ABCB10

ATP binding cassette subfamily B 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 intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The function of this mitochondrial protein is unknown. [provided by RefSeq, Jul 2008]

Known Variants44 total

rsidPosition (GRCh37)AllelesClassClinVar
rs1453563911:229,653,970T/Cuncertain significance
rs3771592081:229,654,000G/Cuncertain significance
rs1170777841:229,654,092G/Auncertain significance
rs12558034991:229,654,114C/Tuncertain significance
rs7798355131:229,661,740G/Auncertain significance
rs5632758261:229,661,757T/Cuncertain significance
rs1404261971:229,666,037C/Tlikely benign
rs1378965581:229,666,042T/Cuncertain significance
rs3740245941:229,666,072C/Tuncertain significance
rs25276376221:229,666,083G/Tuncertain significance
rs575033591:229,667,384G/Tbenign
rs1396897881:229,667,460G/Auncertain significance
rs7719055491:229,675,260C/Tuncertain significance
rs7490262821:229,675,326C/Tuncertain significance
rs3776733801:229,676,373G/Auncertain significance
rs7700194371:229,676,393G/Cuncertain significance
rs7633868111:229,676,410G/Tuncertain significance
rs18384631:229,677,097T/Cintron variant
rs1387085871:229,678,030C/Tuncertain significance
rs1384688151:229,678,039C/Tuncertain significance
rs2006350641:229,678,057A/Guncertain significance
rs13969171361:229,678,075A/Guncertain significance
rs7617875781:229,683,257T/Guncertain significance
rs13352019001:229,683,332T/Auncertain significance
rs25276761371:229,683,382A/Cuncertain significance
rs175846421:229,683,443G/Auncertain significance
rs1491182031:229,685,047G/Auncertain significance
rs7534912261:229,685,094T/Cuncertain significance
rs120808111:229,685,162C/Tbenign
rs41487571:229,693,846A/Cregulatory region variant
rs16633101301:229,693,967C/Tuncertain significance
rs7513880171:229,693,976C/Guncertain significance
rs16633113811:229,693,993C/Tuncertain significance
rs16633126581:229,694,039C/Tuncertain significance
rs16633138851:229,694,072C/Guncertain significance
rs7781247471:229,694,097C/Guncertain significance
rs14679768331:229,694,116C/Tuncertain significance
rs11584188371:229,694,143A/Cuncertain significance
rs9344609601:229,694,196C/Guncertain significance
rs14783693711:229,694,248A/Cuncertain significance
rs12790857621:229,694,290G/Cuncertain significance
rs25277030631:229,694,339C/Tuncertain significance
rs8873569971:229,694,359G/Cuncertain significance
rs10044938201:229,694,371C/Auncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.