Arhgap1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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556 records found for search term Arhgap1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405674758	CV3286387	single nucleotide variant	NM_004308.5(ARHGAP1):c.8C>T (p.Pro3Leu)	not specified [RCV004420367]	uncertain significance	11	46696100	46696100	Human		name
15148589	CV737994	single nucleotide variant	NM_004308.5(ARHGAP1):c.156G>A (p.Pro52=)	not provided [RCV000900750]	benign	11	46695733	46695733	Human		name
405674753	CV3286386	single nucleotide variant	NM_004308.5(ARHGAP1):c.77C>T (p.Ala26Val)	not specified [RCV004420366]	uncertain significance	11	46696031	46696031	Human		name
597741923	CV3573297	single nucleotide variant	NM_004308.5(ARHGAP1):c.450G>A (p.Lys150=)	not specified [RCV004844816]	likely benign	11	46681379	46681379	Human		name
598272818	CV4006717	single nucleotide variant	NM_004308.5(ARHGAP1):c.91A>G (p.Lys31Glu)	not specified [RCV005389488]	uncertain significance	11	46696017	46696017	Human		name
15187413	CV737992	single nucleotide variant	NM_004308.5(ARHGAP1):c.708C>A (p.Pro236=)	not provided [RCV000909083]	benign	11	46680675	46680675	Human		name
15166308	CV752681	single nucleotide variant	NM_004308.5(ARHGAP1):c.915C>T (p.Phe305=)	not provided [RCV000926837]	likely benign	11	46679760	46679760	Human		name
15105686	CV752682	single nucleotide variant	NM_004308.5(ARHGAP1):c.642C>T (p.Asp214=)	not provided [RCV000915598]	likely benign	11	46680741	46680741	Human		name
38467621	CV920827	single nucleotide variant	NM_004308.5(ARHGAP1):c.768G>A (p.Gln256=)	not provided [RCV001200339]	likely benign	11	46680539	46680539	Human		name
405674632	CV3286381	single nucleotide variant	NM_004308.5(ARHGAP1):c.256A>G (p.Ile86Val)	not specified [RCV004420361]	uncertain significance	11	46688234	46688234	Human		name
405674637	CV3286382	single nucleotide variant	NM_004308.5(ARHGAP1):c.284C>T (p.Pro95Leu)	not specified [RCV004420362]	uncertain significance	11	46688206	46688206	Human		name
407531261	CV3461470	single nucleotide variant	NM_004308.5(ARHGAP1):c.202G>C (p.Ala68Pro)	not specified [RCV004657503]	uncertain significance	11	46695687	46695687	Human		name
597768527	CV3573289	single nucleotide variant	NM_004308.5(ARHGAP1):c.218T>C (p.Val73Ala)	not specified [RCV004850706]	uncertain significance	11	46695671	46695671	Human		name
15118792	CV737993	single nucleotide variant	NM_004308.5(ARHGAP1):c.205C>T (p.Arg69Trp)	not provided [RCV000895606]\|not specified [RCV004028453]	likely benign\|uncertain significance	11	46695684	46695684	Human		name
156379937	CV2211676	single nucleotide variant	NM_004308.5(ARHGAP1):c.298G>A (p.Asp100Asn)	not specified [RCV004084565]	uncertain significance	11	46688192	46688192	Human		name
156092718	CV2216849	single nucleotide variant	NM_004308.5(ARHGAP1):c.394G>A (p.Asp132Asn)	not specified [RCV004083275]	uncertain significance	11	46682106	46682106	Human		name
156230994	CV2227566	single nucleotide variant	NM_004308.5(ARHGAP1):c.663G>C (p.Gln221His)	not specified [RCV004092209]	uncertain significance	11	46680720	46680720	Human		name
156053726	CV2269528	single nucleotide variant	NM_004308.5(ARHGAP1):c.412A>T (p.Ser138Cys)	not specified [RCV004124635]	uncertain significance	11	46682088	46682088	Human		name
155904583	CV2353913	single nucleotide variant	NM_004308.5(ARHGAP1):c.563A>G (p.Tyr188Cys)	not specified [RCV004201909]	uncertain significance	11	46681083	46681083	Human		name
401747984	CV2699973	single nucleotide variant	NM_004308.5(ARHGAP1):c.704C>A (p.Pro235His)	not specified [RCV004310406]	uncertain significance	11	46680679	46680679	Human		name
401858408	CV2774044	single nucleotide variant	NM_004308.5(ARHGAP1):c.526C>G (p.Pro176Ala)	not specified [RCV004345652]	uncertain significance	11	46681303	46681303	Human		name
405674741	CV3286383	single nucleotide variant	NM_004308.5(ARHGAP1):c.673G>T (p.Ala225Ser)	not specified [RCV004420363]	uncertain significance	11	46680710	46680710	Human		name
405674745	CV3286384	single nucleotide variant	NM_004308.5(ARHGAP1):c.758A>T (p.Asn253Ile)	not specified [RCV004420364]	uncertain significance	11	46680549	46680549	Human		name
405674749	CV3286385	single nucleotide variant	NM_004308.5(ARHGAP1):c.760C>A (p.Pro254Thr)	not specified [RCV004420365]	uncertain significance	11	46680547	46680547	Human		name
597741758	CV3573265	single nucleotide variant	NM_004308.5(ARHGAP1):c.931C>A (p.Leu311Met)	not specified [RCV004844785]	uncertain significance	11	46679744	46679744	Human		name
597742386	CV3573268	single nucleotide variant	NM_004308.5(ARHGAP1):c.700C>T (p.Arg234Trp)	not specified [RCV004844788]	uncertain significance	11	46680683	46680683	Human		name
597741834	CV3573279	single nucleotide variant	NM_004308.5(ARHGAP1):c.701G>A (p.Arg234Gln)	not specified [RCV004844799]	uncertain significance	11	46680682	46680682	Human		name
597742017	CV3580242	single nucleotide variant	NM_004308.5(ARHGAP1):c.665A>G (p.Lys222Arg)	not specified [RCV004844834]	uncertain significance	11	46680718	46680718	Human		name
15168756	CV724452	single nucleotide variant	NM_004308.5(ARHGAP1):c.787C>T (p.Leu263Phe)	not provided [RCV000883130]	benign	11	46680520	46680520	Human	1	name
15168756	CV724452	single nucleotide variant	NM_004308.5(ARHGAP1):c.787C>T (p.Leu263Phe)	not provided [RCV000883130]	benign	11	46680520	46680521	Human	1	name
156258641	CV2304878	single nucleotide variant	NM_004308.5(ARHGAP1):c.1009C>T (p.His337Tyr)	not specified [RCV004168798]	uncertain significance	11	46679666	46679666	Human		name
156345371	CV2372911	single nucleotide variant	NM_004308.5(ARHGAP1):c.1142A>G (p.His381Arg)	not specified [RCV004223956]	uncertain significance	11	46679215	46679215	Human		name
329372684	CV2428605	single nucleotide variant	NM_004308.5(ARHGAP1):c.1084G>A (p.Glu362Lys)	not specified [RCV004255411]	uncertain significance	11	46679412	46679412	Human		name
405674616	CV3286377	single nucleotide variant	NM_004308.5(ARHGAP1):c.1150C>G (p.Gln384Glu)	not specified [RCV004420357]	uncertain significance	11	46679207	46679207	Human		name
405674620	CV3286378	single nucleotide variant	NM_004308.5(ARHGAP1):c.1192C>T (p.Pro398Ser)	not specified [RCV004420358]	uncertain significance	11	46679165	46679165	Human		name
405674624	CV3286379	single nucleotide variant	NM_004308.5(ARHGAP1):c.1259C>T (p.Thr420Ile)	not specified [RCV004420359]	uncertain significance	11	46679098	46679098	Human		name
405674628	CV3286380	single nucleotide variant	NM_004308.5(ARHGAP1):c.1301C>T (p.Pro434Leu)	not specified [RCV004420360]	uncertain significance	11	46679056	46679056	Human		name
597741710	CV3573255	single nucleotide variant	NM_004308.5(ARHGAP1):c.1109T>C (p.Phe370Ser)	not specified [RCV004844776]	uncertain significance	11	46679387	46679387	Human		name
597741964	CV3580231	single nucleotide variant	NM_004308.5(ARHGAP1):c.1244C>T (p.Pro415Leu)	not specified [RCV004844824]	uncertain significance	11	46679113	46679113	Human		name
598272841	CV4006728	single nucleotide variant	NM_004308.5(ARHGAP1):c.1298G>C (p.Ser433Thr)	not specified [RCV005389495]	uncertain significance	11	46679059	46679059	Human		name
15117050	CV737991	single nucleotide variant	NM_004308.5(ARHGAP1):c.1105C>T (p.Arg369Cys)	not provided [RCV000895311]	likely benign	11	46679391	46679391	Human		name
401916958	CV2812357	single nucleotide variant	NM_018460.4(ARHGAP15):c.474+1G>A	not provided [RCV003429287]	uncertain significance	2	143250601	143250601	Human		name
401928543	CV2820199	single nucleotide variant	NM_024605.4(ARHGAP10):c.251-3C>T	not provided [RCV003439509]	likely benign	4	147822893	147822893	Human		name
15190132	CV777199	single nucleotide variant	NM_018460.4(ARHGAP15):c.475-4G>T	not provided [RCV000954385]	likely benign	2	143435597	143435597	Human		name
8626090	CV81234	single nucleotide variant	NM_033515.2(ARHGAP18):c.787-1G>T	Malignant melanoma [RCV000061312]	not provided	6	129618853	129618853	Human		name
8576608	CV110975	single nucleotide variant	NM_018460.3(ARHGAP15):c.234+620A>G	Lung cancer [RCV000091498]	uncertain significance	2	143202822	143202822	Human		name
8649342	CV125907	single nucleotide variant	NM_024605.4(ARHGAP10):c.1116+21A>G	not provided [RCV000106395]	not provided	4	147906740	147906740	Human		name
15118324	CV779673	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1235+5T>G	not provided [RCV000962357]	benign	15	32633113	32633113	Human		name
8576611	CV110979	single nucleotide variant	NM_018460.3(ARHGAP15):c.704-4471A>G	Lung cancer [RCV000091502]	uncertain significance	2	143482902	143482902	Human		name
8576612	CV110980	single nucleotide variant	NM_018460.3(ARHGAP15):c.826+3974T>C	Lung cancer [RCV000091503]	uncertain significance	2	143491469	143491469	Human		name
8576609	CV110976	single nucleotide variant	NM_018460.3(ARHGAP15):c.474+86541G>A	Lung cancer [RCV000091499]	uncertain significance	2	143337141	143337141	Human		name
8648979	CV110977	single nucleotide variant	NM_018460.3(ARHGAP15):c.475-83608T>C	Lung cancer [RCV000091500]	uncertain significance	2	143351993	143351993	Human		name
8576610	CV110978	single nucleotide variant	NM_018460.3(ARHGAP15):c.475-27933T>A	Lung cancer [RCV000091501]	uncertain significance	2	143407668	143407668	Human		name
8576616	CV110984	single nucleotide variant	NM_018460.3(ARHGAP15):c.1139-5396G>C	Lung cancer [RCV000091507]	uncertain significance	2	143698023	143698023	Human		name
8576617	CV110985	single nucleotide variant	NM_018460.3(ARHGAP15):c.1244+2777A>G	Lung cancer [RCV000091508]	uncertain significance	2	143706301	143706301	Human		name
8576613	CV110981	single nucleotide variant	NM_018460.3(ARHGAP15):c.1004-27015A>G	Lung cancer [RCV000091504]	uncertain significance	2	143597118	143597118	Human		name
8576614	CV110982	single nucleotide variant	NM_018460.3(ARHGAP15):c.1004-11362C>A	Lung cancer [RCV000091505]	uncertain significance	2	143612771	143612771	Human		name
8576615	CV110983	single nucleotide variant	NM_018460.3(ARHGAP15):c.1138+22590A>G	Lung cancer [RCV000091506]	uncertain significance	2	143646857	143646857	Human		name
8576618	CV110986	single nucleotide variant	NM_018460.3(ARHGAP15):c.1245-17783G>C	Lung cancer [RCV000091509]	uncertain significance	2	143750206	143750206	Human		name
8651886	CV128461	single nucleotide variant	NM_001270695.1(ARHGAP12):c.-111+5776G>A	Lung cancer [RCV000108948]	uncertain significance	10	31922907	31922907	Human		name
405273260	CV3210365	deletion	NM_033515.3(ARHGAP18):c.1123-20_1123-13del	ARHGAP18-related disorder [RCV003914589]	likely benign	6	129608065	129608072	Human		name , trait , alternate_id
15123494	CV712351	single nucleotide variant	NM_018287.7(ARHGAP12):c.16A>C (p.Arg6=)	not provided [RCV000963251]	benign	10	31908840	31908840	Human		name
598205280	CV4002851	single nucleotide variant	NM_024605.4(ARHGAP10):c.25A>G (p.Ser9Gly)	not specified [RCV005399440]	uncertain significance	4	147732326	147732326	Human		name
8649341	CV125906	single nucleotide variant	NM_024605.4(ARHGAP10):c.822C>T (p.Val274=)	not provided [RCV000106394]	not provided	4	147875140	147875140	Human		name
156106804	CV2257303	single nucleotide variant	NM_033515.3(ARHGAP18):c.56G>A (p.Gly19Asp)	not specified [RCV004125408]	uncertain significance	6	129710081	129710081	Human		name
156361503	CV2269257	single nucleotide variant	NM_033515.3(ARHGAP18):c.91G>A (p.Ala31Thr)	not specified [RCV004130405]	uncertain significance	6	129710046	129710046	Human		name
156054242	CV2308649	single nucleotide variant	NM_018460.4(ARHGAP15):c.52C>T (p.Arg18Cys)	not specified [RCV004167201]	uncertain significance	2	143155542	143155542	Human		name
156146824	CV2311115	single nucleotide variant	NM_018287.7(ARHGAP12):c.43G>A (p.Val15Met)	not specified [RCV004164106]	uncertain significance	10	31908813	31908813	Human		name
155958814	CV2313838	single nucleotide variant	NM_033515.3(ARHGAP18):c.81C>A (p.Ser27Arg)	not specified [RCV004164159]	uncertain significance	6	129710056	129710056	Human		name
155903362	CV2386487	single nucleotide variant	NM_032900.6(ARHGAP19):c.28G>C (p.Glu10Gln)	not specified [RCV004230850]	uncertain significance	10	97292600	97292600	Human		name
401870246	CV2792319	single nucleotide variant	NM_032900.6(ARHGAP19):c.47C>G (p.Ser16Cys)	not specified [RCV004361498]	uncertain significance	10	97292581	97292581	Human		name
401923526	CV2820200	single nucleotide variant	NM_024605.4(ARHGAP10):c.978G>A (p.Lys326=)	not provided [RCV003435176]	likely benign	4	147881876	147881876	Human		name
401920920	CV2820697	single nucleotide variant	NM_033515.3(ARHGAP18):c.462G>A (p.Thr154=)	not provided [RCV003432044]	likely benign	6	129638484	129638484	Human		name
405684636	CV3282628	single nucleotide variant	NM_032900.6(ARHGAP19):c.29A>C (p.Glu10Ala)	not specified [RCV004422439]	uncertain significance	10	97292599	97292599	Human		name
405684482	CV3286470	single nucleotide variant	NM_033515.3(ARHGAP18):c.73G>C (p.Gly25Arg)	not specified [RCV004422431]	uncertain significance	6	129710064	129710064	Human		name
597742518	CV3580327	single nucleotide variant	NM_024605.4(ARHGAP10):c.55C>T (p.Arg19Trp)	not specified [RCV004844903]	uncertain significance	4	147732356	147732356	Human		name
597742732	CV3580369	single nucleotide variant	NM_024605.4(ARHGAP10):c.28G>C (p.Asp10His)	not specified [RCV004844936]	uncertain significance	4	147732329	147732329	Human		name
597743345	CV3580497	single nucleotide variant	NM_014783.6(ARHGAP11A):c.19G>T (p.Val7Leu)	not specified [RCV004845032]	uncertain significance	15	32616230	32616230	Human		name
597743436	CV3580559	single nucleotide variant	NM_018460.4(ARHGAP15):c.45T>G (p.Asn15Lys)	not specified [RCV004845046]	uncertain significance	2	143155535	143155535	Human		name
597744406	CV3590770	single nucleotide variant	NM_032900.6(ARHGAP19):c.90T>A (p.Asp30Glu)	not specified [RCV004845223]	uncertain significance	10	97266092	97266092	Human		name
598168490	CV4000018	single nucleotide variant	NM_032900.6(ARHGAP19):c.86A>G (p.Asn29Ser)	not specified [RCV005391900]	uncertain significance	10	97266096	97266096	Human		name
598205749	CV4000047	single nucleotide variant	NM_032900.6(ARHGAP19):c.31G>A (p.Val11Met)	not specified [RCV005399514]	uncertain significance	10	97292597	97292597	Human		name
598168278	CV4003236	single nucleotide variant	NM_033515.3(ARHGAP18):c.82C>T (p.His28Tyr)	not specified [RCV005391861]	uncertain significance	6	129710055	129710055	Human		name
15133825	CV710172	single nucleotide variant	NM_033515.3(ARHGAP18):c.94G>A (p.Gly32Arg)	not provided [RCV000965020]	benign	6	129710043	129710043	Human		name
15199651	CV720778	single nucleotide variant	NM_024605.4(ARHGAP10):c.729G>A (p.Arg243=)	not provided [RCV000890692]	benign	4	147875047	147875047	Human		name
156187813	CV2195806	single nucleotide variant	NM_018287.7(ARHGAP12):c.274A>C (p.Thr92Pro)	not specified [RCV004076152]	uncertain significance	10	31908582	31908582	Human		name
156236537	CV2210541	single nucleotide variant	NM_032900.6(ARHGAP19):c.191A>G (p.Asn64Ser)	not specified [RCV004083354]	uncertain significance	10	97265991	97265991	Human		name
156072397	CV2240443	single nucleotide variant	NM_032900.6(ARHGAP19):c.269G>T (p.Gly90Val)	not specified [RCV004117331]	uncertain significance	10	97265913	97265913	Human		name
156191572	CV2255268	single nucleotide variant	NM_032900.6(ARHGAP19):c.236T>C (p.Leu79Pro)	not specified [RCV004117655]	uncertain significance	10	97265946	97265946	Human		name
156123372	CV2276171	single nucleotide variant	NM_033515.3(ARHGAP18):c.124G>A (p.Gly42Ser)	not specified [RCV004141830]	uncertain significance	6	129642008	129642008	Human		name
156177214	CV2317227	single nucleotide variant	NM_024605.4(ARHGAP10):c.134A>G (p.Asn45Ser)	not specified [RCV004178726]	uncertain significance	4	147732435	147732435	Human		name
156327241	CV2332076	single nucleotide variant	NM_024605.4(ARHGAP10):c.197A>G (p.Asp66Gly)	not specified [RCV004189123]	uncertain significance	4	147822769	147822769	Human		name
156171626	CV2355005	single nucleotide variant	NM_033515.3(ARHGAP18):c.116G>A (p.Arg39His)	not specified [RCV004198406]	uncertain significance	6	129642016	129642016	Human		name
156110391	CV2387642	single nucleotide variant	NM_018460.4(ARHGAP15):c.163C>A (p.Pro55Thr)	not specified [RCV004234190]	uncertain significance	2	143155653	143155653	Human		name
329376390	CV2438188	single nucleotide variant	NM_018460.4(ARHGAP15):c.283G>A (p.Gly95Arg)	not specified [RCV004256960]	uncertain significance	2	143216432	143216432	Human		name
329357601	CV2453672	single nucleotide variant	NM_024605.4(ARHGAP10):c.169C>A (p.Gln57Lys)	not specified [RCV004269327]	uncertain significance	4	147822741	147822741	Human		name
401863770	CV2773294	single nucleotide variant	NM_014783.6(ARHGAP11A):c.59G>T (p.Gly20Val)	not specified [RCV004353961]	uncertain significance	15	32616270	32616270	Human		name
401923527	CV2820201	single nucleotide variant	NM_024605.4(ARHGAP10):c.1041C>T (p.Gly347=)	not provided [RCV003435177]	likely benign	4	147906644	147906644	Human		name
401920918	CV2820696	single nucleotide variant	NM_033515.3(ARHGAP18):c.1113T>C (p.Ile371=)	not provided [RCV003432043]	likely benign	6	129611542	129611542	Human		name
405684443	CV3286461	single nucleotide variant	NM_033515.3(ARHGAP18):c.125G>A (p.Gly42Asp)	not specified [RCV004422422]	uncertain significance	6	129642007	129642007	Human		name
405684626	CV3286476	single nucleotide variant	NM_032900.6(ARHGAP19):c.143A>C (p.Lys48Thr)	not specified [RCV004422437]	uncertain significance	10	97266039	97266039	Human		name
407513982	CV3461503	single nucleotide variant	NM_024605.4(ARHGAP10):c.242G>A (p.Arg81Gln)	not specified [RCV004649017]	uncertain significance	4	147822814	147822814	Human		name
407531528	CV3471772	single nucleotide variant	NM_018460.4(ARHGAP15):c.142G>A (p.Asp48Asn)	not specified [RCV004657657]	uncertain significance	2	143155632	143155632	Human		name
407531686	CV3471878	single nucleotide variant	NM_033515.3(ARHGAP18):c.203A>C (p.Asp68Ala)	not specified [RCV004657733]	uncertain significance	6	129641929	129641929	Human		name
597743176	CV3580447	single nucleotide variant	NM_024605.4(ARHGAP10):c.173G>A (p.Arg58Gln)	not specified [RCV004845006]	uncertain significance	4	147822745	147822745	Human		name
597743276	CV3580478	single nucleotide variant	NM_014783.6(ARHGAP11A):c.55T>C (p.Tyr19His)	not specified [RCV004845022]	uncertain significance	15	32616266	32616266	Human		name
597743390	CV3580509	single nucleotide variant	NM_018287.7(ARHGAP12):c.221G>A (p.Arg74His)	not specified [RCV004845039]	uncertain significance	10	31908635	31908635	Human		name
597743398	CV3580512	single nucleotide variant	NM_018287.7(ARHGAP12):c.232A>G (p.Met78Val)	not specified [RCV004845040]	uncertain significance	10	31908624	31908624	Human		name
597743459	CV3580576	single nucleotide variant	NM_018460.4(ARHGAP15):c.226G>A (p.Glu76Lys)	not specified [RCV004845050]	uncertain significance	2	143202194	143202194	Human		name
597744008	CV3590666	single nucleotide variant	NM_033515.3(ARHGAP18):c.232T>C (p.Tyr78His)	not specified [RCV004845149]	uncertain significance	6	129641900	129641900	Human		name
598273054	CV4002842	single nucleotide variant	NM_024605.4(ARHGAP10):c.116T>G (p.Leu39Arg)	not specified [RCV005389546]	uncertain significance	4	147732417	147732417	Human		name
598167348	CV4003016	single nucleotide variant	NM_018287.7(ARHGAP12):c.127G>A (p.Val43Met)	not specified [RCV005391677]	uncertain significance	10	31908729	31908729	Human		name
598205499	CV4003045	single nucleotide variant	NM_018287.7(ARHGAP12):c.275C>T (p.Thr92Met)	not specified [RCV005399473]	likely benign	10	31908581	31908581	Human		name
598168154	CV4003212	single nucleotide variant	NM_033515.3(ARHGAP18):c.238A>C (p.Ile80Leu)	not specified [RCV005391838]	uncertain significance	6	129641894	129641894	Human		name
15166868	CV709183	single nucleotide variant	NM_024605.4(ARHGAP10):c.1215C>T (p.Ala405=)	not provided [RCV000971278]	benign	4	147913126	147913126	Human		name
15184184	CV709184	single nucleotide variant	NM_024605.4(ARHGAP10):c.1842C>T (p.Tyr614=)	not provided [RCV000975052]	benign	4	148023388	148023388	Human		name
15180736	CV720779	single nucleotide variant	NM_024605.4(ARHGAP10):c.1461C>T (p.Ser487=)	not provided [RCV000885598]	benign	4	147965034	147965034	Human		name
15181352	CV725998	single nucleotide variant	NM_014783.6(ARHGAP11A):c.327A>G (p.Leu109=)	not provided [RCV000885747]	benign	15	32624202	32624202	Human		name
15106654	CV784870	single nucleotide variant	NM_014783.6(ARHGAP11A):c.790C>T (p.Leu264=)	not provided [RCV000976670]	likely benign	15	32625561	32625561	Human		name
8629870	CV85017	single nucleotide variant	NM_018460.3(ARHGAP15):c.170C>T (p.Ser57Phe)	Malignant melanoma [RCV000065099]	not provided	2	143202138	143202138	Human		name
8631041	CV86197	single nucleotide variant	NM_024605.3(ARHGAP10):c.1047C>T (p.Ser349=)	Malignant melanoma [RCV000066288]	not provided	4	147906650	147906650	Human		name
8649340	CV125905	single nucleotide variant	NM_024605.4(ARHGAP10):c.716T>A (p.Phe239Tyr)	not provided [RCV000106393]	not provided	4	147875034	147875034	Human		name
156312336	CV2196350	single nucleotide variant	NM_018287.7(ARHGAP12):c.527C>T (p.Ser176Leu)	not specified [RCV004072525]	likely benign	10	31908329	31908329	Human		name
156314735	CV2196687	single nucleotide variant	NM_018287.7(ARHGAP12):c.359C>T (p.Ser120Leu)	not specified [RCV004073947]	uncertain significance	10	31908497	31908497	Human		name
156119329	CV2219252	single nucleotide variant	NM_032900.6(ARHGAP19):c.661A>G (p.Lys221Glu)	not specified [RCV004095131]	uncertain significance	10	97259581	97259581	Human		name
156292208	CV2223486	single nucleotide variant	NM_032900.6(ARHGAP19):c.960G>C (p.Leu320Phe)	not specified [RCV004106054]	uncertain significance	10	97246305	97246305	Human		name
156002658	CV2257985	single nucleotide variant	NM_018287.7(ARHGAP12):c.398A>G (p.Asn133Ser)	not specified [RCV004129793]	uncertain significance	10	31908458	31908458	Human		name
156365485	CV2272118	single nucleotide variant	NM_033515.3(ARHGAP18):c.845A>G (p.Gln282Arg)	not specified [RCV004124901]	uncertain significance	6	129618794	129618794	Human		name
156115358	CV2273333	single nucleotide variant	NM_018287.7(ARHGAP12):c.355C>G (p.Pro119Ala)	not specified [RCV004132116]	uncertain significance	10	31908501	31908501	Human		name
156275698	CV2290701	single nucleotide variant	NM_018460.4(ARHGAP15):c.499T>C (p.Phe167Leu)	not specified [RCV004149224]	uncertain significance	2	143435625	143435625	Human		name
155931641	CV2293637	single nucleotide variant	NM_018287.7(ARHGAP12):c.371A>G (p.Gln124Arg)	not specified [RCV004153148]	uncertain significance	10	31908485	31908485	Human		name
156183972	CV2294841	single nucleotide variant	NM_024605.4(ARHGAP10):c.935A>T (p.Lys312Ile)	not specified [RCV004156003]	uncertain significance	4	147879334	147879334	Human		name
156177427	CV2301237	single nucleotide variant	NM_018460.4(ARHGAP15):c.534G>C (p.Leu178Phe)	not specified [RCV004160140]	uncertain significance	2	143435660	143435660	Human		name
155903494	CV2301650	single nucleotide variant	NM_024605.4(ARHGAP10):c.946G>A (p.Gly316Arg)	not specified [RCV004162552]	uncertain significance	4	147881844	147881844	Human		name
156105496	CV2307397	single nucleotide variant	NM_033515.3(ARHGAP18):c.761G>C (p.Ser254Thr)	not specified [RCV004166077]	uncertain significance	6	129629378	129629378	Human		name
156147494	CV2311161	single nucleotide variant	NM_032900.6(ARHGAP19):c.442A>G (p.Ser148Gly)	not specified [RCV004165971]	uncertain significance	10	97263591	97263591	Human		name
156062009	CV2316419	single nucleotide variant	NM_018460.4(ARHGAP15):c.310A>G (p.Thr104Ala)	not specified [RCV004169912]	uncertain significance	2	143228594	143228594	Human		name
156163324	CV2319622	single nucleotide variant	NM_018460.4(ARHGAP15):c.856G>A (p.Val286Met)	not specified [RCV004185171]	uncertain significance	2	143519295	143519295	Human		name
156162019	CV2323502	single nucleotide variant	NM_018460.4(ARHGAP15):c.497A>G (p.Glu166Gly)	not specified [RCV004165709]	uncertain significance	2	143435623	143435623	Human		name
156305544	CV2338833	single nucleotide variant	NM_033515.3(ARHGAP18):c.983C>T (p.Ala328Val)	not specified [RCV004182388]	likely benign	6	129616273	129616273	Human		name
156330335	CV2339458	single nucleotide variant	NM_024605.4(ARHGAP10):c.881G>A (p.Arg294Gln)	not specified [RCV004194128]	uncertain significance	4	147879280	147879280	Human		name
156041164	CV2342108	single nucleotide variant	NM_033515.3(ARHGAP18):c.908G>A (p.Gly303Asp)	not specified [RCV004191703]	uncertain significance	6	129618731	129618731	Human		name
155974746	CV2342587	single nucleotide variant	NM_032900.6(ARHGAP19):c.985G>T (p.Ala329Ser)	not specified [RCV004196680]	uncertain significance	10	97246280	97246280	Human		name
155920280	CV2343324	single nucleotide variant	NM_033515.3(ARHGAP18):c.970G>A (p.Val324Ile)	not specified [RCV004194940]	likely benign	6	129616286	129616286	Human		name
155985192	CV2345034	single nucleotide variant	NM_032900.6(ARHGAP19):c.719G>A (p.Arg240His)	not specified [RCV004193317]	uncertain significance	10	97259523	97259523	Human		name
156209553	CV2370129	single nucleotide variant	NM_033515.3(ARHGAP18):c.370G>A (p.Gly124Arg)	not specified [RCV004211015]	uncertain significance	6	129638576	129638576	Human		name
155935654	CV2371841	single nucleotide variant	NM_024605.4(ARHGAP10):c.322G>A (p.Val108Ile)	not specified [RCV004221535]	uncertain significance	4	147847160	147847160	Human		name
155989980	CV2371994	single nucleotide variant	NM_018287.7(ARHGAP12):c.788C>T (p.Pro263Leu)	not specified [RCV004221669]	uncertain significance	10	31861555	31861555	Human		name
156076238	CV2375019	single nucleotide variant	NM_018460.4(ARHGAP15):c.637A>G (p.Thr213Ala)	not specified [RCV004230072]	uncertain significance	2	143436976	143436976	Human		name
156347729	CV2382961	single nucleotide variant	NM_033515.3(ARHGAP18):c.424C>T (p.Arg142Trp)	not specified [RCV004217551]	uncertain significance	6	129638522	129638522	Human		name
156204887	CV2385124	single nucleotide variant	NM_033515.3(ARHGAP18):c.604C>G (p.Gln202Glu)	not specified [RCV004228384]	uncertain significance	6	129634054	129634054	Human		name
155998853	CV2396318	single nucleotide variant	NM_018460.4(ARHGAP15):c.752T>C (p.Val251Ala)	not specified [RCV004242050]	uncertain significance	2	143487421	143487421	Human		name
329368627	CV2428085	single nucleotide variant	NM_018287.7(ARHGAP12):c.524G>A (p.Arg175His)	not specified [RCV004254458]	uncertain significance	10	31908332	31908332	Human		name
329359137	CV2435308	single nucleotide variant	NM_018287.7(ARHGAP12):c.575G>T (p.Ser192Ile)	not specified [RCV004252971]	uncertain significance	10	31908281	31908281	Human		name
329401110	CV2446141	single nucleotide variant	NM_018460.4(ARHGAP15):c.600A>T (p.Arg200Ser)	not specified [RCV004264556]	uncertain significance	2	143436939	143436939	Human		name
329391775	CV2453117	single nucleotide variant	NM_032900.6(ARHGAP19):c.344C>T (p.Ser115Phe)	not specified [RCV004279508]	uncertain significance	10	97264885	97264885	Human		name
329352029	CV2455638	single nucleotide variant	NM_032900.6(ARHGAP19):c.317G>A (p.Arg106Gln)	not specified [RCV004276884]	uncertain significance	10	97265865	97265865	Human		name
329396399	CV2462632	single nucleotide variant	NM_033515.3(ARHGAP18):c.385G>C (p.Asp129His)	not specified [RCV004278574]	uncertain significance	6	129638561	129638561	Human		name
329396135	CV2463293	single nucleotide variant	NM_024605.4(ARHGAP10):c.348G>T (p.Leu116Phe)	not specified [RCV004275050]	uncertain significance	4	147847186	147847186	Human		name
329382373	CV2465198	single nucleotide variant	NM_024605.4(ARHGAP10):c.328G>A (p.Glu110Lys)	not specified [RCV004287234]	uncertain significance	4	147847166	147847166	Human		name
401729932	CV2683864	single nucleotide variant	NM_018460.4(ARHGAP15):c.749G>A (p.Arg250Gln)	not specified [RCV004284589]	uncertain significance	2	143487418	143487418	Human		name
401728220	CV2685953	single nucleotide variant	NM_024605.4(ARHGAP10):c.995T>C (p.Ile332Thr)	not specified [RCV004294924]	uncertain significance	4	147881893	147881893	Human		name
401746852	CV2690985	single nucleotide variant	NM_032900.6(ARHGAP19):c.667C>T (p.Arg223Trp)	not specified [RCV004301007]	uncertain significance	10	97259575	97259575	Human		name
401774994	CV2696187	single nucleotide variant	NM_024605.4(ARHGAP10):c.596C>T (p.Pro199Leu)	not specified [RCV004310237]	uncertain significance	4	147864955	147864955	Human		name
401738749	CV2708136	single nucleotide variant	NM_024605.4(ARHGAP10):c.664A>G (p.Asn222Asp)	not specified [RCV004311510]	uncertain significance	4	147866778	147866778	Human		name
401887238	CV2773257	single nucleotide variant	NM_033515.3(ARHGAP18):c.392A>G (p.Gln131Arg)	not specified [RCV004353929]	uncertain significance	6	129638554	129638554	Human		name
401883869	CV2785789	single nucleotide variant	NM_033515.3(ARHGAP18):c.995A>G (p.Gln332Arg)	not specified [RCV004365036]	uncertain significance	6	129616261	129616261	Human		name
401865024	CV2791453	single nucleotide variant	NM_032900.6(ARHGAP19):c.582T>G (p.His194Gln)	not specified [RCV004358842]	uncertain significance	10	97263451	97263451	Human		name
401907664	CV2809522	single nucleotide variant	NM_032900.6(ARHGAP19):c.961C>T (p.His321Tyr)	not provided [RCV003422783]	likely benign	10	97246304	97246304	Human		name
405684641	CV3282629	single nucleotide variant	NM_032900.6(ARHGAP19):c.386T>C (p.Ile129Thr)	not specified [RCV004422440]	uncertain significance	10	97264843	97264843	Human		name
405684644	CV3282630	single nucleotide variant	NM_032900.6(ARHGAP19):c.472C>T (p.Leu158Phe)	not specified [RCV004422441]	uncertain significance	10	97263561	97263561	Human		name
405684649	CV3282631	single nucleotide variant	NM_032900.6(ARHGAP19):c.546G>A (p.Met182Ile)	not specified [RCV004422442]	uncertain significance	10	97263487	97263487	Human		name
405684654	CV3282632	single nucleotide variant	NM_032900.6(ARHGAP19):c.922T>C (p.Phe308Leu)	not specified [RCV004422443]	uncertain significance	10	97256323	97256323	Human		name
405674802	CV3286398	single nucleotide variant	NM_024605.4(ARHGAP10):c.511C>T (p.Arg171Trp)	not specified [RCV004420378]	uncertain significance	4	147864870	147864870	Human		name
405674806	CV3286399	single nucleotide variant	NM_024605.4(ARHGAP10):c.713G>T (p.Arg238Leu)	not specified [RCV004420379]	uncertain significance	4	147875031	147875031	Human		name
405674810	CV3286400	single nucleotide variant	NM_024605.4(ARHGAP10):c.859G>A (p.Val287Ile)	not specified [RCV004420380]	uncertain significance	4	147879258	147879258	Human		name
405674812	CV3286401	single nucleotide variant	NM_014783.6(ARHGAP11A):c.115G>A (p.Ala39Thr)	not specified [RCV004420381]	uncertain significance	15	32616326	32616326	Human		name
405674854	CV3286411	single nucleotide variant	NM_014783.6(ARHGAP11A):c.249A>T (p.Glu83Asp)	not specified [RCV004420391]	uncertain significance	15	32623540	32623540	Human		name
405674944	CV3286434	single nucleotide variant	NM_018287.7(ARHGAP12):c.386T>C (p.Ile129Thr)	not specified [RCV004420414]	likely benign	10	31908470	31908470	Human		name
405674947	CV3286435	single nucleotide variant	NM_018287.7(ARHGAP12):c.488C>T (p.Ser163Leu)	not specified [RCV004420415]	uncertain significance	10	31908368	31908368	Human		name
405674953	CV3286437	single nucleotide variant	NM_018287.7(ARHGAP12):c.590A>G (p.Gln197Arg)	not specified [RCV004420417]	uncertain significance	10	31908266	31908266	Human		name
405674956	CV3286438	single nucleotide variant	NM_018287.7(ARHGAP12):c.932A>C (p.Asn311Thr)	not specified [RCV004420418]	uncertain significance	10	31861411	31861411	Human		name
405674959	CV3286439	single nucleotide variant	NM_018287.7(ARHGAP12):c.985T>C (p.Tyr329His)	not specified [RCV004420419]	uncertain significance	10	31854170	31854170	Human		name
405674968	CV3286441	single nucleotide variant	NM_018460.4(ARHGAP15):c.782G>A (p.Arg261Gln)	not specified [RCV004420421]	uncertain significance	2	143487451	143487451	Human		name
405674972	CV3286442	single nucleotide variant	NM_018460.4(ARHGAP15):c.866G>A (p.Arg289His)	not specified [RCV004420422]	uncertain significance	2	143519305	143519305	Human		name
405684357	CV3286443	single nucleotide variant	NM_018460.4(ARHGAP15):c.992T>C (p.Ile331Thr)	not specified [RCV004422404]	uncertain significance	2	143556474	143556474	Human		name
405684471	CV3286467	single nucleotide variant	NM_033515.3(ARHGAP18):c.556C>G (p.Pro186Ala)	not specified [RCV004422428]	uncertain significance	6	129634102	129634102	Human		name
405684475	CV3286468	single nucleotide variant	NM_033515.3(ARHGAP18):c.574C>G (p.Gln192Glu)	not specified [RCV004422429]	uncertain significance	6	129634084	129634084	Human		name
405684477	CV3286469	single nucleotide variant	NM_033515.3(ARHGAP18):c.725A>G (p.Asn242Ser)	not specified [RCV004422430]	uncertain significance	6	129629414	129629414	Human		name
405684488	CV3286471	single nucleotide variant	NM_033515.3(ARHGAP18):c.784C>A (p.Pro262Thr)	not specified [RCV004422432]	uncertain significance	6	129629355	129629355	Human		name
405684492	CV3286472	single nucleotide variant	NM_033515.3(ARHGAP18):c.901G>A (p.Val301Ile)	not specified [RCV004422433]	uncertain significance	6	129618738	129618738	Human		name
407531274	CV3461481	single nucleotide variant	NM_024605.4(ARHGAP10):c.635A>G (p.His212Arg)	not specified [RCV004657509]	uncertain significance	4	147866749	147866749	Human		name
407531297	CV3461523	single nucleotide variant	NM_024605.4(ARHGAP10):c.805G>A (p.Glu269Lys)	not specified [RCV004657527]	uncertain significance	4	147875123	147875123	Human		name
407482169	CV3461563	single nucleotide variant	NM_014783.6(ARHGAP11A):c.154A>C (p.Asn52His)	not specified [RCV004649054]	uncertain significance	15	32620132	32620132	Human		name
407531452	CV3471709	single nucleotide variant	NM_018287.7(ARHGAP12):c.343A>G (p.Ser115Gly)	not specified [RCV004657610]	uncertain significance	10	31908513	31908513	Human		name
407531464	CV3471730	single nucleotide variant	NM_018287.7(ARHGAP12):c.884C>G (p.Pro295Arg)	not specified [RCV004657625]	uncertain significance	10	31861459	31861459	Human		name
407531478	CV3471741	single nucleotide variant	NM_018287.7(ARHGAP12):c.413C>G (p.Pro138Arg)	not specified [RCV004657632]	uncertain significance	10	31908443	31908443	Human		name
407490939	CV3471793	single nucleotide variant	NM_018460.4(ARHGAP15):c.368A>C (p.Gln123Pro)	not specified [RCV004666739]	uncertain significance	2	143228652	143228652	Human		name
407490950	CV3471804	single nucleotide variant	NM_018460.4(ARHGAP15):c.428A>G (p.His143Arg)	not specified [RCV004666743]	uncertain significance	2	143250554	143250554	Human		name
407531593	CV3471815	single nucleotide variant	NM_018460.4(ARHGAP15):c.655T>G (p.Tyr219Asp)	not specified [RCV004657689]	uncertain significance	2	143436994	143436994	Human		name
407531699	CV3471887	single nucleotide variant	NM_033515.3(ARHGAP18):c.832G>A (p.Asp278Asn)	not specified [RCV004657739]	uncertain significance	6	129618807	129618807	Human		name
407491053	CV3471918	single nucleotide variant	NM_032900.6(ARHGAP19):c.956G>T (p.Arg319Ile)	not specified [RCV004666775]	uncertain significance	10	97246309	97246309	Human		name
597742403	CV3580259	single nucleotide variant	NM_024605.4(ARHGAP10):c.512G>A (p.Arg171Gln)	not specified [RCV004844850]	uncertain significance	4	147864871	147864871	Human		name
597742210	CV3580288	single nucleotide variant	NM_024605.4(ARHGAP10):c.787G>A (p.Ala263Thr)	not specified [RCV004844870]	uncertain significance	4	147875105	147875105	Human		name
597742418	CV3580306	single nucleotide variant	NM_024605.4(ARHGAP10):c.605C>T (p.Ser202Leu)	not specified [RCV004844885]	uncertain significance	4	147866719	147866719	Human		name
597742463	CV3580316	single nucleotide variant	NM_024605.4(ARHGAP10):c.538G>A (p.Glu180Lys)	not specified [RCV004844893]	uncertain significance	4	147864897	147864897	Human		name
597743416	CV3580535	single nucleotide variant	NM_018287.7(ARHGAP12):c.896C>T (p.Thr299Ile)	not specified [RCV004845043]	uncertain significance	10	31861447	31861447	Human		name
597743422	CV3580546	single nucleotide variant	NM_018460.4(ARHGAP15):c.308C>T (p.Ser103Phe)	not specified [RCV004845044]	uncertain significance	2	143228592	143228592	Human		name
597743453	CV3580568	single nucleotide variant	NM_018460.4(ARHGAP15):c.394C>A (p.His132Asn)	not specified [RCV004845049]	uncertain significance	2	143250520	143250520	Human		name
597743469	CV3580587	single nucleotide variant	NM_018460.4(ARHGAP15):c.574C>A (p.Pro192Thr)	not specified [RCV004845052]	uncertain significance	2	143436913	143436913	Human		name
597744002	CV3590661	single nucleotide variant	NM_033515.3(ARHGAP18):c.670C>A (p.Pro224Thr)	not specified [RCV004845148]	uncertain significance	6	129629469	129629469	Human		name
597744142	CV3590692	single nucleotide variant	NM_033515.3(ARHGAP18):c.369C>A (p.Phe123Leu)	not specified [RCV004845174]	uncertain significance	6	129638577	129638577	Human		name
597744240	CV3590716	single nucleotide variant	NM_033515.3(ARHGAP18):c.745G>A (p.Glu249Lys)	not specified [RCV004845192]	uncertain significance	6	129629394	129629394	Human		name
597744289	CV3590727	single nucleotide variant	NM_033515.3(ARHGAP18):c.362A>G (p.Asn121Ser)	not specified [RCV004845201]	uncertain significance	6	129638584	129638584	Human		name
597744315	CV3590741	single nucleotide variant	NM_032900.6(ARHGAP19):c.593A>G (p.Asn198Ser)	not specified [RCV004845206]	uncertain significance	10	97263440	97263440	Human		name
597744380	CV3590765	single nucleotide variant	NM_032900.6(ARHGAP19):c.565G>A (p.Glu189Lys)	not specified [RCV004845218]	uncertain significance	10	97263468	97263468	Human		name
598168336	CV3999986	single nucleotide variant	NM_033515.3(ARHGAP18):c.656C>T (p.Pro219Leu)	not specified [RCV005391874]	likely benign	6	129629483	129629483	Human		name
598168603	CV4000039	single nucleotide variant	NM_032900.6(ARHGAP19):c.455A>G (p.Gln152Arg)	not specified [RCV005391920]	uncertain significance	10	97263578	97263578	Human		name
598205769	CV4000058	single nucleotide variant	NM_032900.6(ARHGAP19):c.452A>G (p.Gln151Arg)	not specified [RCV005399517]	uncertain significance	10	97263581	97263581	Human		name
598205255	CV4002823	single nucleotide variant	NM_024605.4(ARHGAP10):c.533C>G (p.Ser178Cys)	not specified [RCV005399437]	uncertain significance	4	147864892	147864892	Human		name
598273021	CV4002833	single nucleotide variant	NM_024605.4(ARHGAP10):c.706C>T (p.Arg236Trp)	not specified [RCV005389537]	uncertain significance	4	147875024	147875024	Human		name
598167369	CV4003021	single nucleotide variant	NM_018287.7(ARHGAP12):c.547C>G (p.Pro183Ala)	not specified [RCV005391682]	uncertain significance	10	31908309	31908309	Human		name
598167565	CV4003077	single nucleotide variant	NM_018460.4(ARHGAP15):c.950G>A (p.Arg317Gln)	not specified [RCV005391728]	uncertain significance	2	143556432	143556432	Human		name
598205530	CV4003088	single nucleotide variant	NM_018460.4(ARHGAP15):c.435A>C (p.Glu145Asp)	not specified [RCV005399479]	uncertain significance	2	143250561	143250561	Human		name
598167670	CV4003105	single nucleotide variant	NM_018460.4(ARHGAP15):c.910G>A (p.Ala304Thr)	not specified [RCV005391751]	uncertain significance	2	143519349	143519349	Human		name
598168111	CV4003200	single nucleotide variant	NM_033515.3(ARHGAP18):c.758A>C (p.Lys253Thr)	not specified [RCV005391829]	uncertain significance	6	129629381	129629381	Human		name
15118311	CV714383	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1098G>A (p.Pro366=)	not provided [RCV000962355]	benign	15	32629755	32629755	Human		name
15118317	CV714384	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1200G>A (p.Arg400=)	not provided [RCV000962356]	benign	15	32633073	32633073	Human		name
15105690	CV714385	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2709G>A (p.Gln903=)	not provided [RCV000959934]	benign	15	32637482	32637482	Human		name
15118330	CV714386	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2934C>T (p.Asn978=)	not provided [RCV000962358]	benign	15	32637707	32637707	Human		name
15134041	CV754362	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1989T>C (p.Gly663=)	not provided [RCV000920619]	likely benign	15	32636762	32636762	Human		name
8625150	CV80269	single nucleotide variant	NM_018460.3(ARHGAP15):c.355G>A (p.Glu119Lys)	Malignant melanoma [RCV000060345]	not provided	2	143228639	143228639	Human		name
8627623	CV82767	single nucleotide variant	NM_014783.4(ARHGAP11A):c.2997C>T (p.Ala999=)	Malignant melanoma [RCV000062847]	not provided	15	32637770	32637770	Human		name
26902942	CV858324	single nucleotide variant	NM_024605.4(ARHGAP10):c.665A>G (p.Asn222Ser)	Epidermolysis bullosa simplex with nail dystrophy [RCV001089672]\|not provided [RCV004693592]	uncertain significance	4	147866779	147866779	Human	1	name
8633610	CV88825	single nucleotide variant	NM_018287.6(ARHGAP12):c.506C>T (p.Ser169Phe)	Malignant melanoma [RCV000068920]	not provided	10	31908350	31908350	Human		name
8649343	CV125908	single nucleotide variant	NM_024605.4(ARHGAP10):c.1468T>C (p.Ser490Pro)	not provided [RCV000106396]	not provided	4	147965041	147965041	Human		name
8649344	CV125909	single nucleotide variant	NM_024605.4(ARHGAP10):c.2228A>G (p.His743Arg)	not provided [RCV000106397]	not provided	4	148064463	148064463	Human		name
155918018	CV2195640	single nucleotide variant	NM_018460.4(ARHGAP15):c.1280C>T (p.Thr427Met)	not specified [RCV004076007]	uncertain significance	2	143768024	143768024	Human		name
156134646	CV2196039	single nucleotide variant	NM_018287.7(ARHGAP12):c.1642C>T (p.Arg548Cys)	not specified [RCV004072281]	uncertain significance	10	31817877	31817877	Human		name
156065948	CV2197092	single nucleotide variant	NM_032900.6(ARHGAP19):c.1093A>G (p.Thr365Ala)	not specified [RCV004071526]	uncertain significance	10	97244060	97244060	Human		name
156277520	CV2209915	single nucleotide variant	NM_018287.7(ARHGAP12):c.1205T>C (p.Ile402Thr)	not specified [RCV004076364]	uncertain significance	10	31843552	31843552	Human		name
156333891	CV2214677	single nucleotide variant	NM_033515.3(ARHGAP18):c.1376A>C (p.Glu459Ala)	not specified [RCV004090499]	uncertain significance	6	129600838	129600838	Human		name
156225287	CV2219560	single nucleotide variant	NM_024605.4(ARHGAP10):c.1876C>A (p.Pro626Thr)	not specified [RCV004095291]	uncertain significance	4	148046900	148046900	Human		name
156076388	CV2230208	single nucleotide variant	NM_024605.4(ARHGAP10):c.2183T>A (p.Ile728Asn)	not specified [RCV004099836]	uncertain significance	4	148064418	148064418	Human		name
156168201	CV2237297	single nucleotide variant	NM_014783.6(ARHGAP11A):c.752C>T (p.Ala251Val)	not specified [RCV004115017]	uncertain significance	15	32625523	32625523	Human		name
156052089	CV2238157	single nucleotide variant	NM_018460.4(ARHGAP15):c.1354A>G (p.Met452Val)	not specified [RCV004111165]	uncertain significance	2	143768098	143768098	Human		name
156296200	CV2239909	single nucleotide variant	NM_024605.4(ARHGAP10):c.2191C>T (p.Arg731Trp)	not specified [RCV004110462]	uncertain significance	4	148064426	148064426	Human		name
156297856	CV2246948	single nucleotide variant	NM_024605.4(ARHGAP10):c.1780A>T (p.Asn594Tyr)	not specified [RCV004112739]	uncertain significance	4	148023326	148023326	Human		name
155918898	CV2254758	single nucleotide variant	NM_018460.4(ARHGAP15):c.1364A>G (p.Gln455Arg)	not specified [RCV004115228]	uncertain significance	2	143768108	143768108	Human		name
156100752	CV2260281	single nucleotide variant	NM_024605.4(ARHGAP10):c.1811G>A (p.Gly604Asp)	not specified [RCV004129384]	uncertain significance	4	148023357	148023357	Human		name
156023526	CV2273775	single nucleotide variant	NM_018460.4(ARHGAP15):c.1048G>A (p.Val350Ile)	not specified [RCV004132416]	uncertain significance	2	143624177	143624177	Human		name
155906674	CV2279366	single nucleotide variant	NM_024605.4(ARHGAP10):c.1039G>A (p.Gly347Ser)	not specified [RCV004141920]	uncertain significance	4	147906642	147906642	Human		name
156036017	CV2283024	single nucleotide variant	NM_024605.4(ARHGAP10):c.1777C>A (p.Pro593Thr)	not specified [RCV004143645]	uncertain significance	4	148023323	148023323	Human		name
156066557	CV2284588	single nucleotide variant	NM_014783.6(ARHGAP11A):c.797G>A (p.Gly266Asp)	not specified [RCV004140755]	uncertain significance	15	32625568	32625568	Human		name
156203619	CV2300744	single nucleotide variant	NM_024605.4(ARHGAP10):c.1194T>G (p.Ile398Met)	not specified [RCV004155678]	uncertain significance	4	147913105	147913105	Human		name
155950747	CV2302059	single nucleotide variant	NM_033515.3(ARHGAP18):c.1334T>C (p.Leu445Pro)	not specified [RCV004158820]	uncertain significance	6	129605908	129605908	Human		name
155908587	CV2302466	single nucleotide variant	NM_014783.6(ARHGAP11A):c.641C>T (p.Ser214Phe)	not specified [RCV004161196]	uncertain significance	15	32625169	32625169	Human		name
156160477	CV2311671	single nucleotide variant	NM_024605.4(ARHGAP10):c.2122G>C (p.Gly708Arg)	not specified [RCV004170553]	uncertain significance	4	148063242	148063242	Human		name
156270309	CV2312151	single nucleotide variant	NM_018287.7(ARHGAP12):c.1372G>T (p.Ala458Ser)	not specified [RCV004165058]	uncertain significance	10	31839319	31839319	Human		name
156170091	CV2312482	single nucleotide variant	NM_024605.4(ARHGAP10):c.2012A>G (p.Asp671Gly)	not specified [RCV004167448]	uncertain significance	4	148047036	148047036	Human		name
156166633	CV2319953	single nucleotide variant	NM_018287.7(ARHGAP12):c.2408G>A (p.Ser803Asn)	not specified [RCV004167828]	uncertain significance	10	31807791	31807791	Human		name
156354861	CV2324367	single nucleotide variant	NM_032900.6(ARHGAP19):c.1220G>T (p.Arg407Leu)	not specified [RCV004178867]	uncertain significance	10	97235281	97235281	Human		name
155919526	CV2333211	single nucleotide variant	NM_018460.4(ARHGAP15):c.1199C>T (p.Pro400Leu)	not specified [RCV004194498]	uncertain significance	2	143703479	143703479	Human		name
155922832	CV2340692	single nucleotide variant	NM_024605.4(ARHGAP10):c.2206G>A (p.Val736Met)	not specified [RCV004190364]	uncertain significance	4	148064441	148064441	Human		name
156343845	CV2349278	single nucleotide variant	NM_018287.7(ARHGAP12):c.1540A>C (p.Asn514His)	not specified [RCV004199225]	uncertain significance	10	31820479	31820479	Human		name
156225605	CV2352668	single nucleotide variant	NM_024605.4(ARHGAP10):c.2213C>T (p.Pro738Leu)	not specified [RCV004198698]	uncertain significance	4	148064448	148064448	Human		name
156121748	CV2354278	single nucleotide variant	NM_032900.6(ARHGAP19):c.1178T>C (p.Ile393Thr)	not specified [RCV004206700]	uncertain significance	10	97243975	97243975	Human		name
156248278	CV2357124	single nucleotide variant	NM_014783.6(ARHGAP11A):c.748C>A (p.Pro250Thr)	not specified [RCV004206918]	uncertain significance	15	32625519	32625519	Human		name
156003964	CV2357511	single nucleotide variant	NM_018287.7(ARHGAP12):c.2536C>T (p.Arg846Cys)	not specified [RCV004202790]	uncertain significance	10	31807663	31807663	Human		name
156212613	CV2366971	single nucleotide variant	NM_018287.7(ARHGAP12):c.1472C>T (p.Ala491Val)	not specified [RCV004213376]	uncertain significance	10	31826362	31826362	Human		name
156256694	CV2368759	single nucleotide variant	NM_018460.4(ARHGAP15):c.1319G>A (p.Arg440Gln)	not specified [RCV004214639]	uncertain significance	2	143768063	143768063	Human		name
156098480	CV2370780	single nucleotide variant	NM_018287.7(ARHGAP12):c.2243A>T (p.Asn748Ile)	not specified [RCV004209177]	uncertain significance	10	31809014	31809014	Human		name
156266126	CV2372401	single nucleotide variant	NM_024605.4(ARHGAP10):c.2045C>G (p.Ser682Trp)	not specified [RCV004217165]	uncertain significance	4	148063165	148063165	Human		name
156388856	CV2376164	single nucleotide variant	NM_033515.3(ARHGAP18):c.1447G>A (p.Ala483Thr)	not specified [RCV004220393]	uncertain significance	6	129600767	129600767	Human		name
156061856	CV2380293	single nucleotide variant	NM_018460.4(ARHGAP15):c.1159A>G (p.Arg387Gly)	not specified [RCV004224643]	uncertain significance	2	143703439	143703439	Human		name
156083889	CV2395085	single nucleotide variant	NM_033515.3(ARHGAP18):c.1739G>A (p.Arg580Gln)	not specified [RCV004236768]	uncertain significance	6	129584087	129584087	Human		name
156056652	CV2396262	single nucleotide variant	NM_024605.4(ARHGAP10):c.1948G>C (p.Ala650Pro)	not specified [RCV004240213]	uncertain significance	4	148046972	148046972	Human		name
155931233	CV2399806	single nucleotide variant	NM_018287.7(ARHGAP12):c.2282G>A (p.Arg761Gln)	not specified [RCV004603432]	uncertain significance	10	31808733	31808733	Human		name
329382029	CV2424304	single nucleotide variant	NM_024605.4(ARHGAP10):c.1724G>A (p.Arg575Gln)	not specified [RCV004252213]	uncertain significance	4	148023270	148023270	Human		name
329399819	CV2444208	single nucleotide variant	NM_014783.6(ARHGAP11A):c.990G>T (p.Leu330Phe)	not specified [RCV004260937]	uncertain significance	15	32629647	32629647	Human		name
329391363	CV2447997	single nucleotide variant	NM_024605.4(ARHGAP10):c.1136C>T (p.Thr379Ile)	not specified [RCV004260793]	uncertain significance	4	147909751	147909751	Human		name
329362969	CV2449606	single nucleotide variant	NM_032900.6(ARHGAP19):c.1252G>A (p.Ala418Thr)	not specified [RCV004268526]	uncertain significance	10	97235249	97235249	Human		name
329377640	CV2449892	single nucleotide variant	NM_018287.7(ARHGAP12):c.1178C>T (p.Ala393Val)	not specified [RCV004268975]	uncertain significance	10	31843579	31843579	Human		name
329397366	CV2460194	single nucleotide variant	NM_024605.4(ARHGAP10):c.2321A>C (p.Lys774Thr)	not specified [RCV004273291]	uncertain significance	4	148072041	148072041	Human		name
329353635	CV2466965	single nucleotide variant	NM_033515.3(ARHGAP18):c.1198G>A (p.Ala400Thr)	not specified [RCV004282717]	uncertain significance	6	129607977	129607977	Human		name
401731204	CV2674295	single nucleotide variant	NM_014783.6(ARHGAP11A):c.964C>T (p.Leu322Phe)	not specified [RCV004289173]	uncertain significance	15	32629621	32629621	Human		name
401722398	CV2676969	single nucleotide variant	NM_024605.4(ARHGAP10):c.1069G>A (p.Glu357Lys)	not specified [RCV004293571]	uncertain significance	4	147906672	147906672	Human		name
401739795	CV2684175	single nucleotide variant	NM_024605.4(ARHGAP10):c.1192A>G (p.Ile398Val)	not specified [RCV004288847]	uncertain significance	4	147913103	147913103	Human		name
401730702	CV2686668	single nucleotide variant	NM_018287.7(ARHGAP12):c.1708C>T (p.Leu570Phe)	not specified [RCV004300080]	uncertain significance	10	31817811	31817811	Human		name
401734383	CV2688491	single nucleotide variant	NM_024605.4(ARHGAP10):c.1411A>G (p.Met471Val)	not specified [RCV004301465]	uncertain significance	4	147955335	147955335	Human		name
401733591	CV2691347	single nucleotide variant	NM_018460.4(ARHGAP15):c.1225C>T (p.Leu409Phe)	not specified [RCV004303096]	uncertain significance	2	143703505	143703505	Human		name
401759702	CV2701680	single nucleotide variant	NM_024605.4(ARHGAP10):c.1329C>A (p.Asp443Glu)	not specified [RCV004314092]	uncertain significance	4	147946642	147946642	Human		name
401772866	CV2708993	single nucleotide variant	NM_032900.6(ARHGAP19):c.1421C>T (p.Thr474Met)	not specified [RCV004314351]	uncertain significance	10	97229200	97229200	Human		name
401783718	CV2723877	single nucleotide variant	NM_014783.6(ARHGAP11A):c.311A>G (p.His104Arg)	not specified [RCV004326013]	likely benign	15	32624186	32624186	Human		name
401773687	CV2727601	single nucleotide variant	NM_018287.7(ARHGAP12):c.1084G>A (p.Glu362Lys)	not specified [RCV004329786]	uncertain significance	10	31854071	31854071	Human		name
401718326	CV2728533	single nucleotide variant	NM_018287.7(ARHGAP12):c.1373C>T (p.Ala458Val)	not specified [RCV004333436]	uncertain significance	10	31839318	31839318	Human		name
401881429	CV2759412	single nucleotide variant	NM_018460.4(ARHGAP15):c.1372A>G (p.Ile458Val)	not specified [RCV004338412]	uncertain significance	2	143768116	143768116	Human		name
401864233	CV2767560	single nucleotide variant	NM_018287.7(ARHGAP12):c.1676A>G (p.Asn559Ser)	not specified [RCV004343713]	uncertain significance	10	31817843	31817843	Human		name
401881863	CV2774638	single nucleotide variant	NM_033515.3(ARHGAP18):c.1906C>T (p.Arg636Cys)	not specified [RCV004350105]	uncertain significance	6	129578599	129578599	Human		name
401891121	CV2778655	single nucleotide variant	NM_018287.7(ARHGAP12):c.1783A>G (p.Ile595Val)	not specified [RCV004344298]	uncertain significance	10	31814310	31814310	Human		name
401898346	CV2787696	single nucleotide variant	NM_033515.3(ARHGAP18):c.1665G>C (p.Met555Ile)	not specified [RCV004356618]	uncertain significance	6	129599264	129599264	Human		name
401875955	CV2789245	single nucleotide variant	NM_032900.6(ARHGAP19):c.1138G>A (p.Val380Ile)	not specified [RCV004365277]	uncertain significance	10	97244015	97244015	Human		name
405674761	CV3286388	single nucleotide variant	NM_024605.4(ARHGAP10):c.1042G>A (p.Val348Ile)	not specified [RCV004420368]	uncertain significance	4	147906645	147906645	Human		name
405674765	CV3286389	single nucleotide variant	NM_024605.4(ARHGAP10):c.1085A>G (p.Gln362Arg)	not specified [RCV004420369]	uncertain significance	4	147906688	147906688	Human		name
405674768	CV3286390	single nucleotide variant	NM_024605.4(ARHGAP10):c.1096G>A (p.Ala366Thr)	not specified [RCV004420370]	uncertain significance	4	147906699	147906699	Human		name
405674772	CV3286391	single nucleotide variant	NM_024605.4(ARHGAP10):c.1141A>G (p.Ile381Val)	not specified [RCV004420371]	uncertain significance	4	147909756	147909756	Human		name
405674775	CV3286392	single nucleotide variant	NM_024605.4(ARHGAP10):c.1472G>C (p.Arg491Pro)	not specified [RCV004420372]	uncertain significance	4	147965045	147965045	Human		name
405674781	CV3286393	single nucleotide variant	NM_024605.4(ARHGAP10):c.1723C>T (p.Arg575Trp)	not specified [RCV004420373]	uncertain significance	4	148023269	148023269	Human		name
405674788	CV3286395	single nucleotide variant	NM_024605.4(ARHGAP10):c.2143T>A (p.Ser715Thr)	not specified [RCV004420375]	uncertain significance	4	148063263	148063263	Human		name
405674793	CV3286396	single nucleotide variant	NM_024605.4(ARHGAP10):c.2144C>T (p.Ser715Phe)	not specified [RCV004420376]	uncertain significance	4	148063264	148063264	Human		name
405674797	CV3286397	single nucleotide variant	NM_024605.4(ARHGAP10):c.2347G>A (p.Val783Ile)	not specified [RCV004420377]	uncertain significance	4	148072067	148072067	Human		name
405674861	CV3286413	single nucleotide variant	NM_014783.6(ARHGAP11A):c.308A>G (p.Asp103Gly)	not specified [RCV004420393]	uncertain significance	15	32624183	32624183	Human		name
405674865	CV3286414	single nucleotide variant	NM_014783.6(ARHGAP11A):c.338C>T (p.Pro113Leu)	not specified [RCV004420394]	likely benign	15	32624213	32624213	Human		name
405674869	CV3286415	single nucleotide variant	NM_014783.6(ARHGAP11A):c.359T>A (p.Leu120His)	not specified [RCV004420395]	uncertain significance	15	32624234	32624234	Human		name
405674873	CV3286416	single nucleotide variant	NM_014783.6(ARHGAP11A):c.770G>T (p.Gly257Val)	not specified [RCV004420396]	uncertain significance	15	32625541	32625541	Human		name
405674878	CV3286417	single nucleotide variant	NM_014783.6(ARHGAP11A):c.977C>A (p.Ala326Asp)	not specified [RCV004420397]	uncertain significance	15	32629634	32629634	Human		name
405674907	CV3286425	single nucleotide variant	NM_018287.7(ARHGAP12):c.1066A>G (p.Thr356Ala)	not specified [RCV004420405]	uncertain significance	10	31854089	31854089	Human		name
405674912	CV3286426	single nucleotide variant	NM_018287.7(ARHGAP12):c.1127A>G (p.Tyr376Cys)	not specified [RCV004420406]	uncertain significance	10	31852560	31852560	Human		name
405674916	CV3286427	single nucleotide variant	NM_018287.7(ARHGAP12):c.1159G>A (p.Glu387Lys)	not specified [RCV004420407]	uncertain significance	10	31852528	31852528	Human		name
405674920	CV3286428	single nucleotide variant	NM_018287.7(ARHGAP12):c.1643G>A (p.Arg548His)	not specified [RCV004420408]	uncertain significance	10	31817876	31817876	Human		name
405674924	CV3286429	single nucleotide variant	NM_018287.7(ARHGAP12):c.1678G>A (p.Asp560Asn)	not specified [RCV004420409]	uncertain significance	10	31817841	31817841	Human		name
405674928	CV3286430	single nucleotide variant	NM_018287.7(ARHGAP12):c.1889T>C (p.Leu630Ser)	not specified [RCV004420410]	uncertain significance	10	31812769	31812769	Human		name
405674934	CV3286431	single nucleotide variant	NM_018287.7(ARHGAP12):c.2297A>T (p.Lys766Met)	not specified [RCV004420411]	uncertain significance	10	31808718	31808718	Human		name
405674937	CV3286432	single nucleotide variant	NM_018287.7(ARHGAP12):c.2442A>T (p.Lys814Asn)	not specified [RCV004420412]	uncertain significance	10	31807757	31807757	Human		name
405674964	CV3286440	single nucleotide variant	NM_018460.4(ARHGAP15):c.1208G>A (p.Arg403His)	not specified [RCV004420420]	uncertain significance	2	143703488	143703488	Human		name
405684432	CV3286459	single nucleotide variant	NM_033515.3(ARHGAP18):c.1031T>C (p.Leu344Ser)	not specified [RCV004422420]	uncertain significance	6	129616225	129616225	Human		name
405684446	CV3286462	single nucleotide variant	NM_033515.3(ARHGAP18):c.1303C>A (p.Gln435Lys)	not specified [RCV004422423]	uncertain significance	6	129605939	129605939	Human		name
405684450	CV3286463	single nucleotide variant	NM_033515.3(ARHGAP18):c.1708A>G (p.Asn570Asp)	not specified [RCV004422424]	uncertain significance	6	129599221	129599221	Human		name
405684455	CV3286464	single nucleotide variant	NM_033515.3(ARHGAP18):c.1907G>A (p.Arg636His)	not specified [RCV004422425]	uncertain significance	6	129578598	129578598	Human		name
405684466	CV3286466	single nucleotide variant	NM_033515.3(ARHGAP18):c.1941A>T (p.Leu647Phe)	not specified [RCV004422427]	uncertain significance	6	129578564	129578564	Human		name
405684621	CV3286475	single nucleotide variant	NM_032900.6(ARHGAP19):c.1106C>T (p.Thr369Met)	not specified [RCV004422436]	uncertain significance	10	97244047	97244047	Human		name
407513968	CV3461489	single nucleotide variant	NM_024605.4(ARHGAP10):c.1594G>C (p.Ala532Pro)	not specified [RCV004649008]	uncertain significance	4	147966717	147966717	Human		name
407513973	CV3461493	single nucleotide variant	NM_024605.4(ARHGAP10):c.2004C>G (p.Ser668Arg)	not specified [RCV004649011]	uncertain significance	4	148047028	148047028	Human		name
407531283	CV3461498	single nucleotide variant	NM_024605.4(ARHGAP10):c.1294A>T (p.Met432Leu)	not specified [RCV004657516]	uncertain significance	4	147939890	147939890	Human		name
407513992	CV3461513	single nucleotide variant	NM_024605.4(ARHGAP10):c.1111G>A (p.Glu371Lys)	not specified [RCV004649023]	uncertain significance	4	147906714	147906714	Human		name
407514017	CV3461532	single nucleotide variant	NM_024605.4(ARHGAP10):c.1094A>G (p.Glu365Gly)	not specified [RCV004649033]	uncertain significance	4	147906697	147906697	Human		name
407482164	CV3461552	single nucleotide variant	NM_014783.6(ARHGAP11A):c.340C>G (p.Pro114Ala)	not specified [RCV004649047]	uncertain significance	15	32624215	32624215	Human		name
407482187	CV3471626	single nucleotide variant	NM_014783.6(ARHGAP11A):c.907C>A (p.Pro303Thr)	not specified [RCV004649061]	uncertain significance	15	32628772	32628772	Human		name
407531396	CV3471675	single nucleotide variant	NM_018287.7(ARHGAP12):c.1720A>G (p.Ile574Val)	not specified [RCV004657582]	uncertain significance	10	31817799	31817799	Human		name
407531419	CV3471691	single nucleotide variant	NM_018287.7(ARHGAP12):c.1970A>G (p.Asn657Ser)	not specified [RCV004657593]	uncertain significance	10	31810729	31810729	Human		name
407531456	CV3471719	single nucleotide variant	NM_018287.7(ARHGAP12):c.2372T>C (p.Ile791Thr)	not specified [RCV004657617]	uncertain significance	10	31807827	31807827	Human		name
407531492	CV3471751	single nucleotide variant	NM_018287.7(ARHGAP12):c.2027G>C (p.Cys676Ser)	not specified [RCV004657639]	uncertain significance	10	31810672	31810672	Human		name
407531511	CV3471762	single nucleotide variant	NM_018287.7(ARHGAP12):c.2402A>T (p.Tyr801Phe)	not specified [RCV004657648]	uncertain significance	10	31807797	31807797	Human		name
407531544	CV3471782	single nucleotide variant	NM_018460.4(ARHGAP15):c.1108A>T (p.Ser370Cys)	not specified [RCV004657665]	uncertain significance	2	143624237	143624237	Human		name
407531619	CV3471827	single nucleotide variant	NM_018460.4(ARHGAP15):c.1373T>C (p.Ile458Thr)	not specified [RCV004657700]	uncertain significance	2	143768117	143768117	Human		name
407531670	CV3471868	single nucleotide variant	NM_033515.3(ARHGAP18):c.1676G>A (p.Arg559Gln)	not specified [RCV004657725]	uncertain significance	6	129599253	129599253	Human		name
407531718	CV3471898	single nucleotide variant	NM_032900.6(ARHGAP19):c.1063C>T (p.Arg355Trp)	not specified [RCV004657749]	uncertain significance	10	97244090	97244090	Human		name
407531730	CV3471908	single nucleotide variant	NM_032900.6(ARHGAP19):c.1195C>G (p.Gln399Glu)	not specified [RCV004657755]	uncertain significance	10	97235306	97235306	Human		name
407531754	CV3471929	single nucleotide variant	NM_032900.6(ARHGAP19):c.1246A>G (p.Lys416Glu)	not specified [RCV004657768]	uncertain significance	10	97235255	97235255	Human		name
597742073	CV3580253	single nucleotide variant	NM_024605.4(ARHGAP10):c.1789C>T (p.Pro597Ser)	not specified [RCV004844845]	uncertain significance	4	148023335	148023335	Human		name
597742248	CV3580296	single nucleotide variant	NM_024605.4(ARHGAP10):c.1847T>C (p.Leu616Pro)	not specified [RCV004844877]	uncertain significance	4	148023393	148023393	Human		name
597768652	CV3580359	single nucleotide variant	NM_024605.4(ARHGAP10):c.1099C>A (p.Leu367Met)	not specified [RCV004850730]	uncertain significance	4	147906702	147906702	Human		name
597742793	CV3580380	single nucleotide variant	NM_024605.4(ARHGAP10):c.2111C>T (p.Pro704Leu)	not specified [RCV004844946]	uncertain significance	4	148063231	148063231	Human		name
597742857	CV3580390	single nucleotide variant	NM_024605.4(ARHGAP10):c.1045T>C (p.Ser349Pro)	not specified [RCV004844956]	uncertain significance	4	147906648	147906648	Human		name
597742903	CV3580398	single nucleotide variant	NM_024605.4(ARHGAP10):c.1781A>G (p.Asn594Ser)	not specified [RCV004844963]	uncertain significance	4	148023327	148023327	Human		name
597742967	CV3580408	single nucleotide variant	NM_024605.4(ARHGAP10):c.2182A>G (p.Ile728Val)	not specified [RCV004844973]	likely benign	4	148064417	148064417	Human		name
597768673	CV3580419	single nucleotide variant	NM_024605.4(ARHGAP10):c.1518T>A (p.Asn506Lys)	not specified [RCV004850735]	uncertain significance	4	147965091	147965091	Human		name
597743074	CV3580428	single nucleotide variant	NM_024605.4(ARHGAP10):c.2126C>T (p.Ser709Leu)	not specified [RCV004844990]	likely benign	4	148063246	148063246	Human		name
597743138	CV3580440	single nucleotide variant	NM_024605.4(ARHGAP10):c.1271C>T (p.Ser424Leu)	not specified [RCV004845000]	uncertain significance	4	147939867	147939867	Human		name
597743262	CV3580475	single nucleotide variant	NM_014783.6(ARHGAP11A):c.334G>T (p.Ala112Ser)	not specified [RCV004845020]	uncertain significance	15	32624209	32624209	Human		name
597768700	CV3580507	single nucleotide variant	NM_018287.7(ARHGAP12):c.1291G>A (p.Asp431Asn)	not specified [RCV004850741]	uncertain significance	10	31843466	31843466	Human		name
597743384	CV3580508	single nucleotide variant	NM_018287.7(ARHGAP12):c.1228C>T (p.Arg410Trp)	not specified [RCV004845038]	uncertain significance	10	31843529	31843529	Human		name
597743403	CV3580515	single nucleotide variant	NM_018287.7(ARHGAP12):c.1332A>C (p.Glu444Asp)	not specified [RCV004845041]	uncertain significance	10	31839676	31839676	Human		name
597743409	CV3580523	single nucleotide variant	NM_018287.7(ARHGAP12):c.1348T>G (p.Ser450Ala)	not specified [RCV004845042]	uncertain significance	10	31839660	31839660	Human		name
597768705	CV3580528	single nucleotide variant	NM_018287.7(ARHGAP12):c.2455A>G (p.Thr819Ala)	not specified [RCV004850742]	uncertain significance	10	31807744	31807744	Human		name
597743430	CV3580551	single nucleotide variant	NM_018460.4(ARHGAP15):c.1258G>C (p.Ala420Pro)	not specified [RCV004845045]	uncertain significance	2	143768002	143768002	Human		name
597743441	CV3580564	single nucleotide variant	NM_018460.4(ARHGAP15):c.1295T>C (p.Ile432Thr)	not specified [RCV004845047]	uncertain significance	2	143768039	143768039	Human		name
597743464	CV3580582	single nucleotide variant	NM_018460.4(ARHGAP15):c.1136T>A (p.Ile379Asn)	not specified [RCV004845051]	uncertain significance	2	143624265	143624265	Human		name
597744050	CV3590675	single nucleotide variant	NM_033515.3(ARHGAP18):c.1055G>A (p.Arg352Gln)	not specified [RCV004845157]	uncertain significance	6	129611600	129611600	Human		name
597744099	CV3590684	single nucleotide variant	NM_033515.3(ARHGAP18):c.1958A>G (p.Asn653Ser)	not specified [RCV004845166]	uncertain significance	6	129578547	129578547	Human		name
597744148	CV3590697	single nucleotide variant	NM_033515.3(ARHGAP18):c.1037T>G (p.Phe346Cys)	not specified [RCV004845175]	uncertain significance	6	129616219	129616219	Human		name
597744191	CV3590706	single nucleotide variant	NM_033515.3(ARHGAP18):c.1613C>T (p.Thr538Met)	not specified [RCV004845183]	uncertain significance	6	129599316	129599316	Human		name
597744309	CV3590734	single nucleotide variant	NM_033515.3(ARHGAP18):c.1355A>G (p.Asp452Gly)	not specified [RCV004845205]	uncertain significance	6	129605887	129605887	Human		name
597744327	CV3590743	single nucleotide variant	NM_032900.6(ARHGAP19):c.1376G>A (p.Ser459Asn)	not specified [RCV004845208]	uncertain significance	10	97229783	97229783	Human		name
597744348	CV3590750	single nucleotide variant	NM_032900.6(ARHGAP19):c.1216G>A (p.Gly406Arg)	not specified [RCV004845212]	uncertain significance	10	97235285	97235285	Human		name
597744375	CV3590758	single nucleotide variant	NM_032900.6(ARHGAP19):c.1355T>C (p.Ile452Thr)	not specified [RCV004845217]	uncertain significance	10	97229804	97229804	Human		name
597744453	CV3590779	single nucleotide variant	NM_032900.6(ARHGAP19):c.1033T>C (p.Phe345Leu)	not specified [RCV004845232]	uncertain significance	10	97244120	97244120	Human		name
598205697	CV3999977	single nucleotide variant	NM_033515.3(ARHGAP18):c.1423G>C (p.Val475Leu)	not specified [RCV005399505]	uncertain significance	6	129600791	129600791	Human		name
598168444	CV4000007	single nucleotide variant	NM_032900.6(ARHGAP19):c.1072T>A (p.Ser358Thr)	not specified [RCV005391893]	uncertain significance	10	97244081	97244081	Human		name
598168551	CV4000029	single nucleotide variant	NM_032900.6(ARHGAP19):c.1025C>T (p.Thr342Ile)	not specified [RCV005391910]	uncertain significance	10	97244128	97244128	Human		name
598168744	CV4000067	single nucleotide variant	NM_032900.6(ARHGAP19):c.1181G>A (p.Arg394Lys)	not specified [RCV005391943]	uncertain significance	10	97243972	97243972	Human		name
598272920	CV4002806	single nucleotide variant	NM_024605.4(ARHGAP10):c.1055T>C (p.Met352Thr)	not specified [RCV005389513]	uncertain significance	4	147906658	147906658	Human		name
598273208	CV4002904	single nucleotide variant	NM_014783.6(ARHGAP11A):c.335C>T (p.Ala112Val)	not specified [RCV005389600]	uncertain significance	15	32624210	32624210	Human		name
598273286	CV4002938	single nucleotide variant	NM_014783.6(ARHGAP11A):c.983G>A (p.Arg328His)	not specified [RCV005389629]	uncertain significance	15	32629640	32629640	Human		name
598167323	CV4003010	single nucleotide variant	NM_018287.7(ARHGAP12):c.2123A>G (p.Asn708Ser)	not specified [RCV005391672]	uncertain significance	10	31809235	31809235	Human		name
598167418	CV4003034	single nucleotide variant	NM_018287.7(ARHGAP12):c.2149G>A (p.Asp717Asn)	not specified [RCV005391693]	uncertain significance	10	31809108	31809108	Human		name
598167459	CV4003049	single nucleotide variant	NM_018287.7(ARHGAP12):c.1646A>C (p.Gln549Pro)	not specified [RCV005391703]	uncertain significance	10	31817873	31817873	Human		name
598167497	CV4003059	single nucleotide variant	NM_018287.7(ARHGAP12):c.2092G>A (p.Ala698Thr)	not specified [RCV005391712]	uncertain significance	10	31809266	31809266	Human		name
598167537	CV4003069	single nucleotide variant	NM_018287.7(ARHGAP12):c.1688T>C (p.Ile563Thr)	not specified [RCV005391721]	uncertain significance	10	31817831	31817831	Human		name
598167715	CV4003114	single nucleotide variant	NM_018460.4(ARHGAP15):c.1417G>A (p.Glu473Lys)	not specified [RCV005391759]	uncertain significance	2	143768161	143768161	Human		name
598168083	CV4003194	single nucleotide variant	NM_033515.3(ARHGAP18):c.1055G>C (p.Arg352Pro)	not specified [RCV005391824]	uncertain significance	6	129611600	129611600	Human		name
598168204	CV4003222	single nucleotide variant	NM_033515.3(ARHGAP18):c.1547T>A (p.Ile516Asn)	not specified [RCV005391847]	uncertain significance	6	129600667	129600667	Human		name
598168249	CV4003230	single nucleotide variant	NM_033515.3(ARHGAP18):c.1256A>G (p.Tyr419Cys)	not specified [RCV005391855]	uncertain significance	6	129607919	129607919	Human		name
598272880	CV4006739	single nucleotide variant	NM_024605.4(ARHGAP10):c.1727C>T (p.Thr576Met)	not specified [RCV005389504]	uncertain significance	4	148023273	148023273	Human		name
15147483	CV714381	single nucleotide variant	NM_014783.6(ARHGAP11A):c.985A>G (p.Thr329Ala)	not provided [RCV000967348]	benign	15	32629642	32629642	Human		name
15142153	CV714382	single nucleotide variant	NM_014783.6(ARHGAP11A):c.997G>C (p.Asp333His)	not provided [RCV000966433]	benign	15	32629654	32629654	Human		name
15109011	CV720780	single nucleotide variant	NM_024605.4(ARHGAP10):c.2026A>G (p.Ile676Val)	not provided [RCV000893783]	likely benign	4	148047050	148047050	Human		name
8631040	CV86196	single nucleotide variant	NM_024605.3(ARHGAP10):c.1046C>T (p.Ser349Phe)	Malignant melanoma [RCV000066287]	not provided	4	147906649	147906649	Human		name
8631042	CV86198	single nucleotide variant	NM_024605.3(ARHGAP10):c.1984C>T (p.Leu662Phe)	Malignant melanoma [RCV000066289]	not provided	4	148047008	148047008	Human		name
156398996	CV2194919	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1661T>C (p.Ile554Thr)	not specified [RCV004075447]	uncertain significance	15	32636434	32636434	Human		name
155979212	CV2222822	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2935A>G (p.Met979Val)	not specified [RCV004101655]	uncertain significance	15	32637708	32637708	Human		name
156118486	CV2232135	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2472A>T (p.Arg824Ser)	not specified [RCV004093167]	uncertain significance	15	32637245	32637245	Human		name
155945956	CV2238055	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1127A>G (p.Glu376Gly)	not specified [RCV004111082]	uncertain significance	15	32633000	32633000	Human		name
156081730	CV2244346	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1810T>G (p.Ser604Ala)	not specified [RCV004100330]	uncertain significance	15	32636583	32636583	Human		name
155989662	CV2282834	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2960A>T (p.Asn987Ile)	not specified [RCV004143494]	uncertain significance	15	32637733	32637733	Human		name
156000822	CV2296350	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2245C>T (p.Pro749Ser)	not specified [RCV004148107]	uncertain significance	15	32637018	32637018	Human		name
156193616	CV2302003	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1435A>G (p.Thr479Ala)	not specified [RCV004158774]	uncertain significance	15	32635867	32635867	Human		name
156047489	CV2319168	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2549A>C (p.Glu850Ala)	not specified [RCV004178232]	uncertain significance	15	32637322	32637322	Human		name
155976998	CV2324875	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1168G>A (p.Gly390Arg)	not specified [RCV004173100]	uncertain significance	15	32633041	32633041	Human		name
156167179	CV2373662	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1264T>C (p.Ser422Pro)	not specified [RCV004222749]	uncertain significance	15	32633961	32633961	Human		name
156040892	CV2387661	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2465C>T (p.Pro822Leu)	not specified [RCV004234207]	uncertain significance	15	32637238	32637238	Human		name
156003564	CV2396764	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2246C>T (p.Pro749Leu)	not specified [RCV004233912]	likely benign	15	32637019	32637019	Human		name
156253873	CV2397482	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1388G>A (p.Arg463Gln)	not specified [RCV004236957]	uncertain significance	15	32635820	32635820	Human		name
329387991	CV2440322	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2363T>C (p.Leu788Ser)	not specified [RCV004262801]	uncertain significance	15	32637136	32637136	Human		name
329378485	CV2446940	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.80G>A (p.Arg27His)	not specified [RCV004257785]	uncertain significance	15	30626900	30626900	Human		name
329395986	CV2454606	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2387C>T (p.Ser796Phe)	not specified [RCV004268071]	uncertain significance	15	32637160	32637160	Human		name
401773196	CV2709174	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1445T>A (p.Leu482His)	not specified [RCV004316358]	uncertain significance	15	32635877	32635877	Human		name
401738165	CV2714348	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1895C>A (p.Pro632Gln)	not specified [RCV004317887]	uncertain significance	15	32636668	32636668	Human		name
401878803	CV2777902	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2633G>C (p.Gly878Ala)	not specified [RCV004347871]	uncertain significance	15	32637406	32637406	Human		name
401865775	CV2779093	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2633G>T (p.Gly878Val)	not specified [RCV004348724]	uncertain significance	15	32637406	32637406	Human		name
401881894	CV2784874	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2867G>A (p.Gly956Asp)	not specified [RCV004352653]	uncertain significance	15	32637640	32637640	Human		name
405674818	CV3286402	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1162A>G (p.Ile388Val)	not specified [RCV004420382]	uncertain significance	15	32633035	32633035	Human		name
405674822	CV3286403	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1267C>T (p.Pro423Ser)	not specified [RCV004420383]	uncertain significance	15	32633964	32633964	Human		name
405674826	CV3286404	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1409T>C (p.Leu470Ser)	not specified [RCV004420384]	uncertain significance	15	32635841	32635841	Human		name
405674830	CV3286405	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1556T>G (p.Met519Arg)	not specified [RCV004420385]	uncertain significance	15	32636329	32636329	Human		name
405674834	CV3286406	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1678C>A (p.Pro560Thr)	not specified [RCV004420386]	uncertain significance	15	32636451	32636451	Human		name
405674839	CV3286408	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1934A>G (p.Glu645Gly)	not specified [RCV004420388]	uncertain significance	15	32636707	32636707	Human		name
405674843	CV3286409	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2285C>G (p.Ser762Cys)	not specified [RCV004420389]	uncertain significance	15	32637058	32637058	Human		name
405674849	CV3286410	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2338A>G (p.Met780Val)	not specified [RCV004420390]	likely benign	15	32637111	32637111	Human		name
405674858	CV3286412	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2766G>T (p.Glu922Asp)	not specified [RCV004420392]	uncertain significance	15	32637539	32637539	Human		name
405674894	CV3286421	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.54C>G (p.Phe18Leu)	not specified [RCV004420401]	uncertain significance	15	30626874	30626874	Human		name
407484303	CV3461543	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1597G>A (p.Asp533Asn)	not specified [RCV004657534]	uncertain significance	15	32636370	32636370	Human		name
407486424	CV3471636	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2062A>G (p.Ile688Val)	not specified [RCV004666703]	uncertain significance	15	32636835	32636835	Human		name
597743183	CV3580456	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1097C>T (p.Pro366Leu)	not specified [RCV004845007]	uncertain significance	15	32629754	32629754	Human		name
597743212	CV3580465	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1739C>G (p.Thr580Arg)	not specified [RCV004845012]	uncertain significance	15	32636512	32636512	Human		name
597743255	CV3580474	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2743G>A (p.Ala915Thr)	not specified [RCV004845019]	uncertain significance	15	32637516	32637516	Human		name
597743268	CV3580476	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2367A>C (p.Glu789Asp)	not specified [RCV004845021]	uncertain significance	15	32637140	32637140	Human		name
597743282	CV3580482	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2723G>T (p.Cys908Phe)	not specified [RCV004845023]	uncertain significance	15	32637496	32637496	Human		name
597743289	CV3580484	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2677G>A (p.Val893Ile)	not specified [RCV004845024]	likely benign	15	32637450	32637450	Human		name
597743297	CV3580486	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2231T>A (p.Met744Lys)	not specified [RCV004845025]	uncertain significance	15	32637004	32637004	Human		name
597743305	CV3580487	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2687T>A (p.Ile896Asn)	not specified [RCV004845026]	uncertain significance	15	32637460	32637460	Human		name
597743311	CV3580488	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1423G>A (p.Glu475Lys)	not specified [RCV004845027]	uncertain significance	15	32635855	32635855	Human		name
597743319	CV3580489	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1588C>G (p.Gln530Glu)	not specified [RCV004845028]	uncertain significance	15	32636361	32636361	Human		name
597743327	CV3580491	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2252G>A (p.Cys751Tyr)	not specified [RCV004845029]	likely benign	15	32637025	32637025	Human		name
597743333	CV3580493	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2812G>A (p.Val938Met)	not specified [RCV004845030]	uncertain significance	15	32637585	32637585	Human		name
597768693	CV3580494	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1949C>T (p.Thr650Ile)	not specified [RCV004850739]	uncertain significance	15	32636722	32636722	Human		name
597743339	CV3580495	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1570C>T (p.Pro524Ser)	not specified [RCV004845031]	uncertain significance	15	32636343	32636343	Human		name
597743351	CV3580498	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1306C>T (p.Arg436Cys)	not specified [RCV004845033]	uncertain significance	15	32634003	32634003	Human		name
597743932	CV3580603	single nucleotide variant	NM_001006634.3(ARHGAP17):c.287C>T (p.Thr96Met)	not specified [RCV004845062]	uncertain significance	16	24968758	24968758	Human		name
597743878	CV3580615	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1047T>C (p.Ser349=)	not specified [RCV004845072]	likely benign	16	24949484	24949484	Human		name
597743543	CV3580637	single nucleotide variant	NM_001006634.3(ARHGAP17):c.113C>T (p.Thr38Met)	not specified [RCV004845088]	uncertain significance	16	24977300	24977300	Human		name
597743723	CV3590617	single nucleotide variant	NM_001006634.3(ARHGAP17):c.118C>T (p.Arg40Trp)	not specified [RCV004845119]	uncertain significance	16	24977295	24977295	Human		name
597743824	CV3590637	single nucleotide variant	NM_001006634.3(ARHGAP17):c.145C>T (p.Arg49Cys)	not specified [RCV004845137]	uncertain significance	16	24977268	24977268	Human		name
598273121	CV4002871	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1951A>G (p.Ile651Val)	not specified [RCV005389571]	likely benign	15	32636724	32636724	Human		name
598273139	CV4002878	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2104G>T (p.Asp702Tyr)	not specified [RCV005389577]	uncertain significance	15	32636877	32636877	Human		name
598273164	CV4002887	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2315C>T (p.Thr772Ile)	not specified [RCV005389586]	uncertain significance	15	32637088	32637088	Human		name
598273190	CV4002896	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1448T>A (p.Phe483Tyr)	not specified [RCV005389594]	uncertain significance	15	32635880	32635880	Human		name
598273222	CV4002909	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1790T>C (p.Val597Ala)	not specified [RCV005389605]	uncertain significance	15	32636563	32636563	Human		name
598273245	CV4002920	single nucleotide variant	NM_014783.6(ARHGAP11A):c.1996G>A (p.Glu666Lys)	not specified [RCV005389613]	uncertain significance	15	32636769	32636769	Human		name
598205354	CV4002928	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2824C>G (p.Leu942Val)	not specified [RCV005399450]	uncertain significance	15	32637597	32637597	Human		name
598273311	CV4002947	single nucleotide variant	NM_014783.6(ARHGAP11A):c.2515C>T (p.Arg839Cys)	not specified [RCV005389637]	uncertain significance	15	32637288	32637288	Human		name
8627622	CV82766	single nucleotide variant	NM_014783.4(ARHGAP11A):c.2728G>T (p.Glu910Ter)	Malignant melanoma [RCV000062846]	not provided	15	32637501	32637501	Human		name
155928761	CV2369559	single nucleotide variant	NM_001006634.3(ARHGAP17):c.713G>A (p.Arg238Gln)	not specified [RCV004214978]	uncertain significance	16	24959682	24959682	Human		name
401731636	CV2674440	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.247G>A (p.Glu83Lys)	not specified [RCV004289301]	uncertain significance	15	30633536	30633536	Human		name
401729528	CV2690310	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.164C>T (p.Pro55Leu)	not specified [RCV004302305]	uncertain significance	15	30630737	30630737	Human		name
401734156	CV2713350	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.173C>T (p.Ala58Val)	not specified [RCV004318651]	likely benign	15	30630746	30630746	Human		name
401767589	CV2729773	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.211G>A (p.Asp71Asn)	not specified [RCV004332790]	uncertain significance	15	30633500	30633500	Human		name
401779020	CV2733062	single nucleotide variant	NM_014783.6(ARHGAP11A):c.3028G>A (p.Gly1010Arg)	not specified [RCV004331996]	uncertain significance	15	32637801	32637801	Human		name
405684418	CV3286456	single nucleotide variant	NM_001006634.3(ARHGAP17):c.424G>A (p.Ala142Thr)	not specified [RCV004422417]	uncertain significance	16	24968388	24968388	Human		name
405684423	CV3286457	single nucleotide variant	NM_001006634.3(ARHGAP17):c.554A>G (p.Asn185Ser)	not specified [RCV004422418]	uncertain significance	16	24964216	24964216	Human		name
405684429	CV3286458	single nucleotide variant	NM_001006634.3(ARHGAP17):c.919A>G (p.Thr307Ala)	not specified [RCV004422419]	uncertain significance	16	24952976	24952976	Human		name
407531350	CV3471646	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.259C>T (p.Arg87Trp)	not specified [RCV004657558]	uncertain significance	15	30633548	30633548	Human		name
407531384	CV3471666	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.109A>G (p.Thr37Ala)	not specified [RCV004657576]	uncertain significance	15	30626929	30626929	Human		name
597743358	CV3580499	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.234A>C (p.Glu78Asp)	not specified [RCV004845034]	uncertain significance	15	30633523	30633523	Human		name
597743377	CV3580505	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.137T>C (p.Ile46Thr)	not specified [RCV004845037]	uncertain significance	15	30630710	30630710	Human		name
597768697	CV3580506	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.230A>G (p.Glu77Gly)	not specified [RCV004850740]	uncertain significance	15	30633519	30633519	Human		name
598167760	CV4003123	single nucleotide variant	NM_001006634.3(ARHGAP17):c.839G>C (p.Gly280Ala)	not specified [RCV005391767]	uncertain significance	16	24954616	24954616	Human		name
598167932	CV4003153	single nucleotide variant	NM_001006634.3(ARHGAP17):c.608C>T (p.Ala203Val)	not specified [RCV005391796]	uncertain significance	16	24959945	24959945	Human		name
156374745	CV2194796	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2143C>T (p.Pro715Ser)	not specified [RCV004075342]	uncertain significance	16	24931156	24931156	Human		name
156400377	CV2199146	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.508G>C (p.Val170Leu)	not specified [RCV004080539]	uncertain significance	15	30634380	30634380	Human		name
156399466	CV2205137	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2593C>T (p.Pro865Ser)	not specified [RCV004077735]	uncertain significance	16	24920183	24920183	Human		name
156018198	CV2233036	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1633C>G (p.Gln545Glu)	not specified [RCV004103674]	uncertain significance	16	24939455	24939455	Human		name
156124174	CV2234223	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1221G>C (p.Leu407Phe)	not specified [RCV004106303]	uncertain significance	16	24947502	24947502	Human		name
156030218	CV2238389	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1583C>T (p.Pro528Leu)	not specified [RCV004113458]	uncertain significance	16	24939505	24939505	Human		name
156089981	CV2241507	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1240G>A (p.Gly414Arg)	not specified [RCV004104410]	uncertain significance	16	24947483	24947483	Human		name
155948026	CV2245840	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2263C>T (p.Pro755Ser)	not specified [RCV004111688]	uncertain significance	16	24931036	24931036	Human		name
156105605	CV2257214	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1883C>T (p.Thr628Ile)	not specified [RCV004123423]	uncertain significance	16	24935481	24935481	Human		name
156239080	CV2285936	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1135A>T (p.Ile379Phe)	not specified [RCV004143860]	uncertain significance	16	24947588	24947588	Human		name
155907006	CV2302130	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2036C>T (p.Thr679Ile)	not specified [RCV004159146]	uncertain significance	16	24931263	24931263	Human		name
156269603	CV2315015	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2390C>A (p.Pro797Gln)	not specified [RCV004164934]	uncertain significance	16	24930909	24930909	Human		name
155973453	CV2332402	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.769C>G (p.Leu257Val)	not specified [RCV004196134]	uncertain significance	15	30635595	30635595	Human		name
156286379	CV2334927	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1637G>A (p.Ser546Asn)	not specified [RCV004182030]	uncertain significance	16	24939451	24939451	Human		name
156052235	CV2336724	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1606G>A (p.Val536Met)	not specified [RCV004196964]	uncertain significance	16	24939482	24939482	Human		name
155984029	CV2344372	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.631G>A (p.Glu211Lys)	not specified [RCV004195125]	uncertain significance	15	30635159	30635159	Human		name
156243884	CV2347108	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1406G>C (p.Gly469Ala)	not specified [RCV004204590]	uncertain significance	16	24942071	24942071	Human		name
156077155	CV2351012	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1640C>G (p.Ser547Cys)	not specified [RCV004211836]	uncertain significance	16	24939448	24939448	Human		name
155991170	CV2355316	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1612G>A (p.Ala538Thr)	not specified [RCV004203165]	uncertain significance	16	24939476	24939476	Human		name
156147571	CV2377258	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2384C>T (p.Pro795Leu)	not specified [RCV004225448]	uncertain significance	16	24930915	24930915	Human		name
156347943	CV2383011	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.309T>A (p.Asp103Glu)	not specified [RCV004217596]	uncertain significance	15	30634181	30634181	Human		name
156097677	CV2384927	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1897G>A (p.Val633Ile)	not specified [RCV004226164]	uncertain significance	16	24931402	24931402	Human		name
156225691	CV2400942	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.593T>C (p.Ile198Thr)	not specified [RCV004244231]	uncertain significance	15	30635121	30635121	Human		name
329384343	CV2435030	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1781A>G (p.Asn594Ser)	not specified [RCV004252683]	likely benign	16	24935583	24935583	Human		name
329359846	CV2446440	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1889G>A (p.Arg630His)	not provided [RCV004696348]\|not specified [RCV004249557]	uncertain significance	16	24935475	24935475	Human		name
329402236	CV2454078	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1642A>G (p.Arg548Gly)	not specified [RCV004265586]	uncertain significance	16	24939446	24939446	Human		name
329396474	CV2459569	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1815G>C (p.Gln605His)	not specified [RCV004277020]	uncertain significance	16	24935549	24935549	Human		name
329363776	CV2471959	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1420T>C (p.Ser474Pro)	not specified [RCV004280971]	uncertain significance	16	24942057	24942057	Human		name
401771309	CV2675544	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.665T>A (p.Val222Glu)	not specified [RCV004295159]	uncertain significance	15	30635491	30635491	Human		name
401741358	CV2680604	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2256C>G (p.His752Gln)	not specified [RCV004291227]	uncertain significance	16	24931043	24931043	Human		name
401730932	CV2686791	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2546G>A (p.Arg849His)	not specified [RCV004301973]	uncertain significance	16	24920230	24920230	Human		name
401725793	CV2687265	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1408A>C (p.Asn470His)	not specified [RCV004298203]	uncertain significance	16	24942069	24942069	Human		name
401780266	CV2725963	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2275A>G (p.Thr759Ala)	not specified [RCV004324333]	uncertain significance	16	24931024	24931024	Human		name
401870603	CV2755939	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1441C>T (p.Arg481Trp)	not specified [RCV004336027]	uncertain significance	16	24942036	24942036	Human		name
401863574	CV2770718	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1907C>A (p.Pro636His)	not specified [RCV004349762]	uncertain significance	16	24931392	24931392	Human		name
401883866	CV2785788	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1628C>G (p.Pro543Arg)	not specified [RCV004365035]	uncertain significance	16	24939460	24939460	Human		name
401881096	CV2787817	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1654A>G (p.Ser552Gly)	not specified [RCV004358503]	uncertain significance	16	24939434	24939434	Human		name
401884454	CV2789688	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2096G>A (p.Arg699Gln)	not specified [RCV004360279]	uncertain significance	16	24931203	24931203	Human		name
405674886	CV3286419	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.451G>A (p.Glu151Lys)	not specified [RCV004420399]	uncertain significance	15	30634323	30634323	Human		name
405674891	CV3286420	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.521T>G (p.Phe174Cys)	not specified [RCV004420400]	uncertain significance	15	30634393	30634393	Human		name
405674898	CV3286422	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.686A>G (p.Lys229Arg)	not specified [RCV004420402]	uncertain significance	15	30635512	30635512	Human		name
405674901	CV3286423	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.721G>T (p.Val241Leu)	not specified [RCV004420403]	uncertain significance	15	30635547	30635547	Human		name
405674904	CV3286424	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.798C>A (p.Asn266Lys)	not specified [RCV004420404]	likely benign	15	30635624	30635624	Human		name
405684361	CV3286444	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1190G>A (p.Ser397Asn)	not specified [RCV004422405]	uncertain significance	16	24947533	24947533	Human		name
405684364	CV3286445	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1199C>T (p.Ala400Val)	not specified [RCV004422406]	uncertain significance	16	24947524	24947524	Human		name
405684369	CV3286446	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1453A>G (p.Met485Val)	not specified [RCV004422407]	uncertain significance	16	24942024	24942024	Human		name
405684379	CV3286448	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1574C>T (p.Pro525Leu)	not specified [RCV004422409]	uncertain significance	16	24939514	24939514	Human		name
405684384	CV3286449	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1609C>T (p.Pro537Ser)	not specified [RCV004422410]	uncertain significance	16	24939479	24939479	Human		name
405684389	CV3286450	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1699C>G (p.Gln567Glu)	not specified [RCV004422411]	uncertain significance	16	24939389	24939389	Human		name
405684394	CV3286451	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1736C>T (p.Pro579Leu)	not specified [RCV004422412]	uncertain significance	16	24935628	24935628	Human		name
405684400	CV3286452	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2291C>T (p.Pro764Leu)	not specified [RCV004422413]	uncertain significance	16	24931008	24931008	Human		name
405684410	CV3286454	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2600G>A (p.Arg867His)	not specified [RCV004422415]	likely benign	16	24920176	24920176	Human		name
405684415	CV3286455	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2639C>T (p.Ala880Val)	not specified [RCV004422416]	uncertain significance	16	24920137	24920137	Human		name
407490818	CV3471656	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.662G>A (p.Gly221Asp)	not specified [RCV004666707]	uncertain significance	15	30635488	30635488	Human		name
407490980	CV3471847	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1700A>G (p.Gln567Arg)	not specified [RCV004666752]	uncertain significance	16	24939388	24939388	Human		name
407531659	CV3471857	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1913C>T (p.Pro638Leu)	not specified [RCV004657720]	uncertain significance	16	24931386	24931386	Human		name
597743366	CV3580501	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.664G>A (p.Val222Met)	not specified [RCV004845035]	likely benign	15	30635490	30635490	Human		name
597743371	CV3580503	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.490G>A (p.Ala164Thr)	not specified [RCV004845036]	uncertain significance	15	30634362	30634362	Human		name
597768710	CV3580592	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1440G>C (p.Lys480Asn)	not specified [RCV004850743]	uncertain significance	16	24942037	24942037	Human		name
597743885	CV3580613	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1379C>T (p.Pro460Leu)	not specified [RCV004845071]	uncertain significance	16	24942098	24942098	Human		name
597743869	CV3580621	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2512A>G (p.Thr838Ala)	not specified [RCV004845074]	uncertain significance	16	24930787	24930787	Human		name
597743839	CV3580627	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2599C>T (p.Arg867Cys)	not specified [RCV004845079]	uncertain significance	16	24920177	24920177	Human		name
597768726	CV3580647	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2059G>A (p.Gly687Ser)	not specified [RCV004850748]	uncertain significance	16	24931240	24931240	Human		name
597743649	CV3590598	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1332A>C (p.Glu444Asp)	not specified [RCV004845105]	uncertain significance	16	24943772	24943772	Human		name
597743692	CV3590608	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2003C>G (p.Pro668Arg)	not specified [RCV004845113]	uncertain significance	16	24931296	24931296	Human		name
597743767	CV3590627	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2483A>T (p.Asn828Ile)	not specified [RCV004845127]	uncertain significance	16	24930816	24930816	Human		name
598273333	CV4002956	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.505C>T (p.His169Tyr)	not specified [RCV005389645]	uncertain significance	15	30634377	30634377	Human		name
598167177	CV4002976	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.326T>C (p.Leu109Pro)	not specified [RCV005391644]	uncertain significance	15	30634198	30634198	Human		name
598167230	CV4002987	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.446C>G (p.Thr149Arg)	not specified [RCV005391654]	uncertain significance	15	30634318	30634318	Human		name
598167271	CV4002995	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.308A>T (p.Asp103Val)	not specified [RCV005391661]	uncertain significance	15	30634180	30634180	Human		name
598167308	CV4003006	single nucleotide variant	NM_001039841.3(ARHGAP11B):c.752A>T (p.Lys251Met)	not specified [RCV005391669]	uncertain significance	15	30635578	30635578	Human		name
598167820	CV4003134	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2438C>G (p.Pro813Arg)	not specified [RCV005391778]	uncertain significance	16	24930861	24930861	Human		name
598167882	CV4003144	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1799G>T (p.Gly600Val)	not specified [RCV005391788]	uncertain significance	16	24935565	24935565	Human		name
598167987	CV4003164	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1970C>T (p.Ser657Leu)	not specified [RCV005391806]	uncertain significance	16	24931329	24931329	Human		name
598167998	CV4003167	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2135A>G (p.Asn712Ser)	not specified [RCV005391808]	likely benign	16	24931164	24931164	Human		name
598205608	CV4003176	single nucleotide variant	NM_001006634.3(ARHGAP17):c.1509G>T (p.Met503Ile)	not specified [RCV005399491]	uncertain significance	16	24939579	24939579	Human		name
598168059	CV4003186	single nucleotide variant	NM_001006634.3(ARHGAP17):c.2638G>A (p.Ala880Thr)	not specified [RCV005391819]	uncertain significance	16	24920138	24920138	Human		name
11059993	CV226944	deletion	NM_014783.6(ARHGAP11A):c.2370_2371del (p.Thr790_Cys791insTer)	Inborn genetic diseases [RCV000210601]	pathogenic\|likely pathogenic	15	32637143	32637144	Human	1	name

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