Usp22 Variant Search Result - Rat Genome Database

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14 records found for search term Usp22

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597722771	CV3626218	single nucleotide variant	NM_015276.2(USP22):c.38A>G (p.Asp13Gly)	not specified [RCV004888053]	uncertain significance	17	21042798	21042798	Human		name
156400285	CV2199081	single nucleotide variant	NM_015276.2(USP22):c.202G>A (p.Val68Ile)	not specified [RCV004080481]	uncertain significance	17	21028644	21028644	Human		name
405814866	CV3341753	single nucleotide variant	NM_015276.2(USP22):c.274G>C (p.Glu92Gln)	not specified [RCV004484639]	uncertain significance	17	21028572	21028572	Human		name
597798489	CV3626216	single nucleotide variant	NM_015276.2(USP22):c.119C>G (p.Ala40Gly)	not specified [RCV004879220]	uncertain significance	17	21042717	21042717	Human		name
597798491	CV3626217	single nucleotide variant	NM_015276.2(USP22):c.129G>C (p.Gln43His)	not specified [RCV004879221]	uncertain significance	17	21042707	21042707	Human		name
598275189	CV3936540	single nucleotide variant	NM_015276.2(USP22):c.145G>T (p.Gly49Cys)	not specified [RCV005304323]	uncertain significance	17	21042691	21042691	Human		name
401861939	CV2766504	single nucleotide variant	NM_015276.2(USP22):c.517A>G (p.Ile173Val)	not specified [RCV004347126]	uncertain significance	17	21019087	21019087	Human		name
598203780	CV3936539	single nucleotide variant	NM_015276.2(USP22):c.602G>A (p.Arg201Gln)	not specified [RCV005290589]	uncertain significance	17	21018030	21018030	Human		name
156050272	CV2391155	single nucleotide variant	NM_015276.2(USP22):c.1160A>G (p.His387Arg)	not specified [RCV004237179]	uncertain significance	17	21007940	21007940	Human		name
329376870	CV2435726	single nucleotide variant	NM_015276.2(USP22):c.1082C>T (p.Thr361Met)	not specified [RCV004253357]	uncertain significance	17	21011172	21011172	Human		name
401878734	CV2767558	single nucleotide variant	NM_015276.2(USP22):c.1070C>T (p.Ser357Leu)	not specified [RCV004343711]	uncertain significance	17	21011184	21011184	Human		name
407455213	CV3487478	single nucleotide variant	NM_015276.2(USP22):c.1066G>A (p.Val356Met)	not specified [RCV004685484]	likely benign	17	21011188	21011188	Human		name
407455215	CV3487479	single nucleotide variant	NM_015276.2(USP22):c.1297G>A (p.Asp433Asn)	not specified [RCV004685485]	uncertain significance	17	21006921	21006921	Human		name
597722785	CV3626219	single nucleotide variant	NM_015276.2(USP22):c.1289T>C (p.Leu430Pro)	not specified [RCV004888054]	uncertain significance	17	21006929	21006929	Human		name