Nfx1 Variant Search Result - Rat Genome Database

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79 records found for search term Nfx1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405719412	CV3361817	single nucleotide variant	NM_002504.6(NFX1):c.16C>A (p.Pro6Thr)	not specified [RCV004494980]	uncertain significance	9	33290588	33290588	Human		name
596947493	CV3549050	single nucleotide variant	NM_002504.6(NFX1):c.216T>C (p.Ser72=)	not provided [RCV004811374]	likely benign	9	33294610	33294610	Human		name
405719798	CV3358368	single nucleotide variant	NM_002504.6(NFX1):c.34A>G (p.Lys12Glu)	not specified [RCV004495056]	uncertain significance	9	33294428	33294428	Human		name
405719817	CV3358371	single nucleotide variant	NM_002504.6(NFX1):c.60C>G (p.Phe20Leu)	not specified [RCV004495059]	uncertain significance	9	33294454	33294454	Human		name
156313934	CV2196573	single nucleotide variant	NM_002504.6(NFX1):c.140A>C (p.Asn47Thr)	not specified [RCV004073854]	uncertain significance	9	33294534	33294534	Human		name
156125236	CV2283617	single nucleotide variant	NM_002504.6(NFX1):c.134G>C (p.Arg45Thr)	not specified [RCV004140121]	uncertain significance	9	33294528	33294528	Human		name
156338481	CV2370653	single nucleotide variant	NM_002504.6(NFX1):c.224C>T (p.Pro75Leu)	not specified [RCV004209062]	uncertain significance	9	33294618	33294618	Human		name
156041573	CV2387742	single nucleotide variant	NM_002504.6(NFX1):c.254C>T (p.Thr85Met)	not specified [RCV004234275]	uncertain significance	9	33294648	33294648	Human		name
329395657	CV2454440	single nucleotide variant	NM_002504.6(NFX1):c.202G>C (p.Val68Leu)	not specified [RCV004267945]	uncertain significance	9	33294596	33294596	Human		name
329353598	CV2469333	single nucleotide variant	NM_002504.6(NFX1):c.157C>T (p.Pro53Ser)	not specified [RCV004280664]	uncertain significance	9	33294551	33294551	Human		name
401944297	CV2840691	single nucleotide variant	NM_002504.6(NFX1):c.1638A>G (p.Val546=)	not provided [RCV003457167]	likely benign	9	33318780	33318780	Human		name
405719280	CV3361800	single nucleotide variant	NM_002504.6(NFX1):c.152C>T (p.Pro51Leu)	not specified [RCV004494963]	uncertain significance	9	33294546	33294546	Human		name
405720197	CV3361857	single nucleotide variant	NM_002504.6(NFX1):c.244A>C (p.Ser82Arg)	not specified [RCV004495020]	uncertain significance	9	33294638	33294638	Human		name
407526873	CV3451269	single nucleotide variant	NM_002504.6(NFX1):c.142T>C (p.Tyr48His)	not specified [RCV004654972]	uncertain significance	9	33294536	33294536	Human		name
407526882	CV3451274	single nucleotide variant	NM_002504.6(NFX1):c.125G>A (p.Arg42Lys)	not specified [RCV004654975]	uncertain significance	9	33294519	33294519	Human		name
597656774	CV3559179	single nucleotide variant	NM_002504.6(NFX1):c.145A>G (p.Ser49Gly)	not specified [RCV004834346]	uncertain significance	9	33294539	33294539	Human		name
155965161	CV2308470	single nucleotide variant	NM_002504.6(NFX1):c.823A>G (p.Arg275Gly)	not specified [RCV004166758]	uncertain significance	9	33295217	33295217	Human		name
156216643	CV2386083	single nucleotide variant	NM_002504.6(NFX1):c.952C>T (p.Arg318Trp)	not specified [RCV004229140]	uncertain significance	9	33295346	33295346	Human		name
329401678	CV2457307	single nucleotide variant	NM_002504.6(NFX1):c.350G>C (p.Arg117Thr)	not specified [RCV004267151]	uncertain significance	9	33294744	33294744	Human		name
401879530	CV2755187	single nucleotide variant	NM_002504.6(NFX1):c.896A>G (p.Asn299Ser)	not specified [RCV004337379]	uncertain significance	9	33295290	33295290	Human		name
405719892	CV3358380	single nucleotide variant	NM_002504.6(NFX1):c.924G>C (p.Arg308Ser)	not specified [RCV004495068]	uncertain significance	9	33295318	33295318	Human		name
407496955	CV3451272	single nucleotide variant	NM_002504.6(NFX1):c.962A>T (p.Asp321Val)	not specified [RCV004643630]	uncertain significance	9	33295356	33295356	Human		name
597656745	CV3559175	single nucleotide variant	NM_002504.6(NFX1):c.913A>C (p.Lys305Gln)	not specified [RCV004834342]	uncertain significance	9	33295307	33295307	Human		name
597656787	CV3559181	single nucleotide variant	NM_002504.6(NFX1):c.346A>G (p.Ile116Val)	not specified [RCV004834348]	uncertain significance	9	33294740	33294740	Human		name
597656817	CV3559185	single nucleotide variant	NM_002504.6(NFX1):c.947C>T (p.Thr316Ile)	not specified [RCV004834352]	uncertain significance	9	33295341	33295341	Human		name
598192418	CV3997727	single nucleotide variant	NM_002504.6(NFX1):c.814G>A (p.Ala272Thr)	not specified [RCV005374348]	uncertain significance	9	33295208	33295208	Human		name
598192425	CV3997729	single nucleotide variant	NM_002504.6(NFX1):c.949G>A (p.Val317Ile)	not specified [RCV005374349]	uncertain significance	9	33295343	33295343	Human		name
598192439	CV3997732	single nucleotide variant	NM_002504.6(NFX1):c.684G>T (p.Leu228Phe)	not specified [RCV005374351]	uncertain significance	9	33295078	33295078	Human		name
598192451	CV3997735	single nucleotide variant	NM_002504.6(NFX1):c.850G>A (p.Asp284Asn)	not specified [RCV005374353]	uncertain significance	9	33295244	33295244	Human		name
156095737	CV2210296	single nucleotide variant	NM_002504.6(NFX1):c.2086C>T (p.Arg696Trp)	not specified [RCV004089459]	uncertain significance	9	33338560	33338560	Human		name
156159541	CV2236229	single nucleotide variant	NM_002504.6(NFX1):c.1826G>A (p.Ser609Asn)	not specified [RCV004107933]	uncertain significance	9	33319047	33319047	Human		name
155981906	CV2244129	single nucleotide variant	NM_002504.6(NFX1):c.1633G>A (p.Asp545Asn)	not specified [RCV004108587]	uncertain significance	9	33318775	33318775	Human		name
155925639	CV2258587	single nucleotide variant	NM_002504.6(NFX1):c.2194C>T (p.Arg732Cys)	not specified [RCV004116063]	uncertain significance	9	33342824	33342824	Human		name
156362082	CV2265471	single nucleotide variant	NM_002504.6(NFX1):c.1511T>G (p.Leu504Trp)	not specified [RCV004124233]	uncertain significance	9	33313716	33313716	Human		name
156251800	CV2311324	single nucleotide variant	NM_002504.6(NFX1):c.1158A>G (p.Ile386Met)	not specified [RCV004166394]	uncertain significance	9	33301387	33301387	Human		name
156195769	CV2318998	single nucleotide variant	NM_002504.6(NFX1):c.1799C>T (p.Pro600Leu)	not specified [RCV004178090]	uncertain significance	9	33319020	33319020	Human		name
156132637	CV2350163	single nucleotide variant	NM_002504.6(NFX1):c.2824C>G (p.Gln942Glu)	not specified [RCV004200079]	uncertain significance	9	33354180	33354180	Human		name
156228736	CV2352932	single nucleotide variant	NM_002504.6(NFX1):c.1485C>G (p.His495Gln)	not specified [RCV004200977]	uncertain significance	9	33313690	33313690	Human		name
156239450	CV2356347	single nucleotide variant	NM_002504.6(NFX1):c.1405T>A (p.Cys469Ser)	not specified [RCV004206151]	uncertain significance	9	33311134	33311134	Human		name
156068530	CV2356874	single nucleotide variant	NM_002504.6(NFX1):c.2694G>A (p.Met898Ile)	not specified [RCV004204251]	likely benign	9	33352684	33352684	Human		name
156004650	CV2401009	single nucleotide variant	NM_002504.6(NFX1):c.2345T>C (p.Val782Ala)	not specified [RCV004244288]	uncertain significance	9	33347038	33347038	Human		name
329384481	CV2435084	single nucleotide variant	NM_002504.6(NFX1):c.2576C>G (p.Pro859Arg)	not specified [RCV004252729]	uncertain significance	9	33351711	33351711	Human		name
329402740	CV2451307	single nucleotide variant	NM_002504.6(NFX1):c.1945G>A (p.Asp649Asn)	not specified [RCV004272001]	uncertain significance	9	33328619	33328619	Human		name
329394652	CV2461500	single nucleotide variant	NM_002504.6(NFX1):c.1582A>T (p.Asn528Tyr)	not specified [RCV004269427]	uncertain significance	9	33313787	33313787	Human		name
401747366	CV2679081	single nucleotide variant	NM_002504.6(NFX1):c.1238C>T (p.Ala413Val)	not specified [RCV004295076]	uncertain significance	9	33303236	33303236	Human		name
401748640	CV2713139	single nucleotide variant	NM_002504.6(NFX1):c.1341A>T (p.Lys447Asn)	not specified [RCV004316688]	uncertain significance	9	33307264	33307264	Human		name
401783857	CV2720503	single nucleotide variant	NM_002504.6(NFX1):c.1610C>T (p.Ser537Phe)	not specified [RCV004327910]	uncertain significance	9	33318752	33318752	Human		name
401872550	CV2779712	single nucleotide variant	NM_002504.6(NFX1):c.1337A>G (p.Lys446Arg)	not specified [RCV004351399]	likely benign	9	33307260	33307260	Human		name
401896726	CV2788718	single nucleotide variant	NM_002504.6(NFX1):c.2428C>T (p.Arg810Trp)	not specified [RCV004361194]	uncertain significance	9	33351563	33351563	Human		name
405719014	CV3361767	single nucleotide variant	NM_002504.6(NFX1):c.1006G>A (p.Val336Met)	not specified [RCV004494930]	uncertain significance	9	33295400	33295400	Human		name
405719047	CV3361771	single nucleotide variant	NM_002504.6(NFX1):c.1018G>T (p.Val340Leu)	not specified [RCV004494934]	uncertain significance	9	33295412	33295412	Human		name
405719506	CV3361830	single nucleotide variant	NM_002504.6(NFX1):c.1895G>A (p.Cys632Tyr)	not specified [RCV004494993]	uncertain significance	9	33319116	33319116	Human		name
405720100	CV3361869	single nucleotide variant	NM_002504.6(NFX1):c.2845G>A (p.Glu949Lys)	not specified [RCV004495032]	uncertain significance	9	33354864	33354864	Human		name
405720076	CV3361872	single nucleotide variant	NM_002504.6(NFX1):c.2974A>G (p.Lys992Glu)	not specified [RCV004495035]	uncertain significance	9	33364709	33364709	Human		name
407496951	CV3451271	single nucleotide variant	NM_002504.6(NFX1):c.2159G>A (p.Arg720His)	not specified [RCV004643629]	uncertain significance	9	33342789	33342789	Human		name
407526879	CV3451273	single nucleotide variant	NM_002504.6(NFX1):c.2130G>T (p.Lys710Asn)	not specified [RCV004654974]	uncertain significance	9	33342760	33342760	Human		name
407496959	CV3451275	single nucleotide variant	NM_002504.6(NFX1):c.2494T>C (p.Cys832Arg)	not specified [RCV004643631]	uncertain significance	9	33351629	33351629	Human		name
597656767	CV3559178	single nucleotide variant	NM_002504.6(NFX1):c.2681G>A (p.Arg894Gln)	not specified [RCV004834345]	uncertain significance	9	33352671	33352671	Human		name
597656780	CV3559180	single nucleotide variant	NM_002504.6(NFX1):c.2317G>A (p.Ala773Thr)	not specified [RCV004834347]	uncertain significance	9	33344161	33344161	Human		name
597656809	CV3559184	single nucleotide variant	NM_002504.6(NFX1):c.1370G>C (p.Cys457Ser)	not specified [RCV004834351]	uncertain significance	9	33307293	33307293	Human		name
597656832	CV3559187	single nucleotide variant	NM_002504.6(NFX1):c.1874T>A (p.Val625Glu)	not specified [RCV004834354]	uncertain significance	9	33319095	33319095	Human		name
597656839	CV3559188	single nucleotide variant	NM_002504.6(NFX1):c.2804T>C (p.Ile935Thr)	not specified [RCV004834355]	uncertain significance	9	33354160	33354160	Human		name
598238367	CV3997726	single nucleotide variant	NM_002504.6(NFX1):c.2386A>G (p.Thr796Ala)	not specified [RCV005382734]	uncertain significance	9	33347079	33347079	Human		name
598238372	CV3997728	single nucleotide variant	NM_002504.6(NFX1):c.2877A>T (p.Arg959Ser)	not specified [RCV005382735]	uncertain significance	9	33364013	33364013	Human		name
598192431	CV3997730	single nucleotide variant	NM_002504.6(NFX1):c.1646C>G (p.Ser549Cys)	not specified [RCV005374350]	uncertain significance	9	33318788	33318788	Human		name
598238385	CV3997734	single nucleotide variant	NM_002504.6(NFX1):c.2132G>A (p.Cys711Tyr)	not specified [RCV005382737]	uncertain significance	9	33342762	33342762	Human		name
598238391	CV3997736	single nucleotide variant	NM_002504.6(NFX1):c.2321G>A (p.Arg774Lys)	not specified [RCV005382738]	uncertain significance	9	33344165	33344165	Human		name
155905742	CV2393773	single nucleotide variant	NM_002504.6(NFX1):c.3196G>A (p.Val1066Ile)	not specified [RCV004233608]	likely benign	9	33367525	33367525	Human		name
329375258	CV2431435	single nucleotide variant	NM_002504.6(NFX1):c.3164A>G (p.Asn1055Ser)	not specified [RCV004254600]	uncertain significance	9	33366753	33366753	Human		name
401772408	CV2719633	single nucleotide variant	NM_002504.6(NFX1):c.3055A>C (p.Lys1019Gln)	not specified [RCV004327297]	uncertain significance	9	33366644	33366644	Human		name
405719691	CV3361878	single nucleotide variant	NM_002504.6(NFX1):c.3160C>G (p.Arg1054Gly)	not specified [RCV004495041]	uncertain significance	9	33366749	33366749	Human		name
405719740	CV3361885	single nucleotide variant	NM_002504.6(NFX1):c.3308A>G (p.Asn1103Ser)	not specified [RCV004495048]	uncertain significance	9	33369923	33369923	Human		name
405719779	CV3361890	single nucleotide variant	NM_002504.6(NFX1):c.3328G>C (p.Glu1110Gln)	not specified [RCV004495053]	uncertain significance	9	33369943	33369943	Human		name
597656750	CV3559176	single nucleotide variant	NM_002504.6(NFX1):c.3212C>T (p.Thr1071Met)	not specified [RCV004834343]	uncertain significance	9	33367541	33367541	Human		name
597656759	CV3559177	single nucleotide variant	NM_002504.6(NFX1):c.3247C>T (p.Arg1083Trp)	not specified [RCV004834344]	uncertain significance	9	33367576	33367576	Human		name
597656794	CV3559182	single nucleotide variant	NM_002504.6(NFX1):c.3302G>T (p.Ser1101Ile)	not specified [RCV004834349]	uncertain significance	9	33369917	33369917	Human		name
597656825	CV3559186	single nucleotide variant	NM_002504.6(NFX1):c.3090C>A (p.His1030Gln)	not specified [RCV004834353]	uncertain significance	9	33366679	33366679	Human		name
598238379	CV3997731	single nucleotide variant	NM_002504.6(NFX1):c.3223G>A (p.Val1075Met)	not specified [RCV005382736]	uncertain significance	9	33367552	33367552	Human		name
598192445	CV3997733	single nucleotide variant	NM_002504.6(NFX1):c.3298G>A (p.Gly1100Arg)	not specified [RCV005374352]	uncertain significance	9	33369913	33369913	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
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