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/Gnot provided
rs147287216519:22,154,079A/Guncertain significance
rs56272313519:22,154,121T/Cuncertain significance
rs137683546619:22,154,135A/Tuncertain significance
rs78005043419:22,154,174C/Auncertain significance
rs74810945319:22,154,186T/Auncertain significance
rs251332644819:22,154,189T/Cuncertain significance
rs37389626219:22,154,222G/Auncertain significance
rs18070298819:22,154,235C/Tuncertain significance
rs11654207019:22,154,281T/Alikely benign
rs37210098519:22,154,289T/Cuncertain significance
rs75361604919:22,154,297A/Cuncertain significance
rs74612776719:22,154,312C/Tuncertain significance
rs52727833319:22,154,360T/Cuncertain significance
rs57470517119:22,154,439C/Guncertain significance
rs74829388219:22,154,514T/Cuncertain significance
rs76561297819:22,154,548C/Guncertain significance
rs77968148219:22,154,603G/Auncertain significance
rs76508895119:22,154,643C/Tuncertain significance
rs251332796219:22,154,697G/Tuncertain significance
rs130171563119:22,154,825T/Cuncertain significance
rs139633502119:22,154,852T/Cuncertain significance
rs95389660419:22,154,865G/Tuncertain significance
rs77798570219:22,154,900C/Tuncertain significance
rs120566702919:22,154,912T/Cuncertain significance
rs18608530419:22,154,914T/Clikely benign
rs20091894019:22,154,984C/Tuncertain significance
rs251332881519:22,155,015C/Tuncertain significance
rs94150045719:22,155,032T/Cuncertain significance
rs37080497819:22,155,038C/Tuncertain significance
rs142506677619:22,155,063C/Tuncertain significance
rs75547849019:22,155,180C/Tuncertain significance
rs37128855119:22,155,182C/Auncertain significance
rs56491350919:22,155,203T/Cuncertain significance
rs77530937219:22,155,206C/Tuncertain significance
rs36864051819:22,155,228A/Cuncertain significance
rs76573791719:22,155,234T/Cuncertain significance
rs132119043919:22,155,269G/Auncertain significance
rs142774194819:22,155,279C/Tuncertain significance
rs14572263119:22,155,321C/Auncertain significance
rs138522813219:22,155,357G/Cuncertain significance
rs37155642119:22,155,378G/Auncertain significance
rs37589612919:22,155,435C/Auncertain significance
rs20152296619:22,155,438T/Cuncertain significance
rs86675948919:22,155,441G/Auncertain significance
rs74984729419:22,155,452T/Cuncertain significance
rs76025948019:22,155,453G/Auncertain significance
rs19965084919:22,155,495C/Guncertain significance
rs37544708519:22,155,510G/Auncertain significance
rs251332994819:22,155,549T/Cuncertain significance
rs37711924119:22,155,568T/Auncertain significance
rs251333003819:22,155,581T/Cuncertain significance
rs75033367219:22,155,692T/Cuncertain significance
rs251333036919:22,155,734G/Cuncertain significance
rs77183721819:22,155,735C/Guncertain significance
rs128457964319:22,155,745T/Guncertain significance
rs74774721519:22,155,779A/Guncertain significance
rs37145159319:22,155,808C/Guncertain significance
rs36997253619:22,155,854C/Guncertain significance
rs57039662919:22,155,912A/Tuncertain significance
rs102494573319:22,155,921A/Tuncertain significance
rs37562831719:22,156,086C/Tuncertain significance
rs251333145219:22,156,112T/Auncertain significance
rs53344843619:22,156,124T/Cuncertain significance
rs19258857419:22,156,155C/Tuncertain significance
rs145655635119:22,156,160C/Guncertain significance
rs18437885019:22,156,162A/Glikely benign
rs87924263219:22,156,279A/Glikely benign
rs56792205819:22,156,292T/Cuncertain significance
rs6211092519:22,156,303G/Alikely benign
rs138872336319:22,156,305T/Guncertain significance
rs36859913819:22,156,340C/Tuncertain significance
rs77258198219:22,156,353T/Cuncertain significance
rs14201178519:22,156,437T/Guncertain significance
rs76842003319:22,156,544C/Auncertain significance
rs53115093619:22,156,566G/Tuncertain significance
rs37033612819:22,156,574C/Guncertain significance
rs11370733519:22,156,589T/Guncertain significance
rs251333282919:22,156,715C/Tuncertain significance
rs75750839619:22,156,763T/Cuncertain significance
rs36754684019:22,156,774T/Glikely benign
rs197037200419:22,156,810T/Auncertain significance
rs75691718719:22,156,875C/Tuncertain significance
rs145654334519:22,156,908C/Guncertain significance
rs75845198519:22,156,934G/Tuncertain significance
rs104712511619:22,156,959C/Tuncertain significance
rs6174242119:22,156,983T/Alikely benign
rs20218242019:22,157,028C/Auncertain significance
rs20056428219:22,157,056T/Guncertain significance
rs135644353019:22,157,073T/Cuncertain significance
rs75928559119:22,157,097G/Tuncertain significance
rs18497059619:22,157,114A/Tuncertain significance
rs56118599919:22,157,237G/Auncertain significance
rs75790324919:22,157,286T/Guncertain significance
rs77583686519:22,157,349G/Auncertain significance
rs53055951719:22,157,397G/Auncertain significance
rs75463019919:22,157,406C/Auncertain significance
rs197039438819:22,157,496T/Guncertain significance

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

Gene information from NCBI Gene. Variant classifications from ClinVar.