Arhgap30 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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104 records found for search term Arhgap30

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8574974	CV109314	single nucleotide variant	NM_001025598.1(ARHGAP30):c.345+77A>G	Lung cancer [RCV000089839]	uncertain significance	1	161056311	161056311	Human		name
598186001	CV4003268	single nucleotide variant	NM_001025598.2(ARHGAP30):c.5A>G (p.Lys2Arg)	not specified [RCV005395702]	uncertain significance	1	161069620	161069620	Human		name
156004013	CV2400943	single nucleotide variant	NM_001025598.2(ARHGAP30):c.37G>A (p.Ala13Thr)	not specified [RCV004244232]	uncertain significance	1	161069588	161069588	Human		name
401735016	CV2706629	single nucleotide variant	NM_001025598.2(ARHGAP30):c.94G>A (p.Glu32Lys)	not specified [RCV004319209]	uncertain significance	1	161069531	161069531	Human		name
597778072	CV3584082	single nucleotide variant	NM_001025598.2(ARHGAP30):c.94G>C (p.Glu32Gln)	not specified [RCV004852909]	uncertain significance	1	161069531	161069531	Human		name
598129708	CV3887128	single nucleotide variant	NM_001025598.2(ARHGAP30):c.531G>T (p.Leu177=)	not provided [RCV005245188]	likely benign	1	161054371	161054371	Human		name
156381412	CV2215501	single nucleotide variant	NM_001025598.2(ARHGAP30):c.236G>A (p.Arg79His)	not specified [RCV004089290]	uncertain significance	1	161056497	161056497	Human		name
401750601	CV2689468	single nucleotide variant	NM_001025598.2(ARHGAP30):c.221G>A (p.Arg74Gln)	not specified [RCV004308313]	uncertain significance	1	161056512	161056512	Human		name
401933107	CV2806114	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1860G>A (p.Leu620=)	not provided [RCV003409200]	likely benign	1	161049161	161049161	Human		name
156317406	CV2203971	single nucleotide variant	NM_001025598.2(ARHGAP30):c.622C>T (p.Leu208Phe)	not specified [RCV004070014]	uncertain significance	1	161053300	161053300	Human		name
155953199	CV2306378	single nucleotide variant	NM_001025598.2(ARHGAP30):c.683G>C (p.Gly228Ala)	not specified [RCV004163075]	uncertain significance	1	161052779	161052779	Human		name
401744925	CV2698427	single nucleotide variant	NM_001025598.2(ARHGAP30):c.709G>A (p.Ala237Thr)	not specified [RCV004298942]	uncertain significance	1	161052753	161052753	Human		name
401717805	CV2703247	single nucleotide variant	NM_001025598.2(ARHGAP30):c.886G>C (p.Gly296Arg)	not specified [RCV004315613]	uncertain significance	1	161052494	161052494	Human		name
401752935	CV2703520	single nucleotide variant	NM_001025598.2(ARHGAP30):c.707G>A (p.Arg236Gln)	not specified [RCV004317699]	uncertain significance	1	161052755	161052755	Human		name
401893314	CV2765101	single nucleotide variant	NM_001025598.2(ARHGAP30):c.768A>G (p.Ile256Met)	not specified [RCV004337597]	uncertain significance	1	161052694	161052694	Human		name
405685565	CV3282816	single nucleotide variant	NM_001025598.2(ARHGAP30):c.692C>T (p.Ser231Leu)	not specified [RCV004422627]	uncertain significance	1	161052770	161052770	Human		name
407473277	CV3464714	single nucleotide variant	NM_001025598.2(ARHGAP30):c.437A>G (p.Glu146Gly)	not specified [RCV004662703]	uncertain significance	1	161054465	161054465	Human		name
597777787	CV3583959	single nucleotide variant	NM_001025598.2(ARHGAP30):c.403C>T (p.Arg135Trp)	not specified [RCV004852815]	uncertain significance	1	161054648	161054648	Human		name
597777654	CV3583969	single nucleotide variant	NM_001025598.2(ARHGAP30):c.626C>T (p.Thr209Ile)	not specified [RCV004852823]	uncertain significance	1	161053296	161053296	Human		name
597777772	CV3584024	single nucleotide variant	NM_001025598.2(ARHGAP30):c.910C>T (p.Arg304Cys)	not specified [RCV004852854]	uncertain significance	1	161052470	161052470	Human		name
598186047	CV4003275	single nucleotide variant	NM_001025598.2(ARHGAP30):c.514G>A (p.Val172Met)	not specified [RCV005395709]	uncertain significance	1	161054388	161054388	Human		name
598186438	CV4003325	single nucleotide variant	NM_001025598.2(ARHGAP30):c.464T>C (p.Met155Thr)	not specified [RCV005395759]	uncertain significance	1	161054438	161054438	Human		name
155916703	CV2197554	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2437G>A (p.Asp813Asn)	not specified [RCV004081275]	uncertain significance	1	161048584	161048584	Human		name
156019508	CV2230028	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1334G>A (p.Arg445His)	not specified [RCV004105827]	uncertain significance	1	161051400	161051400	Human		name
155921456	CV2240527	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1219T>C (p.Cys407Arg)	not specified [RCV004119187]	uncertain significance	1	161051515	161051515	Human		name
155964943	CV2286802	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2176G>A (p.Ala726Thr)	not specified [RCV004142605]	uncertain significance	1	161048845	161048845	Human		name
155945432	CV2292093	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2843A>G (p.Lys948Arg)	not specified [RCV004160362]	uncertain significance	1	161048178	161048178	Human		name
156299581	CV2306864	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2725T>C (p.Cys909Arg)	not specified [RCV004157396]	uncertain significance	1	161048296	161048296	Human		name
155928321	CV2360000	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2512C>T (p.Arg838Trp)	not specified [RCV004212838]	uncertain significance	1	161048509	161048509	Human		name
156285515	CV2360803	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2711C>G (p.Pro904Arg)	not specified [RCV004213579]	uncertain significance	1	161048310	161048310	Human		name
156073385	CV2365451	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1052G>A (p.Arg351Gln)	not specified [RCV004209527]	uncertain significance	1	161051682	161051682	Human		name
155991917	CV2379257	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1059C>G (p.Ser353Arg)	not specified [RCV004223730]	uncertain significance	1	161051675	161051675	Human		name
156390633	CV2383276	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2207A>C (p.Glu736Ala)	not specified [RCV004222326]	uncertain significance	1	161048814	161048814	Human		name
156079766	CV2384552	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2419T>C (p.Tyr807His)	not specified [RCV004232345]	uncertain significance	1	161048602	161048602	Human		name
156104458	CV2386965	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1676T>G (p.Val559Gly)	not specified [RCV004226723]	uncertain significance	1	161049434	161049434	Human		name
329385348	CV2432092	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1780G>A (p.Ala594Thr)	not specified [RCV004249242]	uncertain significance	1	161049241	161049241	Human		name
329357500	CV2453626	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2492C>T (p.Ala831Val)	not specified [RCV004269288]	uncertain significance	1	161048529	161048529	Human		name
401762601	CV2719992	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2908C>T (p.Arg970Trp)	not specified [RCV004323574]	uncertain significance	1	161048113	161048113	Human		name
401887281	CV2773295	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2768G>A (p.Arg923His)	not specified [RCV004353962]	uncertain significance	1	161048253	161048253	Human		name
401858097	CV2774193	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2804G>A (p.Arg935His)	not specified [RCV004345780]	uncertain significance	1	161048217	161048217	Human		name
401896965	CV2785451	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2934G>C (p.Arg978Ser)	not specified [RCV004362988]	uncertain significance	1	161048087	161048087	Human		name
405685363	CV3282799	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1045A>G (p.Ser349Gly)	not specified [RCV004422610]	uncertain significance	1	161051689	161051689	Human		name
405685367	CV3282800	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1076G>A (p.Ser359Asn)	not specified [RCV004422611]	uncertain significance	1	161051658	161051658	Human		name
405685371	CV3282801	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1363C>T (p.Arg455Trp)	not specified [RCV004422612]	uncertain significance	1	161051371	161051371	Human		name
405685375	CV3282802	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1403T>C (p.Leu468Pro)	not specified [RCV004422613]	uncertain significance	1	161051331	161051331	Human		name
405685381	CV3282803	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1428G>T (p.Lys476Asn)	not specified [RCV004422614]	uncertain significance	1	161049682	161049682	Human		name
405685386	CV3282804	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1453C>A (p.Pro485Thr)	not specified [RCV004422615]	uncertain significance	1	161049657	161049657	Human		name
405685390	CV3282805	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1664A>C (p.Glu555Ala)	not specified [RCV004422616]	uncertain significance	1	161049446	161049446	Human		name
405685397	CV3282806	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1819G>A (p.Glu607Lys)	not specified [RCV004422617]	uncertain significance	1	161049202	161049202	Human		name
405685400	CV3282807	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1856T>C (p.Leu619Pro)	not specified [RCV004422618]	uncertain significance	1	161049165	161049165	Human		name
405685527	CV3282808	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2010C>G (p.Asp670Glu)	not specified [RCV004422619]	uncertain significance	1	161049011	161049011	Human		name
405685531	CV3282809	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2249T>C (p.Ile750Thr)	not specified [RCV004422620]	likely benign	1	161048772	161048772	Human		name
405685535	CV3282810	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2615T>G (p.Val872Gly)	not specified [RCV004422621]	uncertain significance	1	161048406	161048406	Human		name
405685540	CV3282811	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2621G>A (p.Cys874Tyr)	not specified [RCV004422622]	uncertain significance	1	161048400	161048400	Human		name
405685545	CV3282812	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2653A>T (p.Met885Leu)	not specified [RCV004422623]	uncertain significance	1	161048368	161048368	Human		name
405685550	CV3282813	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2737T>A (p.Cys913Ser)	not specified [RCV004422624]	uncertain significance	1	161048284	161048284	Human		name
407473078	CV3464642	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1822G>A (p.Val608Ile)	not specified [RCV004662654]	uncertain significance	1	161049199	161049199	Human		name
407473102	CV3464652	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2969G>C (p.Arg990Thr)	not specified [RCV004662660]	uncertain significance	1	161048052	161048052	Human		name
407499300	CV3464662	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2573A>G (p.Glu858Gly)	not specified [RCV004669257]	uncertain significance	1	161048448	161048448	Human		name
407473157	CV3464673	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1821A>T (p.Glu607Asp)	not specified [RCV004662673]	uncertain significance	1	161049200	161049200	Human		name
407473183	CV3464684	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1945G>A (p.Gly649Arg)	not specified [RCV004662680]	uncertain significance	1	161049076	161049076	Human		name
407473208	CV3464694	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2774C>A (p.Ala925Asp)	not specified [RCV004662686]	uncertain significance	1	161048247	161048247	Human		name
407473244	CV3464705	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1942G>A (p.Gly648Ser)	not specified [RCV004662695]	uncertain significance	1	161049079	161049079	Human		name
407473305	CV3464724	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1717G>A (p.Asp573Asn)	not specified [RCV004662710]	uncertain significance	1	161049304	161049304	Human		name
407499339	CV3468574	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1811A>C (p.Asn604Thr)	not specified [RCV004669249]	uncertain significance	1	161049210	161049210	Human		name
597778196	CV3580659	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1799T>C (p.Val600Ala)	not specified [RCV004852942]	likely benign	1	161049222	161049222	Human		name
597777871	CV3583931	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1367C>G (p.Pro456Arg)	not specified [RCV004852793]	uncertain significance	1	161051367	161051367	Human		name
597777864	CV3583939	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1444G>A (p.Ala482Thr)	not specified [RCV004852795]	uncertain significance	1	161049666	161049666	Human		name
597777659	CV3583977	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2509G>A (p.Glu837Lys)	not specified [RCV004852824]	uncertain significance	1	161048512	161048512	Human		name
597777672	CV3583988	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2357T>A (p.Val786Glu)	not specified [RCV004852828]	uncertain significance	1	161048664	161048664	Human		name
597777707	CV3583998	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1177C>T (p.Arg393Trp)	not specified [RCV004852837]	uncertain significance	1	161051557	161051557	Human		name
597777745	CV3584008	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2645C>T (p.Ser882Phe)	not specified [RCV004852847]	uncertain significance	1	161048376	161048376	Human		name
597777768	CV3584016	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1027G>A (p.Gly343Arg)	not specified [RCV004852853]	uncertain significance	1	161051707	161051707	Human		name
597777969	CV3584055	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2434A>G (p.Lys812Glu)	not specified [RCV004852882]	likely benign	1	161048587	161048587	Human		name
597778041	CV3584074	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2651A>T (p.Glu884Val)	not specified [RCV004852901]	uncertain significance	1	161048370	161048370	Human		name
597778113	CV3584094	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1486C>T (p.Pro496Ser)	not specified [RCV004852920]	uncertain significance	1	161049624	161049624	Human		name
597778153	CV3584105	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2936C>T (p.Ala979Val)	not specified [RCV004852931]	uncertain significance	1	161048085	161048085	Human		name
598185873	CV4003248	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1931C>T (p.Ala644Val)	not specified [RCV005395682]	uncertain significance	1	161049090	161049090	Human		name
598185932	CV4003258	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2122G>C (p.Gly708Arg)	not specified [RCV005395692]	uncertain significance	1	161048899	161048899	Human		name
598186130	CV4003285	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2287G>T (p.Val763Leu)	not specified [RCV005395719]	uncertain significance	1	161048734	161048734	Human		name
598186205	CV4003295	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2948G>C (p.Arg983Pro)	not specified [RCV005395729]	uncertain significance	1	161048073	161048073	Human		name
598186280	CV4003304	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1861G>A (p.Gly621Arg)	not specified [RCV005395738]	uncertain significance	1	161049160	161049160	Human		name
598186355	CV4003314	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2200G>A (p.Val734Met)	not specified [RCV005395748]	uncertain significance	1	161048821	161048821	Human		name
598185416	CV4007119	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1976A>T (p.Glu659Val)	not specified [RCV005395610]	uncertain significance	1	161049045	161049045	Human		name
598185468	CV4007128	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2619C>G (p.Asp873Glu)	not specified [RCV005395619]	uncertain significance	1	161048402	161048402	Human		name
598185512	CV4007135	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1060C>A (p.Pro354Thr)	not specified [RCV005395626]	uncertain significance	1	161051674	161051674	Human		name
598185562	CV4007143	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2332G>A (p.Val778Ile)	not specified [RCV005395634]	uncertain significance	1	161048689	161048689	Human		name
598185679	CV4007162	single nucleotide variant	NM_001025598.2(ARHGAP30):c.2791G>A (p.Val931Ile)	not specified [RCV005395653]	uncertain significance	1	161048230	161048230	Human		name
598185732	CV4007170	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1216C>T (p.Arg406Cys)	not specified [RCV005395661]	uncertain significance	1	161051518	161051518	Human		name
598185796	CV4007180	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1628C>G (p.Pro543Arg)	not specified [RCV005395671]	uncertain significance	1	161049482	161049482	Human		name
8629044	CV84187	single nucleotide variant	NM_001025598.1(ARHGAP30):c.2017G>A (p.Glu673Lys)	Malignant melanoma [RCV000064268]	not provided	1	161049004	161049004	Human		name
8629045	CV84188	single nucleotide variant	NM_001025598.2(ARHGAP30):c.1477G>A (p.Asp493Asn)	not specified [RCV004217525]	uncertain significance\|not provided	1	161049633	161049633	Human		name
156316960	CV2193133	single nucleotide variant	NM_001025598.2(ARHGAP30):c.3175G>A (p.Gly1059Arg)	not specified [RCV004071134]	uncertain significance	1	161047846	161047846	Human		name
156249452	CV2264104	single nucleotide variant	NM_001025598.2(ARHGAP30):c.3122C>T (p.Ala1041Val)	not specified [RCV004138114]	uncertain significance	1	161047899	161047899	Human		name
156071552	CV2337763	single nucleotide variant	NM_001025598.2(ARHGAP30):c.3250C>T (p.Arg1084Cys)	not specified [RCV004183782]	uncertain significance	1	161047771	161047771	Human		name
156235145	CV2346335	single nucleotide variant	NM_001025598.2(ARHGAP30):c.3217C>A (p.Pro1073Thr)	not specified [RCV004203819]	uncertain significance	1	161047804	161047804	Human		name
155935980	CV2379743	single nucleotide variant	NM_001025598.2(ARHGAP30):c.3134G>A (p.Arg1045Gln)	not specified [RCV004219863]	uncertain significance	1	161047887	161047887	Human		name
405685554	CV3282814	single nucleotide variant	NM_001025598.2(ARHGAP30):c.3041G>A (p.Gly1014Glu)	not specified [RCV004422625]	uncertain significance	1	161047980	161047980	Human		name
405685559	CV3282815	single nucleotide variant	NM_001025598.2(ARHGAP30):c.3187C>T (p.Arg1063Trp)	not specified [RCV004422626]	uncertain significance	1	161047834	161047834	Human		name
407473016	CV3468566	single nucleotide variant	NM_001025598.2(ARHGAP30):c.3259T>C (p.Tyr1087His)	not specified [RCV004662640]	uncertain significance	1	161047762	161047762	Human		name
597777826	CV3583949	single nucleotide variant	NM_001025598.2(ARHGAP30):c.3096A>C (p.Arg1032Ser)	not specified [RCV004852805]	uncertain significance	1	161047925	161047925	Human		name
597777894	CV3584035	single nucleotide variant	NM_001025598.2(ARHGAP30):c.3070G>A (p.Gly1024Ser)	not specified [RCV004852862]	uncertain significance	1	161047951	161047951	Human		name
597777935	CV3584046	single nucleotide variant	NM_001025598.2(ARHGAP30):c.3295G>A (p.Glu1099Lys)	not specified [RCV004852873]	uncertain significance	1	161047726	161047726	Human		name
597778009	CV3584065	single nucleotide variant	NM_001025598.2(ARHGAP30):c.3193C>T (p.Arg1065Cys)	not specified [RCV004852892]	uncertain significance	1	161047828	161047828	Human		name

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