CTR9

CTR9 component of Paf1/RNA polymerase II complex

Summary

The protein encoded by this gene is a component of the PAF1 complex, which associates with RNA polymerase II and functions in transcriptional regulation and elongation. This complex also plays a role in the modification of histones. [provided by RefSeq, Oct 2016]

Known Variants535 total

rsidPosition (GRCh37)AllelesClassClinVar
rs11134405711:10,772,422T/C—benign
rs11202670511:10,772,479T/C—likely benign
rs227969611:10,772,555A/G—benign
rs133418711511:10,772,965G/T—likely benign
rs253936513711:10,772,972T/C—uncertain significance
rs140864179911:10,772,977C/T—likely benign
rs75326606811:10,772,989C/G—likely benign
rs213535144511:10,773,002G/A—likely pathogenic
rs253936519211:10,773,003A/G—likely pathogenic
rs77882046411:10,773,004G/A—uncertain significance
rs75820541711:10,773,009G/T—uncertain significance
rs77975487811:10,773,010T/C—uncertain significance
rs36978215411:10,773,013C/A—likely benign
rs139304258511:10,773,016G/T—likely benign
rs227969711:10,773,049A/G—benign
rs648448011:10,773,992C/T—benign
rs19288616411:10,774,124A/G—likely benign
rs213535309011:10,774,223T/C—pathogenic
rs253936659911:10,774,229T/A—likely pathogenic
rs213535312611:10,774,247C/G—pathogenic
rs13885054711:10,774,248G/A—likely benign
rs213535314311:10,774,249G/C—likely pathogenic
rs186282495211:10,774,256A/G—uncertain significance
rs147682420911:10,774,257T/C—likely benign
rs253936663711:10,774,258G/C—likely pathogenic
rs213535317811:10,774,282G/C—likely pathogenic
rs253936666011:10,774,283A/G—likely pathogenic
rs253936666411:10,774,284A/T—uncertain significance
rs186282535811:10,774,297C/T—uncertain significance
rs55396959011:10,774,317G/T—uncertain significance
rs213535321411:10,774,321A/T—uncertain significance
rs77489637111:10,774,333G/C—likely benign
rs11281864911:10,774,449G/A—likely benign
rs11687150811:10,776,448T/C—likely benign
rs77163667011:10,776,513C/Gstop gained—
rs135594403711:10,776,525A/G—likely benign
rs135297133211:10,776,531A/G—likely benign
rs11339737711:10,776,550T/G—uncertain significance
rs118207436011:10,776,594T/C—likely benign
rs186286397811:10,776,596A/G—uncertain significance
rs3558246611:10,776,600A/G—likely benign
rs76636142411:10,776,611C/T—uncertain significance
rs213535605011:10,776,614G/A—likely pathogenic
rs75945060911:10,776,624A/G—likely benign
rs18290318211:10,776,633G/A—benign
rs253936976211:10,776,639T/C—likely benign
rs90124290711:10,776,640G/A—uncertain significance
rs148291713411:10,776,645A/T—uncertain significance
rs75644647011:10,776,646C/A—uncertain significance
rs159001734211:10,776,655A/T—uncertain significance
rs253936981211:10,776,658G/A—uncertain significance
rs213535615711:10,776,673A/G—uncertain significance
rs253936987311:10,776,699C/T—likely benign
rs78032876711:10,776,702C/T—likely benign
rs213535620711:10,776,708G/A—likely benign
rs213535621611:10,776,715A/G—uncertain significance
rs76950272611:10,776,720C/T—likely benign
rs186286594411:10,776,733A/G—not provided
rs253936997011:10,776,753A/G—likely benign
rs186286632311:10,776,763T/A—likely benign
rs5719298511:10,776,877G/C—likely benign
rs11796614711:10,776,938C/T—likely benign
rs491018711:10,777,031T/C—benign
rs11522488911:10,777,166T/C—benign
rs74743194111:10,777,212C/T—benign
rs37111648011:10,777,216A/C—likely benign
rs74896946911:10,777,218T/C—likely benign
rs37439209011:10,777,257A/G—likely benign
rs186287485511:10,777,310A/G—uncertain significance
rs20096736511:10,777,320A/G—likely benign
rs186287523711:10,777,324A/G—uncertain significance
rs253937096711:10,777,331C/T—uncertain significance
rs253937097911:10,777,334C/G—uncertain significance
rs253937098911:10,777,336C/T—uncertain significance
rs186287539311:10,777,340T/G—uncertain significance
rs20171423211:10,777,349G/A—likely benign
rs76631121311:10,777,352C/G—likely benign
rs227062111:10,777,410G/A—benign
rs14524080311:10,777,479C/T—likely benign
rs7341776011:10,777,492T/C—benign
rs77660526711:10,778,281T/A—likely benign
rs76165999111:10,778,288C/G—likely benign
rs186289085611:10,778,290T/C—likely benign
rs253937205911:10,778,314T/A—uncertain significance
rs144958240811:10,778,317A/G—uncertain significance
rs253937208711:10,778,337G/A—uncertain significance
rs186289137411:10,778,340C/G—uncertain significance
rs253937210311:10,778,347A/T—uncertain significance
rs76800991511:10,778,361T/C—likely benign
rs75311805911:10,778,365G/A—uncertain significance
rs13897988611:10,778,378A/G—benign
rs75794097611:10,778,387T/Csplice region variantuncertain significance
rs253937216211:10,778,403T/G—likely benign
rs7518240211:10,778,501A/G—benign
rs648448311:10,778,510T/G—benign
rs14221490011:10,778,650G/A—likely benign
rs18855815011:10,779,846G/Tintron variant—
rs7935456311:10,781,395T/G—benign
rs75816113811:10,781,701G/A—likely benign
rs77984546311:10,781,712T/A—uncertain significance

Showing 100 of 535 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.