ARHGAP15

Rho GTPase activating protein 15

Summary

RHO GTPases (see ARHA; MIM 165390) regulate diverse biologic processes, and their activity is regulated by RHO GTPase-activating proteins (GAPs), such as ARHGAP15 (Seoh et al., 2003 [PubMed 12650940]).[supplied by OMIM, Mar 2008]

Known Variants67 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs354707	2:143,886,437	T/A	regulatory region variant	—
rs144449054	2:143,889,934	G/A	regulatory region variant	—
rs150127285	2:143,913,111	C/T	—	uncertain significance
rs373692174	2:143,913,222	C/A	—	uncertain significance
rs563447271	2:143,914,774	T/C	—	—
rs35713119	2:143,948,355	A/G	—	—
rs35028264	2:143,972,880	G/T	intron variant	—
rs757406465	2:143,974,001	G/A	—	uncertain significance
rs1030218974	2:143,986,163	A/G	—	uncertain significance
rs2468403381	2:144,008,170	G/A	—	uncertain significance
rs2381401	2:144,020,974	C/T	regulatory region variant	—
rs2381459	2:144,056,371	A/G	intron variant	—
rs10460253	2:144,085,491	C/A	—	—
rs10176394	2:144,096,374	T/C	intron variant	—
rs13008966	2:144,117,605	A/C	intron variant	—
rs10496949	2:144,153,344	G/T	—	—
rs62172064	2:144,154,888	T/C	intron variant	—
rs34210137	2:144,154,917	A/T	—	—
rs1320139	2:144,158,177	C/G	intron variant	—
rs140397066	2:144,162,105	A/G	intron variant	—
rs4662330	2:144,186,475	T/C	regulatory region variant	—
rs199653389	2:144,193,166	G/T	—	likely benign
rs766488154	2:144,193,192	A/G	—	uncertain significance
rs2467506710	2:144,193,194	T/C	—	uncertain significance
rs368334646	2:144,193,229	G/C	—	uncertain significance
rs2467512236	2:144,194,508	A/T	—	uncertain significance
rs375998378	2:144,194,545	A/G	—	uncertain significance
rs12691680	2:144,204,338	C/G	—	—
rs35942385	2:144,208,523	G/T	intron variant	—
rs13411140	2:144,215,811	C/T	intron variant	—
rs13024996	2:144,225,215	C/A	intron variant	—
rs4273169	2:144,231,309	G/T	—	—
rs28380327	2:144,232,491	A/T	intron variant	—
rs191784266	2:144,234,080	C/T	regulatory region variant	—
rs751971221	2:144,244,987	G/A	—	uncertain significance
rs868812296	2:144,244,990	T/C	—	uncertain significance
rs778935227	2:144,245,020	G/A	—	uncertain significance
rs35789697	2:144,248,718	G/A	intron variant	—
rs13428598	2:144,250,487	C/T	intron variant	—
rs10191758	2:144,263,280	A/G	regulatory region variant	—
rs4561605	2:144,272,150	C/G	regulatory region variant	—
rs1693959539	2:144,276,864	G/A	—	uncertain significance
rs765197653	2:144,276,874	G/A	—	uncertain significance
rs6736741	2:144,278,534	C/T	intron variant	—
rs4278879	2:144,299,242	T/A	—	—
rs6733817	2:144,300,147	A/G	intron variant	—
rs10084164	2:144,302,613	G/C	—	—
rs6731747	2:144,308,396	T/A	intron variant	—
rs6717024	2:144,308,780	C/G	intron variant	—
rs2467941479	2:144,314,043	T/C	—	uncertain significance
rs10170378	2:144,334,078	C/G	—	—
rs11894956	2:144,336,132	T/A	intron variant	—
rs4662208	2:144,338,448	A/C	intron variant	—
rs4662344	2:144,348,858	T/A	—	—
rs1490866906	2:144,381,746	G/A	—	uncertain significance
rs71350022	2:144,395,796	G/A	—	—
rs10928195	2:144,428,608	C/A	—	—
rs770105549	2:144,461,008	A/G	—	uncertain significance
rs201019600	2:144,461,048	C/T	—	uncertain significance
rs776074764	2:144,461,057	G/A	—	uncertain significance
rs764811617	2:144,461,074	C/T	—	uncertain significance
rs73961845	2:144,478,983	A/G	intron variant	—
rs760147596	2:144,525,593	C/T	—	uncertain significance
rs781102282	2:144,525,632	G/A	—	uncertain significance
rs369327090	2:144,525,667	A/G	—	uncertain significance
rs2467486763	2:144,525,677	A/G	—	uncertain significance
rs1473524669	2:144,525,685	A/G	—	uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.