CEP126

centrosomal protein 126

Summary

Involved in cilium assembly; cytoplasmic microtubule organization; and mitotic spindle organization. Located in centrosome; ciliary base; and midbody. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants72 total

rsidPosition (GRCh37)AllelesClassClinVar
rs14560653811:101,786,028A/T—uncertain significance
rs75795582511:101,786,074C/T—uncertain significance
rs86579804711:101,786,092C/G—uncertain significance
rs125588013611:101,786,130C/G—uncertain significance
rs20046575211:101,793,439A/T—uncertain significance
rs7822006011:101,793,458G/A—uncertain significance
rs14038725711:101,814,989A/C—benign
rs14588648111:101,815,013G/A—uncertain significance
rs78140988211:101,815,129C/T—uncertain significance
rs75649022011:101,815,130G/A—uncertain significance
rs14214123911:101,818,803C/G—benign
rs1122508611:101,828,924G/A—benign
rs14634947311:101,828,970A/G—likely benign
rs130858249611:101,828,979G/A—uncertain significance
rs37171428111:101,829,059C/G—uncertain significance
rs6174207011:101,829,070C/T—benign
rs213710869811:101,829,095C/A—uncertain significance
rs86755830411:101,832,489T/C—likely benign
rs54296513811:101,832,598C/T—likely benign
rs37554630411:101,832,599G/A—likely benign
rs249620540411:101,832,604A/G—uncertain significance
rs36991967211:101,832,643C/T—uncertain significance
rs6174217211:101,832,689A/T—benign
rs124971053111:101,832,772G/A—uncertain significance
rs105419503711:101,832,787G/C—uncertain significance
rs14590474311:101,832,825G/T—uncertain significance
rs77077961811:101,832,835G/C—uncertain significance
rs6174575911:101,832,880T/C—benign
rs75218661311:101,832,922A/T—uncertain significance
rs194098467311:101,832,936C/A—uncertain significance
rs117847127311:101,832,995C/G—uncertain significance
rs13876411911:101,833,122T/G—uncertain significance
rs57319061911:101,833,148C/T—likely benign
rs77491044011:101,833,280T/G—uncertain significance
rs115873925311:101,833,312C/T—uncertain significance
rs75128953411:101,833,357C/G—uncertain significance
rs75618575311:101,833,400C/T—uncertain significance
rs134550062311:101,833,468G/A—uncertain significance
rs77401432711:101,833,495A/G—uncertain significance
rs54397560511:101,833,585G/A—uncertain significance
rs6174454211:101,833,632A/C—uncertain significance
rs249620822411:101,833,673C/T—uncertain significance
rs122229090411:101,833,807G/A—uncertain significance
rs14487549311:101,833,825A/G—uncertain significance
rs37366996411:101,833,852G/A—uncertain significance
rs710961411:101,833,894C/T—benign
rs14331709911:101,833,975C/G—uncertain significance
rs37140696011:101,834,021G/A—uncertain significance
rs74931286211:101,834,070C/G—benign
rs37570930211:101,834,095G/A—likely benign
rs76232774811:101,834,108C/G—uncertain significance
rs117890629411:101,834,273A/G—uncertain significance
rs53960353611:101,834,306A/G—uncertain significance
rs36994973911:101,834,357C/G—uncertain significance
rs194101798411:101,834,390T/C—uncertain significance
rs6174643411:101,834,428A/G—uncertain significance
rs76139926511:101,834,437C/T—uncertain significance
rs14263525611:101,834,474C/T—uncertain significance
rs37077427911:101,834,522C/T—uncertain significance
rs15095208211:101,834,568G/C—uncertain significance
rs249621055611:101,834,587C/G—uncertain significance
rs14315495511:101,834,591A/G—uncertain significance
rs11710925111:101,837,235T/Cintron variant—
rs147835529011:101,849,083A/G—uncertain significance
rs15027496311:101,849,120G/A—likely benign
rs20157286711:101,849,189A/G—uncertain significance
rs711142911:101,857,590T/C—benign
rs20093752411:101,857,610G/A—uncertain significance
rs36940774611:101,857,620C/T—uncertain significance
rs77149326511:101,863,521C/A—uncertain significance
rs159129764411:101,863,581T/G—likely benign
rs129241261511:101,868,334A/G—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.