ZNF208

zinc finger protein 208

Summary

Zinc finger proteins (ZNFs), such as ZNF208, bind DNA and, through this binding, regulate gene transcription. Most ZNFs contain conserved C2H2 motifs and are classified as Kruppel-type zinc fingers. A conserved protein motif, termed the Kruppel-associated box (KRAB) domain, mediates protein-protein interactions (Eichler et al., 1998 [PubMed 9724325]). See ZNF91 (MIM 603971) for further information on ZNFs.[supplied by OMIM, Aug 2009]

Known Variants105 total

rsidPosition (GRCh37)AllelesClassClinVar
rs53781590919:22,131,094G/A——
rs226290919:22,135,270A/Cintron variant—
rs74777987219:22,153,993C/G—not provided
rs147287216519:22,154,079A/G—uncertain significance
rs56272313519:22,154,121T/C—uncertain significance
rs137683546619:22,154,135A/T—uncertain significance
rs78005043419:22,154,174C/A—uncertain significance
rs74810945319:22,154,186T/A—uncertain significance
rs251332644819:22,154,189T/C—uncertain significance
rs37389626219:22,154,222G/A—uncertain significance
rs18070298819:22,154,235C/T—uncertain significance
rs11654207019:22,154,281T/A—likely benign
rs37210098519:22,154,289T/C—uncertain significance
rs75361604919:22,154,297A/C—uncertain significance
rs74612776719:22,154,312C/T—uncertain significance
rs52727833319:22,154,360T/C—uncertain significance
rs57470517119:22,154,439C/G—uncertain significance
rs74829388219:22,154,514T/C—uncertain significance
rs76561297819:22,154,548C/G—uncertain significance
rs77968148219:22,154,603G/A—uncertain significance
rs76508895119:22,154,643C/T—uncertain significance
rs251332796219:22,154,697G/T—uncertain significance
rs130171563119:22,154,825T/C—uncertain significance
rs139633502119:22,154,852T/C—uncertain significance
rs95389660419:22,154,865G/T—uncertain significance
rs77798570219:22,154,900C/T—uncertain significance
rs120566702919:22,154,912T/C—uncertain significance
rs18608530419:22,154,914T/C—likely benign
rs20091894019:22,154,984C/T—uncertain significance
rs251332881519:22,155,015C/T—uncertain significance
rs94150045719:22,155,032T/C—uncertain significance
rs37080497819:22,155,038C/T—uncertain significance
rs142506677619:22,155,063C/T—uncertain significance
rs75547849019:22,155,180C/T—uncertain significance
rs37128855119:22,155,182C/A—uncertain significance
rs56491350919:22,155,203T/C—uncertain significance
rs77530937219:22,155,206C/T—uncertain significance
rs36864051819:22,155,228A/C—uncertain significance
rs76573791719:22,155,234T/C—uncertain significance
rs132119043919:22,155,269G/A—uncertain significance
rs142774194819:22,155,279C/T—uncertain significance
rs14572263119:22,155,321C/A—uncertain significance
rs138522813219:22,155,357G/C—uncertain significance
rs37155642119:22,155,378G/A—uncertain significance
rs37589612919:22,155,435C/A—uncertain significance
rs20152296619:22,155,438T/C—uncertain significance
rs86675948919:22,155,441G/A—uncertain significance
rs74984729419:22,155,452T/C—uncertain significance
rs76025948019:22,155,453G/A—uncertain significance
rs19965084919:22,155,495C/G—uncertain significance
rs37544708519:22,155,510G/A—uncertain significance
rs251332994819:22,155,549T/C—uncertain significance
rs37711924119:22,155,568T/A—uncertain significance
rs251333003819:22,155,581T/C—uncertain significance
rs75033367219:22,155,692T/C—uncertain significance
rs251333036919:22,155,734G/C—uncertain significance
rs77183721819:22,155,735C/G—uncertain significance
rs128457964319:22,155,745T/G—uncertain significance
rs74774721519:22,155,779A/G—uncertain significance
rs37145159319:22,155,808C/G—uncertain significance
rs36997253619:22,155,854C/G—uncertain significance
rs57039662919:22,155,912A/T—uncertain significance
rs102494573319:22,155,921A/T—uncertain significance
rs37562831719:22,156,086C/T—uncertain significance
rs251333145219:22,156,112T/A—uncertain significance
rs53344843619:22,156,124T/C—uncertain significance
rs19258857419:22,156,155C/T—uncertain significance
rs145655635119:22,156,160C/G—uncertain significance
rs18437885019:22,156,162A/G—likely benign
rs87924263219:22,156,279A/G—likely benign
rs56792205819:22,156,292T/C—uncertain significance
rs6211092519:22,156,303G/A—likely benign
rs138872336319:22,156,305T/G—uncertain significance
rs36859913819:22,156,340C/T—uncertain significance
rs77258198219:22,156,353T/C—uncertain significance
rs14201178519:22,156,437T/G—uncertain significance
rs76842003319:22,156,544C/A—uncertain significance
rs53115093619:22,156,566G/T—uncertain significance
rs37033612819:22,156,574C/G—uncertain significance
rs11370733519:22,156,589T/G—uncertain significance
rs251333282919:22,156,715C/T—uncertain significance
rs75750839619:22,156,763T/C—uncertain significance
rs36754684019:22,156,774T/G—likely benign
rs197037200419:22,156,810T/A—uncertain significance
rs75691718719:22,156,875C/T—uncertain significance
rs145654334519:22,156,908C/G—uncertain significance
rs75845198519:22,156,934G/T—uncertain significance
rs104712511619:22,156,959C/T—uncertain significance
rs6174242119:22,156,983T/A—likely benign
rs20218242019:22,157,028C/A—uncertain significance
rs20056428219:22,157,056T/G—uncertain significance
rs135644353019:22,157,073T/C—uncertain significance
rs75928559119:22,157,097G/T—uncertain significance
rs18497059619:22,157,114A/T—uncertain significance
rs56118599919:22,157,237G/A—uncertain significance
rs75790324919:22,157,286T/G—uncertain significance
rs77583686519:22,157,349G/A—uncertain significance
rs53055951719:22,157,397G/A—uncertain significance
rs75463019919:22,157,406C/A—uncertain significance
rs197039438819:22,157,496T/G—uncertain significance

Showing 100 of 105 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.