ANXA11

annexin A11

Summary

This gene encodes a member of the annexin family, a group of calcium-dependent phospholipid-binding proteins. Annexins have unique N-terminal domains and conserved C-terminal domains, which contain calcium-dependent phospholipid-binding sites. The encoded protein is a 56-kD antigen recognized by sera from patients with various autoimmune diseases. Several transcript variants encoding two different isoforms have been identified. [provided by RefSeq, Dec 2015]

Known Variants282 total

rsidPosition (GRCh37)AllelesClassClinVar
rs195360010:81,911,725C/T3 prime UTR variant—
rs709156510:81,913,561C/T3 prime UTR variant—
rs20010417510:81,915,605C/A—likely benign
rs213235206310:81,915,616T/C—uncertain significance
rs131848914110:81,915,646C/T—uncertain significance
rs74703926010:81,915,647G/A—uncertain significance
rs77720798010:81,915,656C/T—uncertain significance
rs158941050810:81,915,658G/T—uncertain significance
rs76270566910:81,915,686G/A—likely benign
rs278968710:81,915,790C/T—benign
rs3607386510:81,916,055C/Tregulatory region variant—
rs1277537410:81,917,320G/A—benign
rs75522665510:81,917,390C/T—likely benign
rs74813435010:81,917,392C/T—uncertain significance
rs7995090010:81,917,393G/A—benign
rs77808297210:81,917,398G/A—uncertain significance
rs14392143810:81,917,405C/G—uncertain significance
rs74966854410:81,917,406G/A—likely benign
rs249254734710:81,917,412C/T—likely benign
rs14649593710:81,917,430C/T—likely benign
rs14664473310:81,917,431C/T—uncertain significance
rs36813271510:81,917,432G/A—uncertain significance
rs75020933310:81,917,451G/A—likely benign
rs14295687210:81,917,462C/T—uncertain significance
rs96100361410:81,917,473C/T—uncertain significance
rs180293210:81,917,486C/T—benign
rs77928273210:81,917,490A/C—uncertain significance
rs213235835010:81,917,492T/C—uncertain significance
rs14200172110:81,917,500C/T—uncertain significance
rs15067149710:81,917,501G/A—benign
rs141024915210:81,917,516C/T—uncertain significance
rs76188568710:81,917,539G/A—likely benign
rs1276714210:81,917,629T/C—benign
rs7772437510:81,917,706A/C—benign
rs107924210:81,917,708G/A—benign
rs37140565110:81,917,717A/G—uncertain significance
rs77321781810:81,917,719A/G—uncertain significance
rs100093105610:81,917,730G/T—uncertain significance
rs14011599010:81,917,747C/G—likely benign
rs19987059210:81,917,756G/C—benign
rs37409537710:81,917,799G/A—likely benign
rs386251810:81,917,957T/C—benign
rs257334610:81,918,041G/C——
rs11255006710:81,918,776A/C—benign
rs56158763710:81,918,859C/T—uncertain significance
rs6186001810:81,918,880G/A—likely benign
rs14668378810:81,918,886C/T—uncertain significance
rs13919300110:81,918,887G/A—likely benign
rs75994799210:81,918,889A/T—uncertain significance
rs76804333410:81,918,897C/T—uncertain significance
rs37538385910:81,918,898G/A—uncertain significance
rs75307128510:81,918,904T/C—uncertain significance
rs7466614110:81,918,908C/T—benign
rs75329065310:81,918,914A/G—likely benign
rs136339573910:81,918,921C/T—uncertain significance
rs74586409910:81,918,922G/A—uncertain significance
rs184540763710:81,918,927G/A—uncertain significance
rs96295728610:81,918,941C/G—uncertain significance
rs77196211610:81,918,945T/C—uncertain significance
rs184540878110:81,918,954A/T—uncertain significance
rs74676193410:81,918,955T/C—likely benign
rs7581029510:81,918,956G/A—benign
rs278477310:81,919,800T/Cintron variant—
rs278477410:81,921,553T/C—benign
rs249207228910:81,921,680G/A—likely benign
rs249207231610:81,921,684G/A—likely benign
rs213237864010:81,921,686C/T—uncertain significance
rs74957380010:81,921,702T/G—uncertain significance
rs89418570210:81,921,703G/A—uncertain significance
rs140647409310:81,921,704G/A—likely benign
rs141632089410:81,921,705G/A—uncertain significance
rs141660933610:81,921,707C/T—likely benign
rs37219664410:81,921,708C/T—uncertain significance
rs53960572110:81,921,709G/A—uncertain significance
rs14622270410:81,921,715G/A—benign
rs19996315810:81,921,722C/A—likely benign
rs249207333710:81,921,724G/T—uncertain significance
rs14316571610:81,921,728C/T—likely benign
rs213237921110:81,921,740G/C—likely benign
rs75524318410:81,921,752T/C—likely benign
rs13918658310:81,921,759C/T—likely benign
rs75751364110:81,921,760G/A—uncertain significance
rs3441401510:81,921,766C/T—benign
rs77233385310:81,921,769C/T—uncertain significance
rs74755631110:81,921,771G/A—likely benign
rs14145693810:81,921,773C/T—likely benign
rs96470800310:81,921,776A/G—likely benign
rs105596517810:81,921,779C/T—likely benign
rs76949514510:81,921,785C/T—uncertain significance
rs7666636910:81,921,792G/C—benign
rs4555743310:81,921,802C/T—likely benign
rs230441010:81,921,810T/C—benign
rs224516810:81,921,918T/C—benign
rs3518057610:81,922,971G/A—benign
rs77053139410:81,923,085G/T—likely benign
rs184558914410:81,923,101T/A—uncertain significance
rs76704979510:81,923,110C/T—uncertain significance
rs76063784210:81,923,122C/T—uncertain significance
rs54106292010:81,923,123G/A—benign
rs37329607510:81,923,130A/G—uncertain significance

Showing 100 of 282 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.