Fcer2 Variant Search Result - Rat Genome Database

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39 records found for search term Fcer2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401908396	CV2815338	single nucleotide variant	NM_001220500.2(FCER2):c.228T>G (p.Gly76=)	not provided [RCV003423274]	likely benign	19	7697552	7697552	Human		name
8637125	CV92351	single nucleotide variant	NM_002002.4(FCER2):c.544A>G (p.Lys182Glu)	Malignant melanoma [RCV000072449]	not provided	19	7690483	7690483	Human		name
156165113	CV2195991	single nucleotide variant	NM_001220500.2(FCER2):c.59G>A (p.Arg20His)	not specified [RCV004072241]	uncertain significance	19	7698818	7698818	Human		name
156001512	CV2257859	single nucleotide variant	NM_001220500.2(FCER2):c.92C>T (p.Thr31Ile)	not specified [RCV004127901]	uncertain significance	19	7698785	7698785	Human		name
401739236	CV2673249	single nucleotide variant	NM_001220500.2(FCER2):c.28G>A (p.Glu10Lys)	not specified [RCV004286053]	uncertain significance	19	7698849	7698849	Human		name
405724429	CV3260607	single nucleotide variant	NM_001220500.2(FCER2):c.83G>A (p.Gly28Glu)	not specified [RCV004389209]	uncertain significance	19	7698794	7698794	Human		name
405724436	CV3260608	single nucleotide variant	NM_001220500.2(FCER2):c.97G>A (p.Ala33Thr)	not specified [RCV004389210]	uncertain significance	19	7698780	7698780	Human		name
597724387	CV3675842	single nucleotide variant	NM_001220500.2(FCER2):c.47G>A (p.Arg16Gln)	not specified [RCV004919090]	uncertain significance	19	7698830	7698830	Human		name
598228782	CV3958999	single nucleotide variant	NM_001220500.2(FCER2):c.46C>T (p.Arg16Trp)	not specified [RCV005341973]	uncertain significance	19	7698831	7698831	Human		name
156373112	CV2204802	single nucleotide variant	NM_001220500.2(FCER2):c.110G>A (p.Gly37Glu)	not specified [RCV004075056]	uncertain significance	19	7698767	7698767	Human		name
156388521	CV2231873	single nucleotide variant	NM_001220500.2(FCER2):c.146C>T (p.Thr49Ile)	not specified [RCV004098671]	uncertain significance	19	7698400	7698400	Human		name
156314858	CV2253323	single nucleotide variant	NM_001220500.2(FCER2):c.262A>G (p.Ile88Val)	not specified [RCV004123156]	uncertain significance	19	7697290	7697290	Human		name
405724404	CV3260604	single nucleotide variant	NM_001220500.2(FCER2):c.208A>G (p.Asn70Asp)	not specified [RCV004389206]	likely benign	19	7697572	7697572	Human		name
407482598	CV3442707	single nucleotide variant	NM_001220500.2(FCER2):c.274C>G (p.Leu92Val)	not specified [RCV004618407]	uncertain significance	19	7697278	7697278	Human		name
598228774	CV3958996	single nucleotide variant	NM_001220500.2(FCER2):c.257C>T (p.Thr86Met)	not specified [RCV005341972]	uncertain significance	19	7697295	7697295	Human		name
15166174	CV742216	deletion	NM_001220500.2(FCER2):c.954del (p.Leu319fs)	not provided [RCV000904385]	likely benign	19	7689205	7689205	Human		name
156290911	CV2226253	single nucleotide variant	NM_001220500.2(FCER2):c.586G>A (p.Gly196Arg)	not specified [RCV004099501]	uncertain significance	19	7690441	7690441	Human		name
156072559	CV2233379	single nucleotide variant	NM_001220500.2(FCER2):c.520T>A (p.Cys174Ser)	not specified [RCV004105744]	uncertain significance	19	7690507	7690507	Human		name
156083163	CV2244452	single nucleotide variant	NM_001220500.2(FCER2):c.343G>A (p.Gly115Arg)	not specified [RCV004100417]	likely benign	19	7697049	7697049	Human		name
156219930	CV2254100	single nucleotide variant	NM_001220500.2(FCER2):c.458A>C (p.Gln153Pro)	not specified [RCV004129545]	uncertain significance	19	7696836	7696836	Human		name
156245588	CV2310399	single nucleotide variant	NM_001220500.2(FCER2):c.824G>A (p.Arg275His)	not specified [RCV004163440]	uncertain significance	19	7689335	7689335	Human		name
156068152	CV2345930	single nucleotide variant	NM_001220500.2(FCER2):c.656C>T (p.Ser219Phe)	not specified [RCV004198967]	uncertain significance	19	7690231	7690231	Human		name
156126305	CV2350276	single nucleotide variant	NM_001220500.2(FCER2):c.616G>A (p.Glu206Lys)	not specified [RCV004202232]	uncertain significance	19	7690411	7690411	Human		name
156012126	CV2358855	single nucleotide variant	NM_001220500.2(FCER2):c.916C>T (p.Pro306Ser)	not specified [RCV004212201]	uncertain significance	19	7689243	7689243	Human		name
156197317	CV2400727	single nucleotide variant	NM_001220500.2(FCER2):c.424C>T (p.Arg142Trp)	not specified [RCV004242395]	uncertain significance	19	7696870	7696870	Human		name
401726805	CV2674551	single nucleotide variant	NM_001220500.2(FCER2):c.305T>C (p.Leu102Ser)	not specified [RCV004291429]	uncertain significance	19	7697247	7697247	Human		name
401768210	CV2675163	single nucleotide variant	NM_001220500.2(FCER2):c.800G>C (p.Arg267Pro)	not specified [RCV004289938]	uncertain significance	19	7689359	7689359	Human		name
401729370	CV2690184	single nucleotide variant	NM_001220500.2(FCER2):c.788G>A (p.Arg263Gln)	not specified [RCV004302196]	likely benign	19	7689371	7689371	Human		name
401762144	CV2699535	single nucleotide variant	NM_001220500.2(FCER2):c.812C>A (p.Ala271Asp)	not specified [RCV004299742]	uncertain significance	19	7689347	7689347	Human		name
405724421	CV3260606	single nucleotide variant	NM_001220500.2(FCER2):c.736G>T (p.Ala246Ser)	not specified [RCV004389208]	uncertain significance	19	7689423	7689423	Human		name
407482577	CV3442703	single nucleotide variant	NM_001220500.2(FCER2):c.892G>A (p.Glu298Lys)	not specified [RCV004618403]	uncertain significance	19	7689267	7689267	Human		name
407482584	CV3442704	single nucleotide variant	NM_001220500.2(FCER2):c.652G>A (p.Gly218Ser)	not specified [RCV004618404]	uncertain significance	19	7690235	7690235	Human		name
407482590	CV3442705	single nucleotide variant	NM_001220500.2(FCER2):c.644G>C (p.Ser215Thr)	not specified [RCV004618405]	uncertain significance	19	7690243	7690243	Human		name
407482595	CV3442706	single nucleotide variant	NM_001220500.2(FCER2):c.937C>T (p.Pro313Ser)	not specified [RCV004618406]	uncertain significance	19	7689222	7689222	Human		name
597724353	CV3675839	single nucleotide variant	NM_001220500.2(FCER2):c.850C>T (p.Arg284Trp)	not specified [RCV004919087]	uncertain significance	19	7689309	7689309	Human		name
597724374	CV3675841	single nucleotide variant	NM_001220500.2(FCER2):c.563G>A (p.Arg188Gln)	not specified [RCV004919089]	uncertain significance	19	7690464	7690464	Human		name
598271842	CV3958997	single nucleotide variant	NM_001220500.2(FCER2):c.928G>A (p.Gly310Ser)	not specified [RCV005327832]	likely benign	19	7689231	7689231	Human		name
598228790	CV3959000	single nucleotide variant	NM_001220500.2(FCER2):c.691G>C (p.Glu231Gln)	not specified [RCV005341974]	uncertain significance	19	7690196	7690196	Human		name
598228798	CV3959001	single nucleotide variant	NM_001220500.2(FCER2):c.707A>G (p.Asp236Gly)	not specified [RCV005341975]	uncertain significance	19	7690180	7690180	Human		name

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