Arhgef17 Variant Search Result - Rat Genome Database

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244 records found for search term Arhgef17

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401909707	CV2813521	single nucleotide variant	NM_014786.4(ARHGEF17):c.24C>G (p.Pro8=)	not provided [RCV003398124]	likely benign	11	73308662	73308662	Human		name
156336315	CV2333653	single nucleotide variant	NM_014786.4(ARHGEF17):c.95A>G (p.Asp32Gly)	not specified [RCV004192493]	uncertain significance	11	73308733	73308733	Human		name
401934056	CV2813522	single nucleotide variant	NM_014786.4(ARHGEF17):c.525A>C (p.Thr175=)	not provided [RCV003410915]	likely benign	11	73309163	73309163	Human		name
405698721	CV3279362	single nucleotide variant	NM_014786.4(ARHGEF17):c.44C>T (p.Ser15Leu)	not specified [RCV004425014]	uncertain significance	11	73308682	73308682	Human		name
407467877	CV3465084	single nucleotide variant	NM_014786.4(ARHGEF17):c.50A>C (p.Lys17Thr)	not specified [RCV004660905]	uncertain significance	11	73308688	73308688	Human		name
597771441	CV3581544	single nucleotide variant	NM_014786.4(ARHGEF17):c.34C>T (p.Arg12Cys)	not specified [RCV004851338]	uncertain significance	11	73308672	73308672	Human		name
156005823	CV2281685	single nucleotide variant	NM_014786.4(ARHGEF17):c.202G>A (p.Ala68Thr)	not specified [RCV004147838]	uncertain significance	11	73308840	73308840	Human		name
156181286	CV2384062	single nucleotide variant	NM_014786.4(ARHGEF17):c.130T>A (p.Cys44Ser)	not specified [RCV004225425]	uncertain significance	11	73308768	73308768	Human		name
401748743	CV2694492	single nucleotide variant	NM_014786.4(ARHGEF17):c.121C>T (p.Arg41Cys)	not specified [RCV004304978]	uncertain significance	11	73308759	73308759	Human		name
401863038	CV2765931	single nucleotide variant	NM_014786.4(ARHGEF17):c.232C>T (p.Leu78Phe)	not specified [RCV004337957]	uncertain significance	11	73308870	73308870	Human		name
401934057	CV2813524	single nucleotide variant	NM_014786.4(ARHGEF17):c.2679G>A (p.Leu893=)	not provided [RCV003410916]	likely benign	11	73311317	73311317	Human		name
405698587	CV3279337	single nucleotide variant	NM_014786.4(ARHGEF17):c.200C>A (p.Ala67Asp)	not specified [RCV004424989]	uncertain significance	11	73308838	73308838	Human		name
405698605	CV3279340	single nucleotide variant	NM_014786.4(ARHGEF17):c.214C>T (p.Pro72Ser)	not specified [RCV004424992]	uncertain significance	11	73308852	73308852	Human		name
405698623	CV3279343	single nucleotide variant	NM_014786.4(ARHGEF17):c.239C>T (p.Pro80Leu)	not specified [RCV004424995]	uncertain significance	11	73308877	73308877	Human		name
405698630	CV3279344	single nucleotide variant	NM_014786.4(ARHGEF17):c.260G>A (p.Arg87Gln)	not specified [RCV004424996]	uncertain significance	11	73308898	73308898	Human		name
407467687	CV3468934	single nucleotide variant	NM_014786.4(ARHGEF17):c.296C>T (p.Ala99Val)	not specified [RCV004660834]	uncertain significance	11	73308934	73308934	Human		name
597771797	CV3581614	single nucleotide variant	NM_014786.4(ARHGEF17):c.152G>C (p.Arg51Pro)	not specified [RCV004851408]	likely benign	11	73308790	73308790	Human		name
597772303	CV3581725	single nucleotide variant	NM_014786.4(ARHGEF17):c.193C>T (p.Pro65Ser)	not specified [RCV004851506]	uncertain significance	11	73308831	73308831	Human		name
597772523	CV3581771	single nucleotide variant	NM_014786.4(ARHGEF17):c.275C>T (p.Pro92Leu)	not specified [RCV004851547]	uncertain significance	11	73308913	73308913	Human		name
597772617	CV3581794	single nucleotide variant	NM_014786.4(ARHGEF17):c.292T>C (p.Ser98Pro)	not specified [RCV004851564]	uncertain significance	11	73308930	73308930	Human		name
598168765	CV3897463	single nucleotide variant	NM_014786.4(ARHGEF17):c.269A>G (p.Asp90Gly)	not specified [RCV005262675]	uncertain significance	11	73308907	73308907	Human		name
598168886	CV3897482	single nucleotide variant	NM_014786.4(ARHGEF17):c.252G>T (p.Gln84His)	not specified [RCV005262694]	uncertain significance	11	73308890	73308890	Human		name
598169091	CV3897512	single nucleotide variant	NM_014786.4(ARHGEF17):c.103A>G (p.Thr35Ala)	not specified [RCV005262724]	uncertain significance	11	73308741	73308741	Human		name
598159823	CV3901154	single nucleotide variant	NM_014786.4(ARHGEF17):c.181C>G (p.Leu61Val)	not specified [RCV005260835]	uncertain significance	11	73308819	73308819	Human		name
8634363	CV89583	single nucleotide variant	NM_014786.3(ARHGEF17):c.2136C>T (p.Val712=)	Malignant melanoma [RCV000069680]	not provided	11	73310774	73310774	Human		name
156152313	CV2265899	single nucleotide variant	NM_014786.4(ARHGEF17):c.417G>C (p.Arg139Ser)	not specified [RCV004126753]	uncertain significance	11	73309055	73309055	Human		name
156272635	CV2297240	single nucleotide variant	NM_014786.4(ARHGEF17):c.709G>A (p.Ala237Thr)	not specified [RCV004151120]	uncertain significance	11	73309347	73309347	Human		name
156058836	CV2322966	single nucleotide variant	NM_014786.4(ARHGEF17):c.835G>A (p.Asp279Asn)	not specified [RCV004185407]	uncertain significance	11	73309473	73309473	Human		name
156055776	CV2326608	single nucleotide variant	NM_014786.4(ARHGEF17):c.455G>A (p.Ser152Asn)	not specified [RCV004183149]	uncertain significance	11	73309093	73309093	Human		name
155973201	CV2334412	single nucleotide variant	NM_014786.4(ARHGEF17):c.919A>T (p.Arg307Trp)	not specified [RCV004188387]	uncertain significance	11	73309557	73309557	Human		name
156228256	CV2388429	single nucleotide variant	NM_014786.4(ARHGEF17):c.997C>G (p.Pro333Ala)	not specified [RCV004236921]	uncertain significance	11	73309635	73309635	Human		name
329396648	CV2462848	single nucleotide variant	NM_014786.4(ARHGEF17):c.373A>C (p.Ser125Arg)	not specified [RCV004272404]	uncertain significance	11	73309011	73309011	Human		name
401758943	CV2694355	single nucleotide variant	NM_014786.4(ARHGEF17):c.660C>G (p.Phe220Leu)	not specified [RCV004304546]	uncertain significance	11	73309298	73309298	Human		name
401884416	CV2761723	single nucleotide variant	NM_014786.4(ARHGEF17):c.484G>C (p.Ala162Pro)	not specified [RCV004337335]	uncertain significance	11	73309122	73309122	Human		name
401895783	CV2778908	single nucleotide variant	NM_014786.4(ARHGEF17):c.478C>A (p.Pro160Thr)	not specified [RCV004346787]	uncertain significance	11	73309116	73309116	Human		name
401909711	CV2813525	single nucleotide variant	NM_014786.4(ARHGEF17):c.3006G>A (p.Ser1002=)	not provided [RCV003398126]	likely benign	11	73311644	73311644	Human		name
401909713	CV2813526	single nucleotide variant	NM_014786.4(ARHGEF17):c.3252G>A (p.Ser1084=)	not provided [RCV003398127]	likely benign	11	73346942	73346942	Human		name
401909715	CV2813527	single nucleotide variant	NM_014786.4(ARHGEF17):c.6150T>C (p.Gly2050=)	not provided [RCV003398128]	likely benign	11	73367738	73367738	Human		name
405698760	CV3279369	single nucleotide variant	NM_014786.4(ARHGEF17):c.538G>A (p.Ala180Thr)	not specified [RCV004425021]	uncertain significance	11	73309176	73309176	Human		name
405698799	CV3279375	single nucleotide variant	NM_014786.4(ARHGEF17):c.676G>A (p.Gly226Arg)	not specified [RCV004425027]	uncertain significance	11	73309314	73309314	Human		name
407507341	CV3468869	single nucleotide variant	NM_014786.4(ARHGEF17):c.588G>C (p.Arg196Ser)	not specified [RCV004671691]	uncertain significance	11	73309226	73309226	Human		name
407467706	CV3468945	single nucleotide variant	NM_014786.4(ARHGEF17):c.340G>T (p.Ala114Ser)	not specified [RCV004660844]	uncertain significance	11	73308978	73308978	Human		name
407467730	CV3468955	single nucleotide variant	NM_014786.4(ARHGEF17):c.341C>A (p.Ala114Glu)	not specified [RCV004660852]	uncertain significance	11	73308979	73308979	Human		name
407507431	CV3468987	single nucleotide variant	NM_014786.4(ARHGEF17):c.616C>T (p.Arg206Trp)	not specified [RCV004671720]	uncertain significance	11	73309254	73309254	Human		name
597771355	CV3581525	single nucleotide variant	NM_014786.4(ARHGEF17):c.415A>G (p.Arg139Gly)	not specified [RCV004851319]	uncertain significance	11	73309053	73309053	Human		name
597771400	CV3581535	single nucleotide variant	NM_014786.4(ARHGEF17):c.636T>G (p.Asp212Glu)	not specified [RCV004851329]	uncertain significance	11	73309274	73309274	Human		name
597772000	CV3581667	single nucleotide variant	NM_014786.4(ARHGEF17):c.704C>T (p.Ser235Phe)	not specified [RCV004851447]	uncertain significance	11	73309342	73309342	Human		name
597772107	CV3581688	single nucleotide variant	NM_014786.4(ARHGEF17):c.935G>A (p.Gly312Glu)	not specified [RCV004851468]	uncertain significance	11	73309573	73309573	Human		name
597772362	CV3581736	single nucleotide variant	NM_014786.4(ARHGEF17):c.430G>A (p.Asp144Asn)	not specified [RCV004851517]	uncertain significance	11	73309068	73309068	Human		name
597771197	CV3584906	single nucleotide variant	NM_014786.4(ARHGEF17):c.632C>G (p.Ala211Gly)	not specified [RCV004851284]	uncertain significance	11	73309270	73309270	Human		name
597771311	CV3584974	single nucleotide variant	NM_014786.4(ARHGEF17):c.559C>T (p.Pro187Ser)	not specified [RCV004851309]	uncertain significance	11	73309197	73309197	Human		name
598128887	CV3886688	single nucleotide variant	NM_014786.4(ARHGEF17):c.4932G>T (p.Ser1644=)	not provided [RCV005244348]	likely benign	11	73362670	73362670	Human		name
598160065	CV3897334	single nucleotide variant	NM_014786.4(ARHGEF17):c.668C>T (p.Pro223Leu)	not specified [RCV005260902]	uncertain significance	11	73309306	73309306	Human		name
598168948	CV3897492	single nucleotide variant	NM_014786.4(ARHGEF17):c.443C>G (p.Pro148Arg)	not specified [RCV005262704]	uncertain significance	11	73309081	73309081	Human		name
15106590	CV713158	single nucleotide variant	NM_014786.4(ARHGEF17):c.716C>A (p.Ser239Tyr)	not provided [RCV000960110]	benign	11	73309354	73309354	Human		name
15154129	CV713159	single nucleotide variant	NM_014786.4(ARHGEF17):c.4743C>T (p.Pro1581=)	not provided [RCV000968679]	benign	11	73362481	73362481	Human		name
15169780	CV724719	single nucleotide variant	NM_014786.4(ARHGEF17):c.4779C>T (p.Asp1593=)	not provided [RCV000883340]	benign	11	73362517	73362517	Human		name
156143897	CV2200121	single nucleotide variant	NM_014786.4(ARHGEF17):c.2846G>A (p.Arg949Gln)	not specified [RCV004069693]	likely benign	11	73311484	73311484	Human		name
156139464	CV2202907	single nucleotide variant	NM_014786.4(ARHGEF17):c.1909T>G (p.Ser637Ala)	not specified [RCV004069181]	uncertain significance	11	73310547	73310547	Human		name
156327388	CV2217268	single nucleotide variant	NM_014786.4(ARHGEF17):c.1624C>T (p.Arg542Trp)	not specified [RCV004087716]	uncertain significance	11	73310262	73310262	Human		name
156194259	CV2223331	single nucleotide variant	NM_014786.4(ARHGEF17):c.1945G>C (p.Gly649Arg)	not specified [RCV004105935]	uncertain significance	11	73310583	73310583	Human		name
155938949	CV2225262	single nucleotide variant	NM_014786.4(ARHGEF17):c.1400T>C (p.Ile467Thr)	not specified [RCV004098911]	uncertain significance	11	73310038	73310038	Human		name
156185868	CV2236077	single nucleotide variant	NM_014786.4(ARHGEF17):c.1384C>G (p.Leu462Val)	not specified [RCV004114234]	uncertain significance	11	73310022	73310022	Human		name
156073047	CV2240622	single nucleotide variant	NM_014786.4(ARHGEF17):c.1643C>T (p.Thr548Ile)	not specified [RCV004119263]	uncertain significance	11	73310281	73310281	Human		name
155950430	CV2242913	single nucleotide variant	NM_014786.4(ARHGEF17):c.2630G>A (p.Gly877Asp)	not specified [RCV004107501]	uncertain significance	11	73311268	73311268	Human		name
156166497	CV2243611	single nucleotide variant	NM_014786.4(ARHGEF17):c.1646G>C (p.Cys549Ser)	not specified [RCV004114338]	uncertain significance	11	73310284	73310284	Human		name
155981670	CV2244102	single nucleotide variant	NM_014786.4(ARHGEF17):c.1162C>T (p.Arg388Cys)	not specified [RCV004108569]	likely benign	11	73309800	73309800	Human		name
155912791	CV2245645	single nucleotide variant	NM_014786.4(ARHGEF17):c.1229C>T (p.Ser410Phe)	not specified [RCV004111531]	uncertain significance	11	73309867	73309867	Human		name
155925552	CV2258560	single nucleotide variant	NM_014786.4(ARHGEF17):c.2930C>G (p.Ser977Cys)	not specified [RCV004116041]	uncertain significance	11	73311568	73311568	Human		name
156158061	CV2314503	single nucleotide variant	NM_014786.4(ARHGEF17):c.2804G>A (p.Arg935Gln)	not specified [RCV004168601]	likely benign	11	73311442	73311442	Human		name
156277478	CV2330838	single nucleotide variant	NM_014786.4(ARHGEF17):c.1170C>A (p.Ser390Arg)	not provided [RCV005242340]\|not specified [RCV004185893]	likely benign\|uncertain significance	11	73309808	73309808	Human		name
155917607	CV2332846	single nucleotide variant	NM_014786.4(ARHGEF17):c.2755C>T (p.Arg919Cys)	not specified [RCV004192110]	uncertain significance	11	73311393	73311393	Human		name
156034210	CV2338623	single nucleotide variant	NM_014786.4(ARHGEF17):c.2119C>T (p.Arg707Cys)	not specified [RCV004182207]	uncertain significance	11	73310757	73310757	Human		name
155977253	CV2342869	single nucleotide variant	NM_014786.4(ARHGEF17):c.1811G>A (p.Arg604His)	not provided [RCV003396842]\|not specified [RCV004189903]	likely benign\|uncertain significance	11	73310449	73310449	Human		name
155985138	CV2344492	single nucleotide variant	NM_014786.4(ARHGEF17):c.2333G>T (p.Gly778Val)	not specified [RCV004599597]	uncertain significance	11	73310971	73310971	Human		name
155907939	CV2354529	single nucleotide variant	NM_014786.4(ARHGEF17):c.1660A>G (p.Met554Val)	not specified [RCV004202509]	likely benign	11	73310298	73310298	Human		name
156402002	CV2367804	single nucleotide variant	NM_014786.4(ARHGEF17):c.2872C>T (p.Arg958Cys)	not specified [RCV004222919]	uncertain significance	11	73311510	73311510	Human		name
156263389	CV2377214	single nucleotide variant	NM_014786.4(ARHGEF17):c.1003G>A (p.Ala335Thr)	not specified [RCV004231882]	uncertain significance	11	73309641	73309641	Human		name
156045070	CV2381691	single nucleotide variant	NM_014786.4(ARHGEF17):c.2497C>T (p.Arg833Cys)	not specified [RCV004232155]	uncertain significance	11	73311135	73311135	Human		name
156084980	CV2390474	single nucleotide variant	NM_014786.4(ARHGEF17):c.2446G>A (p.Asp816Asn)	not specified [RCV004239015]	uncertain significance	11	73311084	73311084	Human		name
155928364	CV2391713	single nucleotide variant	NM_014786.4(ARHGEF17):c.1655A>G (p.Lys552Arg)	not specified [RCV004241868]	uncertain significance	11	73310293	73310293	Human		name
329367266	CV2427326	single nucleotide variant	NM_014786.4(ARHGEF17):c.1403C>T (p.Ala468Val)	not specified [RCV004248186]	uncertain significance	11	73310041	73310041	Human		name
329397498	CV2466255	single nucleotide variant	NM_014786.4(ARHGEF17):c.1534G>A (p.Gly512Ser)	not specified [RCV004279881]	uncertain significance	11	73310172	73310172	Human		name
329399042	CV2471866	single nucleotide variant	NM_014786.4(ARHGEF17):c.1891C>T (p.Arg631Trp)	not specified [RCV004280897]	uncertain significance	11	73310529	73310529	Human		name
401736959	CV2679191	single nucleotide variant	NM_014786.4(ARHGEF17):c.1003G>T (p.Ala335Ser)	not specified [RCV004285750]	uncertain significance	11	73309641	73309641	Human		name
401739479	CV2684087	single nucleotide variant	NM_014786.4(ARHGEF17):c.2183G>C (p.Gly728Ala)	not specified [RCV004295679]	uncertain significance	11	73310821	73310821	Human		name
401760352	CV2709793	single nucleotide variant	NM_014786.4(ARHGEF17):c.1392T>G (p.Asn464Lys)	not specified [RCV004320773]	uncertain significance	11	73310030	73310030	Human		name
401753366	CV2722444	single nucleotide variant	NM_014786.4(ARHGEF17):c.1153G>T (p.Ala385Ser)	not specified [RCV004322838]	uncertain significance	11	73309791	73309791	Human		name
401899822	CV2758874	single nucleotide variant	NM_014786.4(ARHGEF17):c.2852G>A (p.Arg951Gln)	not specified [RCV004339962]	uncertain significance	11	73311490	73311490	Human		name
401888951	CV2761581	single nucleotide variant	NM_014786.4(ARHGEF17):c.2609G>A (p.Arg870Gln)	not specified [RCV004337209]	likely benign	11	73311247	73311247	Human		name
401887744	CV2770403	single nucleotide variant	NM_014786.4(ARHGEF17):c.2180C>G (p.Ala727Gly)	not specified [RCV004358049]	uncertain significance	11	73310818	73310818	Human		name
401885990	CV2771554	single nucleotide variant	NM_014786.4(ARHGEF17):c.1099G>A (p.Gly367Arg)	not specified [RCV004348581]	uncertain significance	11	73309737	73309737	Human		name
401878926	CV2773806	single nucleotide variant	NM_014786.4(ARHGEF17):c.1250G>A (p.Arg417His)	not specified [RCV004358256]	uncertain significance	11	73309888	73309888	Human		name
401895962	CV2779798	single nucleotide variant	NM_014786.4(ARHGEF17):c.1679G>A (p.Arg560His)	not specified [RCV004353429]	uncertain significance	11	73310317	73310317	Human		name
401884946	CV2786627	single nucleotide variant	NM_014786.4(ARHGEF17):c.2759G>A (p.Arg920Gln)	not specified [RCV004363766]	uncertain significance	11	73311397	73311397	Human		name
401909709	CV2813523	single nucleotide variant	NM_014786.4(ARHGEF17):c.1735G>C (p.Glu579Gln)	not provided [RCV003398125]	likely benign	11	73310373	73310373	Human		name
405698520	CV3279326	single nucleotide variant	NM_014786.4(ARHGEF17):c.1043C>T (p.Ser348Phe)	not specified [RCV004424978]	uncertain significance	11	73309681	73309681	Human		name
405698524	CV3279327	single nucleotide variant	NM_014786.4(ARHGEF17):c.1123G>C (p.Val375Leu)	not specified [RCV004424979]	uncertain significance	11	73309761	73309761	Human		name
405698538	CV3279329	single nucleotide variant	NM_014786.4(ARHGEF17):c.1136C>T (p.Ser379Leu)	not specified [RCV004424981]	uncertain significance	11	73309774	73309774	Human		name
405698542	CV3279330	single nucleotide variant	NM_014786.4(ARHGEF17):c.1157G>A (p.Gly386Asp)	not specified [RCV004424982]	uncertain significance	11	73309795	73309795	Human		name
405698549	CV3279331	single nucleotide variant	NM_014786.4(ARHGEF17):c.1368T>G (p.Ser456Arg)	not specified [RCV004424983]	uncertain significance	11	73310006	73310006	Human		name
405698563	CV3279333	single nucleotide variant	NM_014786.4(ARHGEF17):c.1669C>T (p.Arg557Cys)	not specified [RCV004424985]	uncertain significance	11	73310307	73310307	Human		name
405698567	CV3279334	single nucleotide variant	NM_014786.4(ARHGEF17):c.1684A>G (p.Ser562Gly)	not specified [RCV004424986]	likely benign	11	73310322	73310322	Human		name
405698574	CV3279335	single nucleotide variant	NM_014786.4(ARHGEF17):c.1733C>T (p.Ala578Val)	not specified [RCV004424987]	uncertain significance	11	73310371	73310371	Human		name
405698581	CV3279336	single nucleotide variant	NM_014786.4(ARHGEF17):c.1946G>A (p.Gly649Glu)	not specified [RCV004424988]	uncertain significance	11	73310584	73310584	Human		name
405698593	CV3279338	single nucleotide variant	NM_014786.4(ARHGEF17):c.2071G>A (p.Gly691Arg)	not specified [RCV004424990]	uncertain significance	11	73310709	73310709	Human		name
405698598	CV3279339	single nucleotide variant	NM_014786.4(ARHGEF17):c.2087C>T (p.Ser696Leu)	not specified [RCV004424991]	uncertain significance	11	73310725	73310725	Human		name
405698609	CV3279341	single nucleotide variant	NM_014786.4(ARHGEF17):c.2221C>T (p.Arg741Cys)	not specified [RCV004424993]	uncertain significance	11	73310859	73310859	Human		name
405698619	CV3279342	single nucleotide variant	NM_014786.4(ARHGEF17):c.2395G>T (p.Val799Phe)	not specified [RCV004424994]	uncertain significance	11	73311033	73311033	Human		name
405698636	CV3279345	single nucleotide variant	NM_014786.4(ARHGEF17):c.2687C>T (p.Pro896Leu)	not specified [RCV004424997]	uncertain significance	11	73311325	73311325	Human		name
405698642	CV3279346	single nucleotide variant	NM_014786.4(ARHGEF17):c.2706C>G (p.Asn902Lys)	not specified [RCV004424998]	uncertain significance	11	73311344	73311344	Human		name
405698651	CV3279348	single nucleotide variant	NM_014786.4(ARHGEF17):c.2812G>A (p.Glu938Lys)	not specified [RCV004425000]	uncertain significance	11	73311450	73311450	Human		name
405698656	CV3279349	single nucleotide variant	NM_014786.4(ARHGEF17):c.2972C>T (p.Pro991Leu)	not specified [RCV004425001]	uncertain significance	11	73311610	73311610	Human		name
407507472	CV3465094	single nucleotide variant	NM_014786.4(ARHGEF17):c.1042T>C (p.Ser348Pro)	not specified [RCV004671737]	uncertain significance	11	73309680	73309680	Human		name
407467883	CV3465101	single nucleotide variant	NM_014786.4(ARHGEF17):c.1162C>G (p.Arg388Gly)	not specified [RCV004660917]	uncertain significance	11	73309800	73309800	Human		name
407467894	CV3465110	single nucleotide variant	NM_014786.4(ARHGEF17):c.1448C>T (p.Ser483Leu)	not specified [RCV004660922]	uncertain significance	11	73310086	73310086	Human		name
407467654	CV3468880	single nucleotide variant	NM_014786.4(ARHGEF17):c.1675C>G (p.Pro559Ala)	not specified [RCV004660798]	uncertain significance	11	73310313	73310313	Human		name
407507366	CV3468888	single nucleotide variant	NM_014786.4(ARHGEF17):c.1054G>A (p.Val352Ile)	not specified [RCV004671698]	uncertain significance	11	73309692	73309692	Human		name
407468009	CV3468889	single nucleotide variant	NM_014786.4(ARHGEF17):c.2294C>T (p.Pro765Leu)	not specified [RCV004660803]	uncertain significance	11	73310932	73310932	Human		name
407507369	CV3468891	single nucleotide variant	NM_014786.4(ARHGEF17):c.1229C>G (p.Ser410Cys)	not specified [RCV004671699]	uncertain significance	11	73309867	73309867	Human		name
407467986	CV3468908	single nucleotide variant	NM_014786.4(ARHGEF17):c.1759G>A (p.Val587Ile)	not specified [RCV004660816]	uncertain significance	11	73310397	73310397	Human		name
407507387	CV3468913	single nucleotide variant	NM_014786.4(ARHGEF17):c.1127G>A (p.Ser376Asn)	not specified [RCV004671707]	uncertain significance	11	73309765	73309765	Human		name
407467756	CV3468966	single nucleotide variant	NM_014786.4(ARHGEF17):c.2816G>A (p.Gly939Asp)	not specified [RCV004660861]	uncertain significance	11	73311454	73311454	Human		name
597771577	CV3581573	single nucleotide variant	NM_014786.4(ARHGEF17):c.1006C>T (p.Pro336Ser)	not specified [RCV004851367]	uncertain significance	11	73309644	73309644	Human		name
597771631	CV3581583	single nucleotide variant	NM_014786.4(ARHGEF17):c.2570T>A (p.Leu857Gln)	not specified [RCV004851377]	uncertain significance	11	73311208	73311208	Human		name
597771901	CV3581634	single nucleotide variant	NM_014786.4(ARHGEF17):c.2938C>T (p.Pro980Ser)	not specified [RCV004851428]	uncertain significance	11	73311576	73311576	Human		name
597771938	CV3581641	single nucleotide variant	NM_014786.4(ARHGEF17):c.2756G>A (p.Arg919His)	not specified [RCV004851435]	uncertain significance	11	73311394	73311394	Human		name
597771955	CV3581658	single nucleotide variant	NM_014786.4(ARHGEF17):c.1396G>T (p.Asp466Tyr)	not specified [RCV004851438]	uncertain significance	11	73310034	73310034	Human		name
597772157	CV3581698	single nucleotide variant	NM_014786.4(ARHGEF17):c.2192A>G (p.Tyr731Cys)	not specified [RCV004851478]	uncertain significance	11	73310830	73310830	Human		name
597772247	CV3581715	single nucleotide variant	NM_014786.4(ARHGEF17):c.2983C>T (p.His995Tyr)	not specified [RCV004851496]	uncertain significance	11	73311621	73311621	Human		name
597772514	CV3581764	single nucleotide variant	NM_014786.4(ARHGEF17):c.1639T>C (p.Phe547Leu)	not specified [RCV004851545]	uncertain significance	11	73310277	73310277	Human		name
597772519	CV3581767	single nucleotide variant	NM_014786.4(ARHGEF17):c.2783G>C (p.Arg928Pro)	not specified [RCV004851546]	uncertain significance	11	73311421	73311421	Human		name
597771189	CV3584895	single nucleotide variant	NM_014786.4(ARHGEF17):c.1221T>G (p.Ser407Arg)	not specified [RCV004851282]	uncertain significance	11	73309859	73309859	Human		name
597771201	CV3584912	single nucleotide variant	NM_014786.4(ARHGEF17):c.2869G>A (p.Val957Ile)	not specified [RCV004851285]	uncertain significance	11	73311507	73311507	Human		name
597771211	CV3584934	single nucleotide variant	NM_014786.4(ARHGEF17):c.2266G>A (p.Asp756Asn)	not specified [RCV004851287]	uncertain significance	11	73310904	73310904	Human		name
597771216	CV3584944	single nucleotide variant	NM_014786.4(ARHGEF17):c.1987G>A (p.Gly663Ser)	not specified [RCV004851288]	uncertain significance	11	73310625	73310625	Human		name
597771221	CV3584954	single nucleotide variant	NM_014786.4(ARHGEF17):c.1753C>G (p.Leu585Val)	not specified [RCV004851289]	uncertain significance	11	73310391	73310391	Human		name
597771265	CV3584964	single nucleotide variant	NM_014786.4(ARHGEF17):c.2237C>T (p.Thr746Ile)	not specified [RCV004851299]	uncertain significance	11	73310875	73310875	Human		name
598128977	CV3886780	single nucleotide variant	NM_014786.4(ARHGEF17):c.2324T>C (p.Met775Thr)	not provided [RCV005244440]	likely benign	11	73310962	73310962	Human		name
598159997	CV3897313	single nucleotide variant	NM_014786.4(ARHGEF17):c.2008C>T (p.Pro670Ser)	not specified [RCV005260882]	uncertain significance	11	73310646	73310646	Human		name
598160240	CV3897372	single nucleotide variant	NM_014786.4(ARHGEF17):c.1786C>T (p.Arg596Cys)	not specified [RCV005260940]	uncertain significance	11	73310424	73310424	Human		name
598160287	CV3897383	single nucleotide variant	NM_014786.4(ARHGEF17):c.2714T>G (p.Leu905Arg)	not specified [RCV005260950]	uncertain significance	11	73311352	73311352	Human		name
598160378	CV3897402	single nucleotide variant	NM_014786.4(ARHGEF17):c.2635A>T (p.Thr879Ser)	not specified [RCV005260969]	uncertain significance	11	73311273	73311273	Human		name
598168465	CV3897412	single nucleotide variant	NM_014786.4(ARHGEF17):c.1819G>T (p.Ala607Ser)	not specified [RCV005262626]	uncertain significance	11	73310457	73310457	Human		name
598168523	CV3897423	single nucleotide variant	NM_014786.4(ARHGEF17):c.2911G>A (p.Val971Met)	not specified [RCV005262636]	uncertain significance	11	73311549	73311549	Human		name
598168634	CV3897441	single nucleotide variant	NM_014786.4(ARHGEF17):c.2434C>T (p.Arg812Cys)	not specified [RCV005262654]	likely benign	11	73311072	73311072	Human		name
598168699	CV3897452	single nucleotide variant	NM_014786.4(ARHGEF17):c.1443C>G (p.Asp481Glu)	not specified [RCV005262664]	uncertain significance	11	73310081	73310081	Human		name
598169002	CV3897501	single nucleotide variant	NM_014786.4(ARHGEF17):c.2795A>C (p.Gln932Pro)	not specified [RCV005262713]	uncertain significance	11	73311433	73311433	Human		name
598159636	CV3901102	single nucleotide variant	NM_014786.4(ARHGEF17):c.1526C>G (p.Ser509Cys)	not specified [RCV005260784]	uncertain significance	11	73310164	73310164	Human		name
598159751	CV3901133	single nucleotide variant	NM_014786.4(ARHGEF17):c.2150C>G (p.Ser717Cys)	not specified [RCV005260815]	uncertain significance	11	73310788	73310788	Human		name
598159859	CV3901164	single nucleotide variant	NM_014786.4(ARHGEF17):c.1024C>T (p.Arg342Trp)	not specified [RCV005260845]	uncertain significance	11	73309662	73309662	Human		name
156234649	CV2193323	single nucleotide variant	NM_014786.4(ARHGEF17):c.4061C>T (p.Pro1354Leu)	not specified [RCV004072829]	uncertain significance	11	73357301	73357301	Human		name
156332506	CV2220692	single nucleotide variant	NM_014786.4(ARHGEF17):c.3343G>C (p.Asp1115His)	not specified [RCV004097866]	uncertain significance	11	73352902	73352902	Human		name
156220444	CV2222298	single nucleotide variant	NM_014786.4(ARHGEF17):c.3749G>A (p.Arg1250His)	not specified [RCV004105315]	uncertain significance	11	73356260	73356260	Human		name
156195263	CV2223416	single nucleotide variant	NM_014786.4(ARHGEF17):c.6070A>G (p.Met2024Val)	not specified [RCV004105999]	uncertain significance	11	73367658	73367658	Human		name
156340995	CV2225734	single nucleotide variant	NM_014786.4(ARHGEF17):c.4772C>A (p.Ala1591Asp)	not specified [RCV004103150]	uncertain significance	11	73362510	73362510	Human		name
156362894	CV2265629	single nucleotide variant	NM_014786.4(ARHGEF17):c.3388C>G (p.Gln1130Glu)	not specified [RCV004124358]	uncertain significance	11	73352947	73352947	Human		name
156251090	CV2273369	single nucleotide variant	NM_014786.4(ARHGEF17):c.4399G>A (p.Asp1467Asn)	not specified [RCV004132142]	uncertain significance	11	73360512	73360512	Human		name
156264803	CV2275345	single nucleotide variant	NM_014786.4(ARHGEF17):c.4442A>G (p.Asp1481Gly)	not specified [RCV004135234]	uncertain significance	11	73361109	73361109	Human		name
156123404	CV2276173	single nucleotide variant	NM_014786.4(ARHGEF17):c.4844C>T (p.Ser1615Leu)	not specified [RCV004141832]	uncertain significance	11	73362582	73362582	Human		name
156274919	CV2330636	single nucleotide variant	NM_014786.4(ARHGEF17):c.3796C>T (p.Arg1266Cys)	not specified [RCV004183665]	uncertain significance	11	73356307	73356307	Human		name
156276698	CV2330773	single nucleotide variant	NM_014786.4(ARHGEF17):c.5122A>G (p.Met1708Val)	not specified [RCV004185835]	uncertain significance	11	73363331	73363331	Human		name
156087480	CV2337724	single nucleotide variant	NM_014786.4(ARHGEF17):c.3782C>T (p.Ala1261Val)	not specified [RCV004183745]	uncertain significance	11	73356293	73356293	Human		name
155977662	CV2342917	single nucleotide variant	NM_014786.4(ARHGEF17):c.5587G>A (p.Val1863Met)	not specified [RCV004189949]	uncertain significance	11	73365426	73365426	Human		name
155903585	CV2353608	single nucleotide variant	NM_014786.4(ARHGEF17):c.4135C>T (p.Arg1379Cys)	not specified [RCV004199585]	uncertain significance	11	73359881	73359881	Human		name
156198205	CV2362770	single nucleotide variant	NM_014786.4(ARHGEF17):c.5269G>A (p.Asp1757Asn)	not specified [RCV004208887]	uncertain significance	11	73363769	73363769	Human		name
155927368	CV2365916	single nucleotide variant	NM_014786.4(ARHGEF17):c.3823A>G (p.Ile1275Val)	not specified [RCV004207531]	uncertain significance	11	73356334	73356334	Human		name
156102760	CV2386862	single nucleotide variant	NM_014786.4(ARHGEF17):c.6152G>A (p.Arg2051Gln)	not specified [RCV004233498]	uncertain significance	11	73367740	73367740	Human		name
155970247	CV2392181	single nucleotide variant	NM_014786.4(ARHGEF17):c.4759G>A (p.Asp1587Asn)	not specified [RCV004242529]	uncertain significance	11	73362497	73362497	Human		name
329358897	CV2425432	single nucleotide variant	NM_014786.4(ARHGEF17):c.3049G>A (p.Gly1017Ser)	not specified [RCV004251087]	uncertain significance	11	73311687	73311687	Human		name
329357720	CV2427814	single nucleotide variant	NM_014786.4(ARHGEF17):c.3452C>T (p.Ser1151Leu)	not specified [RCV004252590]	uncertain significance	11	73353011	73353011	Human		name
329364563	CV2443694	single nucleotide variant	NM_014786.4(ARHGEF17):c.5039C>T (p.Thr1680Ile)	not specified [RCV004255995]	uncertain significance	11	73363248	73363248	Human		name
329378204	CV2459045	single nucleotide variant	NM_014786.4(ARHGEF17):c.4563C>G (p.Ser1521Arg)	not specified [RCV004272516]	uncertain significance	11	73362108	73362108	Human		name
401755439	CV2682485	single nucleotide variant	NM_014786.4(ARHGEF17):c.4279T>C (p.Tyr1427His)	not specified [RCV004290507]	uncertain significance	11	73360392	73360392	Human		name
401742838	CV2697877	single nucleotide variant	NM_014786.4(ARHGEF17):c.3104C>T (p.Pro1035Leu)	not specified [RCV004300589]	likely benign	11	73311742	73311742	Human		name
401765084	CV2701822	single nucleotide variant	NM_014786.4(ARHGEF17):c.5219C>G (p.Ser1740Cys)	not specified [RCV004314211]	uncertain significance	11	73363428	73363428	Human		name
401734633	CV2709560	single nucleotide variant	NM_014786.4(ARHGEF17):c.3896C>T (p.Ala1299Val)	not specified [RCV004318792]	uncertain significance	11	73357029	73357029	Human		name
401762742	CV2710298	single nucleotide variant	NM_014786.4(ARHGEF17):c.4342T>C (p.Ser1448Pro)	not specified [RCV004317481]	uncertain significance	11	73360455	73360455	Human		name
401763165	CV2710465	single nucleotide variant	NM_014786.4(ARHGEF17):c.5870G>A (p.Arg1957Gln)	not specified [RCV004319404]	uncertain significance	11	73365822	73365822	Human		name
401742246	CV2718701	single nucleotide variant	NM_014786.4(ARHGEF17):c.4870G>C (p.Gly1624Arg)	not specified [RCV004328458]	uncertain significance	11	73362608	73362608	Human		name
401767423	CV2727159	single nucleotide variant	NM_014786.4(ARHGEF17):c.5696T>C (p.Val1899Ala)	not specified [RCV004325513]	uncertain significance	11	73365535	73365535	Human		name
401862816	CV2755442	single nucleotide variant	NM_014786.4(ARHGEF17):c.5660A>G (p.His1887Arg)	not specified [RCV004340033]	uncertain significance	11	73365499	73365499	Human		name
401888665	CV2758012	single nucleotide variant	NM_014786.4(ARHGEF17):c.3145G>A (p.Ala1049Thr)	not specified [RCV004339181]	uncertain significance	11	73311783	73311783	Human		name
401889592	CV2758230	single nucleotide variant	NM_014786.4(ARHGEF17):c.3724C>T (p.Arg1242Trp)	not specified [RCV004341594]	uncertain significance	11	73356235	73356235	Human		name
401891691	CV2780671	single nucleotide variant	NM_014786.4(ARHGEF17):c.4798G>C (p.Ala1600Pro)	not specified [RCV004352017]	uncertain significance	11	73362536	73362536	Human		name
401897341	CV2790039	single nucleotide variant	NM_014786.4(ARHGEF17):c.3581G>A (p.Arg1194His)	not specified [RCV004363992]	uncertain significance	11	73355871	73355871	Human		name
405698661	CV3279350	single nucleotide variant	NM_014786.4(ARHGEF17):c.3010G>A (p.Glu1004Lys)	not specified [RCV004425002]	uncertain significance	11	73311648	73311648	Human		name
405698665	CV3279351	single nucleotide variant	NM_014786.4(ARHGEF17):c.3197T>C (p.Met1066Thr)	not specified [RCV004425003]	uncertain significance	11	73346887	73346887	Human		name
405698670	CV3279352	single nucleotide variant	NM_014786.4(ARHGEF17):c.3303C>G (p.Asn1101Lys)	not specified [RCV004425004]	uncertain significance	11	73352862	73352862	Human		name
405698674	CV3279353	single nucleotide variant	NM_014786.4(ARHGEF17):c.3307G>A (p.Val1103Met)	not specified [RCV004425005]	uncertain significance	11	73352866	73352866	Human		name
405698685	CV3279355	single nucleotide variant	NM_014786.4(ARHGEF17):c.3745G>A (p.Glu1249Lys)	not specified [RCV004425007]	uncertain significance	11	73356256	73356256	Human		name
405698690	CV3279356	single nucleotide variant	NM_014786.4(ARHGEF17):c.3859C>T (p.Arg1287Trp)	not specified [RCV004425008]	uncertain significance	11	73356727	73356727	Human		name
405698696	CV3279357	single nucleotide variant	NM_014786.4(ARHGEF17):c.4015A>G (p.Ser1339Gly)	not specified [RCV004425009]	uncertain significance	11	73357255	73357255	Human		name
405698713	CV3279360	single nucleotide variant	NM_014786.4(ARHGEF17):c.4365C>G (p.His1455Gln)	not specified [RCV004425012]	uncertain significance	11	73360478	73360478	Human		name
405698717	CV3279361	single nucleotide variant	NM_014786.4(ARHGEF17):c.4376G>A (p.Arg1459His)	not specified [RCV004425013]	uncertain significance	11	73360489	73360489	Human		name
405698727	CV3279363	single nucleotide variant	NM_014786.4(ARHGEF17):c.4567G>C (p.Gly1523Arg)	not specified [RCV004425015]	uncertain significance	11	73362112	73362112	Human		name
405698732	CV3279364	single nucleotide variant	NM_014786.4(ARHGEF17):c.4780G>A (p.Glu1594Lys)	not specified [RCV004425016]	uncertain significance	11	73362518	73362518	Human		name
405698739	CV3279365	single nucleotide variant	NM_014786.4(ARHGEF17):c.4867C>G (p.Leu1623Val)	not specified [RCV004425017]	uncertain significance	11	73362605	73362605	Human		name
405698745	CV3279366	single nucleotide variant	NM_014786.4(ARHGEF17):c.5009C>T (p.Pro1670Leu)	not specified [RCV004425018]	uncertain significance	11	73363218	73363218	Human		name
405698750	CV3279367	single nucleotide variant	NM_014786.4(ARHGEF17):c.5175C>A (p.Ser1725Arg)	not specified [RCV004425019]	uncertain significance	11	73363384	73363384	Human		name
405698755	CV3279368	single nucleotide variant	NM_014786.4(ARHGEF17):c.5189T>C (p.Leu1730Pro)	not specified [RCV004425020]	uncertain significance	11	73363398	73363398	Human		name
405698767	CV3279370	single nucleotide variant	NM_014786.4(ARHGEF17):c.5513G>A (p.Arg1838Gln)	not specified [RCV004425022]	uncertain significance	11	73364563	73364563	Human		name
405698773	CV3279371	single nucleotide variant	NM_014786.4(ARHGEF17):c.5755G>A (p.Ala1919Thr)	not specified [RCV004425023]	uncertain significance	11	73365707	73365707	Human		name
405698782	CV3279372	single nucleotide variant	NM_014786.4(ARHGEF17):c.5975C>T (p.Pro1992Leu)	not specified [RCV004425024]	uncertain significance	11	73365927	73365927	Human		name
405698786	CV3279373	single nucleotide variant	NM_014786.4(ARHGEF17):c.6005A>T (p.Lys2002Met)	not specified [RCV004425025]	uncertain significance	11	73367593	73367593	Human		name
405698792	CV3279374	single nucleotide variant	NM_014786.4(ARHGEF17):c.6120T>A (p.Ser2040Arg)	not specified [RCV004425026]	uncertain significance	11	73367708	73367708	Human		name
407467857	CV3465074	single nucleotide variant	NM_014786.4(ARHGEF17):c.3071C>T (p.Pro1024Leu)	not specified [RCV004660898]	uncertain significance	11	73311709	73311709	Human		name
407507502	CV3465121	single nucleotide variant	NM_014786.4(ARHGEF17):c.6039G>C (p.Trp2013Cys)	not specified [RCV004671746]	uncertain significance	11	73367627	73367627	Human		name
407468002	CV3468895	single nucleotide variant	NM_014786.4(ARHGEF17):c.4865G>T (p.Gly1622Val)	not specified [RCV004660807]	uncertain significance	11	73362603	73362603	Human		name
407507377	CV3468900	single nucleotide variant	NM_014786.4(ARHGEF17):c.4815G>T (p.Gln1605His)	not specified [RCV004671702]	uncertain significance	11	73362553	73362553	Human		name
407507395	CV3468923	single nucleotide variant	NM_014786.4(ARHGEF17):c.4862C>T (p.Pro1621Leu)	not specified [RCV004671710]	uncertain significance	11	73362600	73362600	Human		name
407467783	CV3468976	single nucleotide variant	NM_014786.4(ARHGEF17):c.4526G>A (p.Cys1509Tyr)	not specified [RCV004660870]	uncertain significance	11	73362071	73362071	Human		name
407507449	CV3468997	single nucleotide variant	NM_014786.4(ARHGEF17):c.5282A>G (p.Asp1761Gly)	not specified [RCV004671725]	uncertain significance	11	73363782	73363782	Human		name
407507459	CV3469007	single nucleotide variant	NM_014786.4(ARHGEF17):c.4373C>T (p.Ala1458Val)	not specified [RCV004671728]	uncertain significance	11	73360486	73360486	Human		name
597771478	CV3581552	single nucleotide variant	NM_014786.4(ARHGEF17):c.4378C>G (p.Leu1460Val)	not specified [RCV004851346]	uncertain significance	11	73360491	73360491	Human		name
597771530	CV3581563	single nucleotide variant	NM_014786.4(ARHGEF17):c.3965G>A (p.Arg1322Gln)	not specified [RCV004851357]	uncertain significance	11	73357098	73357098	Human		name
597771685	CV3581593	single nucleotide variant	NM_014786.4(ARHGEF17):c.3527G>A (p.Arg1176His)	not specified [RCV004851387]	uncertain significance	11	73355606	73355606	Human		name
597771739	CV3581603	single nucleotide variant	NM_014786.4(ARHGEF17):c.4528C>G (p.Pro1510Ala)	not specified [RCV004851397]	uncertain significance	11	73362073	73362073	Human		name
597771849	CV3581624	single nucleotide variant	NM_014786.4(ARHGEF17):c.5506C>G (p.Gln1836Glu)	not specified [RCV004851418]	uncertain significance	11	73364556	73364556	Human		name
597771943	CV3581648	single nucleotide variant	NM_014786.4(ARHGEF17):c.3757A>G (p.Lys1253Glu)	not specified [RCV004851436]	uncertain significance	11	73356268	73356268	Human		name
597772055	CV3581678	single nucleotide variant	NM_014786.4(ARHGEF17):c.3395G>A (p.Arg1132Gln)	not specified [RCV004851458]	uncertain significance	11	73352954	73352954	Human		name
597772210	CV3581708	single nucleotide variant	NM_014786.4(ARHGEF17):c.3065C>A (p.Pro1022Gln)	not specified [RCV004851489]	uncertain significance	11	73311703	73311703	Human		name
597772420	CV3581747	single nucleotide variant	NM_014786.4(ARHGEF17):c.5932G>A (p.Ala1978Thr)	not specified [RCV004851528]	likely benign	11	73365884	73365884	Human		name
597772480	CV3581758	single nucleotide variant	NM_014786.4(ARHGEF17):c.6025C>T (p.Arg2009Trp)	not specified [RCV004851539]	uncertain significance	11	73367613	73367613	Human		name
597772528	CV3581777	single nucleotide variant	NM_014786.4(ARHGEF17):c.4339G>A (p.Asp1447Asn)	not specified [RCV004851548]	uncertain significance	11	73360452	73360452	Human		name
597772562	CV3581784	single nucleotide variant	NM_014786.4(ARHGEF17):c.3755A>G (p.Asn1252Ser)	not specified [RCV004851554]	uncertain significance	11	73356266	73356266	Human		name
597772646	CV3581801	single nucleotide variant	NM_014786.4(ARHGEF17):c.4893G>C (p.Glu1631Asp)	not specified [RCV004851570]	uncertain significance	11	73362631	73362631	Human		name
597771184	CV3584894	single nucleotide variant	NM_014786.4(ARHGEF17):c.5651G>C (p.Cys1884Ser)	not specified [RCV004851281]	uncertain significance	11	73365490	73365490	Human		name
597771192	CV3584902	single nucleotide variant	NM_014786.4(ARHGEF17):c.4124A>G (p.Lys1375Arg)	not specified [RCV004851283]	uncertain significance	11	73359870	73359870	Human		name
597771206	CV3584923	single nucleotide variant	NM_014786.4(ARHGEF17):c.4283C>T (p.Ala1428Val)	not specified [RCV004851286]	uncertain significance	11	73360396	73360396	Human		name
598128843	CV3886642	single nucleotide variant	NM_014786.4(ARHGEF17):c.5110G>A (p.Gly1704Ser)	not provided [RCV005244302]	likely benign	11	73363319	73363319	Human		name
598128999	CV3886802	single nucleotide variant	NM_014786.4(ARHGEF17):c.4715G>A (p.Arg1572Lys)	not provided [RCV005244462]	likely benign	11	73362453	73362453	Human		name
598129197	CV3888490	single nucleotide variant	NM_014786.4(ARHGEF17):c.4685G>C (p.Arg1562Pro)	not provided [RCV005244664]	uncertain significance	11	73362230	73362230	Human		name
598160034	CV3897324	single nucleotide variant	NM_014786.4(ARHGEF17):c.3719C>T (p.Ala1240Val)	not specified [RCV005260892]	uncertain significance	11	73356230	73356230	Human		name
598160112	CV3897344	single nucleotide variant	NM_014786.4(ARHGEF17):c.4959C>G (p.Ser1653Arg)	not specified [RCV005260912]	uncertain significance	11	73362697	73362697	Human		name
598160162	CV3897355	single nucleotide variant	NM_014786.4(ARHGEF17):c.4523G>A (p.Ser1508Asn)	not specified [RCV005260923]	uncertain significance	11	73362068	73362068	Human		name
598160195	CV3897363	single nucleotide variant	NM_014786.4(ARHGEF17):c.6042C>A (p.His2014Gln)	not specified [RCV005260931]	uncertain significance	11	73367630	73367630	Human		name
598160329	CV3897392	single nucleotide variant	NM_014786.4(ARHGEF17):c.4175A>G (p.Lys1392Arg)	not specified [RCV005260959]	uncertain significance	11	73359921	73359921	Human		name
598168579	CV3897432	single nucleotide variant	NM_014786.4(ARHGEF17):c.5641G>T (p.Ala1881Ser)	not specified [RCV005262645]	uncertain significance	11	73365480	73365480	Human		name
598168826	CV3897472	single nucleotide variant	NM_014786.4(ARHGEF17):c.5983C>G (p.Pro1995Ala)	not specified [RCV005262684]	likely benign	11	73365935	73365935	Human		name
598169136	CV3897521	single nucleotide variant	NM_014786.4(ARHGEF17):c.5161T>G (p.Phe1721Val)	not specified [RCV005262733]	uncertain significance	11	73363370	73363370	Human		name
598159595	CV3901091	single nucleotide variant	NM_014786.4(ARHGEF17):c.5827G>A (p.Val1943Ile)	not specified [RCV005260773]	uncertain significance	11	73365779	73365779	Human		name
598159928	CV3901183	single nucleotide variant	NM_014786.4(ARHGEF17):c.3767G>A (p.Arg1256Gln)	not specified [RCV005260863]	uncertain significance	11	73356278	73356278	Human		name
598159963	CV3901193	single nucleotide variant	NM_014786.4(ARHGEF17):c.4282G>A (p.Ala1428Thr)	not specified [RCV005260872]	uncertain significance	11	73360395	73360395	Human		name

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