Nfx1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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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
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

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InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

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Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

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