CASZ1

castor zinc finger 1

Summary

The protein encoded by this gene is a zinc finger transcription factor. The encoded protein may function as a tumor suppressor, and single nucleotide polymorphisms in this gene are associated with blood pressure variation. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]

Known Variants369 total

rsidPosition (GRCh37)AllelesClassClinVar
rs21246604281:10,699,003G/A—uncertain significance
rs21246604381:10,699,008G/A—likely benign
rs12490269331:10,699,011G/C—likely benign
rs12196296561:10,699,019T/A—uncertain significance
rs25219839771:10,699,036G/T—uncertain significance
rs9233568801:10,699,042A/G—uncertain significance
rs25219841901:10,699,045G/C—uncertain significance
rs9834905301:10,699,054G/A—uncertain significance
rs1845114371:10,699,066G/C—benign
rs7503744321:10,699,072C/T—uncertain significance
rs7560315811:10,699,074C/T—likely benign
rs7722304801:10,699,110C/A—likely benign
rs13809268321:10,699,115A/G—uncertain significance
rs12973139301:10,699,117T/G—uncertain significance
rs25219858931:10,699,124A/G—uncertain significance
rs2016587681:10,699,125G/T—benign
rs25219872921:10,699,157C/T—uncertain significance
rs13078277401:10,699,158G/T—uncertain significance
rs25219880071:10,699,169C/T—uncertain significance
rs7702931691:10,699,173G/C—uncertain significance
rs15574506101:10,699,176G/C—uncertain significance
rs25219885661:10,699,177T/C—uncertain significance
rs2002592101:10,699,188G/C—uncertain significance
rs9929918071:10,699,226G/A—uncertain significance
rs25219906741:10,699,247C/T—uncertain significance
rs10397368011:10,699,275G/C—likely benign
rs7800157041:10,699,278G/A—likely benign
rs10040246751:10,699,302C/T—likely benign
rs8672353831:10,699,331C/A—uncertain significance
rs9410752211:10,699,332G/A—likely benign
rs16421139451:10,699,339C/T—uncertain significance
rs10150212041:10,699,357A/T—uncertain significance
rs11605681021:10,699,374C/A—likely benign
rs7472475441:10,699,391G/C—uncertain significance
rs1899594541:10,699,401C/G—likely benign
rs9257266471:10,699,406C/T—uncertain significance
rs16421172381:10,699,410G/A—likely benign
rs12717876191:10,699,444G/A—uncertain significance
rs7746535111:10,699,445G/A—uncertain significance
rs7671285751:10,699,452C/G—likely benign
rs25219952471:10,699,462T/G—uncertain significance
rs7575925741:10,699,522G/A—uncertain significance
rs3768321731:10,699,587G/A—likely benign
rs9953180301:10,699,619T/C—uncertain significance
rs14167472071:10,699,634A/G—uncertain significance
rs7525869991:10,699,644G/A—likely benign
rs11580054711:10,699,662T/C—likely benign
rs16421320531:10,699,714A/T—uncertain significance
rs2015291181:10,699,740C/A—likely benign
rs3731111461:10,699,760G/C—uncertain significance
rs11939695491:10,699,774T/A—uncertain significance
rs9694874181:10,699,830G/A—likely benign
rs5457447741:10,699,884G/C—likely benign
rs16421427051:10,699,992C/G—uncertain significance
rs7462103101:10,700,023G/A—uncertain significance
rs3676808431:10,700,043G/A—likely benign
rs1815577541:10,700,044A/C—likely benign
rs1402158621:10,700,088C/T—benign
rs5586279951:10,700,102T/G—likely benign
rs7681189531:10,700,108T/C—uncertain significance
rs7667865731:10,700,128C/T—likely benign
rs5617741451:10,700,176G/T——
rs111216011:10,702,712T/C—benign
rs356190521:10,702,814A/G—benign
rs14417274661:10,702,903G/A—uncertain significance
rs2007293711:10,702,906T/C—likely benign
rs3698800591:10,702,909C/T—likely benign
rs3687879861:10,702,920C/T—likely benign
rs1156285121:10,702,941G/A—benign
rs7470595841:10,702,960C/T—uncertain significance
rs11899806781:10,702,961G/A—uncertain significance
rs7702071901:10,702,991C/T—uncertain significance
rs1835588781:10,702,992G/A—likely benign
rs7573603871:10,703,070G/A—likely benign
rs747229711:10,703,083G/C—benign
rs7792048421:10,703,208G/C—likely benign
rs7715887671:10,703,223G/C—likely benign
rs5319018111:10,703,233C/T—uncertain significance
rs7524993601:10,703,234G/A—uncertain significance
rs12372031081:10,703,243T/C—uncertain significance
rs1880452661:10,703,274C/T—likely benign
rs3725484831:10,703,275G/A—uncertain significance
rs7553538241:10,703,277G/A—likely benign
rs13257855071:10,703,308G/A—uncertain significance
rs16422666901:10,703,314T/C—uncertain significance
rs25220397181:10,703,364G/A—likely benign
rs48459401:10,704,888G/C—benign
rs1157396671:10,704,968C/T—likely benign
rs12155398381:10,705,008T/G—uncertain significance
rs7454484431:10,705,027C/T—uncertain significance
rs7699410581:10,705,036G/A—uncertain significance
rs25220495491:10,705,045T/C—uncertain significance
rs3755658401:10,705,100C/T—uncertain significance
rs3694721991:10,705,101G/A—likely benign
rs48459411:10,705,110A/G—benign
rs13830458111:10,705,139C/T—uncertain significance
rs3686009491:10,705,160G/C—likely benign
rs2842421:10,706,091G/C—benign
rs1456496741:10,706,167A/G—benign
rs2000620801:10,706,209A/G—likely benign

Showing 100 of 369 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.