Stox2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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85 records found for search term Stox2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405779494	CV3330829	single nucleotide variant	NM_020225.3(STOX2):c.22A>G (p.Thr8Ala)	not specified [RCV004458407]	uncertain significance	4	183906812	183906812	Human		name
405779522	CV3330834	single nucleotide variant	NM_020225.3(STOX2):c.56C>T (p.Ser19Leu)	not specified [RCV004458412]	uncertain significance	4	183906846	183906846	Human		name
405779533	CV3330836	single nucleotide variant	NM_020225.3(STOX2):c.67T>G (p.Ser23Ala)	not specified [RCV004458414]	uncertain significance	4	183906857	183906857	Human		name
156154939	CV2328709	single nucleotide variant	NM_020225.3(STOX2):c.142G>C (p.Ala48Pro)	not specified [RCV004177945]	uncertain significance	4	183906932	183906932	Human		name
401753193	CV2674809	single nucleotide variant	NM_020225.3(STOX2):c.171T>G (p.Asp57Glu)	not specified [RCV004294088]	uncertain significance	4	184001329	184001329	Human		name
401928646	CV2820290	single nucleotide variant	NM_020225.3(STOX2):c.2325C>T (p.Asn775=)	not provided [RCV003439559]	likely benign	4	184011163	184011163	Human		name
407530155	CV3485601	single nucleotide variant	NM_020225.3(STOX2):c.178C>G (p.Pro60Ala)	not specified [RCV004681698]	uncertain significance	4	184001336	184001336	Human		name
598251754	CV3915955	single nucleotide variant	NM_020225.3(STOX2):c.115C>G (p.Arg39Gly)	not specified [RCV005277953]	uncertain significance	4	183906905	183906905	Human		name
598251767	CV3915959	single nucleotide variant	NM_020225.3(STOX2):c.172G>A (p.Val58Ile)	not specified [RCV005277956]	uncertain significance	4	184001330	184001330	Human		name
8631118	CV86274	single nucleotide variant	NM_020225.1(STOX2):c.1863G>A (p.Lys621=)	Malignant melanoma [RCV000066365]	not provided	4	184010701	184010701	Human		name
155940717	CV2232209	single nucleotide variant	NM_020225.3(STOX2):c.823T>G (p.Phe275Val)	not specified [RCV004105002]	uncertain significance	4	184009661	184009661	Human		name
156074192	CV2248158	single nucleotide variant	NM_020225.3(STOX2):c.342A>T (p.Glu114Asp)	not specified [RCV004117554]	uncertain significance	4	184009180	184009180	Human		name
156083558	CV2289602	single nucleotide variant	NM_020225.3(STOX2):c.836A>G (p.Lys279Arg)	not specified [RCV004148527]	uncertain significance	4	184009674	184009674	Human		name
156077706	CV2318608	single nucleotide variant	NM_020225.3(STOX2):c.898G>A (p.Glu300Lys)	not specified [RCV004173507]	uncertain significance	4	184009736	184009736	Human		name
155920575	CV2343372	single nucleotide variant	NM_020225.3(STOX2):c.962A>G (p.Asp321Gly)	not specified [RCV004194986]	uncertain significance	4	184009800	184009800	Human		name
156088313	CV2359226	single nucleotide variant	NM_020225.3(STOX2):c.567G>T (p.Arg189Ser)	not specified [RCV004212520]	uncertain significance	4	184009405	184009405	Human		name
156162083	CV2371638	single nucleotide variant	NM_020225.3(STOX2):c.436A>G (p.Ile146Val)	not specified [RCV004216879]	uncertain significance	4	184009274	184009274	Human		name
156041218	CV2384422	single nucleotide variant	NM_020225.3(STOX2):c.970G>A (p.Val324Met)	not specified [RCV004229840]	uncertain significance	4	184009808	184009808	Human		name
329376785	CV2455082	single nucleotide variant	NM_020225.3(STOX2):c.697C>A (p.Gln233Lys)	not specified [RCV004272331]	uncertain significance	4	184009535	184009535	Human		name
329360900	CV2463095	single nucleotide variant	NM_020225.3(STOX2):c.743A>G (p.Tyr248Cys)	not specified [RCV004272901]	uncertain significance	4	184009581	184009581	Human		name
405779516	CV3330833	single nucleotide variant	NM_020225.3(STOX2):c.298C>T (p.His100Tyr)	not specified [RCV004458411]	uncertain significance	4	184001456	184001456	Human		name
405779527	CV3330835	single nucleotide variant	NM_020225.3(STOX2):c.605G>A (p.Cys202Tyr)	not specified [RCV004458413]	uncertain significance	4	184009443	184009443	Human		name
407530156	CV3485602	single nucleotide variant	NM_020225.3(STOX2):c.851C>G (p.Ala284Gly)	not specified [RCV004681699]	uncertain significance	4	184009689	184009689	Human		name
597758085	CV3615012	single nucleotide variant	NM_020225.3(STOX2):c.997C>T (p.Leu333Phe)	not specified [RCV004868731]	uncertain significance	4	184009835	184009835	Human		name
597758095	CV3615014	single nucleotide variant	NM_020225.3(STOX2):c.854A>G (p.Asn285Ser)	not specified [RCV004868733]	uncertain significance	4	184009692	184009692	Human		name
597758101	CV3615015	single nucleotide variant	NM_020225.3(STOX2):c.688T>C (p.Ser230Pro)	not specified [RCV004868734]	uncertain significance	4	184009526	184009526	Human		name
597758127	CV3615021	single nucleotide variant	NM_020225.3(STOX2):c.920C>G (p.Pro307Arg)	not specified [RCV004868739]	uncertain significance	4	184009758	184009758	Human		name
598208132	CV3915965	single nucleotide variant	NM_020225.3(STOX2):c.518C>G (p.Pro173Arg)	not specified [RCV005291401]	uncertain significance	4	184009356	184009356	Human		name
598208137	CV3915966	single nucleotide variant	NM_020225.3(STOX2):c.728C>G (p.Thr243Ser)	not specified [RCV005291402]	uncertain significance	4	184009566	184009566	Human		name
598251778	CV3915969	single nucleotide variant	NM_020225.3(STOX2):c.995C>T (p.Ala332Val)	not specified [RCV005277958]	uncertain significance	4	184009833	184009833	Human		name
598208148	CV3915970	single nucleotide variant	NM_020225.3(STOX2):c.689C>G (p.Ser230Cys)	not specified [RCV005291405]	uncertain significance	4	184009527	184009527	Human		name
598251783	CV3915971	single nucleotide variant	NM_020225.3(STOX2):c.905C>T (p.Thr302Met)	not specified [RCV005277959]	uncertain significance	4	184009743	184009743	Human		name
156188654	CV2205829	single nucleotide variant	NM_020225.3(STOX2):c.1705G>A (p.Ala569Thr)	not specified [RCV004076228]	uncertain significance	4	184010543	184010543	Human		name
155980503	CV2263662	single nucleotide variant	NM_020225.3(STOX2):c.2213G>A (p.Arg738Gln)	not specified [RCV004135662]	uncertain significance	4	184011051	184011051	Human		name
155976287	CV2266281	single nucleotide variant	NM_020225.3(STOX2):c.1006A>C (p.Lys336Gln)	not specified [RCV004129112]	uncertain significance	4	184009844	184009844	Human		name
156339518	CV2271427	single nucleotide variant	NM_020225.3(STOX2):c.1574A>T (p.Gln525Leu)	not specified [RCV004136532]	uncertain significance	4	184010412	184010412	Human		name
155962091	CV2285613	single nucleotide variant	NM_020225.3(STOX2):c.1772G>T (p.Cys591Phe)	not specified [RCV004141480]	uncertain significance	4	184010610	184010610	Human		name
155999989	CV2296260	single nucleotide variant	NM_020225.3(STOX2):c.2696G>A (p.Arg899Gln)	not specified [RCV004154164]	uncertain significance	4	184017199	184017199	Human		name
156277195	CV2316591	single nucleotide variant	NM_020225.3(STOX2):c.2651C>T (p.Ala884Val)	not specified [RCV004171839]	uncertain significance	4	184017154	184017154	Human		name
156112274	CV2353413	single nucleotide variant	NM_020225.3(STOX2):c.2276G>A (p.Arg759His)	not specified [RCV004205872]	uncertain significance	4	184011114	184011114	Human		name
155908138	CV2354573	single nucleotide variant	NM_020225.3(STOX2):c.2491G>A (p.Asp831Asn)	not specified [RCV004202548]	uncertain significance	4	184011329	184011329	Human		name
155929343	CV2356770	single nucleotide variant	NM_020225.3(STOX2):c.2133G>T (p.Leu711Phe)	not specified [RCV004202114]	uncertain significance	4	184010971	184010971	Human		name
156346231	CV2377964	single nucleotide variant	NM_020225.3(STOX2):c.1229G>A (p.Gly410Asp)	not specified [RCV004230529]	uncertain significance	4	184010067	184010067	Human		name
156187243	CV2378052	single nucleotide variant	NM_020225.3(STOX2):c.1583T>C (p.Ile528Thr)	not specified [RCV004232613]	uncertain significance	4	184010421	184010421	Human		name
156392124	CV2378298	single nucleotide variant	NM_020225.3(STOX2):c.2231C>T (p.Pro744Leu)	not specified [RCV004226329]	uncertain significance	4	184011069	184011069	Human		name
156134567	CV2379662	single nucleotide variant	NM_020225.3(STOX2):c.2650G>A (p.Ala884Thr)	not specified [RCV004219789]	likely benign	4	184017153	184017153	Human		name
156041044	CV2387676	single nucleotide variant	NM_020225.3(STOX2):c.2249C>T (p.Ala750Val)	not specified [RCV004234219]	likely benign	4	184011087	184011087	Human		name
329399227	CV2469999	single nucleotide variant	NM_020225.3(STOX2):c.1726G>C (p.Gly576Arg)	not specified [RCV004287279]	uncertain significance	4	184010564	184010564	Human		name
401737596	CV2679922	single nucleotide variant	NM_020225.3(STOX2):c.1697C>T (p.Pro566Leu)	not specified [RCV004284205]	uncertain significance	4	184010535	184010535	Human		name
401739539	CV2684099	single nucleotide variant	NM_020225.3(STOX2):c.1510T>G (p.Ser504Ala)	not specified [RCV004295691]	uncertain significance	4	184010348	184010348	Human		name
401772197	CV2687445	single nucleotide variant	NM_020225.3(STOX2):c.2032G>A (p.Gly678Arg)	not specified [RCV004300690]	uncertain significance	4	184010870	184010870	Human		name
401733227	CV2691240	single nucleotide variant	NM_020225.3(STOX2):c.1270C>G (p.His424Asp)	not specified [RCV004303007]	uncertain significance	4	184010108	184010108	Human		name
401778211	CV2700697	single nucleotide variant	NM_020225.3(STOX2):c.1031G>A (p.Arg344Lys)	not specified [RCV004313410]	uncertain significance	4	184009869	184009869	Human		name
401765122	CV2701874	single nucleotide variant	NM_020225.3(STOX2):c.2459A>C (p.Lys820Thr)	not specified [RCV004307836]	uncertain significance	4	184011297	184011297	Human		name
401862353	CV2775238	single nucleotide variant	NM_020225.3(STOX2):c.1690A>G (p.Lys564Glu)	not specified [RCV004348365]	uncertain significance	4	184010528	184010528	Human		name
401892499	CV2782091	single nucleotide variant	NM_020225.3(STOX2):c.1257T>G (p.Asp419Glu)	not specified [RCV004359086]	uncertain significance	4	184010095	184010095	Human		name
405779451	CV3330822	single nucleotide variant	NM_020225.3(STOX2):c.1062C>A (p.Ser354Arg)	not specified [RCV004458400]	uncertain significance	4	184009900	184009900	Human		name
405779460	CV3330823	single nucleotide variant	NM_020225.3(STOX2):c.1205C>T (p.Pro402Leu)	not specified [RCV004458401]	uncertain significance	4	184010043	184010043	Human		name
405779466	CV3330824	single nucleotide variant	NM_020225.3(STOX2):c.1379G>A (p.Arg460Lys)	not specified [RCV004458402]	uncertain significance	4	184010217	184010217	Human		name
405779471	CV3330825	single nucleotide variant	NM_020225.3(STOX2):c.1400T>C (p.Val467Ala)	not specified [RCV004458403]	uncertain significance	4	184010238	184010238	Human		name
405779477	CV3330826	single nucleotide variant	NM_020225.3(STOX2):c.2003C>T (p.Ser668Leu)	not specified [RCV004458404]	uncertain significance	4	184010841	184010841	Human		name
405779482	CV3330827	single nucleotide variant	NM_020225.3(STOX2):c.2149C>A (p.His717Asn)	not specified [RCV004458405]	uncertain significance	4	184010987	184010987	Human		name
405779499	CV3330830	single nucleotide variant	NM_020225.3(STOX2):c.2527C>T (p.Arg843Trp)	not specified [RCV004458408]	uncertain significance	4	184011365	184011365	Human		name
405779505	CV3330831	single nucleotide variant	NM_020225.3(STOX2):c.2584C>T (p.Arg862Cys)	not specified [RCV004458409]	uncertain significance	4	184011422	184011422	Human		name
405779509	CV3330832	single nucleotide variant	NM_020225.3(STOX2):c.2750A>T (p.Asn917Ile)	not specified [RCV004458410]	uncertain significance	4	184017253	184017253	Human		name
407496558	CV3485600	single nucleotide variant	NM_020225.3(STOX2):c.1738G>A (p.Glu580Lys)	not specified [RCV004668176]	uncertain significance	4	184010576	184010576	Human		name
407496562	CV3485603	single nucleotide variant	NM_020225.3(STOX2):c.1588G>A (p.Asp530Asn)	not specified [RCV004668177]	uncertain significance	4	184010426	184010426	Human		name
407496567	CV3485604	single nucleotide variant	NM_020225.3(STOX2):c.1756G>A (p.Gly586Ser)	not specified [RCV004668178]	uncertain significance	4	184010594	184010594	Human		name
597758090	CV3615013	single nucleotide variant	NM_020225.3(STOX2):c.1939T>C (p.Ser647Pro)	not specified [RCV004868732]	uncertain significance	4	184010777	184010777	Human		name
597758107	CV3615016	single nucleotide variant	NM_020225.3(STOX2):c.1462A>G (p.Lys488Glu)	not specified [RCV004868735]	uncertain significance	4	184010300	184010300	Human		name
597758113	CV3615018	single nucleotide variant	NM_020225.3(STOX2):c.1853G>A (p.Gly618Glu)	not specified [RCV004868736]	uncertain significance	4	184010691	184010691	Human		name
597758118	CV3615019	single nucleotide variant	NM_020225.3(STOX2):c.1130G>A (p.Arg377Gln)	not specified [RCV004868737]	uncertain significance	4	184009968	184009968	Human		name
597758123	CV3615020	single nucleotide variant	NM_020225.3(STOX2):c.1523C>T (p.Thr508Met)	not specified [RCV004868738]	uncertain significance	4	184010361	184010361	Human		name
597758132	CV3615022	single nucleotide variant	NM_020225.3(STOX2):c.2717C>T (p.Thr906Ile)	not specified [RCV004868740]	uncertain significance	4	184017220	184017220	Human		name
597758137	CV3615023	single nucleotide variant	NM_020225.3(STOX2):c.1771T>C (p.Cys591Arg)	not specified [RCV004868741]	uncertain significance	4	184010609	184010609	Human		name
598208113	CV3915956	single nucleotide variant	NM_020225.3(STOX2):c.2705C>T (p.Ala902Val)	not specified [RCV005291396]	uncertain significance	4	184017208	184017208	Human		name
598251759	CV3915957	single nucleotide variant	NM_020225.3(STOX2):c.2205G>T (p.Leu735Phe)	not specified [RCV005277954]	uncertain significance	4	184011043	184011043	Human		name
598251764	CV3915958	single nucleotide variant	NM_020225.3(STOX2):c.2361C>G (p.Asn787Lys)	not specified [RCV005277955]	uncertain significance	4	184011199	184011199	Human		name
598251773	CV3915960	single nucleotide variant	NM_020225.3(STOX2):c.1996G>A (p.Ala666Thr)	not specified [RCV005277957]	uncertain significance	4	184010834	184010834	Human		name
598208117	CV3915961	single nucleotide variant	NM_020225.3(STOX2):c.2395G>A (p.Val799Ile)	not specified [RCV005291397]	uncertain significance	4	184011233	184011233	Human		name
598208125	CV3915963	single nucleotide variant	NM_020225.3(STOX2):c.1562A>G (p.Gln521Arg)	not specified [RCV005291399]	uncertain significance	4	184010400	184010400	Human		name
598208128	CV3915964	single nucleotide variant	NM_020225.3(STOX2):c.1742G>A (p.Ser581Asn)	not specified [RCV005291400]	uncertain significance	4	184010580	184010580	Human		name
598208141	CV3915967	single nucleotide variant	NM_020225.3(STOX2):c.2507A>G (p.Gln836Arg)	not specified [RCV005291403]	uncertain significance	4	184011345	184011345	Human		name
598208144	CV3915968	single nucleotide variant	NM_020225.3(STOX2):c.2716A>G (p.Thr906Ala)	not specified [RCV005291404]	uncertain significance	4	184017219	184017219	Human		name
8631117	CV86273	single nucleotide variant	NM_020225.1(STOX2):c.1388C>T (p.Ser463Phe)	Malignant melanoma [RCV000066364]	not provided	4	184010226	184010226	Human		name

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