ATP11A

ATPase phospholipid transporting 11A

Summary

The protein encoded by this gene is an integral membrane ATPase. The encoded protein is probably phosphorylated in its intermediate state and likely drives the transport of ions such as calcium across membranes. [provided by RefSeq, Apr 2022]

Known Variants141 total

rsidPosition (GRCh37)AllelesClassClinVar
rs213942515313:113,344,741G/A—pathogenic
rs188501194513:113,344,755C/G—uncertain significance
rs28257613:113,358,864A/C——
rs1287614313:113,366,291T/Cregulatory region variant—
rs7357645913:113,378,290C/Gintron variant—
rs57413515013:113,420,174C/G——
rs20030953513:113,439,489A/G—uncertain significance
rs75315663513:113,439,517C/T—likely benign
rs214013820313:113,459,358C/G—pathogenic
rs36868104913:113,459,369G/A—benign
rs14203341513:113,460,559A/G—likely benign
rs4128862613:113,464,927T/A—likely benign
rs207846582313:113,464,955A/T—uncertain significance
rs20038575313:113,464,993T/C—uncertain significance
rs55061742913:113,465,005G/A—uncertain significance
rs18970939313:113,465,006G/A—uncertain significance
rs37246477313:113,465,017C/T—uncertain significance
rs75268642113:113,465,020A/C—uncertain significance
rs36784679913:113,465,030G/A—uncertain significance
rs77043507413:113,470,452T/C—uncertain significance
rs20186100513:113,470,496G/A—uncertain significance
rs19966086113:113,473,626C/T—likely benign
rs37314496113:113,473,669G/A—uncertain significance
rs116469622913:113,473,720A/G—uncertain significance
rs53567182313:113,477,671G/A—likely benign
rs14108726313:113,478,674G/A—likely benign
rs11465267513:113,478,695A/G—benign
rs250301714613:113,479,785T/A—uncertain significance
rs75869835613:113,479,788G/A—uncertain significance
rs13818358913:113,479,876G/A—likely benign
rs20024902313:113,479,886A/T—uncertain significance
rs14669889913:113,481,024C/T—uncertain significance
rs207894353613:113,481,026G/A—uncertain significance
rs119180257413:113,481,052T/G—uncertain significance
rs14424822513:113,481,088C/T—benign
rs127906142813:113,481,095C/G—uncertain significance
rs55235698413:113,481,106C/T—likely benign
rs76246009113:113,481,134G/A—likely benign
rs250162256113:113,481,161G/T—uncertain significance
rs207908098113:113,485,755T/A—uncertain significance
rs74973760313:113,485,776G/A—uncertain significance
rs7411830813:113,485,814G/A—benign
rs13999108313:113,485,851G/A—uncertain significance
rs14347426813:113,487,177C/T—uncertain significance
rs37324519713:113,487,178G/A—uncertain significance
rs13853209513:113,487,196G/A—likely benign
rs78003725413:113,487,243G/A—uncertain significance
rs37352421613:113,487,265C/T—uncertain significance
rs76655420613:113,487,270G/A—uncertain significance
rs20036952513:113,487,277A/T—uncertain significance
rs14363432213:113,487,286T/G—likely benign
rs78122495113:113,487,301C/T—uncertain significance
rs15106717913:113,487,316C/T—likely benign
rs18892619213:113,487,347G/A—benign
rs75734949013:113,488,914C/T—uncertain significance
rs207923069913:113,490,550G/A—uncertain significance
rs41515913:113,493,317T/Gintron variant—
rs118390619313:113,496,595A/C—uncertain significance
rs76765235613:113,496,656T/C—uncertain significance
rs77942946713:113,496,683G/A—uncertain significance
rs14189952013:113,496,687C/T—likely benign
rs13966242113:113,496,688G/A—uncertain significance
rs77751007813:113,505,348C/T—uncertain significance
rs147734527013:113,505,378T/C—uncertain significance
rs128967523413:113,505,391T/C—uncertain significance
rs76687934013:113,505,453C/T—uncertain significance
rs207975376513:113,505,486A/G—uncertain significance
rs37315882513:113,505,513G/T—uncertain significance
rs6174030613:113,508,611A/G—benign
rs75257837113:113,508,624G/C—uncertain significance
rs14200847513:113,508,641G/A—likely benign
rs207986050013:113,508,672A/T—uncertain significance
rs37564610913:113,508,679C/T—uncertain significance
rs13991781713:113,508,685C/T—uncertain significance
rs140462189313:113,508,687G/T—uncertain significance
rs250193436913:113,508,708C/G—uncertain significance
rs6174163713:113,508,722C/T—benign
rs14998904513:113,508,725G/A—benign
rs6174165013:113,508,755C/G—uncertain significance
rs14794211913:113,508,816G/A—uncertain significance
rs77016582413:113,508,843G/A—uncertain significance
rs55416269513:113,509,433G/A——
rs250195008513:113,510,314G/T—uncertain significance
rs37401334413:113,510,347G/A—uncertain significance
rs7882151013:113,510,357C/T—benign
rs6174742113:113,510,360G/A—benign
rs20037789913:113,510,402G/A—likely benign
rs14394920913:113,512,134T/A—benign
rs76343351913:113,512,145T/A—uncertain significance
rs14176509013:113,512,221G/A—likely benign
rs18242061513:113,512,467G/A—uncertain significance
rs159419553613:113,512,496C/T—likely benign
rs74768246113:113,512,566A/C—uncertain significance
rs14267446613:113,512,574C/T—benign
rs15062542413:113,513,709C/T—likely benign
rs250199735513:113,514,606G/T—uncertain significance
rs77343671013:113,514,610G/A—uncertain significance
rs14161103613:113,516,758G/A—likely benign
rs14533512613:113,516,761G/A—uncertain significance
rs36866844313:113,516,780G/A—uncertain significance

Showing 100 of 141 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.