BTBD17

BTB domain containing 17

Summary

Predicted to be involved in negative regulation of viral genome replication and response to virus. Predicted to be located in cytoplasm and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants77 total

rsidPosition (GRCh37)AllelesClassClinVar
rs250985728217:72,352,814A/G—likely benign
rs250985729517:72,352,823G/A—likely benign
rs250985730117:72,352,826T/G—likely benign
rs77022069217:72,352,828C/T—uncertain significance
rs13851845217:72,352,838G/A—likely benign
rs77404798817:72,352,847C/G—likely benign
rs120105770517:72,352,850G/A—likely benign
rs125840462117:72,352,852G/T—uncertain significance
rs20144640117:72,352,859G/A—likely benign
rs146621742317:72,352,916G/A—likely benign
rs77046082417:72,352,973C/G—likely benign
rs77822809317:72,352,976C/G—uncertain significance
rs99626453917:72,352,997C/G—likely benign
rs250985755717:72,353,026C/T—uncertain significance
rs125334224817:72,353,048C/G—likely benign
rs205489534517:72,353,060C/G—likely benign
rs205489545317:72,353,063T/C—likely benign
rs125037234717:72,353,068C/T—uncertain significance
rs100485221417:72,353,075C/G—likely benign
rs136713964117:72,353,081C/T—likely benign
rs89368798717:72,353,083C/T—uncertain significance
rs57626992317:72,353,085G/A—uncertain significance
rs77423226817:72,353,086C/G—uncertain significance
rs214431884517:72,353,093A/C—likely benign
rs205489631017:72,353,096A/T—likely benign
rs250985770317:72,353,117A/G—likely benign
rs205489672117:72,353,120G/A—likely benign
rs214431892717:72,353,123C/T—likely benign
rs250985773917:72,353,132G/T—likely benign
rs75296651717:72,353,135G/C—likely benign
rs120315982017:72,353,147C/T—likely benign
rs86852845917:72,353,185C/A—uncertain significance
rs76762548517:72,353,195A/G—likely benign
rs77568635317:72,353,198C/T—likely benign
rs250985797717:72,353,231G/A—likely benign
rs250985807317:72,353,276G/A—likely benign
rs53700070017:72,353,305C/T—uncertain significance
rs250985814117:72,353,309G/A—likely benign
rs20097642517:72,353,324G/T—uncertain significance
rs19161789517:72,353,331G/A—uncertain significance
rs36869701417:72,353,348C/G—likely benign
rs250985822617:72,353,351G/A—likely benign
rs205490115417:72,353,393G/C—likely benign
rs250985831817:72,353,414T/G—likely benign
rs77671012017:72,353,429C/A—likely benign
rs205490218917:72,353,450T/A—likely benign
rs118278349217:72,353,461G/C—uncertain significance
rs139036430017:72,353,465G/A—likely benign
rs205490250317:72,353,468T/G—likely benign
rs250985846117:72,353,483C/G—likely benign
rs250985858217:72,353,543C/G—likely benign
rs250985862617:72,353,552T/C—likely benign
rs250985863317:72,353,555A/G—likely benign
rs250985865417:72,353,567C/G—likely benign
rs250985870917:72,353,588C/G—uncertain significance
rs92214142017:72,353,603G/A—likely benign
rs126614631617:72,353,630G/C—likely benign
rs127601149917:72,353,677C/G—uncertain significance
rs205490613217:72,353,701C/T—likely benign
rs205490675617:72,353,741T/G—likely benign
rs147094507317:72,353,762G/A—likely benign
rs56600704917:72,353,777G/C—likely benign
rs53450831117:72,353,785G/A—likely benign
rs94107729317:72,353,844A/G—uncertain significance
rs37696124917:72,353,845C/T—uncertain significance
rs78033574917:72,356,112T/C—uncertain significance
rs141795760117:72,356,135C/T—uncertain significance
rs37682553517:72,356,241C/T—uncertain significance
rs37414817017:72,356,267C/T—uncertain significance
rs77870308517:72,356,280C/T—uncertain significance
rs76842638317:72,356,298G/A—uncertain significance
rs250986127417:72,356,311C/A—uncertain significance
rs14286961817:72,356,322G/C—uncertain significance
rs20034558717:72,356,363C/T—uncertain significance
rs14166131017:72,356,759A/Tdownstream gene variant—
rs14744027717:72,357,907T/A—uncertain significance
rs250986202617:72,357,939G/C—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.