ATAD5

ATPase family AAA domain containing 5

Summary

Enables DNA clamp unloader activity. Involved in positive regulation of DNA replication and positive regulation of cell cycle G2/M phase transition. Part of Elg1 RFC-like complex. Biomarker of neurilemmoma. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants130 total

rsidPosition (GRCh37)AllelesClassClinVar
rs7481516017:29,157,158A/Tupstream gene variant—
rs53535702017:29,159,402C/G—uncertain significance
rs99979617:29,159,404G/C—benign
rs130181676217:29,161,188A/T—uncertain significance
rs20068446817:29,161,196A/G—uncertain significance
rs991005117:29,161,202A/T—benign
rs13983908517:29,161,253A/C—likely benign
rs190556029417:29,161,269C/G—uncertain significance
rs75166755017:29,161,327A/G—likely benign
rs78176301517:29,161,345C/T—likely benign
rs381678017:29,161,358C/T—benign
rs56005595217:29,161,476T/C—uncertain significance
rs1108013417:29,161,503A/G—benign
rs14790944417:29,161,517G/A—likely benign
rs74919027717:29,161,650C/T—uncertain significance
rs76642855917:29,161,698A/C—uncertain significance
rs77954877517:29,161,765G/A—likely benign
rs121333835917:29,161,800A/C—uncertain significance
rs122167233517:29,161,816G/A—likely benign
rs1782621917:29,161,845G/A—benign
rs77944945217:29,161,876T/A—uncertain significance
rs14300613217:29,161,990T/C—benign
rs18641718117:29,161,991G/A—likely benign
rs14951019617:29,162,041C/T—likely benign
rs14161804217:29,162,076C/T—uncertain significance
rs57198870117:29,162,088C/A—uncertain significance
rs76661548017:29,162,090A/G—uncertain significance
rs14840089017:29,162,115T/C—uncertain significance
rs37350966117:29,162,121G/A—uncertain significance
rs76251359817:29,162,164A/T—uncertain significance
rs1165562317:29,162,173T/C—benign
rs18842525017:29,162,193A/G—uncertain significance
rs7890975317:29,162,212T/G—benign
rs77456230617:29,162,285A/G—uncertain significance
rs14148344017:29,162,340C/T—uncertain significance
rs156767668617:29,162,379A/G—uncertain significance
rs75677904017:29,162,382A/G—uncertain significance
rs77833446217:29,162,408G/A—uncertain significance
rs123447702517:29,162,412G/A—uncertain significance
rs250997648417:29,162,501G/A—uncertain significance
rs14544411717:29,162,546A/G—uncertain significance
rs14914075317:29,162,694C/A—uncertain significance
rs97548950517:29,162,769A/G—uncertain significance
rs99061126717:29,162,813A/G—uncertain significance
rs14321314917:29,162,826A/C—uncertain significance
rs75089575117:29,162,864T/C—uncertain significance
rs14806540917:29,162,868C/T—uncertain significance
rs190571646917:29,162,955A/G—uncertain significance
rs142766285217:29,162,984A/G—uncertain significance
rs78061881017:29,163,000C/T—uncertain significance
rs20180445617:29,163,012G/A—uncertain significance
rs376441917:29,164,023C/G——
rs146716032617:29,164,229A/C—uncertain significance
rs75566322217:29,164,247C/T—uncertain significance
rs989003217:29,165,934C/T——
rs990475317:29,167,235A/C——
rs376442117:29,167,653A/C—benign
rs250998524717:29,167,731G/A—uncertain significance
rs74968675117:29,167,735T/A—uncertain significance
rs7946138717:29,168,077G/T——
rs7563763017:29,168,078A/C——
rs7694760017:29,168,079G/T——
rs11752921017:29,168,080T/C——
rs14621672317:29,170,934T/C—uncertain significance
rs13796025617:29,170,962C/T—uncertain significance
rs14946349717:29,171,026A/T—uncertain significance
rs37638214117:29,171,048A/G—uncertain significance
rs76468747117:29,171,895A/G—uncertain significance
rs6207064517:29,180,996C/Aintron variant—
rs36777671817:29,182,188T/C—likely benign
rs20168402617:29,182,208C/T—uncertain significance
rs14880666117:29,182,253G/A—uncertain significance
rs136897306117:29,183,996C/G—uncertain significance
rs190732547117:29,184,029G/A—uncertain significance
rs75898484317:29,184,112C/T—likely benign
rs37728117317:29,184,115T/G—likely benign
rs76591892917:29,185,236A/C—uncertain significance
rs37736693317:29,185,307C/G—uncertain significance
rs92516168617:29,185,318C/A—uncertain significance
rs76908312917:29,185,335A/G—uncertain significance
rs18769658017:29,185,350T/C—likely benign
rs989609517:29,187,497A/G—benign
rs251001994817:29,187,498G/A—uncertain significance
rs3591007017:29,187,582C/T—benign
rs76921323617:29,187,613A/G—uncertain significance
rs7620751617:29,192,715G/T—likely benign
rs20049473517:29,192,716C/T—likely benign
rs14034426517:29,192,802A/C—uncertain significance
rs76349823317:29,195,423A/C—uncertain significance
rs120197921217:29,196,322C/G—uncertain significance
rs254406913517:29,196,580A/G—uncertain significance
rs75512220417:29,203,396A/T—uncertain significance
rs55525592517:29,203,493T/C—likely benign
rs18680032017:29,203,520A/C—likely benign
rs98267326317:29,203,524C/T—uncertain significance
rs123799263317:29,204,511G/A—uncertain significance
rs75858701917:29,204,523G/A—uncertain significance
rs6174536617:29,205,072T/C—benign
rs136716677417:29,205,106C/T—uncertain significance
rs650521617:29,206,421G/Tintron variant—

Showing 100 of 130 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.