PIK3AP1

phosphoinositide-3-kinase adaptor protein 1

Summary

Predicted to enable phosphatidylinositol 3-kinase regulatory subunit binding activity and signaling receptor binding activity. Predicted to be involved in positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction; regulation of inflammatory response; and regulation of innate immune response. Predicted to be located in membrane. Predicted to be active in cytosol. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants399 total

rsidPosition (GRCh37)AllelesClassClinVar
rs74617280710:98,355,365G/C—uncertain significance
rs20182460610:98,355,373G/A—benign
rs14040489110:98,355,374G/A—uncertain significance
rs133472019510:98,355,383G/A—uncertain significance
rs77664979010:98,355,385C/T—likely benign
rs126186696610:98,355,386G/A—uncertain significance
rs213417261410:98,355,408G/T—likely benign
rs74709630810:98,362,018A/T—likely benign
rs78141349410:98,362,022C/A—likely benign
rs74815491810:98,362,023A/G—likely benign
rs184891155810:98,362,031T/C—uncertain significance
rs76959613010:98,362,043G/A—uncertain significance
rs139079604710:98,362,045G/A—likely benign
rs53945841510:98,362,054C/T—benign
rs134207362110:98,362,055G/A—uncertain significance
rs213418108910:98,362,058G/A—uncertain significance
rs14545970310:98,362,060C/T—benign
rs4558754210:98,362,062C/T—conflicting classifications of pathogenicity
rs77723319910:98,362,078G/C—likely benign
rs146294978410:98,362,080G/A—uncertain significance
rs14938180510:98,362,086T/C—conflicting classifications of pathogenicity
rs155495192610:98,362,092G/T—uncertain significance
rs137088195410:98,362,099A/G—likely benign
rs116490755710:98,362,103A/G—uncertain significance
rs117311054010:98,362,109G/T—uncertain significance
rs140419022410:98,362,114G/A—likely benign
rs76563436110:98,362,124C/T—uncertain significance
rs75081951210:98,362,125G/A—uncertain significance
rs14737601710:98,362,146C/A—likely benign
rs37405419710:98,362,158A/G—uncertain significance
rs78147062910:98,362,174G/A—benign
rs128316285610:98,363,723T/A—likely benign
rs117797656710:98,363,730T/C—uncertain significance
rs14810718710:98,363,739G/A—likely benign
rs37615260510:98,363,740T/G—uncertain significance
rs76780745910:98,363,757G/A—likely benign
rs75284465410:98,363,763C/A—likely benign
rs249362009410:98,363,767C/G—uncertain significance
rs119862690110:98,363,772G/A—likely benign
rs77777189210:98,363,779C/T—uncertain significance
rs75378556410:98,363,780G/A—uncertain significance
rs184895643610:98,363,781G/C—likely benign
rs213418343210:98,363,790G/A—likely benign
rs56963262310:98,363,791C/T—benign
rs74563621910:98,363,792G/A—uncertain significance
rs11397624810:98,363,800G/C—uncertain significance
rs11190259310:98,363,813G/A—benign
rs129343049510:98,363,823A/G—likely benign
rs184895760910:98,363,826T/C—likely benign
rs75393598910:98,369,451G/C—likely benign
rs213418947510:98,369,452C/T—likely benign
rs75024370810:98,369,454C/A—likely benign
rs135690693710:98,369,455C/T—likely benign
rs129235073210:98,369,458C/T—likely benign
rs36877596410:98,369,492G/A—uncertain significance
rs184907148010:98,369,504C/T—uncertain significance
rs75463354410:98,369,507C/T—uncertain significance
rs74765465310:98,369,518C/T—likely benign
rs20159527510:98,369,519G/A—uncertain significance
rs94562134710:98,369,523T/G—likely benign
rs155495290110:98,369,531A/G—uncertain significance
rs374823610:98,369,536G/A—benign
rs77590985010:98,369,537C/T—uncertain significance
rs213418961110:98,369,539T/C—likely benign
rs76085651710:98,369,540T/A—uncertain significance
rs126107760510:98,369,552C/T—uncertain significance
rs146067477910:98,369,555T/A—uncertain significance
rs14106786010:98,369,563T/C—benign
rs75042365010:98,369,564C/A—uncertain significance
rs76620805210:98,369,566A/G—likely benign
rs184907573610:98,369,573A/G—uncertain significance
rs37186571010:98,369,574C/T—uncertain significance
rs119696774710:98,369,583G/T—uncertain significance
rs158948482510:98,369,588T/C—uncertain significance
rs20027000910:98,369,604T/C—uncertain significance
rs77741925710:98,369,611C/T—likely benign
rs77576111210:98,369,630A/T—likely benign
rs75246645510:98,376,379C/G—likely benign
rs249364433810:98,376,384G/C—likely benign
rs74734954910:98,376,425C/T—uncertain significance
rs76900219010:98,376,427C/T—likely benign
rs136437989510:98,376,444T/A—uncertain significance
rs77331149610:98,376,445G/A—likely benign
rs76297150610:98,376,455C/T—uncertain significance
rs4129916710:98,376,471G/A—uncertain significance
rs76740556510:98,376,478A/G—likely benign
rs36929185310:98,380,096C/T—likely benign
rs74586855610:98,380,104G/T—uncertain significance
rs77187293710:98,380,119C/T—uncertain significance
rs77545865110:98,380,120G/A—uncertain significance
rs20068446710:98,380,130C/T—likely benign
rs184305951710:98,380,135G/A—uncertain significance
rs1278497510:98,380,137C/T—benign
rs213420110710:98,380,143T/C—uncertain significance
rs75307121210:98,380,169G/A—likely benign
rs213420116110:98,380,178C/T—likely benign
rs77551384810:98,380,187G/A—benign
rs213420118010:98,380,189T/C—uncertain significance
rs213420118110:98,380,193A/G—likely benign
rs76864346610:98,380,233C/T—uncertain significance

Showing 100 of 399 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.