PREX1

phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 1

Summary

The protein encoded by this gene acts as a guanine nucleotide exchange factor for the RHO family of small GTP-binding proteins (RACs). It has been shown to bind to and activate RAC1 by exchanging bound GDP for free GTP. The encoded protein, which is found mainly in the cytoplasm, is activated by phosphatidylinositol-3,4,5-trisphosphate and the beta-gamma subunits of heterotrimeric G proteins. [provided by RefSeq, Jul 2008]

Known Variants123 total

rsidPosition (GRCh37)AllelesClassClinVar
rs138067253420:47,242,431C/Tuncertain significance
rs7916446520:47,244,417C/Tbenign
rs14010350620:47,244,418G/Auncertain significance
rs251562963420:47,244,426C/Auncertain significance
rs97651786420:47,246,047G/Auncertain significance
rs251563345820:47,246,074A/Cuncertain significance
rs393619220:47,246,077C/Gbenign
rs14343666020:47,246,087C/Tuncertain significance
rs393619320:47,246,127G/Abenign
rs56383925720:47,247,291C/Auncertain significance
rs14589584120:47,247,300G/Auncertain significance
rs126038972020:47,247,307G/Cuncertain significance
rs76935484220:47,247,316G/Auncertain significance
rs11165492720:47,248,885C/Alikely benign
rs14466403620:47,249,077C/Tbenign
rs481084620:47,249,591T/G
rs20139920220:47,251,303C/Tuncertain significance
rs37586881420:47,253,042C/Tuncertain significance
rs53195097120:47,253,074C/Auncertain significance
rs14903486820:47,253,124G/Alikely benign
rs14509162020:47,253,168C/Auncertain significance
rs77680505520:47,253,195C/Tuncertain significance
rs11667129920:47,253,196G/Alikely benign
rs74939217620:47,256,312T/Guncertain significance
rs14383026520:47,256,372T/Clikely benign
rs208939520520:47,256,379T/Cuncertain significance
rs208941901620:47,258,718G/Auncertain significance
rs74689972020:47,260,956T/Auncertain significance
rs37606973820:47,262,392T/Cuncertain significance
rs74749093020:47,262,417C/Tuncertain significance
rs601250420:47,262,549C/Tbenign
rs37631138120:47,262,552C/Guncertain significance
rs118827914920:47,265,854C/Tuncertain significance
rs228128720:47,265,918G/Abenign
rs251567226320:47,265,956C/Tuncertain significance
rs37431961520:47,265,958C/Guncertain significance
rs18660657420:47,265,959G/Auncertain significance
rs77058613720:47,265,995A/Guncertain significance
rs20125374120:47,266,012C/Auncertain significance
rs75840508620:47,266,086C/Auncertain significance
rs138965692020:47,266,096G/Auncertain significance
rs11320227720:47,266,104G/Alikely benign
rs75374856020:47,266,543G/Cuncertain significance
rs251567545720:47,267,461T/Cuncertain significance
rs37320016120:47,267,515C/Tuncertain significance
rs53281328720:47,267,545T/Clikely benign
rs74749094520:47,267,593T/Cuncertain significance
rs76143508920:47,267,959C/Tlikely benign
rs75202582120:47,267,969C/Tuncertain significance
rs251567668820:47,267,983A/Guncertain significance
rs251567685820:47,268,046T/Auncertain significance
rs11736296820:47,268,093C/Gbenign
rs14298682120:47,268,121G/Tuncertain significance
rs160104661920:47,269,204T/Guncertain significance
rs20030485920:47,269,225T/Cuncertain significance
rs13992140720:47,269,919T/Cuncertain significance
rs14621067820:47,269,963T/Clikely benign
rs37125590520:47,269,970C/Tuncertain significance
rs37371029420:47,269,981T/Cuncertain significance
rs19313146620:47,271,858C/Tuncertain significance
rs11280619620:47,271,866C/Tlikely benign
rs37752074320:47,271,867G/Auncertain significance
rs14491094320:47,271,868A/Cuncertain significance
rs78042260120:47,271,907G/Cuncertain significance
rs37323151120:47,273,606G/Auncertain significance
rs251568668720:47,273,659A/Cuncertain significance
rs14684711420:47,274,697C/Tuncertain significance
rs15039444120:47,276,464C/Tuncertain significance
rs208957822620:47,276,518T/Cuncertain significance
rs75315356020:47,276,587C/Auncertain significance
rs121885450120:47,282,838T/Cuncertain significance
rs14652609420:47,282,861C/Tbenign
rs1108625820:47,292,329T/G
rs14174321420:47,292,761C/Tlikely benign
rs36878643820:47,295,943A/Guncertain significance
rs19984487720:47,296,196A/Guncertain significance
rs77655457220:47,305,300G/Auncertain significance
rs76970415420:47,305,307T/Cuncertain significance
rs148785171020:47,307,502T/Auncertain significance
rs13946360820:47,307,600G/Alikely benign
rs609524120:47,308,798G/Aintron variant
rs601937820:47,309,716C/Tintron variant
rs251575460720:47,317,406T/Guncertain significance
rs96012914920:47,317,407G/Tuncertain significance
rs481086420:47,319,142G/Cregulatory region variant
rs286966920:47,321,449T/Cintron variant
rs77269763520:47,324,949T/Cuncertain significance
rs601938620:47,326,440T/Gintron variant
rs606682520:47,340,117A/Gregulatory region variant
rs606331220:47,343,059G/Tintron variant
rs77774325520:47,351,146A/Cuncertain significance
rs606683520:47,355,009T/Cregulatory region variant
rs14502624120:47,361,630C/Alikely benign
rs209010164920:47,361,635A/Guncertain significance
rs56056431120:47,375,302T/C
rs242608720:47,379,811G/Aregulatory region variant
rs14925797620:47,384,301C/Aintron variant
rs612546220:47,388,649C/G
rs7524098520:47,391,484G/Aintron variant
rs609090720:47,410,231G/Aintron variant

Showing 100 of 123 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.