ABCC12

ATP binding cassette subfamily C member 12

Summary

This gene is a member of the superfamily of ATP-binding cassette (ABC) transporters and the encoded protein contains two ATP-binding domains and 12 transmembrane regions. 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 gene is a member of the MRP subfamily which is involved in multi-drug resistance. This gene and another subfamily member are arranged head-to-tail on chromosome 16q12.1. Increased expression of this gene is associated with breast cancer. [provided by RefSeq, Jul 2008]

Known Variants84 total

rsidPosition (GRCh37)AllelesClassClinVar
rs75324208916:48,117,670C/Guncertain significance
rs6173384916:48,117,674C/Tbenign
rs254351228716:48,117,693G/Cuncertain significance
rs132391742016:48,117,873G/Tuncertain significance
rs76618136616:48,117,879C/Tuncertain significance
rs196247446816:48,117,974A/Cuncertain significance
rs75669022016:48,119,548G/Auncertain significance
rs20088267216:48,119,571C/Tuncertain significance
rs137262211716:48,119,575T/Guncertain significance
rs90933161016:48,121,862G/Auncertain significance
rs1694578716:48,121,900T/Gbenign
rs254353178416:48,121,925C/Tuncertain significance
rs196269885016:48,121,940T/Cuncertain significance
rs76733412716:48,122,563C/Tlikely benign
rs147277829816:48,122,564T/Cuncertain significance
rs254353648916:48,122,622A/Tuncertain significance
rs74718194716:48,122,632T/Guncertain significance
rs20060747616:48,122,636G/Auncertain significance
rs76291927516:48,125,078T/Cuncertain significance
rs77443463616:48,125,079C/Tlikely benign
rs159730173716:48,125,089G/Cuncertain significance
rs20000376316:48,125,092C/Guncertain significance
rs36908964816:48,130,742G/Tuncertain significance
rs20008939916:48,130,769C/Auncertain significance
rs138937341516:48,130,784C/Guncertain significance
rs4128092116:48,134,842G/Alikely benign
rs77517062716:48,134,871G/Auncertain significance
rs254358166416:48,138,074A/Guncertain significance
rs20027601516:48,138,090C/Tuncertain significance
rs7280214216:48,138,111A/Guncertain significance
rs77675568516:48,138,182G/Auncertain significance
rs15080413716:48,138,264T/Cuncertain significance
rs805747416:48,138,272T/Abenign
rs53615036716:48,139,076A/Cuncertain significance
rs54542123416:48,139,105A/Guncertain significance
rs14345356216:48,139,174A/Glikely benign
rs15115031616:48,139,232G/Alikely benign
rs92253553816:48,141,242C/Auncertain significance
rs77630242316:48,141,283C/Tuncertain significance
rs76196973816:48,142,359G/Auncertain significance
rs77525085016:48,142,429G/Tuncertain significance
rs93962749816:48,145,410G/Auncertain significance
rs254360341916:48,145,494A/Glikely benign
rs101534895416:48,145,720T/Auncertain significance
rs20185207516:48,145,749A/Cuncertain significance
rs77376283016:48,145,796A/Guncertain significance
rs37295827416:48,149,459G/Auncertain significance
rs76294197016:48,149,470G/Alikely benign
rs75654929516:48,149,484T/Auncertain significance
rs76202662616:48,149,520G/Auncertain significance
rs76782414616:48,149,528A/Guncertain significance
rs76659990416:48,151,221C/Auncertain significance
rs76572275716:48,151,228G/Auncertain significance
rs20189668316:48,155,630T/Guncertain significance
rs254363359216:48,155,730C/Tuncertain significance
rs75250758016:48,155,735C/Tuncertain significance
rs254364005416:48,158,137G/Cuncertain significance
rs75624772816:48,158,164C/Tuncertain significance
rs131470601216:48,162,509T/Cuncertain significance
rs75891412516:48,162,599T/Cuncertain significance
rs14540784416:48,162,633T/Cuncertain significance
rs254365286016:48,162,645T/Cuncertain significance
rs76794156316:48,164,767A/Guncertain significance
rs116082986616:48,164,786C/Tuncertain significance
rs36991047216:48,167,600C/Tuncertain significance
rs115797400316:48,167,744T/Cuncertain significance
rs254367973216:48,172,229T/Cuncertain significance
rs75727128316:48,172,231T/Cuncertain significance
rs125724833216:48,173,091T/Cuncertain significance
rs76060189516:48,173,133T/Auncertain significance
rs77296258016:48,173,177G/Tuncertain significance
rs99617442216:48,173,202C/Tuncertain significance
rs116533089816:48,173,246A/Guncertain significance
rs14180726916:48,174,765C/Alikely benign
rs56697022816:48,175,174G/Alikely benign
rs14989675016:48,175,200C/Tuncertain significance
rs20010330816:48,177,848T/Guncertain significance
rs104557730016:48,177,923G/Auncertain significance
rs6070290816:48,177,934G/Abenign
rs1694589416:48,180,110C/Tintron variant
rs75455253616:48,180,264T/Auncertain significance
rs101509604316:48,180,298T/Auncertain significance
rs254370852616:48,180,313A/Tuncertain significance
rs97359706016:48,180,317A/Guncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.