ARHGAP23

Rho GTPase activating protein 23

Summary

The RHO (see ARHA; MIM 165390) family of small GTPases are involved in signal transduction through transmembrane receptors, and they are inactive in the GDP-bound form and active in the GTP-bound form. GTPase-activating proteins, such as ARHGAP23, inactivate RHO family proteins by stimulating their hydrolysis of GTP (Katoh and Katoh, 2004 [PubMed 15254754]).[supplied by OMIM, Mar 2008]

Known Variants128 total

rsidPosition (GRCh37)AllelesClassClinVar
rs75800613017:36,584,772C/Tuncertain significance
rs77731087317:36,584,785C/Tuncertain significance
rs1245001717:36,604,610C/G
rs963073217:36,606,861G/Acoding sequence variant
rs203937301217:36,614,377C/Guncertain significance
rs37094076817:36,614,410C/Tuncertain significance
rs88895939017:36,614,412C/Auncertain significance
rs76195155317:36,614,434A/Guncertain significance
rs131795517917:36,614,439G/Auncertain significance
rs74857988617:36,617,167C/Tuncertain significance
rs126247910917:36,619,162A/Guncertain significance
rs100318501417:36,619,591A/Guncertain significance
rs254439932517:36,619,597C/Tuncertain significance
rs101011982317:36,622,505C/Tuncertain significance
rs145601892317:36,622,558A/Guncertain significance
rs254441909917:36,622,562C/Tuncertain significance
rs254441951417:36,622,585A/Guncertain significance
rs126844849517:36,622,586G/Auncertain significance
rs94965608217:36,622,615C/Tlikely benign
rs75870162717:36,622,666A/Guncertain significance
rs76444570817:36,622,675C/Tuncertain significance
rs54640908317:36,622,709C/Tuncertain significance
rs75496134517:36,622,717C/Tuncertain significance
rs77192903117:36,622,724C/Tuncertain significance
rs86837652817:36,622,750C/Tuncertain significance
rs131853952717:36,622,751G/Auncertain significance
rs77599618417:36,622,819C/Tuncertain significance
rs53521316217:36,622,855C/Tuncertain significance
rs76431657517:36,622,879C/Tuncertain significance
rs77698828517:36,622,904G/Auncertain significance
rs91953052617:36,622,952A/Guncertain significance
rs254442639017:36,622,964A/Guncertain significance
rs148678696717:36,622,967G/Tuncertain significance
rs117529959517:36,622,976C/Tuncertain significance
rs142607687917:36,622,981G/Auncertain significance
rs134708918017:36,622,994G/Auncertain significance
rs76350873017:36,623,021G/Tuncertain significance
rs100050833817:36,623,029G/Auncertain significance
rs119522382817:36,623,044C/Tuncertain significance
rs95456294217:36,623,086C/Tuncertain significance
rs76652092317:36,623,173A/Guncertain significance
rs19976674117:36,623,183G/Auncertain significance
rs92110439717:36,623,302C/Tuncertain significance
rs93998179317:36,623,336C/Tuncertain significance
rs75256067217:36,623,350C/Tuncertain significance
rs52872045517:36,623,351G/Auncertain significance
rs57166243917:36,623,383G/Auncertain significance
rs159779753117:36,623,407C/Guncertain significance
rs97017409917:36,623,411C/Tuncertain significance
rs77759575217:36,623,420G/Auncertain significance
rs56225767417:36,623,425G/Tuncertain significance
rs142435882717:36,623,447A/Cuncertain significance
rs13828911217:36,623,507G/Alikely benign
rs37053346217:36,623,534C/Tuncertain significance
rs53717131317:36,625,496C/Tuncertain significance
rs134848538017:36,625,520G/Auncertain significance
rs117236632217:36,625,783G/Auncertain significance
rs76486813017:36,625,785C/Tuncertain significance
rs147868959117:36,625,854C/Tuncertain significance
rs75115240717:36,626,101C/Tuncertain significance
rs86692499717:36,626,102G/Auncertain significance
rs254446426017:36,628,116T/Guncertain significance
rs76390465917:36,628,155C/Tuncertain significance
rs140631215317:36,633,851G/Auncertain significance
rs137960091917:36,633,863C/Tuncertain significance
rs92645033817:36,633,868C/Tuncertain significance
rs127873884217:36,633,871G/Cuncertain significance
rs254449293117:36,633,893A/Guncertain significance
rs89256913217:36,633,898C/Tuncertain significance
rs76106328317:36,633,910G/Auncertain significance
rs140516389317:36,633,962C/Tuncertain significance
rs78007205317:36,633,976G/Auncertain significance
rs74925143117:36,634,006G/Auncertain significance
rs91397813717:36,634,107G/Clikely benign
rs138998817417:36,635,694C/Guncertain significance
rs19123843817:36,635,717T/Cuncertain significance
rs77741364917:36,636,023C/Tuncertain significance
rs139760062017:36,636,038G/Auncertain significance
rs126037779717:36,636,050G/Auncertain significance
rs76142204217:36,636,080C/Tuncertain significance
rs130446996317:36,636,097A/Cuncertain significance
rs203999126417:36,636,102G/Cuncertain significance
rs20177635917:36,636,116G/Auncertain significance
rs129267235817:36,636,123G/Cuncertain significance
rs147215467417:36,638,307A/Guncertain significance
rs76930023917:36,638,317A/Guncertain significance
rs76902496117:36,638,338C/Tuncertain significance
rs11303819317:36,638,544C/Tregulatory region variant
rs76099656117:36,638,845G/Auncertain significance
rs99513297917:36,638,887C/Tuncertain significance
rs136090578417:36,638,893C/Tuncertain significance
rs118134367217:36,642,303C/Tuncertain significance
rs75003854617:36,642,304G/Auncertain significance
rs143038952217:36,642,319A/Guncertain significance
rs254453501617:36,642,365G/Tuncertain significance
rs76993352117:36,646,385C/Tuncertain significance
rs118987774417:36,646,388G/Cuncertain significance
rs76726945817:36,646,403C/Tuncertain significance
rs123748605717:36,646,748G/Auncertain significance
rs19225607717:36,647,753G/Auncertain significance

Showing 100 of 128 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.