Arhgap20 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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92 records found for search term Arhgap20

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8652533	CV129108	single nucleotide variant	NM_001258415.1(ARHGAP20):c.896-710G>C	Lung cancer [RCV000109595]	uncertain significance	11	110592865	110592865	Human		name
8652534	CV129109	single nucleotide variant	NM_001258415.1(ARHGAP20):c.896-6231C>T	Lung cancer [RCV000109596]	uncertain significance	11	110598386	110598386	Human		name
598168890	CV4000091	single nucleotide variant	NM_001384657.1(ARHGAP20):c.13T>C (p.Ser5Pro)	not specified [RCV005391966]	uncertain significance	11	110712219	110712219	Human		name
329397866	CV2466387	single nucleotide variant	NM_001384657.1(ARHGAP20):c.59C>T (p.Ser20Phe)	not specified [RCV004273951]	uncertain significance	11	110712173	110712173	Human		name
401717741	CV2706819	single nucleotide variant	NM_001384657.1(ARHGAP20):c.86G>T (p.Gly29Val)	not specified [RCV004321454]	uncertain significance	11	110712146	110712146	Human		name
401749083	CV2713716	single nucleotide variant	NM_001384657.1(ARHGAP20):c.32T>C (p.Leu11Pro)	not specified [RCV004321070]	uncertain significance	11	110712200	110712200	Human		name
598205812	CV4000102	single nucleotide variant	NM_001384657.1(ARHGAP20):c.65C>T (p.Thr22Ile)	not specified [RCV005399524]	uncertain significance	11	110712167	110712167	Human		name
156003330	CV2293455	single nucleotide variant	NM_001384657.1(ARHGAP20):c.202G>A (p.Ala68Thr)	not specified [RCV004152698]	uncertain significance	11	110630779	110630779	Human		name
156199015	CV2312961	single nucleotide variant	NM_001384657.1(ARHGAP20):c.152T>C (p.Ile51Thr)	not specified [RCV004159468]	uncertain significance	11	110690583	110690583	Human		name
156159522	CV2314616	single nucleotide variant	NM_001384657.1(ARHGAP20):c.280C>T (p.Leu94Phe)	not specified [RCV004168697]	uncertain significance	11	110630701	110630701	Human		name
156035934	CV2335032	single nucleotide variant	NM_001384657.1(ARHGAP20):c.271C>G (p.Arg91Gly)	not specified [RCV004184573]	uncertain significance	11	110630710	110630710	Human		name
155976687	CV2342804	single nucleotide variant	NM_001384657.1(ARHGAP20):c.187A>G (p.Arg63Gly)	not specified [RCV004189845]	uncertain significance	11	110690548	110690548	Human		name
156122187	CV2354314	single nucleotide variant	NM_001384657.1(ARHGAP20):c.272G>A (p.Arg91Gln)	not specified [RCV004206731]	uncertain significance	11	110630709	110630709	Human		name
156402572	CV2361702	single nucleotide variant	NM_001384657.1(ARHGAP20):c.101A>G (p.Lys34Arg)	not specified [RCV004223185]	uncertain significance	11	110712131	110712131	Human		name
405684677	CV3282637	single nucleotide variant	NM_001384657.1(ARHGAP20):c.263T>C (p.Ile88Thr)	not specified [RCV004422448]	uncertain significance	11	110630718	110630718	Human		name
407491112	CV3471972	single nucleotide variant	NM_001384657.1(ARHGAP20):c.118C>G (p.Leu40Val)	not specified [RCV004666791]	uncertain significance	11	110690617	110690617	Human		name
9687054	CV171495	single nucleotide variant	NM_001384657.1(ARHGAP20):c.464T>C (p.Val155Ala)	Prostate cancer [RCV000149273]	uncertain significance	11	110624201	110624201	Human	2	name
155917357	CV2202346	single nucleotide variant	NM_001384657.1(ARHGAP20):c.953A>C (p.Gln318Pro)	not specified [RCV004078270]	uncertain significance	11	110606572	110606572	Human		name
155924293	CV2248742	single nucleotide variant	NM_001384657.1(ARHGAP20):c.946G>A (p.Ala316Thr)	not specified [RCV004121900]	uncertain significance	11	110606579	110606579	Human		name
156068295	CV2345948	single nucleotide variant	NM_001384657.1(ARHGAP20):c.934A>T (p.Ser312Cys)	not specified [RCV004198984]	uncertain significance	11	110606591	110606591	Human		name
401782838	CV2707520	single nucleotide variant	NM_001384657.1(ARHGAP20):c.902G>T (p.Arg301Leu)	not specified [RCV004312892]	uncertain significance	11	110606623	110606623	Human		name
401855818	CV2757491	single nucleotide variant	NM_001384657.1(ARHGAP20):c.604G>A (p.Ala202Thr)	not specified [RCV004340875]	uncertain significance	11	110614587	110614587	Human		name
401863060	CV2765908	single nucleotide variant	NM_001384657.1(ARHGAP20):c.550A>C (p.Ile184Leu)	not specified [RCV004337937]	uncertain significance	11	110614641	110614641	Human		name
401877362	CV2769428	single nucleotide variant	NM_001384657.1(ARHGAP20):c.902G>A (p.Arg301Gln)	not specified [RCV004357413]	uncertain significance	11	110606623	110606623	Human		name
401890516	CV2778821	single nucleotide variant	NM_001384657.1(ARHGAP20):c.949G>C (p.Ala317Pro)	not specified [RCV004346718]	uncertain significance	11	110606576	110606576	Human		name
405684701	CV3282642	single nucleotide variant	NM_001384657.1(ARHGAP20):c.913T>C (p.Cys305Arg)	not specified [RCV004422453]	uncertain significance	11	110606612	110606612	Human		name
407531827	CV3471980	single nucleotide variant	NM_001384657.1(ARHGAP20):c.864C>G (p.Phe288Leu)	not specified [RCV004657805]	uncertain significance	11	110606661	110606661	Human		name
597745389	CV3590852	single nucleotide variant	NM_001384657.1(ARHGAP20):c.665C>T (p.Ala222Val)	not specified [RCV004845267]	uncertain significance	11	110611352	110611352	Human		name
597705673	CV3590875	single nucleotide variant	NM_001384657.1(ARHGAP20):c.740A>G (p.Asn247Ser)	not specified [RCV004840267]	uncertain significance	11	110609019	110609019	Human		name
598205834	CV4000128	single nucleotide variant	NM_001384657.1(ARHGAP20):c.366C>G (p.Asn122Lys)	not specified [RCV005399527]	uncertain significance	11	110624299	110624299	Human		name
598205845	CV4000159	single nucleotide variant	NM_001384657.1(ARHGAP20):c.451A>G (p.Met151Val)	not specified [RCV005399530]	uncertain significance	11	110624214	110624214	Human		name
155926652	CV2230655	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2528G>A (p.Arg843Gln)	not specified [RCV004097604]	uncertain significance	11	110580418	110580418	Human		name
155982166	CV2233155	single nucleotide variant	NM_001384657.1(ARHGAP20):c.1786G>A (p.Val596Ile)	not specified [RCV004103768]	uncertain significance	11	110581160	110581160	Human		name
156163955	CV2270228	single nucleotide variant	NM_001384657.1(ARHGAP20):c.1519T>C (p.Phe507Leu)	not specified [RCV004135450]	uncertain significance	11	110583634	110583634	Human		name
156303643	CV2308417	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2387C>G (p.Ser796Cys)	not specified [RCV004166717]	uncertain significance	11	110580559	110580559	Human		name
156190390	CV2325480	single nucleotide variant	NM_001384657.1(ARHGAP20):c.1255G>A (p.Glu419Lys)	not specified [RCV004179931]	uncertain significance	11	110590698	110590698	Human		name
156308338	CV2332301	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2629C>T (p.Leu877Phe)	not specified [RCV004182471]	uncertain significance	11	110580317	110580317	Human		name
156067102	CV2340946	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2564G>T (p.Arg855Leu)	not specified [RCV004181440]	uncertain significance	11	110580382	110580382	Human		name
156179261	CV2374658	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2564G>A (p.Arg855His)	not specified [RCV004225275]	uncertain significance	11	110580382	110580382	Human		name
156069029	CV2381210	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2011C>T (p.Arg671Trp)	not specified [RCV004227280]	uncertain significance	11	110580935	110580935	Human		name
329355576	CV2434308	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2125G>A (p.Asp709Asn)	not specified [RCV004251980]	uncertain significance	11	110580821	110580821	Human		name
329354140	CV2447184	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2368G>A (p.Val790Met)	not specified [RCV004262487]	likely benign	11	110580578	110580578	Human		name
401751422	CV2672447	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2279G>A (p.Ser760Asn)	not specified [RCV004285701]	uncertain significance	11	110580667	110580667	Human		name
401732320	CV2678067	single nucleotide variant	NM_001384657.1(ARHGAP20):c.1030A>G (p.Ser344Gly)	not specified [RCV004296587]	uncertain significance	11	110592090	110592090	Human		name
401739624	CV2684124	single nucleotide variant	NM_001384657.1(ARHGAP20):c.1672C>T (p.Leu558Phe)	not specified [RCV004288804]	uncertain significance	11	110582369	110582369	Human		name
401746171	CV2695515	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2086A>C (p.Ser696Arg)	not specified [RCV004305695]	uncertain significance	11	110580860	110580860	Human		name
401783308	CV2716268	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2992G>T (p.Val998Phe)	not specified [RCV004323486]	uncertain significance	11	110579954	110579954	Human		name
401857387	CV2760134	single nucleotide variant	NM_001384657.1(ARHGAP20):c.1591G>A (p.Glu531Lys)	not specified [RCV004345532]	uncertain significance	11	110583562	110583562	Human		name
401877672	CV2761256	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2785C>T (p.Leu929Phe)	not specified [RCV004341133]	uncertain significance	11	110580161	110580161	Human		name
401884732	CV2761956	single nucleotide variant	NM_001384657.1(ARHGAP20):c.1022G>A (p.Arg341Gln)	not specified [RCV004339579]	uncertain significance	11	110592098	110592098	Human		name
401856179	CV2764432	single nucleotide variant	NM_001384657.1(ARHGAP20):c.1976C>T (p.Pro659Leu)	not specified [RCV004339001]	uncertain significance	11	110580970	110580970	Human		name
401869272	CV2776153	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2550A>G (p.Ile850Met)	not specified [RCV004353242]	uncertain significance	11	110580396	110580396	Human		name
401896367	CV2781154	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2654T>A (p.Leu885His)	not specified [RCV004352206]	uncertain significance	11	110580292	110580292	Human		name
405684658	CV3282633	single nucleotide variant	NM_001384657.1(ARHGAP20):c.1295C>G (p.Ser432Cys)	not specified [RCV004422444]	uncertain significance	11	110590658	110590658	Human		name
405684668	CV3282635	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2005C>A (p.Pro669Thr)	not specified [RCV004422446]	uncertain significance	11	110580941	110580941	Human		name
405684673	CV3282636	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2549T>C (p.Ile850Thr)	not specified [RCV004422447]	uncertain significance	11	110580397	110580397	Human		name
405684682	CV3282638	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2894T>G (p.Val965Gly)	not specified [RCV004422449]	uncertain significance	11	110580052	110580052	Human		name
407531787	CV3471951	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2365C>T (p.His789Tyr)	not specified [RCV004657784]	uncertain significance	11	110580581	110580581	Human		name
407531840	CV3471988	single nucleotide variant	NM_001384657.1(ARHGAP20):c.1346A>C (p.Asp449Ala)	not specified [RCV004657811]	uncertain significance	11	110586285	110586285	Human		name
597744566	CV3590808	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2425A>G (p.Met809Val)	not specified [RCV004845254]	likely benign	11	110580521	110580521	Human		name
597705339	CV3590819	single nucleotide variant	NM_001384657.1(ARHGAP20):c.1822G>A (p.Gly608Ser)	not specified [RCV004840231]	uncertain significance	11	110581124	110581124	Human		name
597705496	CV3590842	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2054A>G (p.Tyr685Cys)	not specified [RCV004840248]	uncertain significance	11	110580892	110580892	Human		name
597705664	CV3590868	single nucleotide variant	NM_001384657.1(ARHGAP20):c.1042G>A (p.Asp348Asn)	not specified [RCV004840266]	uncertain significance	11	110592078	110592078	Human		name
597705684	CV3590879	single nucleotide variant	NM_001384657.1(ARHGAP20):c.1402A>C (p.Asn468His)	not specified [RCV004840268]	uncertain significance	11	110586229	110586229	Human		name
597705748	CV3590888	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2122A>G (p.Ile708Val)	not specified [RCV004840274]	uncertain significance	11	110580824	110580824	Human		name
597705834	CV3590897	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2524C>T (p.His842Tyr)	not specified [RCV004840282]	uncertain significance	11	110580422	110580422	Human		name
597745368	CV3590898	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2705G>A (p.Ser902Asn)	not specified [RCV004845271]	uncertain significance	11	110580241	110580241	Human		name
598168808	CV4000077	single nucleotide variant	NM_001384657.1(ARHGAP20):c.1659A>C (p.Glu553Asp)	not specified [RCV005391953]	uncertain significance	11	110582382	110582382	Human		name
598168986	CV4000113	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2616C>G (p.Ser872Arg)	not specified [RCV005391982]	uncertain significance	11	110580330	110580330	Human		name
598169015	CV4000121	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2570T>A (p.Leu857Gln)	not specified [RCV005391989]	uncertain significance	11	110580376	110580376	Human		name
598169026	CV4000123	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2552A>T (p.Glu851Val)	not specified [RCV005391991]	uncertain significance	11	110580394	110580394	Human		name
598169075	CV4000137	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2241A>T (p.Gln747His)	not specified [RCV005392002]	uncertain significance	11	110580705	110580705	Human		name
598169129	CV4000146	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2821C>T (p.Pro941Ser)	not specified [RCV005392011]	uncertain significance	11	110580125	110580125	Human		name
598169178	CV4000155	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2396T>C (p.Val799Ala)	not specified [RCV005392020]	uncertain significance	11	110580550	110580550	Human		name
156389090	CV2229921	single nucleotide variant	NM_001384657.1(ARHGAP20):c.3152A>G (p.Lys1051Arg)	not specified [RCV004105466]	uncertain significance	11	110579794	110579794	Human		name
156205425	CV2249875	single nucleotide variant	NM_001384657.1(ARHGAP20):c.3221C>A (p.Pro1074His)	not specified [RCV004122854]	uncertain significance	11	110579725	110579725	Human		name
156384183	CV2371314	single nucleotide variant	NM_001384657.1(ARHGAP20):c.3373C>A (p.Pro1125Thr)	not specified [RCV004223325]	uncertain significance	11	110579573	110579573	Human		name
155996219	CV2393156	single nucleotide variant	NM_001384657.1(ARHGAP20):c.3181G>A (p.Glu1061Lys)	not specified [RCV004226633]	uncertain significance	11	110579765	110579765	Human		name
156149738	CV2394599	single nucleotide variant	NM_001384657.1(ARHGAP20):c.3404T>A (p.Leu1135Gln)	not specified [RCV004240947]	uncertain significance	11	110579542	110579542	Human		name
329377633	CV2435983	single nucleotide variant	NM_001384657.1(ARHGAP20):c.3526C>T (p.Pro1176Ser)	not specified [RCV004255205]	uncertain significance	11	110579420	110579420	Human		name
401860516	CV2758510	single nucleotide variant	NM_001384657.1(ARHGAP20):c.3137A>G (p.Lys1046Arg)	not specified [RCV004335560]	uncertain significance	11	110579809	110579809	Human		name
401864584	CV2781872	single nucleotide variant	NM_001384657.1(ARHGAP20):c.3266A>G (p.Glu1089Gly)	not specified [RCV004356815]	uncertain significance	11	110579680	110579680	Human		name
405684688	CV3282639	single nucleotide variant	NM_001384657.1(ARHGAP20):c.2998G>A (p.Gly1000Arg)	not specified [RCV004422450]	uncertain significance	11	110579948	110579948	Human		name
405684693	CV3282640	single nucleotide variant	NM_001384657.1(ARHGAP20):c.3035G>A (p.Arg1012His)	not specified [RCV004422451]	likely benign	11	110579911	110579911	Human		name
405684697	CV3282641	single nucleotide variant	NM_001384657.1(ARHGAP20):c.3553A>G (p.Arg1185Gly)	not specified [RCV004422452]	uncertain significance	11	110579393	110579393	Human		name
407531771	CV3471940	single nucleotide variant	NM_001384657.1(ARHGAP20):c.3007G>A (p.Gly1003Ser)	not specified [RCV004657776]	uncertain significance	11	110579939	110579939	Human		name
407531803	CV3471962	single nucleotide variant	NM_001384657.1(ARHGAP20):c.3349G>A (p.Asp1117Asn)	not specified [RCV004657792]	uncertain significance	11	110579597	110579597	Human		name
407491138	CV3471999	single nucleotide variant	NM_001384657.1(ARHGAP20):c.3191T>C (p.Ile1064Thr)	not specified [RCV004666800]	likely benign	11	110579755	110579755	Human		name
597744498	CV3590789	single nucleotide variant	NM_001384657.1(ARHGAP20):c.3506C>T (p.Ala1169Val)	not specified [RCV004845241]	likely benign	11	110579440	110579440	Human		name
597705406	CV3590831	single nucleotide variant	NM_001384657.1(ARHGAP20):c.3447C>A (p.Ser1149Arg)	not specified [RCV004840238]	uncertain significance	11	110579499	110579499	Human		name
598168852	CV4000085	single nucleotide variant	NM_001384657.1(ARHGAP20):c.3378C>A (p.Phe1126Leu)	not specified [RCV005391960]	uncertain significance	11	110579568	110579568	Human		name
598169054	CV4000132	single nucleotide variant	NM_001384657.1(ARHGAP20):c.3514C>T (p.Pro1172Ser)	not specified [RCV005391997]	uncertain significance	11	110579432	110579432	Human		name

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