740715611:41,978,850G/A—benign
rs1154610721:41,978,890C/T—benign
rs16424939531:41,978,924T/G—likely benign
rs797915941:41,978,953G/T—benign
rs6151771:41,979,156A/G—benign
rs1400353361:41,979,162C/T—benign
rs787936081:41,979,163G/A—benign
rs5272784411:41,979,184G/A—benign
rs1506449751:41,979,243C/T—likely benign
rs21490473921:41,979,247G/T—uncertain significance
rs1490328631:41,984,079C/T—likely benign
rs351227331:41,990,461G/A—benign
rs12919981921:41,990,565C/T—uncertain significance
rs6533691:42,002,376A/Tregulatory region variant—
rs1144983791:42,045,427C/T—benign
rs1410958311:42,045,432G/A—likely benign
rs21491032921:42,045,469G/A—benign
rs99431711:42,045,741C/T—benign
rs357303801:42,045,747C/T—benign
rs349708841:42,045,770G/A—likely benign
rs13226740511:42,046,146G/A—likely benign
rs25219433051:42,046,182T/C—likely benign
rs16443896001:42,046,348T/C—uncertain significance
rs357844701:42,046,485C/T—benign
rs356241001:42,046,491A/G—benign
rs5775477041:42,046,530G/A—likely benign
rs121326971:42,046,613G/T—benign
rs617324951:42,046,782C/A—benign
rs28105651:42,046,812C/T—benign
rs1439628781:42,046,899C/T—likely benign
rs1429854411:42,047,058T/C—likely benign
rs2001639481:42,047,061C/T—likely benign
rs5430761901:42,047,163C/T—likely benign
rs173634721:42,047,208C/G—benign
rs7550091161:42,047,211G/T—likely benign
rs412694731:42,047,300A/T—benign
rs412694751:42,047,370C/T—likely benign
rs1434761881:42,047,535G/T—likely benign
rs7759686301:42,047,694A/G—likely benign
rs1476505651:42,047,957G/A—likely benign
rs1420435721:42,048,122C/T—likely benign
rs1404632631:42,048,228C/T—likely benign
rs1474236951:42,048,230G/A—likely benign
rs7550414281:42,048,361A/C—uncertain significance
rs360862471:42,048,387C/T—likely benign
rs99430821:42,048,456G/A—benign
rs7678787291:42,048,540G/A—likely benign
rs28105661:42,048,745T/C—benign
rs29846941:42,049,032G/A—benign
rs1485124201:42,049,134G/A—likely benign
rs24758421:42,049,140C/G—benign
rs412694771:42,049,250G/T—likely benign
rs2016837361:42,049,278G/A—benign
rs1463249751:42,049,386C/T—likely benign
rs1416365661:42,049,422G/C—likely benign
rs357983501:42,049,542G/A—benign
rs1408486371:42,050,000G/T—likely benign
rs1387853921:42,050,007G/A—likely benign
rs617736801:42,050,055T/G—benign
rs3696418111:42,050,181C/T—likely benign
rs1475454201:42,050,343T/A—likely benign
rs752025911:42,050,364G/T—benign
rs21463151:42,050,366T/C—benign
rs1162665511:42,050,432C/T—benign
rs7520101:42,093,015C/Tregulatory region variant—
rs20773541:42,180,082T/A——
rs66003871:42,182,588G/Tintron variant—
rs7102391:42,198,576G/C——
rs7102361:42,202,168C/Tintron variant—
rs127593271:42,222,840G/Aupstream gene variant—
rs23655711:42,230,597C/Aintron variant—
rs561127421:42,253,210T/C——
rs3494231:42,297,124C/Tintron variant—
rs6980471:42,333,603C/A——
rs7834341:42,333,858G/A——
rs1141378541:42,355,082G/Cintron variant—

Showing 100 of 109 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.