ZNF143

zinc finger protein 143

Summary

Enables DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in positive regulation of snRNA transcription by RNA polymerase II. Predicted to be located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants123 total

rsidPosition (GRCh37)AllelesClassClinVar
rs75677880911:9,492,878G/A—uncertain significance
rs14827776211:9,492,890G/A—uncertain significance
rs74683745711:9,492,900G/A—likely benign
rs19951748411:9,492,924G/T—likely benign
rs6174761011:9,492,961G/A—uncertain significance
rs711968011:9,493,100G/T—benign
rs711970111:9,493,151G/A—benign
rs5957195511:9,494,036T/A—benign
rs1236132811:9,494,066C/T—benign
rs185664996711:9,494,209A/G—likely benign
rs74796894511:9,494,219A/G—likely benign
rs185665087311:9,494,220A/G—uncertain significance
rs159050865011:9,494,234C/G—uncertain significance
rs14260175011:9,494,245T/C—uncertain significance
rs249448546811:9,494,259T/G—uncertain significance
rs94849120011:9,494,261G/T—uncertain significance
rs15098469511:9,494,278C/G—uncertain significance
rs249448620611:9,494,302A/G—uncertain significance
rs18188405511:9,494,332A/G—benign
rs36902987911:9,495,484A/C—likely benign
rs37256884411:9,495,490G/A—uncertain significance
rs249450078311:9,495,553G/A—uncertain significance
rs249450080011:9,495,554T/C—uncertain significance
rs185673911411:9,495,563C/T—uncertain significance
rs14361530911:9,495,564T/C—likely benign
rs227890011:9,495,961A/T—benign
rs185677377711:9,496,129G/A—uncertain significance
rs75435518511:9,496,132G/A—conflicting classifications of pathogenicity
rs77964573111:9,496,170C/T—likely benign
rs1077003411:9,499,574C/Tintron variant—
rs7340626811:9,499,820G/A—benign
rs89319926411:9,499,920C/T—likely benign
rs96367188111:9,499,952G/A—uncertain significance
rs20124042311:9,499,965G/A—likely benign
rs75230865011:9,499,971G/A—likely benign
rs77730129011:9,499,985C/T—uncertain significance
rs15031899511:9,499,994A/T—uncertain significance
rs76341041111:9,500,055G/A—likely benign
rs20147682611:9,500,079G/A—likely benign
rs36783196311:9,500,088A/G—likely benign
rs7340626911:9,500,138A/G—benign
rs91570809811:9,500,139G/C—uncertain significance
rs11560288211:9,500,140C/T—benign
rs134853944211:9,500,148A/T—likely benign
rs75339101711:9,500,149A/G—likely benign
rs55926831611:9,500,150T/C—likely benign
rs7758945111:9,500,940C/G—benign
rs13796373211:9,501,026T/C—uncertain significance
rs36916445211:9,501,041G/C—uncertain significance
rs77941907411:9,501,079G/A—uncertain significance
rs18164040111:9,501,111T/C—benign
rs7702268411:9,501,268T/C—benign
rs1104238211:9,501,274G/T—benign
rs1229326411:9,516,186T/C—benign
rs147104018611:9,516,253G/C—uncertain significance
rs184790190311:9,516,304C/G—uncertain significance
rs7340627911:9,517,657A/G—benign
rs6170866911:9,519,174T/C—benign
rs249388658011:9,519,231T/G—uncertain significance
rs37392078911:9,519,250T/G—likely benign
rs14815182011:9,519,280G/A—likely benign
rs1690684911:9,519,298A/G—benign
rs139063184711:9,519,306A/G—uncertain significance
rs36947975711:9,519,322A/G—likely benign
rs18919179811:9,519,355T/C—benign
rs87894706711:9,519,375C/T—benign
rs6074804111:9,519,409G/A—benign
rs1084024911:9,519,420T/C—benign
rs376387711:9,519,464G/A—benign
rs376387611:9,519,534C/T—benign
rs7933012211:9,522,465T/C—benign
rs7506156211:9,522,494C/A—benign
rs1104239511:9,522,498C/G—benign
rs229042511:9,522,567T/C—benign
rs20173329411:9,522,648C/T—likely benign
rs14733402211:9,522,663C/T—likely benign
rs74913569911:9,522,677G/A—uncertain significance
rs77417072511:9,522,689C/T—uncertain significance
rs77576933411:9,522,712G/A—likely benign
rs76077929411:9,522,714T/A—uncertain significance
rs156505186311:9,522,745T/C—uncertain significance
rs76714677611:9,522,801T/C—likely benign
rs18277993311:9,522,802G/A—uncertain significance
rs7577032111:9,529,962G/A—benign
rs11409559711:9,530,014G/A—benign
rs37020573411:9,530,205A/G—uncertain significance
rs249399061511:9,530,308C/T—likely benign
rs37355409811:9,530,311G/A—likely benign
rs74824960311:9,530,329G/A—likely benign
rs77364690911:9,530,339A/T—uncertain significance
rs104016607311:9,530,373C/T—uncertain significance
rs249399192211:9,530,403T/G—likely benign
rs76529663611:9,530,410C/T—likely benign
rs3497221311:9,534,001G/A—benign
rs139429718511:9,534,031C/T—uncertain significance
rs36863780011:9,534,039A/G—uncertain significance
rs14878636111:9,534,103G/A—benign
rs74624952211:9,534,110A/G—likely benign
rs36761210411:9,534,132G/A—uncertain significance
rs78109119111:9,537,754A/G—uncertain significance

Showing 100 of 123 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.