ZNF106

zinc finger protein 106

Summary

Enables RNA binding activity. Predicted to be involved in insulin receptor signaling pathway. Predicted to be located in nuclear speck and nucleolus. Predicted to be active in cytosol and membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants100 total

rsidPosition (GRCh37)AllelesClassClinVar
rs2836455915:42,706,287T/Cdownstream gene variant—
rs11506209815:42,709,996A/C—benign
rs76705756615:42,710,064G/A—uncertain significance
rs13825484415:42,710,122C/T—uncertain significance
rs123253533615:42,714,172T/G—uncertain significance
rs254831795215:42,714,752T/C—uncertain significance
rs18382896115:42,717,090C/T—uncertain significance
rs77511530215:42,717,117T/C—uncertain significance
rs254832234215:42,717,192T/C—uncertain significance
rs14973293215:42,720,268C/T—uncertain significance
rs254832594015:42,720,286C/A—uncertain significance
rs14573799415:42,720,322C/T—uncertain significance
rs14137190515:42,727,660C/G—likely benign
rs254833705115:42,727,701C/G—uncertain significance
rs254833706015:42,727,704T/C—likely benign
rs77381229815:42,731,255C/T—uncertain significance
rs77772758315:42,731,364G/C—uncertain significance
rs75170006415:42,731,528C/G—uncertain significance
rs15124245815:42,731,622G/A—uncertain significance
rs95415699715:42,731,648T/G—uncertain significance
rs254834351615:42,731,751C/G—uncertain significance
rs76633256115:42,731,771A/G—likely benign
rs254834360415:42,731,792T/C—uncertain significance
rs37468904215:42,731,875T/A—uncertain significance
rs55867691815:42,734,376C/G—uncertain significance
rs11359062715:42,734,482C/A—uncertain significance
rs20112102015:42,734,585T/C—conflicting classifications of pathogenicity
rs14628235615:42,734,609G/C—uncertain significance
rs13942446615:42,736,454T/G—uncertain significance
rs254835219915:42,737,042G/A—uncertain significance
rs11681289015:42,737,078C/T—benign
rs143160876815:42,737,177G/A—uncertain significance
rs75158122715:42,740,343G/C—uncertain significance
rs75536527815:42,740,418C/T—uncertain significance
rs74564433615:42,740,468G/C—uncertain significance
rs77982168715:42,740,491T/A—uncertain significance
rs74781614315:42,740,505T/C—likely benign
rs77363847515:42,740,512A/G—uncertain significance
rs14264063415:42,740,541G/A—uncertain significance
rs126835176515:42,740,558C/G—uncertain significance
rs77984569915:42,740,571C/T—uncertain significance
rs254835715515:42,740,708G/T—uncertain significance
rs20000605215:42,740,719C/G—uncertain significance
rs254835720215:42,740,724G/A—uncertain significance
rs254835725015:42,740,751T/G—uncertain significance
rs74889885915:42,740,763C/T—uncertain significance
rs254835733715:42,740,773C/T—uncertain significance
rs205586177215:42,740,812G/T—uncertain significance
rs116279418115:42,740,881G/A—uncertain significance
rs254835922915:42,742,032T/G—uncertain significance
rs126098547515:42,742,036C/A—uncertain significance
rs140681876715:42,742,066G/A—uncertain significance
rs13786181015:42,742,110C/T—uncertain significance
rs14270543115:42,742,118G/T—uncertain significance
rs55856471015:42,742,128C/T—uncertain significance
rs143443596115:42,742,135G/A—uncertain significance
rs15058829615:42,742,344T/C—uncertain significance
rs74720786315:42,742,455T/C—uncertain significance
rs127105508215:42,742,459G/A—uncertain significance
rs55027999115:42,742,483T/C—uncertain significance
rs74909438715:42,742,564C/T—uncertain significance
rs56661127215:42,742,719T/C—uncertain significance
rs37507612715:42,742,794C/T—likely benign
rs20140800215:42,742,800G/T—uncertain significance
rs120451687615:42,742,801T/C—uncertain significance
rs15132038515:42,742,897A/G—uncertain significance
rs7340275815:42,742,905T/C—uncertain significance
rs37654937415:42,742,939T/C—likely benign
rs74884569515:42,742,957A/G—uncertain significance
rs76881027415:42,743,122C/T—uncertain significance
rs55067247815:42,743,182T/G—uncertain significance
rs20173827415:42,743,209G/A—uncertain significance
rs14777079115:42,743,222T/G—uncertain significance
rs254836212515:42,743,331G/A—uncertain significance
rs76868534215:42,743,340G/A—uncertain significance
rs54387441715:42,743,379G/A—likely benign
rs254836220915:42,743,380C/T—likely benign
rs20140167315:42,743,457T/G—uncertain significance
rs14132259815:42,743,496G/A—uncertain significance
rs76714074815:42,743,556C/T—uncertain significance
rs254836269915:42,743,590T/C—uncertain significance
rs76901204315:42,743,712C/A—uncertain significance
rs127390073015:42,743,751T/C—uncertain significance
rs20118832915:42,743,764A/C—uncertain significance
rs254836314115:42,743,767C/T—uncertain significance
rs254836346915:42,743,919G/T—uncertain significance
rs74592421515:42,743,923G/A—likely benign
rs75045792715:42,743,941C/T—likely benign
rs1244011815:42,744,094A/Gmissense variant—
rs14295027715:42,744,100G/C—uncertain significance
rs54087372515:42,745,557C/G——
rs77412059015:42,749,178T/C—uncertain significance
rs123346629315:42,749,247T/C—uncertain significance
rs99976297215:42,749,252T/C—uncertain significance
rs74563087715:42,749,282C/T—uncertain significance
rs18480603815:42,749,349T/G—uncertain significance
rs205625680315:42,749,376A/C—uncertain significance
rs75202128715:42,749,387A/T—uncertain significance
rs6202231315:42,749,476C/Tregulatory region variant—
rs1244324615:42,752,830A/Gupstream gene variant—

Gene information from NCBI Gene. Variant classifications from ClinVar.