ABCA10

ATP binding cassette subfamily A member 10

Summary

The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, and White). This encoded protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. This gene is clustered among 4 other ABC1 family members on 17q24, but neither the substrate nor the function of this gene is known. [provided by RefSeq, Jul 2008]

Known Variants88 total

rsidPosition (GRCh37)AllelesClassClinVar
rs137020160217:67,145,026A/Cuncertain significance
rs118866254617:67,146,129C/Auncertain significance
rs14658463217:67,146,173C/Auncertain significance
rs13794589117:67,146,204T/Auncertain significance
rs76227016817:67,148,200C/Tuncertain significance
rs76563729817:67,148,205G/Auncertain significance
rs75069354317:67,148,212G/Auncertain significance
rs125109704117:67,148,241A/Cuncertain significance
rs127756375417:67,148,323A/Guncertain significance
rs207413614317:67,148,521A/Guncertain significance
rs37747954917:67,148,603C/Tuncertain significance
rs20137501517:67,149,465C/Tuncertain significance
rs14584171117:67,149,540G/Cuncertain significance
rs76844028317:67,149,650C/Guncertain significance
rs14695934717:67,149,666G/Alikely benign
rs93709166317:67,150,017G/Auncertain significance
rs250938124617:67,150,057G/Auncertain significance
rs76113556917:67,150,074T/Cuncertain significance
rs14416024817:67,150,094C/Guncertain significance
rs77835465817:67,150,144A/Cuncertain significance
rs105294242517:67,151,250G/Auncertain significance
rs14055460717:67,152,011C/Tuncertain significance
rs15047284917:67,152,020C/Tuncertain significance
rs53753092317:67,152,031G/Auncertain significance
rs37424819017:67,152,992T/Guncertain significance
rs137324369217:67,161,155T/Auncertain significance
rs144515058217:67,161,173T/Cuncertain significance
rs76613260917:67,170,501A/Guncertain significance
rs250940676417:67,170,523T/Cuncertain significance
rs77418298317:67,170,809T/Cuncertain significance
rs250940739017:67,170,813T/Cuncertain significance
rs75079276617:67,170,846C/Guncertain significance
rs15058402017:67,170,870A/Guncertain significance
rs14275677617:67,171,593T/Cuncertain significance
rs116136757717:67,171,648T/Cuncertain significance
rs76726939017:67,178,295C/Tlikely benign
rs75103336617:67,178,412G/Cuncertain significance
rs250942321517:67,181,657T/Cuncertain significance
rs209529748317:67,181,710T/Cuncertain significance
rs120260081417:67,181,744C/Tuncertain significance
rs15031612217:67,181,767A/Guncertain significance
rs138847424817:67,183,847G/Auncertain significance
rs20056591717:67,183,865G/Cuncertain significance
rs75387278917:67,183,906G/Auncertain significance
rs250942676817:67,183,937G/Cuncertain significance
rs13952050217:67,183,939G/Tuncertain significance
rs13875813117:67,184,008C/Auncertain significance
rs14627528917:67,186,600T/Auncertain significance
rs78133513417:67,187,325T/Auncertain significance
rs77638011117:67,187,395G/Auncertain significance
rs90452796117:67,187,449T/Cuncertain significance
rs250943389117:67,188,711G/Cuncertain significance
rs250943419317:67,188,794T/Cuncertain significance
rs36774660817:67,189,293G/Auncertain significance
rs54611487317:67,189,301C/Auncertain significance
rs20197669517:67,189,361C/Auncertain significance
rs37467077817:67,189,368T/Cuncertain significance
rs37600428217:67,189,672T/Guncertain significance
rs77430012317:67,189,690T/Cuncertain significance
rs77309653317:67,190,020C/Tuncertain significance
rs77932739717:67,190,089C/Tuncertain significance
rs207448375217:67,190,552A/Guncertain significance
rs156806510417:67,193,244C/Tuncertain significance
rs14881816817:67,197,668G/Auncertain significance
rs76685648017:67,197,675C/Auncertain significance
rs250944807017:67,197,710T/Cuncertain significance
rs119826541117:67,210,893T/Clikely benign
rs144803223817:67,210,938C/Tuncertain significance
rs13815032817:67,212,003C/Auncertain significance
rs77064879017:67,212,020G/Auncertain significance
rs75853912417:67,212,084C/Auncertain significance
rs76974664717:67,212,093C/Tlikely benign
rs14367831517:67,212,098A/Guncertain significance
rs14851187217:67,212,123T/Cuncertain significance
rs77516004217:67,212,141T/Guncertain significance
rs76571570017:67,212,401A/Guncertain significance
rs14186718417:67,212,409A/Tuncertain significance
rs91269892017:67,212,422G/Auncertain significance
rs117982127817:67,212,426T/Cuncertain significance
rs77601655417:67,212,457C/Tuncertain significance
rs56014032117:67,215,774T/Auncertain significance
rs14323188217:67,215,836G/Cuncertain significance
rs250947173417:67,215,843A/Guncertain significance
rs250947174117:67,215,846G/Auncertain significance
rs15100761517:67,218,018T/Guncertain significance
rs14956865217:67,218,733C/Tuncertain significance
rs14320406517:67,218,763C/Guncertain significance
rs37546880117:67,218,799T/Cuncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.