Cyb561 Variant Search Result - Rat Genome Database

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89 records found for search term Cyb561

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405283766	CV3199680	single nucleotide variant	NM_001915.4(CYB561):c.-13-2648G>A	CYB561-related disorder [RCV003979347]	benign	17	63440208	63440208	Human		name , trait , alternate_id
405288355	CV3197323	single nucleotide variant	NM_001915.4(CYB561):c.24C>T (p.Ala8=)	CYB561-related disorder [RCV003982419]	likely benign	17	63437524	63437524	Human		name , trait , alternate_id
405280553	CV3195606	single nucleotide variant	NM_001915.4(CYB561):c.207G>A (p.Leu69=)	CYB561-related disorder [RCV003906847]	benign	17	63436148	63436148	Human		name , trait , alternate_id
405260497	CV3204096	single nucleotide variant	NM_001915.4(CYB561):c.561C>T (p.Leu187=)	CYB561-related disorder [RCV003943967]	likely benign	17	63435088	63435088	Human		name , trait , alternate_id
405286963	CV3205560	single nucleotide variant	NM_001915.4(CYB561):c.606C>T (p.Asn202=)	CYB561-related disorder [RCV003959705]	likely benign	17	63434552	63434552	Human		name , trait , alternate_id
405290656	CV3207609	single nucleotide variant	NM_001915.4(CYB561):c.318C>T (p.Phe106=)	CYB561-related disorder [RCV003927176]	likely benign	17	63435775	63435775	Human		name , trait , alternate_id
405665903	CV3239394	single nucleotide variant	NM_001915.4(CYB561):c.44A>T (p.Tyr15Phe)	not specified [RCV004367638]	uncertain significance	17	63437504	63437504	Human		name
598236837	CV3956220	single nucleotide variant	NM_001915.4(CYB561):c.98C>T (p.Ala33Val)	not specified [RCV005320518]	uncertain significance	17	63437450	63437450	Human		name
156284056	CV2317508	single nucleotide variant	NM_001915.4(CYB561):c.278T>C (p.Phe93Ser)	not specified [RCV004172466]	uncertain significance	17	63436077	63436077	Human		name
597656028	CV3657947	single nucleotide variant	NM_001915.4(CYB561):c.235G>T (p.Ala79Ser)	not specified [RCV004911075]	uncertain significance	17	63436120	63436120	Human		name
597656020	CV3657948	single nucleotide variant	NM_001915.4(CYB561):c.236C>G (p.Ala79Gly)	not specified [RCV004911076]	uncertain significance	17	63436119	63436119	Human		name
13828198	CV581700	single nucleotide variant	NM_001915.4(CYB561):c.262G>A (p.Gly88Arg)	Orthostatic hypotension 2 [RCV000721911]	pathogenic	17	63436093	63436093	Human	1	name
13828199	CV581701	single nucleotide variant	NM_001915.4(CYB561):c.131G>A (p.Trp44Ter)	Orthostatic hypotension 2 [RCV000721912]	pathogenic	17	63437417	63437417	Human	1	name
156116763	CV2209110	single nucleotide variant	NM_001915.4(CYB561):c.439G>C (p.Gly147Arg)	not specified [RCV004093337]	uncertain significance	17	63435210	63435210	Human		name
155918454	CV2236833	single nucleotide variant	NM_001915.4(CYB561):c.343G>A (p.Ala115Thr)	not specified [RCV004112594]	uncertain significance	17	63435750	63435750	Human		name
156001384	CV2284476	single nucleotide variant	NM_001915.4(CYB561):c.640G>A (p.Ala214Thr)	not specified [RCV004140662]	uncertain significance	17	63434518	63434518	Human		name
156285643	CV2345599	single nucleotide variant	NM_001915.4(CYB561):c.337G>A (p.Gly113Ser)	not specified [RCV004205552]	uncertain significance	17	63435756	63435756	Human		name
156143316	CV2358566	single nucleotide variant	NM_001915.4(CYB561):c.464G>A (p.Arg155His)	not specified [RCV004207448]	uncertain significance	17	63435185	63435185	Human		name
156288192	CV2370619	single nucleotide variant	NM_001915.4(CYB561):c.457C>T (p.Arg153Trp)	not specified [RCV004215941]	uncertain significance	17	63435192	63435192	Human		name
155930698	CV2399706	single nucleotide variant	NM_001915.4(CYB561):c.319G>A (p.Asp107Asn)	not specified [RCV004245525]	uncertain significance	17	63435774	63435774	Human		name
329358513	CV2425279	single nucleotide variant	NM_001915.4(CYB561):c.728C>T (p.Thr243Met)	not specified [RCV004250948]	uncertain significance	17	63434430	63434430	Human		name
329399948	CV2444401	single nucleotide variant	NM_001915.4(CYB561):c.463C>T (p.Arg155Cys)	not specified [RCV004263144]	uncertain significance	17	63435186	63435186	Human		name
401872169	CV2754288	single nucleotide variant	NM_001915.4(CYB561):c.418T>C (p.Phe140Leu)	not specified [RCV004334466]	uncertain significance	17	63435231	63435231	Human		name
401872172	CV2754289	single nucleotide variant	NM_001915.4(CYB561):c.424T>C (p.Phe142Leu)	not specified [RCV004334467]	uncertain significance	17	63435225	63435225	Human		name
401861264	CV2755509	single nucleotide variant	NM_001915.4(CYB561):c.514G>A (p.Val172Met)	not specified [RCV004340093]	uncertain significance	17	63435135	63435135	Human		name
405665907	CV3239395	single nucleotide variant	NM_001915.4(CYB561):c.650A>G (p.Tyr217Cys)	not specified [RCV004367639]	uncertain significance	17	63434508	63434508	Human		name
405665912	CV3239396	single nucleotide variant	NM_001915.4(CYB561):c.676C>T (p.Arg226Trp)	not specified [RCV004367640]	uncertain significance	17	63434482	63434482	Human		name
405665917	CV3239397	single nucleotide variant	NM_001915.4(CYB561):c.701C>G (p.Ala234Gly)	not specified [RCV004367641]	uncertain significance	17	63434457	63434457	Human		name
598236843	CV3956221	single nucleotide variant	NM_001915.4(CYB561):c.739A>G (p.Ser247Gly)	not specified [RCV005320519]	uncertain significance	17	63434419	63434419	Human		name
598236848	CV3956222	single nucleotide variant	NM_001915.4(CYB561):c.502T>C (p.Phe168Leu)	not specified [RCV005320520]	uncertain significance	17	63435147	63435147	Human		name
405665930	CV3239400	single nucleotide variant	NM_153611.6(CYB561A3):c.-9G>A	not specified [RCV004367644]	likely benign	11	61356722	61356722	Human		name
155986389	CV2345503	single nucleotide variant	NM_153611.6(CYB561A3):c.-12T>C	not specified [RCV004198268]	uncertain significance	11	61356725	61356725	Human		name
156400114	CV2198975	single nucleotide variant	NM_182580.3(CYB561D1):c.148+307T>C	not specified [RCV004080386]	uncertain significance	1	109494594	109494594	Human		name
156075079	CV2247989	single nucleotide variant	NM_182580.3(CYB561D1):c.148+283G>C	not specified [RCV004121415]	uncertain significance	1	109494570	109494570	Human		name
155986545	CV2247990	single nucleotide variant	NM_182580.3(CYB561D1):c.148+287T>C	not specified [RCV004121416]	likely benign	1	109494574	109494574	Human		name
156287762	CV2327349	single nucleotide variant	NM_153611.6(CYB561A3):c.-15-491A>G	not specified [RCV004174783]	uncertain significance	11	61357219	61357219	Human		name
155926862	CV2365832	single nucleotide variant	NM_182580.3(CYB561D1):c.148+253G>A	not specified [RCV004214367]	likely benign	1	109494540	109494540	Human		name
405867492	CV2842267	single nucleotide variant	NM_182580.3(CYB561D1):c.148+293A>T	EBV-positive nodal T- and NK-cell lymphoma [RCV004560216]	likely benign	1	109494580	109494580	Human		name
405665937	CV3239401	single nucleotide variant	NM_182580.3(CYB561D1):c.148+282G>T	not specified [RCV004367645]	uncertain significance	1	109494569	109494569	Human		name
405665944	CV3239402	single nucleotide variant	NM_182580.3(CYB561D1):c.148+319G>A	not specified [RCV004367646]	uncertain significance	1	109494606	109494606	Human		name
401725771	CV2687250	single nucleotide variant	NM_182580.3(CYB561D1):c.18A>G (p.Val6=)	not specified [RCV004298191]	likely benign	1	109494157	109494157	Human		name
598236857	CV3956224	single nucleotide variant	NM_182580.3(CYB561D1):c.7C>T (p.Pro3Ser)	not specified [RCV005320522]	uncertain significance	1	109494146	109494146	Human		name
156335136	CV2333484	single nucleotide variant	NM_153611.6(CYB561A3):c.13C>T (p.Arg5Trp)	not specified [RCV004190181]	likely benign	11	61356701	61356701	Human		name
597655977	CV3657953	single nucleotide variant	NM_153611.6(CYB561A3):c.14G>A (p.Arg5Gln)	not specified [RCV004911081]	uncertain significance	11	61356700	61356700	Human		name
597655568	CV3657961	single nucleotide variant	NM_182580.3(CYB561D1):c.192C>T (p.Cys64=)	not specified [RCV004911089]	likely benign	1	109495761	109495761	Human		name
401782452	CV2719822	single nucleotide variant	NM_182580.3(CYB561D1):c.32C>T (p.Ala11Val)	not specified [RCV004329242]	uncertain significance	1	109494171	109494171	Human		name
407473529	CV3419997	single nucleotide variant	NM_153611.6(CYB561A3):c.44C>T (p.Ser15Phe)	not specified [RCV004616220]	uncertain significance	11	61356670	61356670	Human		name
597655998	CV3657950	single nucleotide variant	NM_153611.6(CYB561A3):c.97G>A (p.Gly33Ser)	not specified [RCV004911078]	uncertain significance	11	61356617	61356617	Human		name
156074755	CV2248196	single nucleotide variant	NM_153611.6(CYB561A3):c.212C>T (p.Ser71Leu)	not specified [RCV004117588]	uncertain significance	11	61353965	61353965	Human		name
155963707	CV2308303	single nucleotide variant	NM_182580.3(CYB561D1):c.243C>G (p.Phe81Leu)	not specified [RCV004164792]	uncertain significance	1	109495812	109495812	Human		name
156212671	CV2378443	single nucleotide variant	NM_182580.3(CYB561D1):c.124A>G (p.Thr42Ala)	not specified [RCV004226455]	uncertain significance	1	109494263	109494263	Human		name
401781826	CV2678314	single nucleotide variant	NM_182580.3(CYB561D1):c.251G>A (p.Cys84Tyr)	not specified [RCV004290305]	uncertain significance	1	109495820	109495820	Human		name
405665926	CV3239399	single nucleotide variant	NM_153611.6(CYB561A3):c.182G>A (p.Gly61Asp)	not specified [RCV004367643]	uncertain significance	11	61356532	61356532	Human		name
407452302	CV3420000	single nucleotide variant	NM_182580.3(CYB561D1):c.257G>A (p.Arg86Gln)	not specified [RCV004608349]	uncertain significance	1	109495826	109495826	Human		name
597655989	CV3657951	single nucleotide variant	NM_153611.6(CYB561A3):c.122T>G (p.Ile41Ser)	not specified [RCV004911079]	uncertain significance	11	61356592	61356592	Human		name
597655968	CV3657954	single nucleotide variant	NM_182580.3(CYB561D1):c.271C>T (p.Arg91Trp)	not specified [RCV004911082]	uncertain significance	1	109495840	109495840	Human		name
598236852	CV3956223	single nucleotide variant	NM_153611.6(CYB561A3):c.185C>T (p.Ala62Val)	not specified [RCV005320521]	uncertain significance	11	61353992	61353992	Human		name
156066806	CV2193416	single nucleotide variant	NM_153611.6(CYB561A3):c.319C>T (p.His107Tyr)	not specified [RCV004072912]	uncertain significance	11	61353858	61353858	Human		name
155922692	CV2219073	single nucleotide variant	NM_153611.6(CYB561A3):c.334A>G (p.Asn112Asp)	not specified [RCV004087236]	uncertain significance	11	61353843	61353843	Human		name
156127234	CV2223773	single nucleotide variant	NM_182580.3(CYB561D1):c.451C>A (p.Pro151Thr)	not specified [RCV004093849]	uncertain significance	1	109496020	109496020	Human		name
156079919	CV2226584	single nucleotide variant	NM_153611.6(CYB561A3):c.682C>G (p.Pro228Ala)	not specified [RCV004101835]	uncertain significance	11	61351014	61351014	Human		name
155910938	CV2303711	single nucleotide variant	NM_182580.3(CYB561D1):c.320G>T (p.Gly107Val)	not specified [RCV004161778]	uncertain significance	1	109495889	109495889	Human		name
156188627	CV2375401	single nucleotide variant	NM_182580.3(CYB561D1):c.467T>C (p.Val156Ala)	not specified [RCV004232796]	uncertain significance	1	109496036	109496036	Human		name
156227567	CV2392749	single nucleotide variant	NM_153611.6(CYB561A3):c.385G>A (p.Ala129Thr)	not specified [RCV004247120]	uncertain significance	11	61353792	61353792	Human		name
329349762	CV2435245	single nucleotide variant	NM_153611.6(CYB561A3):c.445C>T (p.Arg149Cys)	not specified [RCV004252880]	uncertain significance	11	61353088	61353088	Human		name
329349899	CV2462519	single nucleotide variant	NM_153611.6(CYB561A3):c.673C>T (p.Arg225Cys)	not specified [RCV004276690]	uncertain significance	11	61351023	61351023	Human		name
405665949	CV3239403	single nucleotide variant	NM_182580.3(CYB561D1):c.571C>G (p.Gln191Glu)	not specified [RCV004367647]	uncertain significance	1	109496140	109496140	Human		name
407452306	CV3419998	single nucleotide variant	NM_182580.3(CYB561D1):c.305T>C (p.Leu102Pro)	not specified [RCV004608347]	uncertain significance	1	109495874	109495874	Human		name
407452300	CV3420001	single nucleotide variant	NM_182580.3(CYB561D1):c.349C>T (p.Arg117Cys)	not specified [RCV004608350]	uncertain significance	1	109495918	109495918	Human		name
597693306	CV3657952	single nucleotide variant	NM_153611.6(CYB561A3):c.554A>C (p.Asn185Thr)	not specified [RCV004911080]	uncertain significance	11	61351142	61351142	Human		name
597655959	CV3657955	single nucleotide variant	NM_182580.3(CYB561D1):c.481C>T (p.Arg161Cys)	not specified [RCV004911083]	uncertain significance	1	109496050	109496050	Human		name
597655948	CV3657956	single nucleotide variant	NM_182580.3(CYB561D1):c.668C>T (p.Pro223Leu)	not specified [RCV004911084]	uncertain significance	1	109496237	109496237	Human		name
597655940	CV3657957	single nucleotide variant	NM_182580.3(CYB561D1):c.539C>T (p.Thr180Met)	not specified [RCV004911085]	uncertain significance	1	109496108	109496108	Human		name
597655931	CV3657958	single nucleotide variant	NM_182580.3(CYB561D1):c.446T>C (p.Leu149Pro)	not specified [RCV004911086]	uncertain significance	1	109496015	109496015	Human		name
597655554	CV3657960	single nucleotide variant	NM_182580.3(CYB561D1):c.626C>T (p.Pro209Leu)	not specified [RCV004911088]	uncertain significance	1	109496195	109496195	Human		name
598236861	CV3956225	single nucleotide variant	NM_182580.3(CYB561D1):c.419T>G (p.Val140Gly)	not specified [RCV005320523]	likely benign	1	109495988	109495988	Human		name
598236866	CV3956226	single nucleotide variant	NM_182580.3(CYB561D1):c.464G>T (p.Arg155Met)	not specified [RCV005320524]	uncertain significance	1	109496033	109496033	Human		name
598236870	CV3956227	single nucleotide variant	NM_001291284.2(CYB561D2):c.336C>T (p.Gly112=)	not specified [RCV005320525]	likely benign	3	50353411	50353411	Human		name
405665954	CV3239404	single nucleotide variant	NM_001291284.2(CYB561D2):c.236G>A (p.Arg79Gln)	not specified [RCV004367648]	uncertain significance	3	50353311	50353311	Human		name
405665959	CV3239405	single nucleotide variant	NM_001291284.2(CYB561D2):c.250C>T (p.Arg84Cys)	not specified [RCV004367649]	uncertain significance	3	50353325	50353325	Human		name
407477426	CV3420002	single nucleotide variant	NM_001291284.2(CYB561D2):c.254G>A (p.Cys85Tyr)	not specified [RCV004608351]	uncertain significance	3	50353329	50353329	Human		name
156342429	CV2275257	single nucleotide variant	NM_001291284.2(CYB561D2):c.583G>C (p.Ala195Pro)	not specified [RCV004137040]	uncertain significance	3	50353658	50353658	Human		name
401728288	CV2685988	single nucleotide variant	NM_001291284.2(CYB561D2):c.391G>A (p.Ala131Thr)	not specified [RCV004297005]	uncertain significance	3	50353466	50353466	Human		name
401899788	CV2762302	single nucleotide variant	NM_001291284.2(CYB561D2):c.355C>T (p.Arg119Trp)	not specified [RCV004335418]	likely benign	3	50353430	50353430	Human		name
405665964	CV3239406	single nucleotide variant	NM_001291284.2(CYB561D2):c.356G>T (p.Arg119Leu)	not specified [RCV004367650]	uncertain significance	3	50353431	50353431	Human		name
405665970	CV3239407	single nucleotide variant	NM_001291284.2(CYB561D2):c.458C>T (p.Ala153Val)	not specified [RCV004367651]	uncertain significance	3	50353533	50353533	Human		name
405665974	CV3239408	single nucleotide variant	NM_001291284.2(CYB561D2):c.647A>T (p.Tyr216Phe)	not specified [RCV004367652]	uncertain significance	3	50353722	50353722	Human		name
407477432	CV3420003	single nucleotide variant	NM_001291284.2(CYB561D2):c.446G>A (p.Arg149Gln)	not specified [RCV004608352]	uncertain significance	3	50353521	50353521	Human		name
597655577	CV3657962	single nucleotide variant	NM_001291284.2(CYB561D2):c.431C>T (p.Pro144Leu)	not specified [RCV004911090]	uncertain significance	3	50353506	50353506	Human		name

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