Arhgap23 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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198 records found for search term Arhgap23

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597744897	CV3587239	single nucleotide variant	NM_001199417.2(ARHGAP23):c.5A>G (p.Asn2Ser)	not specified [RCV004845340]	uncertain significance	17	38428490	38428490	Human		name
156397626	CV2197328	single nucleotide variant	NM_001199417.2(ARHGAP23):c.56C>T (p.Pro19Leu)	not specified [RCV004081073]	uncertain significance	17	38428541	38428541	Human		name
329358641	CV2425297	single nucleotide variant	NM_001199417.2(ARHGAP23):c.43C>T (p.Pro15Ser)	not specified [RCV004250964]	uncertain significance	17	38428528	38428528	Human		name
405685160	CV3282733	single nucleotide variant	NM_001199417.2(ARHGAP23):c.95C>G (p.Pro32Arg)	not specified [RCV004422544]	uncertain significance	17	38458133	38458133	Human		name
156329396	CV2342398	single nucleotide variant	NM_001199417.2(ARHGAP23):c.157G>A (p.Gly53Ser)	not specified [RCV004194011]	uncertain significance	17	38458195	38458195	Human		name
156129204	CV2364594	single nucleotide variant	NM_001199417.2(ARHGAP23):c.244C>T (p.Arg82Cys)	not specified [RCV004219489]	uncertain significance	17	38460923	38460923	Human		name
156054118	CV2385730	single nucleotide variant	NM_001199417.2(ARHGAP23):c.130C>A (p.Leu44Met)	not specified [RCV004226482]	uncertain significance	17	38458168	38458168	Human		name
155998647	CV2396272	single nucleotide variant	NM_001199417.2(ARHGAP23):c.152A>G (p.Gln51Arg)	not specified [RCV004240221]	uncertain significance	17	38458190	38458190	Human		name
156228982	CV2400164	single nucleotide variant	NM_001199417.2(ARHGAP23):c.128C>T (p.Thr43Met)	not specified [RCV004242965]	uncertain significance	17	38458166	38458166	Human		name
401914389	CV2811277	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2406G>C (p.Ala802=)	not provided [RCV003428245]	likely benign	17	38477866	38477866	Human		name
598207085	CV3997055	single nucleotide variant	NM_001199417.2(ARHGAP23):c.265C>T (p.Arg89Trp)	not specified [RCV005399761]	uncertain significance	17	38462857	38462857	Human		name
156371160	CV2204454	single nucleotide variant	NM_001199417.2(ARHGAP23):c.980G>A (p.Arg327His)	not specified [RCV004079261]	uncertain significance	17	38466663	38466663	Human		name
156121047	CV2233838	single nucleotide variant	NM_001199417.2(ARHGAP23):c.955C>T (p.Arg319Trp)	not specified [RCV004102055]	uncertain significance	17	38466638	38466638	Human		name
156202703	CV2234525	single nucleotide variant	NM_001199417.2(ARHGAP23):c.827G>A (p.Arg276Gln)	not specified [RCV004100719]	uncertain significance	17	38466510	38466510	Human		name
155914003	CV2242570	single nucleotide variant	NM_001199417.2(ARHGAP23):c.751C>T (p.Arg251Cys)	not specified [RCV004113637]	uncertain significance	17	38466434	38466434	Human		name
156158464	CV2262482	single nucleotide variant	NM_001199417.2(ARHGAP23):c.742A>G (p.Ser248Gly)	not specified [RCV004128915]	uncertain significance	17	38466425	38466425	Human		name
156154123	CV2266053	single nucleotide variant	NM_001199417.2(ARHGAP23):c.800C>T (p.Pro267Leu)	not specified [RCV004126867]	uncertain significance	17	38466483	38466483	Human		name
156260007	CV2277879	single nucleotide variant	NM_001199417.2(ARHGAP23):c.785C>T (p.Ser262Leu)	not specified [RCV004147289]	uncertain significance	17	38466468	38466468	Human		name
156133803	CV2284611	single nucleotide variant	NM_001199417.2(ARHGAP23):c.581C>T (p.Thr194Ile)	not specified [RCV004140774]	uncertain significance	17	38466264	38466264	Human		name
156077533	CV2291645	single nucleotide variant	NM_001199417.2(ARHGAP23):c.638C>T (p.Ser213Leu)	not specified [RCV004155932]	uncertain significance	17	38466321	38466321	Human		name
156058843	CV2305281	single nucleotide variant	NM_001199417.2(ARHGAP23):c.634A>G (p.Thr212Ala)	not specified [RCV004171201]	uncertain significance	17	38466317	38466317	Human		name
156292101	CV2339998	single nucleotide variant	NM_001199417.2(ARHGAP23):c.931C>T (p.Arg311Trp)	not specified [RCV004192248]	uncertain significance	17	38466614	38466614	Human		name
156006264	CV2394141	single nucleotide variant	NM_001199417.2(ARHGAP23):c.826C>T (p.Arg276Trp)	not specified [RCV004236340]	uncertain significance	17	38466509	38466509	Human		name
329352979	CV2468137	single nucleotide variant	NM_001199417.2(ARHGAP23):c.329A>G (p.His110Arg)	not specified [RCV004275729]	uncertain significance	17	38462921	38462921	Human		name
401723455	CV2674957	single nucleotide variant	NM_001199417.2(ARHGAP23):c.793C>T (p.Arg265Trp)	not specified [RCV004296266]	uncertain significance	17	38466476	38466476	Human		name
401757859	CV2685599	single nucleotide variant	NM_001199417.2(ARHGAP23):c.662G>A (p.Ser221Asn)	not specified [RCV004294610]	uncertain significance	17	38466345	38466345	Human		name
401732861	CV2691132	single nucleotide variant	NM_001199417.2(ARHGAP23):c.451A>G (p.Ile151Val)	not specified [RCV004301127]	uncertain significance	17	38463350	38463350	Human		name
401772266	CV2719588	single nucleotide variant	NM_001199417.2(ARHGAP23):c.457C>T (p.Pro153Ser)	not specified [RCV004327260]	uncertain significance	17	38463356	38463356	Human		name
401866271	CV2762588	single nucleotide variant	NM_001199417.2(ARHGAP23):c.691C>T (p.Arg231Cys)	not specified [RCV004338112]	likely benign	17	38466374	38466374	Human		name
401914326	CV2811278	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3786G>C (p.Ser1262=)	not provided [RCV003428246]	likely benign	17	38510282	38510282	Human		name
405685143	CV3282730	single nucleotide variant	NM_001199417.2(ARHGAP23):c.661A>G (p.Ser221Gly)	not specified [RCV004422541]	uncertain significance	17	38466344	38466344	Human		name
405685148	CV3282731	single nucleotide variant	NM_001199417.2(ARHGAP23):c.895C>T (p.Arg299Trp)	not specified [RCV004422542]	uncertain significance	17	38466578	38466578	Human		name
407531943	CV3468139	single nucleotide variant	NM_001199417.2(ARHGAP23):c.709C>T (p.Arg237Cys)	not specified [RCV004657863]	uncertain significance	17	38466392	38466392	Human		name
407531977	CV3468161	single nucleotide variant	NM_001199417.2(ARHGAP23):c.924G>T (p.Met308Ile)	not specified [RCV004657881]	uncertain significance	17	38466607	38466607	Human		name
407532142	CV3468208	single nucleotide variant	NM_001199417.2(ARHGAP23):c.886G>A (p.Val296Ile)	not specified [RCV004657915]	uncertain significance	17	38466569	38466569	Human		name
407532036	CV3468232	single nucleotide variant	NM_001199417.2(ARHGAP23):c.954C>G (p.Asp318Glu)	not specified [RCV004657932]	uncertain significance	17	38466637	38466637	Human		name
597744845	CV3587185	single nucleotide variant	NM_001199417.2(ARHGAP23):c.910C>T (p.Arg304Trp)	not specified [RCV004845330]	uncertain significance	17	38466593	38466593	Human		name
598206979	CV3997036	single nucleotide variant	NM_001199417.2(ARHGAP23):c.943G>A (p.Ala315Thr)	not specified [RCV005399742]	uncertain significance	17	38466626	38466626	Human		name
598207442	CV3997118	single nucleotide variant	NM_001199417.2(ARHGAP23):c.307G>A (p.Val103Met)	not specified [RCV005399824]	uncertain significance	17	38462899	38462899	Human		name
598207725	CV3997168	single nucleotide variant	NM_001199417.2(ARHGAP23):c.941G>C (p.Ser314Thr)	not specified [RCV005399874]	uncertain significance	17	38466624	38466624	Human		name
598207835	CV3997186	single nucleotide variant	NM_001199417.2(ARHGAP23):c.944C>T (p.Ala315Val)	not specified [RCV005399892]	uncertain significance	17	38466627	38466627	Human		name
598207892	CV3997195	single nucleotide variant	NM_001199417.2(ARHGAP23):c.678T>A (p.Ser226Arg)	not specified [RCV005399901]	uncertain significance	17	38466361	38466361	Human		name
598172973	CV3997216	single nucleotide variant	NM_001199417.2(ARHGAP23):c.617C>T (p.Thr206Ile)	not specified [RCV005393120]	uncertain significance	17	38466300	38466300	Human		name
156400686	CV2207077	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1105G>A (p.Ala369Thr)	not specified [RCV004085682]	uncertain significance	17	38466788	38466788	Human		name
156378599	CV2207762	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1931G>A (p.Arg644His)	not specified [RCV004084200]	uncertain significance	17	38469861	38469861	Human		name
156292224	CV2223487	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1496G>A (p.Arg499His)	not specified [RCV004106055]	uncertain significance	17	38467179	38467179	Human		name
156062642	CV2232031	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1043G>T (p.Arg348Leu)	not specified [RCV004093083]	uncertain significance	17	38466726	38466726	Human		name
156086920	CV2241280	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2908C>T (p.Arg970Cys)	not specified [RCV004102430]	uncertain significance	17	38486062	38486062	Human		name
156302616	CV2241784	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1028A>G (p.Gln343Arg)	not specified [RCV004106719]	uncertain significance	17	38466711	38466711	Human		name
155979082	CV2266593	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2628G>C (p.Lys876Asn)	not specified [RCV004131142]	uncertain significance	17	38479882	38479882	Human		name
156142829	CV2268751	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2162C>T (p.Ala721Val)	not specified [RCV004124142]	uncertain significance	17	38477622	38477622	Human		name
156119567	CV2275828	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2607G>C (p.Gln869His)	not specified [RCV004139495]	uncertain significance	17	38479861	38479861	Human		name
156131088	CV2279905	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1523A>C (p.Gln508Pro)	not specified [RCV004144495]	uncertain significance	17	38467206	38467206	Human		name
156124284	CV2285745	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1823G>A (p.Arg608His)	not specified [RCV004141888]	uncertain significance	17	38469542	38469542	Human		name
155998297	CV2287134	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1784G>A (p.Arg595His)	not specified [RCV004145000]	uncertain significance	17	38469279	38469279	Human		name
156104358	CV2291722	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1052C>T (p.Ser351Leu)	not specified [RCV004158006]	uncertain significance	17	38466735	38466735	Human		name
156347243	CV2297875	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2602A>C (p.Thr868Pro)	not specified [RCV004157812]	uncertain significance	17	38479856	38479856	Human		name
155957342	CV2304144	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1483C>G (p.Pro495Ala)	not specified [RCV004170178]	uncertain significance	17	38467166	38467166	Human		name
156345945	CV2308971	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1459G>A (p.Asp487Asn)	not specified [RCV004169253]	uncertain significance	17	38467142	38467142	Human		name
156160504	CV2311673	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2555G>A (p.Gly852Asp)	not specified [RCV004170555]	uncertain significance	17	38479809	38479809	Human		name
155973461	CV2332403	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1825C>T (p.Arg609Cys)	not specified [RCV004196135]	uncertain significance	17	38469544	38469544	Human		name
155918076	CV2332934	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1378C>T (p.Pro460Ser)	not specified [RCV004192191]	uncertain significance	17	38467061	38467061	Human		name
156287231	CV2336060	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1097G>T (p.Gly366Val)	not specified [RCV004189661]	uncertain significance	17	38466780	38466780	Human		name
156087468	CV2337723	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2621G>A (p.Gly874Glu)	not specified [RCV004183744]	uncertain significance	17	38479875	38479875	Human		name
155976932	CV2342836	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1426C>T (p.Arg476Trp)	not specified [RCV004189873]	uncertain significance	17	38467109	38467109	Human		name
156112232	CV2387898	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1760C>T (p.Pro587Leu)	not specified [RCV004236448]	uncertain significance	17	38469255	38469255	Human		name
156007701	CV2390005	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2909G>A (p.Arg970His)	not specified [RCV004238620]	uncertain significance	17	38486063	38486063	Human		name
155967038	CV2391301	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1259G>A (p.Arg420Gln)	not specified [RCV004237666]	uncertain significance	17	38466942	38466942	Human		name
155926617	CV2395743	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2684A>G (p.Asn895Ser)	not specified [RCV004235276]	uncertain significance	17	38482076	38482076	Human		name
329359043	CV2425482	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2167C>T (p.Arg723Trp)	not specified [RCV004252926]	uncertain significance	17	38477627	38477627	Human		name
329354692	CV2444713	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2261C>T (p.Ala754Val)	not specified [RCV004258967]	uncertain significance	17	38477721	38477721	Human		name
329391545	CV2452903	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2477T>C (p.Leu826Pro)	not specified [RCV004277543]	uncertain significance	17	38479476	38479476	Human		name
401721156	CV2673620	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2924A>G (p.Asn975Ser)	not specified [RCV004282355]	uncertain significance	17	38486078	38486078	Human		name
401723473	CV2674964	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1120C>T (p.Arg374Cys)	not specified [RCV004296272]	uncertain significance	17	38466803	38466803	Human		name
401767773	CV2677811	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2026C>T (p.His676Tyr)	not specified [RCV004294309]	uncertain significance	17	38471914	38471914	Human		name
401772648	CV2687765	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2275G>A (p.Gly759Ser)	not specified [RCV004302751]	uncertain significance	17	38477735	38477735	Human		name
401769193	CV2693504	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2305G>A (p.Glu769Lys)	not specified [RCV004295445]	uncertain significance	17	38477765	38477765	Human		name
401744182	CV2696952	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2197C>T (p.Arg733Trp)	not specified [RCV004292946]	uncertain significance	17	38477657	38477657	Human		name
401722708	CV2703471	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2970G>T (p.Glu990Asp)	not specified [RCV004317657]	uncertain significance	17	38486124	38486124	Human		name
401738026	CV2714295	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1162C>T (p.Arg388Cys)	not specified [RCV004315979]	uncertain significance	17	38466845	38466845	Human		name
401737509	CV2718121	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1987T>G (p.Trp663Gly)	not specified [RCV004315834]	uncertain significance	17	38471875	38471875	Human		name
401781958	CV2722357	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1930C>T (p.Arg644Cys)	not specified [RCV004322767]	uncertain significance	17	38469860	38469860	Human		name
401784404	CV2730329	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2543G>A (p.Arg848His)	not specified [RCV004333296]	uncertain significance	17	38479797	38479797	Human		name
401767050	CV2730752	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1427G>A (p.Arg476Gln)	not specified [RCV004331609]	uncertain significance	17	38467110	38467110	Human		name
401895735	CV2771107	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1610C>T (p.Ala537Val)	not specified [RCV004346111]	uncertain significance	17	38467293	38467293	Human		name
401869714	CV2772496	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1523A>G (p.Gln508Arg)	not specified [RCV004355274]	uncertain significance	17	38467206	38467206	Human		name
401882794	CV2778645	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2150G>A (p.Arg717Gln)	not specified [RCV004344289]	uncertain significance	17	38477610	38477610	Human		name
401899105	CV2783656	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2170G>C (p.Ala724Pro)	not specified [RCV004360592]	uncertain significance	17	38477630	38477630	Human		name
401895371	CV2786412	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2881C>T (p.Pro961Ser)	not specified [RCV004362000]	uncertain significance	17	38482652	38482652	Human		name
401898915	CV2792115	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2875C>T (p.Arg959Cys)	not specified [RCV004361339]	uncertain significance	17	38482646	38482646	Human		name
401935750	CV2811276	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1583G>A (p.Arg528His)	not provided [RCV003413211]	likely benign	17	38467266	38467266	Human		name
405685001	CV3282703	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1040A>G (p.His347Arg)	not specified [RCV004422514]	uncertain significance	17	38466723	38466723	Human		name
405685006	CV3282704	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1057G>A (p.Asp353Asn)	not specified [RCV004422515]	uncertain significance	17	38466740	38466740	Human		name
405685010	CV3282705	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1070G>A (p.Arg357Gln)	not specified [RCV004422516]	uncertain significance	17	38466753	38466753	Human		name
405685016	CV3282706	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1249A>G (p.Ile417Val)	not specified [RCV004422517]	uncertain significance	17	38466932	38466932	Human		name
405685021	CV3282707	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1412C>T (p.Pro471Leu)	not specified [RCV004422518]	uncertain significance	17	38467095	38467095	Human		name
405685025	CV3282708	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1487C>T (p.Pro496Leu)	not specified [RCV004422519]	uncertain significance	17	38467170	38467170	Human		name
405685032	CV3282709	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1501G>T (p.Val501Phe)	not specified [RCV004422520]	uncertain significance	17	38467184	38467184	Human		name
405685043	CV3282711	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1894C>T (p.Arg632Cys)	not specified [RCV004422522]	uncertain significance	17	38469613	38469613	Human		name
405685048	CV3282712	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2192A>G (p.Lys731Arg)	not specified [RCV004422523]	uncertain significance	17	38477652	38477652	Human		name
405685053	CV3282713	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2209G>A (p.Gly737Arg)	not specified [RCV004422524]	uncertain significance	17	38477669	38477669	Human		name
405685059	CV3282714	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2454C>G (p.Asn818Lys)	not specified [RCV004422525]	uncertain significance	17	38479453	38479453	Human		name
405685063	CV3282715	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2528C>T (p.Ser843Phe)	not specified [RCV004422526]	uncertain significance	17	38479782	38479782	Human		name
405685068	CV3282716	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2585C>T (p.Ala862Val)	not specified [RCV004422527]	uncertain significance	17	38479839	38479839	Human		name
405685072	CV3282717	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2674A>G (p.Ile892Val)	not specified [RCV004422528]	uncertain significance	17	38482066	38482066	Human		name
405685077	CV3282718	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2705C>T (p.Ala902Val)	not specified [RCV004422529]	uncertain significance	17	38482097	38482097	Human		name
405685083	CV3282719	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2833G>A (p.Gly945Ser)	not specified [RCV004422530]	uncertain significance	17	38482604	38482604	Human		name
407531954	CV3468145	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1516G>A (p.Ala506Thr)	not specified [RCV004657869]	uncertain significance	17	38467199	38467199	Human		name
407531991	CV3468168	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1214C>T (p.Pro405Leu)	not specified [RCV004657888]	uncertain significance	17	38466897	38466897	Human		name
407491235	CV3468176	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1757C>T (p.Ser586Phe)	not specified [RCV004666824]	uncertain significance	17	38469252	38469252	Human		name
407491258	CV3468188	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1843G>A (p.Ala615Thr)	not specified [RCV004666829]	uncertain significance	17	38469562	38469562	Human		name
407532155	CV3468198	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1280A>G (p.Gln427Arg)	not specified [RCV004657909]	uncertain significance	17	38466963	38466963	Human		name
407532109	CV3468229	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2540C>G (p.Ser847Cys)	not specified [RCV004657929]	uncertain significance	17	38479794	38479794	Human		name
407532034	CV3468234	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1915C>T (p.Arg639Trp)	not specified [RCV004657934]	uncertain significance	17	38469634	38469634	Human		name
407491210	CV3472055	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2356T>C (p.Tyr786His)	not specified [RCV004666817]	uncertain significance	17	38477816	38477816	Human		name
597744865	CV3587199	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2222C>T (p.Ala741Val)	not specified [RCV004845334]	uncertain significance	17	38477682	38477682	Human		name
597744873	CV3587205	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1426C>G (p.Arg476Gly)	not specified [RCV004845335]	uncertain significance	17	38467109	38467109	Human		name
597744882	CV3587222	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1216T>G (p.Ser406Ala)	not specified [RCV004845337]	uncertain significance	17	38466899	38466899	Human		name
597744907	CV3587246	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2798G>A (p.Arg933Gln)	not specified [RCV004845342]	uncertain significance	17	38482569	38482569	Human		name
597744915	CV3587259	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2683A>C (p.Asn895His)	not specified [RCV004845344]	uncertain significance	17	38482075	38482075	Human		name
597744919	CV3587270	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2213C>T (p.Pro738Leu)	not specified [RCV004845345]	uncertain significance	17	38477673	38477673	Human		name
597744924	CV3587277	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2512C>T (p.Pro838Ser)	not specified [RCV004845346]	uncertain significance	17	38479766	38479766	Human		name
597744938	CV3587297	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1213C>T (p.Pro405Ser)	not specified [RCV004845349]	uncertain significance	17	38466896	38466896	Human		name
597744946	CV3587311	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1945C>T (p.Arg649Trp)	not specified [RCV004845351]	uncertain significance	17	38469875	38469875	Human		name
597744951	CV3587316	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1121G>A (p.Arg374His)	not specified [RCV004845352]	uncertain significance	17	38466804	38466804	Human		name
597744956	CV3587321	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2138G>A (p.Arg713His)	not specified [RCV004845353]	uncertain significance	17	38477598	38477598	Human		name
597744965	CV3587335	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1832C>T (p.Ser611Phe)	not specified [RCV004845355]	uncertain significance	17	38469551	38469551	Human		name
597744970	CV3587343	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2200C>T (p.Arg734Trp)	not specified [RCV004845356]	uncertain significance	17	38477660	38477660	Human		name
598206815	CV3997004	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2689A>C (p.Lys897Gln)	not specified [RCV005399709]	uncertain significance	17	38482081	38482081	Human		name
598206870	CV3997016	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2216C>T (p.Ala739Val)	not specified [RCV005399721]	uncertain significance	17	38477676	38477676	Human		name
598207023	CV3997044	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2519C>G (p.Ala840Gly)	not specified [RCV005399750]	uncertain significance	17	38479773	38479773	Human		name
598207129	CV3997065	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2840A>G (p.Asn947Ser)	not specified [RCV005399771]	uncertain significance	17	38482611	38482611	Human		name
598207353	CV3997105	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1826G>A (p.Arg609His)	not specified [RCV005399811]	uncertain significance	17	38469545	38469545	Human		name
598207429	CV3997116	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2170G>T (p.Ala724Ser)	not specified [RCV005399822]	uncertain significance	17	38477630	38477630	Human		name
598207436	CV3997117	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2873A>G (p.Asn958Ser)	not specified [RCV005399823]	uncertain significance	17	38482644	38482644	Human		name
598207465	CV3997122	single nucleotide variant	NM_001199417.2(ARHGAP23):c.2011G>T (p.Ala671Ser)	not specified [RCV005399828]	uncertain significance	17	38471899	38471899	Human		name
598207772	CV3997176	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1732C>G (p.Pro578Ala)	not specified [RCV005399882]	uncertain significance	17	38469227	38469227	Human		name
598207970	CV3997207	single nucleotide variant	NM_001199417.2(ARHGAP23):c.1829C>T (p.Ser610Phe)	not specified [RCV005399913]	uncertain significance	17	38469548	38469548	Human		name
156399418	CV2205106	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4108G>A (p.Glu1370Lys)	not specified [RCV004077706]	uncertain significance	17	38510604	38510604	Human		name
156326030	CV2209537	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4204A>C (p.Ser1402Arg)	not specified [RCV004093653]	uncertain significance	17	38510700	38510700	Human		name
156150159	CV2213050	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4207T>G (p.Trp1403Gly)	not specified [RCV004091626]	uncertain significance	17	38510703	38510703	Human		name
156380319	CV2218101	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3032G>C (p.Arg1011Pro)	not specified [RCV004086532]	uncertain significance	17	38490147	38490147	Human		name
155913238	CV2245784	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3973C>G (p.Arg1325Gly)	not specified [RCV004111644]	uncertain significance	17	38510469	38510469	Human		name
155973871	CV2269890	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3256G>A (p.Val1086Met)	not specified [RCV004127114]	uncertain significance	17	38491512	38491512	Human		name
155992267	CV2286183	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4465C>G (p.Gln1489Glu)	not specified [RCV004146151]	uncertain significance	17	38510961	38510961	Human		name
156168531	CV2315392	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3485A>G (p.Glu1162Gly)	not specified [RCV004167359]	uncertain significance	17	38509981	38509981	Human		name
156074789	CV2321719	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4018G>A (p.Ala1340Thr)	not specified [RCV004179717]	uncertain significance	17	38510514	38510514	Human		name
156355145	CV2324420	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3989G>A (p.Gly1330Asp)	not specified [RCV004178911]	uncertain significance	17	38510485	38510485	Human		name
156280064	CV2325407	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4207T>C (p.Trp1403Arg)	not specified [RCV004177770]	uncertain significance	17	38510703	38510703	Human		name
156062545	CV2353800	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3986A>G (p.Asp1329Gly)	not specified [RCV004201805]	uncertain significance	17	38510482	38510482	Human		name
156145804	CV2357889	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4288C>T (p.Pro1430Ser)	not specified [RCV004209679]	uncertain significance	17	38510784	38510784	Human		name
156001636	CV2378835	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3870G>C (p.Glu1290Asp)	not specified [RCV004231277]	uncertain significance	17	38510366	38510366	Human		name
156347588	CV2382932	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3047C>T (p.Thr1016Met)	not specified [RCV004217524]	uncertain significance	17	38490162	38490162	Human		name
329361930	CV2468451	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3662T>C (p.Val1221Ala)	not specified [RCV004277757]	uncertain significance	17	38510158	38510158	Human		name
329353440	CV2469278	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3770A>G (p.Asp1257Gly)	not specified [RCV004280615]	uncertain significance	17	38510266	38510266	Human		name
401722213	CV2680865	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3995G>A (p.Gly1332Asp)	not specified [RCV004293511]	uncertain significance	17	38510491	38510491	Human		name
401769715	CV2689904	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3331G>A (p.Asp1111Asn)	not specified [RCV004297797]	uncertain significance	17	38498426	38498426	Human		name
401774416	CV2691728	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3808G>A (p.Gly1270Arg)	not specified [RCV004299185]	uncertain significance	17	38510304	38510304	Human		name
401731774	CV2712150	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4238C>T (p.Pro1413Leu)	not specified [RCV004311874]	uncertain significance	17	38510734	38510734	Human		name
401752670	CV2723313	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3755C>T (p.Thr1252Ile)	not specified [RCV004329534]	uncertain significance	17	38510251	38510251	Human		name
401860911	CV2758681	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3407C>T (p.Pro1136Leu)	not specified [RCV004337748]	uncertain significance	17	38498502	38498502	Human		name
401862819	CV2779027	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4028C>T (p.Pro1343Leu)	not specified [RCV004348676]	uncertain significance	17	38510524	38510524	Human		name
405685090	CV3282720	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3029C>T (p.Ala1010Val)	not specified [RCV004422531]	uncertain significance	17	38490144	38490144	Human		name
405685095	CV3282721	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3106G>A (p.Val1036Met)	not specified [RCV004422532]	uncertain significance	17	38490507	38490507	Human		name
405685102	CV3282722	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3458C>T (p.Ala1153Val)	not specified [RCV004422533]	uncertain significance	17	38509954	38509954	Human		name
405685105	CV3282723	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3556G>C (p.Gly1186Arg)	not specified [RCV004422534]	uncertain significance	17	38510052	38510052	Human		name
405685108	CV3282724	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3563G>C (p.Ser1188Thr)	not specified [RCV004422535]	uncertain significance	17	38510059	38510059	Human		name
405685113	CV3282725	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3911G>A (p.Arg1304Gln)	not specified [RCV004422536]	uncertain significance	17	38510407	38510407	Human		name
405685118	CV3282726	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4274T>C (p.Leu1425Pro)	not specified [RCV004422537]	uncertain significance	17	38510770	38510770	Human		name
405685124	CV3282727	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4394C>A (p.Pro1465Gln)	not specified [RCV004422538]	uncertain significance	17	38510890	38510890	Human		name
405685129	CV3282728	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4394C>T (p.Pro1465Leu)	not specified [RCV004422539]	uncertain significance	17	38510890	38510890	Human		name
405685134	CV3282729	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4442G>A (p.Arg1481His)	not specified [RCV004422540]	uncertain significance	17	38510938	38510938	Human		name
407491231	CV3468154	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3796G>A (p.Gly1266Ser)	not specified [RCV004666823]	uncertain significance	17	38510292	38510292	Human		name
407491244	CV3468181	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4126C>T (p.Leu1376Phe)	not specified [RCV004666826]	uncertain significance	17	38510622	38510622	Human		name
407532122	CV3468217	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4417T>G (p.Ser1473Ala)	not specified [RCV004657923]	likely benign	17	38510913	38510913	Human		name
407491744	CV3468228	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3031C>T (p.Arg1011Trp)	not specified [RCV004666843]	uncertain significance	17	38490146	38490146	Human		name
407532031	CV3468233	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4333T>G (p.Ser1445Ala)	not specified [RCV004657933]	uncertain significance	17	38510829	38510829	Human		name
597744855	CV3587192	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4310G>A (p.Arg1437Gln)	not specified [RCV004845332]	uncertain significance	17	38510806	38510806	Human		name
597744860	CV3587193	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3850C>T (p.His1284Tyr)	not specified [RCV004845333]	uncertain significance	17	38510346	38510346	Human		name
597744877	CV3587217	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3974G>T (p.Arg1325Leu)	not specified [RCV004845336]	uncertain significance	17	38510470	38510470	Human		name
597745411	CV3587227	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4249C>T (p.Leu1417Phe)	not specified [RCV004845338]	uncertain significance	17	38510745	38510745	Human		name
597744892	CV3587236	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4159C>T (p.Arg1387Cys)	not specified [RCV004845339]	uncertain significance	17	38510655	38510655	Human		name
597744910	CV3587253	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4144G>A (p.Asp1382Asn)	not specified [RCV004845343]	uncertain significance	17	38510640	38510640	Human		name
597744928	CV3587284	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4373C>T (p.Pro1458Leu)	not specified [RCV004845347]	uncertain significance	17	38510869	38510869	Human		name
597744933	CV3587290	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4009G>A (p.Gly1337Ser)	not specified [RCV004845348]	uncertain significance	17	38510505	38510505	Human		name
597744942	CV3587306	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3397C>T (p.Pro1133Ser)	not specified [RCV004845350]	uncertain significance	17	38498492	38498492	Human		name
597744961	CV3587328	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3143A>T (p.Lys1048Ile)	not specified [RCV004845354]	uncertain significance	17	38490544	38490544	Human		name
598206844	CV3997010	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4445C>T (p.Ser1482Leu)	not specified [RCV005399715]	uncertain significance	17	38510941	38510941	Human		name
598206925	CV3997026	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4370C>T (p.Ala1457Val)	not specified [RCV005399732]	uncertain significance	17	38510866	38510866	Human		name
598207174	CV3997075	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4291C>T (p.Pro1431Ser)	not specified [RCV005399781]	uncertain significance	17	38510787	38510787	Human		name
598207286	CV3997094	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3665C>T (p.Ala1222Val)	not specified [RCV005399800]	uncertain significance	17	38510161	38510161	Human		name
598207448	CV3997119	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3049C>A (p.Leu1017Met)	not specified [RCV005399825]	uncertain significance	17	38490164	38490164	Human		name
598207491	CV3997127	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4397C>T (p.Pro1466Leu)	not specified [RCV005399833]	uncertain significance	17	38510893	38510893	Human		name
598207524	CV3997134	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3161G>A (p.Arg1054Gln)	not specified [RCV005399840]	uncertain significance	17	38491417	38491417	Human		name
598207554	CV3997140	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3795C>G (p.Ser1265Arg)	not specified [RCV005399846]	uncertain significance	17	38510291	38510291	Human		name
598207575	CV3997144	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3971C>T (p.Ala1324Val)	not specified [RCV005399850]	uncertain significance	17	38510467	38510467	Human		name
598207617	CV3997151	single nucleotide variant	NM_001199417.2(ARHGAP23):c.3133C>T (p.His1045Tyr)	not specified [RCV005399857]	uncertain significance	17	38490534	38490534	Human		name
598207671	CV3997159	single nucleotide variant	NM_001199417.2(ARHGAP23):c.4165C>T (p.Arg1389Trp)	not specified [RCV005399865]	uncertain significance	17	38510661	38510661	Human		name

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