PIK3R2

phosphoinositide-3-kinase regulatory subunit 2

Summary

Phosphatidylinositol 3-kinase (PI3K) is a lipid kinase that phosphorylates phosphatidylinositol and similar compounds, creating second messengers important in growth signaling pathways. PI3K functions as a heterodimer of a regulatory and a catalytic subunit. The protein encoded by this gene is a regulatory component of PI3K. Three transcript variants, one protein coding and the other two non-protein coding, have been found for this gene. [provided by RefSeq, Apr 2019]

Known Variants370 total

rsidPosition (GRCh37)AllelesClassClinVar
rs14824514619:18,266,672C/T—likely benign
rs76090006919:18,266,685C/T—uncertain significance
rs14293331719:18,266,699C/T—benign
rs137155550819:18,266,718G/A—uncertain significance
rs75139233819:18,266,720G/T—uncertain significance
rs130874875919:18,266,723C/G—uncertain significance
rs99102292519:18,266,725G/A—likely benign
rs76749547219:18,266,731G/A—uncertain significance
rs8023302719:18,266,735C/T—conflicting classifications of pathogenicity
rs77951924919:18,266,744C/A—likely benign
rs75469301119:18,266,745G/A—uncertain significance
rs251355578719:18,266,746G/A—likely benign
rs92980997319:18,266,748C/T—uncertain significance
rs77838360419:18,266,749G/A—likely benign
rs91834180019:18,266,761G/A—likely benign
rs11216578019:18,266,771G/A—uncertain significance
rs77117256519:18,266,776C/T—likely benign
rs147626381719:18,266,792C/T—uncertain significance
rs76223823119:18,266,793G/A—benign
rs76807544519:18,266,796C/T—conflicting classifications of pathogenicity
rs76173556119:18,266,797G/A—likely benign
rs75041132519:18,266,808C/T—uncertain significance
rs76057793919:18,266,809G/A—likely benign
rs89302843419:18,266,815C/T—likely benign
rs214794492919:18,266,821C/T—likely benign
rs214794495619:18,266,827T/G—likely benign
rs102226089019:18,266,834C/T—uncertain significance
rs214794499619:18,266,838G/A—uncertain significance
rs214794500319:18,266,840C/G—uncertain significance
rs214794501319:18,266,843C/A—benign
rs146882458119:18,266,848C/T—likely benign
rs20137095719:18,266,849G/A—benign
rs95354228419:18,266,863C/T—likely benign
rs137359829419:18,266,864G/A—uncertain significance
rs55747694019:18,266,866C/T—likely benign
rs53847966419:18,266,873G/A—uncertain significance
rs156863313519:18,266,875G/A—likely benign
rs137450859819:18,266,882C/T—uncertain significance
rs37444899319:18,266,883G/A—conflicting classifications of pathogenicity
rs214794515719:18,266,888C/T—uncertain significance
rs91852064119:18,266,905C/T—likely benign
rs37085373419:18,266,929C/T—likely benign
rs75517127519:18,266,930G/A—likely benign
rs76041653619:18,266,943G/A—uncertain significance
rs56548581419:18,266,947C/T—likely benign
rs127018380219:18,266,948G/A—uncertain significance
rs75913957819:18,266,954C/T—likely benign
rs53239130819:18,266,955G/A—uncertain significance
rs147245457819:18,266,956C/T—likely benign
rs75243088019:18,266,960C/T—uncertain significance
rs98653555719:18,266,963G/T—uncertain significance
rs159996219119:18,266,964G/T—uncertain significance
rs106479651819:18,266,967C/T—uncertain significance
rs75198422819:18,266,969C/T—uncertain significance
rs122760178919:18,266,973C/T—uncertain significance
rs55460996919:18,266,975C/G—uncertain significance
rs20165577919:18,266,980C/T—likely benign
rs75626746219:18,266,981G/A—uncertain significance
rs18764024819:18,266,990C/T—likely benign
rs36797168619:18,266,991G/A—likely benign
rs77450232819:18,266,993G/A—benign
rs95201829719:18,266,994A/C—uncertain significance
rs77069494419:18,267,000C/A—likely benign
rs77667649019:18,267,002C/T—uncertain significance
rs19968304719:18,267,009C/T—likely benign
rs77488335919:18,267,018A/G—likely benign
rs20123502619:18,267,029G/T—likely benign
rs11532086719:18,267,234C/T—likely benign
rs18611690119:18,271,076A/C—likely benign
rs121901226919:18,271,273C/T—likely benign
rs77419672919:18,271,283C/T—uncertain significance
rs76716020719:18,271,285C/T—likely benign
rs251356001719:18,271,286A/G—uncertain significance
rs20035766719:18,271,287C/T—uncertain significance
rs14884336319:18,271,294C/T—uncertain significance
rs214794924619:18,271,296A/C—uncertain significance
rs251356002719:18,271,298T/C—likely benign
rs55367315719:18,271,304G/A—uncertain significance
rs124210096719:18,271,330T/C—likely benign
rs54239808919:18,271,337C/T—likely benign
rs92013906519:18,271,338T/C—conflicting classifications of pathogenicity
rs251356010519:18,271,347A/C—uncertain significance
rs76832956719:18,271,352G/A—uncertain significance
rs77401903019:18,271,357G/A—likely benign
rs75461379919:18,271,362T/C—conflicting classifications of pathogenicity
rs125243971319:18,271,381C/T—likely benign
rs76571095119:18,271,390C/T—likely benign
rs36867980619:18,271,408G/A—benign
rs75590275019:18,271,724C/G—likely benign
rs14387387319:18,271,764C/T—benign
rs214794980719:18,271,766C/T—likely benign
rs77044587519:18,271,771C/G—uncertain significance
rs37695238819:18,271,790G/T—likely benign
rs19973546019:18,271,796A/G—likely benign
rs214794990919:18,271,799G/C—likely benign
rs37328814419:18,271,847C/T—likely benign
rs74646448119:18,271,853T/C—likely benign
rs77621067119:18,271,859C/T—likely benign
rs251356119719:18,271,865C/T—likely benign
rs214795006419:18,271,873T/C—uncertain significance

Showing 100 of 370 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.