ZSCAN10

zinc finger and SCAN domain containing 10

Summary

Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in negative regulation of DNA-templated transcription and regulation of transcription by RNA polymerase II. Predicted to be located in nucleoplasm. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants66 total

rsidPosition (GRCh37)AllelesClassClinVar
rs14105997616:3,139,109G/T—uncertain significance
rs18536418216:3,139,190C/A—likely benign
rs75688441016:3,139,193C/G—uncertain significance
rs250701027716:3,139,240C/G—uncertain significance
rs75006469916:3,139,267G/A—uncertain significance
rs118223752416:3,139,271G/T—uncertain significance
rs19061591716:3,139,284C/T—likely benign
rs57169569416:3,139,289C/G—uncertain significance
rs77604873216:3,139,315C/T—uncertain significance
rs57396118216:3,139,329G/T—uncertain significance
rs91166637616:3,139,347A/G—likely benign
rs144408685216:3,139,390C/T—uncertain significance
rs118166279416:3,139,512C/G—uncertain significance
rs250701241916:3,139,552T/C—uncertain significance
rs125744784116:3,139,618T/G—uncertain significance
rs141954927616:3,139,625G/A—uncertain significance
rs75773912016:3,139,765C/T—uncertain significance
rs116441414816:3,139,804T/G—uncertain significance
rs20198272116:3,139,840C/T—uncertain significance
rs101299617316:3,139,868C/T—uncertain significance
rs56533013816:3,139,879C/T—uncertain significance
rs118871476616:3,139,904C/T—uncertain significance
rs105421625216:3,139,934C/A—uncertain significance
rs76222971216:3,139,977C/A—uncertain significance
rs20149531116:3,139,999G/T—likely benign
rs120257918816:3,140,032G/A—uncertain significance
rs37037662716:3,140,167A/T—uncertain significance
rs130332555116:3,140,185G/T—pathogenic
rs37092007316:3,140,201G/A—uncertain significance
rs250701689916:3,140,318C/A—uncertain significance
rs75866625316:3,140,345C/T—uncertain significance
rs76071429916:3,140,402A/T—uncertain significance
rs75670240116:3,140,434A/G—uncertain significance
rs215121486316:3,140,459T/A—uncertain significance
rs15016189116:3,140,506C/T—likely benign
rs13839663516:3,140,515G/A—uncertain significance
rs20015275716:3,140,540C/G—uncertain significance
rs250701852016:3,140,573T/C—likely benign
rs20088185016:3,140,594C/T—uncertain significance
rs75977879416:3,140,596T/C—uncertain significance
rs14069087016:3,140,601C/T—benign
rs11164363716:3,140,632G/T—uncertain significance
rs7277256116:3,141,560C/T—likely benign
rs75848740616:3,141,561G/A—uncertain significance
rs18448930616:3,141,571C/G—uncertain significance
rs76008720416:3,141,790C/T—uncertain significance
rs129533642716:3,141,805G/A—likely benign
rs77927618416:3,141,806G/A—uncertain significance
rs215121593016:3,141,809A/G—uncertain significance
rs74915811716:3,142,133G/A—likely benign
rs195708860616:3,142,157G/A—uncertain significance
rs14368085916:3,142,181G/A—uncertain significance
rs250702429016:3,142,229C/T—uncertain significance
rs250702437416:3,142,253C/T—uncertain significance
rs75333011416:3,142,275C/T—likely benign
rs76311497916:3,142,301G/A—uncertain significance
rs75597987216:3,142,568C/T—uncertain significance
rs75730398416:3,142,632G/A—uncertain significance
rs6173555416:3,142,669C/T—benign
rs77014363216:3,142,742C/T—uncertain significance
rs77179577316:3,142,749G/A—uncertain significance
rs76026963716:3,142,760G/A—uncertain significance
rs77633916616:3,142,763C/T—uncertain significance
rs13805363816:3,142,819G/C—benign
rs1164497816:3,142,911C/G—benign
rs1713620816:3,145,048T/Cregulatory region variant—

Gene information from NCBI Gene. Variant classifications from ClinVar.