Iffo2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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55 records found for search term Iffo2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405791882	CV3267374	single nucleotide variant	NM_001136265.2(IFFO2):c.23G>A (p.Gly8Glu)	not specified [RCV004400010]	uncertain significance	1	18956310	18956310	Human		name
155926050	CV2230550	single nucleotide variant	NM_001136265.2(IFFO2):c.64G>T (p.Gly22Cys)	not specified [RCV004097520]	uncertain significance	1	18956269	18956269	Human		name
156017053	CV2295486	single nucleotide variant	NM_001136265.2(IFFO2):c.38C>T (p.Ala13Val)	not specified [RCV004160599]	uncertain significance	1	18956295	18956295	Human		name
156063780	CV2321104	single nucleotide variant	NM_001136265.2(IFFO2):c.28A>G (p.Met10Val)	not specified [RCV004174927]	uncertain significance	1	18956305	18956305	Human		name
156050757	CV2378500	single nucleotide variant	NM_001136265.2(IFFO2):c.67G>A (p.Gly23Arg)	not specified [RCV004228554]	uncertain significance	1	18956266	18956266	Human		name
407466030	CV3444461	single nucleotide variant	NM_001136265.2(IFFO2):c.88G>A (p.Gly30Ser)	not specified [RCV004635529]	uncertain significance	1	18956245	18956245	Human		name
597762885	CV3683154	single nucleotide variant	NM_001136265.2(IFFO2):c.86G>A (p.Gly29Asp)	not specified [RCV004926217]	uncertain significance	1	18956247	18956247	Human		name
155917092	CV2366826	single nucleotide variant	NM_001136265.2(IFFO2):c.154T>A (p.Ser52Thr)	not specified [RCV004210814]	uncertain significance	1	18956179	18956179	Human		name
405791879	CV3267373	single nucleotide variant	NM_001136265.2(IFFO2):c.154T>G (p.Ser52Ala)	not specified [RCV004400009]	uncertain significance	1	18956179	18956179	Human		name
405791885	CV3267375	single nucleotide variant	NM_001136265.2(IFFO2):c.293A>G (p.Tyr98Cys)	not specified [RCV004400011]	uncertain significance	1	18956040	18956040	Human		name
407466038	CV3444463	single nucleotide variant	NM_001136265.2(IFFO2):c.151G>T (p.Gly51Cys)	not specified [RCV004635531]	uncertain significance	1	18956182	18956182	Human		name
597762881	CV3683153	single nucleotide variant	NM_001136265.2(IFFO2):c.184G>C (p.Val62Leu)	not specified [RCV004926216]	uncertain significance	1	18956149	18956149	Human		name
597762911	CV3683159	single nucleotide variant	NM_001136265.2(IFFO2):c.188G>A (p.Arg63His)	not specified [RCV004926222]	uncertain significance	1	18956145	18956145	Human		name
598267707	CV3979124	single nucleotide variant	NM_001136265.2(IFFO2):c.290G>A (p.Arg97His)	not specified [RCV005349564]	uncertain significance	1	18956043	18956043	Human		name
156377334	CV2207040	single nucleotide variant	NM_001136265.2(IFFO2):c.824C>G (p.Pro275Arg)	not specified [RCV004085653]	uncertain significance	1	18918501	18918501	Human		name
155902191	CV2274641	single nucleotide variant	NM_001136265.2(IFFO2):c.334G>A (p.Glu112Lys)	not specified [RCV004139022]	uncertain significance	1	18955999	18955999	Human		name
156140298	CV2280822	single nucleotide variant	NM_001136265.2(IFFO2):c.467G>T (p.Arg156Leu)	not specified [RCV004145083]	uncertain significance	1	18955866	18955866	Human		name
156164635	CV2319722	single nucleotide variant	NM_001136265.2(IFFO2):c.734A>G (p.Gln245Arg)	not specified [RCV004187259]	uncertain significance	1	18919766	18919766	Human		name
156280149	CV2325424	single nucleotide variant	NM_001136265.2(IFFO2):c.932G>A (p.Arg311Gln)	not specified [RCV004177783]	uncertain significance	1	18918393	18918393	Human		name
156262875	CV2368567	single nucleotide variant	NM_001136265.2(IFFO2):c.364G>C (p.Gly122Arg)	not specified [RCV004221353]	uncertain significance	1	18955969	18955969	Human		name
156269890	CV2379426	single nucleotide variant	NM_001136265.2(IFFO2):c.424G>C (p.Gly142Arg)	not specified [RCV004223877]	uncertain significance	1	18955909	18955909	Human		name
329402335	CV2454153	single nucleotide variant	NM_001136265.2(IFFO2):c.978G>T (p.Lys326Asn)	not specified [RCV004265646]	uncertain significance	1	18917028	18917028	Human		name
329360375	CV2458702	single nucleotide variant	NM_001136265.2(IFFO2):c.379A>C (p.Ser127Arg)	not specified [RCV004268362]	uncertain significance	1	18955954	18955954	Human		name
401757233	CV2675185	single nucleotide variant	NM_001136265.2(IFFO2):c.378C>A (p.Ser126Arg)	not specified [RCV004289958]	uncertain significance	1	18955955	18955955	Human		name
401868643	CV2767296	single nucleotide variant	NM_001136265.2(IFFO2):c.682G>A (p.Ala228Thr)	not specified [RCV004349464]	uncertain significance	1	18921105	18921105	Human		name
401886507	CV2771304	single nucleotide variant	NM_001136265.2(IFFO2):c.355C>A (p.Pro119Thr)	not specified [RCV004346277]	uncertain significance	1	18955978	18955978	Human		name
401872235	CV2779604	single nucleotide variant	NM_001136265.2(IFFO2):c.942A>C (p.Glu314Asp)	not specified [RCV004351312]	uncertain significance	1	18918383	18918383	Human		name
405791892	CV3267377	single nucleotide variant	NM_001136265.2(IFFO2):c.693G>T (p.Met231Ile)	not specified [RCV004400013]	uncertain significance	1	18921094	18921094	Human		name
407466034	CV3444462	single nucleotide variant	NM_001136265.2(IFFO2):c.606C>G (p.Ile202Met)	not specified [RCV004635530]	uncertain significance	1	18955727	18955727	Human		name
407466042	CV3444464	single nucleotide variant	NM_001136265.2(IFFO2):c.329G>T (p.Gly110Val)	not specified [RCV004635532]	uncertain significance	1	18956004	18956004	Human		name
597762900	CV3683157	single nucleotide variant	NM_001136265.2(IFFO2):c.355C>T (p.Pro119Ser)	not specified [RCV004926220]	uncertain significance	1	18955978	18955978	Human		name
597762905	CV3683158	single nucleotide variant	NM_001136265.2(IFFO2):c.382G>A (p.Gly128Ser)	not specified [RCV004926221]	uncertain significance	1	18955951	18955951	Human		name
598206444	CV3979121	single nucleotide variant	NM_001136265.2(IFFO2):c.970C>T (p.Pro324Ser)	not specified [RCV005337783]	uncertain significance	1	18917036	18917036	Human		name
598267697	CV3979122	single nucleotide variant	NM_001136265.2(IFFO2):c.424G>T (p.Gly142Cys)	not specified [RCV005349562]	uncertain significance	1	18955909	18955909	Human		name
598267702	CV3979123	single nucleotide variant	NM_001136265.2(IFFO2):c.505C>T (p.Arg169Cys)	not specified [RCV005349563]	uncertain significance	1	18955828	18955828	Human		name
156389613	CV2226447	single nucleotide variant	NM_001136265.2(IFFO2):c.1036C>T (p.Arg346Trp)	not specified [RCV004099655]	uncertain significance	1	18916970	18916970	Human		name
156341250	CV2268239	single nucleotide variant	NM_001136265.2(IFFO2):c.1525G>A (p.Glu509Lys)	not specified [RCV004138541]	uncertain significance	1	18908590	18908590	Human		name
155985649	CV2282361	single nucleotide variant	NM_001136265.2(IFFO2):c.1523G>A (p.Arg508His)	not specified [RCV004133183]	uncertain significance	1	18908592	18908592	Human		name
156132819	CV2350198	single nucleotide variant	NM_001136265.2(IFFO2):c.1423C>T (p.Arg475Trp)	not specified [RCV004200112]	uncertain significance	1	18910367	18910367	Human		name
155910746	CV2366622	single nucleotide variant	NM_001136265.2(IFFO2):c.1522C>T (p.Arg508Cys)	not specified [RCV004210635]	uncertain significance	1	18908593	18908593	Human		name
156050183	CV2378394	single nucleotide variant	NM_001136265.2(IFFO2):c.1402G>A (p.Val468Met)	not specified [RCV004226413]	uncertain significance	1	18910388	18910388	Human		name
329358712	CV2425345	single nucleotide variant	NM_001136265.2(IFFO2):c.1196G>C (p.Cys399Ser)	not specified [RCV004251009]	uncertain significance	1	18911991	18911991	Human		name
329370485	CV2435620	single nucleotide variant	NM_001136265.2(IFFO2):c.1457C>T (p.Pro486Leu)	not specified [RCV004254869]	uncertain significance	1	18908658	18908658	Human		name
329363497	CV2442222	single nucleotide variant	NM_001136265.2(IFFO2):c.1073C>A (p.Thr358Asn)	not specified [RCV004264714]	uncertain significance	1	18916933	18916933	Human		name
401771102	CV2700857	single nucleotide variant	NM_001136265.2(IFFO2):c.1145C>T (p.Thr382Met)	not specified [RCV004307131]	uncertain significance	1	18912042	18912042	Human		name
401763684	CV2717088	single nucleotide variant	NM_001136265.2(IFFO2):c.1208T>A (p.Ile403Asn)	not specified [RCV004330112]	uncertain significance	1	18911979	18911979	Human		name
401857199	CV2755637	single nucleotide variant	NM_001136265.2(IFFO2):c.1087C>T (p.Arg363Cys)	not specified [RCV004342023]	uncertain significance	1	18916919	18916919	Human		name
405791874	CV3267371	single nucleotide variant	NM_001136265.2(IFFO2):c.1201C>T (p.Pro401Ser)	not specified [RCV004400007]	uncertain significance	1	18911986	18911986	Human		name
405791876	CV3267372	single nucleotide variant	NM_001136265.2(IFFO2):c.1277C>T (p.Thr426Met)	not specified [RCV004400008]	uncertain significance	1	18911424	18911424	Human		name
597762895	CV3683156	single nucleotide variant	NM_001136265.2(IFFO2):c.1519G>A (p.Glu507Lys)	not specified [RCV004926219]	uncertain significance	1	18908596	18908596	Human		name
597762918	CV3683160	single nucleotide variant	NM_001136265.2(IFFO2):c.1436G>C (p.Gly479Ala)	not specified [RCV004926223]	uncertain significance	1	18910354	18910354	Human		name
597762923	CV3683161	single nucleotide variant	NM_001136265.2(IFFO2):c.1048G>T (p.Asp350Tyr)	not specified [RCV004926224]	uncertain significance	1	18916958	18916958	Human		name
597762928	CV3683162	single nucleotide variant	NM_001136265.2(IFFO2):c.1049A>T (p.Asp350Val)	not specified [RCV004926225]	uncertain significance	1	18916957	18916957	Human		name
598267713	CV3979125	single nucleotide variant	NM_001136265.2(IFFO2):c.1289A>C (p.Glu430Ala)	not specified [RCV005349565]	uncertain significance	1	18911412	18911412	Human		name
598267718	CV3979126	single nucleotide variant	NM_001136265.2(IFFO2):c.1433A>G (p.Lys478Arg)	not specified [RCV005349566]	uncertain significance	1	18910357	18910357	Human		name

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