Usp38 Variant Search Result - Rat Genome Database

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78 records found for search term Usp38

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329362707	CV2467115	single nucleotide variant	NM_032557.6(USP38):c.7A>G (p.Lys3Glu)	not specified [RCV004282845]	uncertain significance	4	143185457	143185457	Human		name
405800679	CV3338198	single nucleotide variant	NM_032557.6(USP38):c.64G>T (p.Val22Leu)	not specified [RCV004477397]	uncertain significance	4	143185514	143185514	Human		name
407528810	CV3487609	single nucleotide variant	NM_032557.6(USP38):c.90G>C (p.Glu30Asp)	not specified [RCV004680580]	uncertain significance	4	143185540	143185540	Human		name
405800649	CV3338182	single nucleotide variant	NM_032557.6(USP38):c.105G>C (p.Glu35Asp)	not specified [RCV004477381]	uncertain significance	4	143185555	143185555	Human		name
405800669	CV3338193	single nucleotide variant	NM_032557.6(USP38):c.294G>C (p.Arg98Ser)	not specified [RCV004477392]	uncertain significance	4	143185744	143185744	Human		name
407528818	CV3487614	single nucleotide variant	NM_032557.6(USP38):c.265C>T (p.Leu89Phe)	not specified [RCV004680584]	uncertain significance	4	143185715	143185715	Human		name
597798904	CV3623036	single nucleotide variant	NM_032557.6(USP38):c.151G>C (p.Glu51Gln)	not specified [RCV004879414]	uncertain significance	4	143185601	143185601	Human		name
156079097	CV2248435	single nucleotide variant	NM_032557.6(USP38):c.376C>G (p.Leu126Val)	not specified [RCV004119574]	uncertain significance	4	143185826	143185826	Human		name
156163800	CV2323632	single nucleotide variant	NM_032557.6(USP38):c.481G>A (p.Gly161Arg)	not specified [RCV004165819]	uncertain significance	4	143185931	143185931	Human		name
156285399	CV2345574	single nucleotide variant	NM_032557.6(USP38):c.856G>A (p.Val286Met)	not specified [RCV004205528]	uncertain significance	4	143195753	143195753	Human		name
401777945	CV2704473	single nucleotide variant	NM_032557.6(USP38):c.644C>T (p.Pro215Leu)	not specified [RCV004313218]	uncertain significance	4	143186094	143186094	Human		name
401719646	CV2729298	single nucleotide variant	NM_032557.6(USP38):c.428T>A (p.Leu143His)	not specified [RCV004332709]	uncertain significance	4	143185878	143185878	Human		name
405800675	CV3338196	single nucleotide variant	NM_032557.6(USP38):c.376C>T (p.Leu126Phe)	not specified [RCV004477395]	uncertain significance	4	143185826	143185826	Human		name
405800677	CV3338197	single nucleotide variant	NM_032557.6(USP38):c.518G>A (p.Arg173Gln)	not specified [RCV004477396]	uncertain significance	4	143185968	143185968	Human		name
405800681	CV3338199	single nucleotide variant	NM_032557.6(USP38):c.797G>A (p.Ser266Asn)	not specified [RCV004477398]	uncertain significance	4	143187940	143187940	Human		name
405800682	CV3338200	single nucleotide variant	NM_032557.6(USP38):c.997G>C (p.Val333Leu)	not specified [RCV004477399]	uncertain significance	4	143197871	143197871	Human		name
407528816	CV3487613	single nucleotide variant	NM_032557.6(USP38):c.367C>G (p.Leu123Val)	not specified [RCV004680583]	uncertain significance	4	143185817	143185817	Human		name
597798895	CV3623029	single nucleotide variant	NM_032557.6(USP38):c.336G>T (p.Lys112Asn)	not specified [RCV004879410]	uncertain significance	4	143185786	143185786	Human		name
597798897	CV3623030	single nucleotide variant	NM_032557.6(USP38):c.751G>C (p.Val251Leu)	not specified [RCV004879411]	uncertain significance	4	143187894	143187894	Human		name
598275302	CV3932834	single nucleotide variant	NM_032557.6(USP38):c.444C>G (p.Ser148Arg)	not specified [RCV005304436]	uncertain significance	4	143185894	143185894	Human		name
598204244	CV3932835	single nucleotide variant	NM_032557.6(USP38):c.851A>G (p.Gln284Arg)	not specified [RCV005290660]	uncertain significance	4	143195748	143195748	Human		name
598204256	CV3932837	single nucleotide variant	NM_032557.6(USP38):c.686C>A (p.Ala229Glu)	not specified [RCV005290662]	uncertain significance	4	143187829	143187829	Human		name
598275304	CV3932839	single nucleotide variant	NM_032557.6(USP38):c.398G>T (p.Arg133Leu)	not specified [RCV005304438]	uncertain significance	4	143185848	143185848	Human		name
156398344	CV2200689	single nucleotide variant	NM_032557.6(USP38):c.1997C>G (p.Ala666Gly)	not specified [RCV004081347]	uncertain significance	4	143213973	143213973	Human		name
156128897	CV2238491	single nucleotide variant	NM_032557.6(USP38):c.2446C>T (p.Leu816Phe)	not specified [RCV004107115]	uncertain significance	4	143214422	143214422	Human		name
156247218	CV2276840	single nucleotide variant	NM_032557.6(USP38):c.1939C>G (p.Gln647Glu)	not specified [RCV004140188]	uncertain significance	4	143213915	143213915	Human		name
156091973	CV2300100	single nucleotide variant	NM_032557.6(USP38):c.2129C>T (p.Pro710Leu)	not specified [RCV004151298]	uncertain significance	4	143214105	143214105	Human		name
155942476	CV2301187	single nucleotide variant	NM_032557.6(USP38):c.2135G>C (p.Gly712Ala)	not specified [RCV004160095]	uncertain significance	4	143214111	143214111	Human		name
156007972	CV2390045	single nucleotide variant	NM_032557.6(USP38):c.2086G>A (p.Glu696Lys)	not specified [RCV004238649]	uncertain significance	4	143214062	143214062	Human		name
329355641	CV2445558	single nucleotide variant	NM_032557.6(USP38):c.1520T>A (p.Ile507Lys)	not specified [RCV004257604]	uncertain significance	4	143212340	143212340	Human		name
329352384	CV2452946	single nucleotide variant	NM_032557.6(USP38):c.1651C>G (p.Pro551Ala)	not specified [RCV004277578]	uncertain significance	4	143213627	143213627	Human		name
329394607	CV2461441	single nucleotide variant	NM_032557.6(USP38):c.2396C>T (p.Ser799Phe)	not specified [RCV004267587]	uncertain significance	4	143214372	143214372	Human		name
401752077	CV2682693	single nucleotide variant	NM_032557.6(USP38):c.2026A>G (p.Lys676Glu)	not specified [RCV004281674]	uncertain significance	4	143214002	143214002	Human		name
401782336	CV2686709	single nucleotide variant	NM_032557.6(USP38):c.1368G>A (p.Met456Ile)	not specified [RCV004300116]	uncertain significance	4	143206191	143206191	Human		name
401729193	CV2690095	single nucleotide variant	NM_032557.6(USP38):c.2870G>A (p.Gly957Asp)	not specified [RCV004300330]	uncertain significance	4	143214846	143214846	Human		name
401748317	CV2698349	single nucleotide variant	NM_032557.6(USP38):c.1162T>C (p.Tyr388His)	not specified [RCV004304891]	uncertain significance	4	143203519	143203519	Human		name
401760586	CV2706007	single nucleotide variant	NM_032557.6(USP38):c.2326G>C (p.Val776Leu)	not specified [RCV004320918]	uncertain significance	4	143214302	143214302	Human		name
401781173	CV2726444	single nucleotide variant	NM_032557.6(USP38):c.1286T>C (p.Leu429Ser)	not specified [RCV004328644]	uncertain significance	4	143206109	143206109	Human		name
401876518	CV2782948	single nucleotide variant	NM_032557.6(USP38):c.2585C>G (p.Ala862Gly)	not specified [RCV004361743]	uncertain significance	4	143214561	143214561	Human		name
405800650	CV3338183	single nucleotide variant	NM_032557.6(USP38):c.1366A>G (p.Met456Val)	not specified [RCV004477382]	uncertain significance	4	143206189	143206189	Human		name
405800652	CV3338184	single nucleotide variant	NM_032557.6(USP38):c.1687C>G (p.Gln563Glu)	not specified [RCV004477383]	uncertain significance	4	143213663	143213663	Human		name
405800654	CV3338185	single nucleotide variant	NM_032557.6(USP38):c.1823A>T (p.Gln608Leu)	not specified [RCV004477384]	uncertain significance	4	143213799	143213799	Human		name
405800656	CV3338186	single nucleotide variant	NM_032557.6(USP38):c.1874C>G (p.Ser625Cys)	not specified [RCV004477385]	uncertain significance	4	143213850	143213850	Human		name
405800658	CV3338187	single nucleotide variant	NM_032557.6(USP38):c.2222A>G (p.Asn741Ser)	not specified [RCV004477386]	uncertain significance	4	143214198	143214198	Human		name
405800660	CV3338188	single nucleotide variant	NM_032557.6(USP38):c.2393C>G (p.Thr798Ser)	not specified [RCV004477387]	uncertain significance	4	143214369	143214369	Human		name
405800662	CV3338189	single nucleotide variant	NM_032557.6(USP38):c.2512G>T (p.Val838Leu)	not specified [RCV004477388]	uncertain significance	4	143214488	143214488	Human		name
405800664	CV3338190	single nucleotide variant	NM_032557.6(USP38):c.2521C>G (p.Leu841Val)	not specified [RCV004477389]	uncertain significance	4	143214497	143214497	Human		name
405800666	CV3338191	single nucleotide variant	NM_032557.6(USP38):c.2678G>A (p.Arg893Lys)	not specified [RCV004477390]	uncertain significance	4	143214654	143214654	Human		name
405800667	CV3338192	single nucleotide variant	NM_032557.6(USP38):c.2849A>G (p.His950Arg)	not specified [RCV004477391]	uncertain significance	4	143214825	143214825	Human		name
407528802	CV3487605	single nucleotide variant	NM_032557.6(USP38):c.1741G>A (p.Gly581Ser)	not specified [RCV004680576]	likely benign	4	143213717	143213717	Human		name
407528804	CV3487606	single nucleotide variant	NM_032557.6(USP38):c.2935G>A (p.Ala979Thr)	not specified [RCV004680577]	uncertain significance	4	143214911	143214911	Human		name
407528806	CV3487607	single nucleotide variant	NM_032557.6(USP38):c.2533G>A (p.Val845Ile)	not specified [RCV004680578]	uncertain significance	4	143214509	143214509	Human		name
407528812	CV3487610	single nucleotide variant	NM_032557.6(USP38):c.2759G>C (p.Arg920Thr)	not specified [RCV004680581]	uncertain significance	4	143214735	143214735	Human		name
407464618	CV3487611	single nucleotide variant	NM_032557.6(USP38):c.1256A>G (p.Gln419Arg)	not specified [RCV004688552]	uncertain significance	4	143206079	143206079	Human		name
407528814	CV3487612	single nucleotide variant	NM_032557.6(USP38):c.1816A>C (p.Thr606Pro)	not specified [RCV004680582]	uncertain significance	4	143213792	143213792	Human		name
407528820	CV3487615	single nucleotide variant	NM_032557.6(USP38):c.1882A>G (p.Asn628Asp)	not specified [RCV004680585]	uncertain significance	4	143213858	143213858	Human		name
597798887	CV3623023	single nucleotide variant	NM_032557.6(USP38):c.1258A>G (p.Ser420Gly)	not specified [RCV004879406]	uncertain significance	4	143206081	143206081	Human		name
597798889	CV3623024	single nucleotide variant	NM_032557.6(USP38):c.2599A>G (p.Ser867Gly)	not specified [RCV004879407]	likely benign	4	143214575	143214575	Human		name
597723940	CV3623025	single nucleotide variant	NM_032557.6(USP38):c.1916G>C (p.Ser639Thr)	not specified [RCV004888125]	uncertain significance	4	143213892	143213892	Human		name
597798891	CV3623027	single nucleotide variant	NM_032557.6(USP38):c.1682C>A (p.Ser561Tyr)	not specified [RCV004879408]	uncertain significance	4	143213658	143213658	Human		name
597798893	CV3623028	single nucleotide variant	NM_032557.6(USP38):c.2551A>G (p.Ile851Val)	not specified [RCV004879409]	likely benign	4	143214527	143214527	Human		name
597798899	CV3623031	single nucleotide variant	NM_032557.6(USP38):c.1163A>G (p.Tyr388Cys)	not specified [RCV004879412]	uncertain significance	4	143203520	143203520	Human		name
597723951	CV3623032	single nucleotide variant	NM_032557.6(USP38):c.1735A>C (p.Ser579Arg)	not specified [RCV004888126]	uncertain significance	4	143213711	143213711	Human		name
597723962	CV3623033	single nucleotide variant	NM_032557.6(USP38):c.2521C>A (p.Leu841Ile)	not specified [RCV004888127]	uncertain significance	4	143214497	143214497	Human		name
597723974	CV3623034	single nucleotide variant	NM_032557.6(USP38):c.1429A>C (p.Asn477His)	not specified [RCV004888128]	uncertain significance	4	143209589	143209589	Human		name
597798902	CV3623035	single nucleotide variant	NM_032557.6(USP38):c.1091A>C (p.Asn364Thr)	not specified [RCV004879413]	uncertain significance	4	143203448	143203448	Human		name
597723995	CV3623038	single nucleotide variant	NM_032557.6(USP38):c.1967A>T (p.Glu656Val)	not specified [RCV004888130]	uncertain significance	4	143213943	143213943	Human		name
597798906	CV3623039	single nucleotide variant	NM_032557.6(USP38):c.2891T>C (p.Leu964Pro)	not specified [RCV004879415]	uncertain significance	4	143214867	143214867	Human		name
598204251	CV3932836	single nucleotide variant	NM_032557.6(USP38):c.2899A>G (p.Asn967Asp)	not specified [RCV005290661]	uncertain significance	4	143214875	143214875	Human		name
598275303	CV3932838	single nucleotide variant	NM_032557.6(USP38):c.2104G>A (p.Val702Ile)	not specified [RCV005304437]	uncertain significance	4	143214080	143214080	Human		name
598275305	CV3932840	single nucleotide variant	NM_032557.6(USP38):c.1909T>C (p.Ser637Pro)	not specified [RCV005304439]	uncertain significance	4	143213885	143213885	Human		name
156146213	CV2218884	single nucleotide variant	NM_032557.6(USP38):c.3028C>T (p.Arg1010Trp)	not specified [RCV004085115]	uncertain significance	4	143220355	143220355	Human		name
156087540	CV2366402	single nucleotide variant	NM_032557.6(USP38):c.3029G>A (p.Arg1010Gln)	not specified [RCV004212449]	uncertain significance	4	143220356	143220356	Human		name
329366763	CV2441869	single nucleotide variant	NM_032557.6(USP38):c.3017C>T (p.Ser1006Leu)	not specified [RCV004262061]	uncertain significance	4	143220344	143220344	Human		name
401891929	CV2777142	single nucleotide variant	NM_032557.6(USP38):c.3037G>A (p.Gly1013Arg)	not specified [RCV004354190]	uncertain significance	4	143220364	143220364	Human		name
405800671	CV3338194	single nucleotide variant	NM_032557.6(USP38):c.3076A>G (p.Thr1026Ala)	not specified [RCV004477393]	uncertain significance	4	143220403	143220403	Human		name
405800673	CV3338195	single nucleotide variant	NM_032557.6(USP38):c.3121G>A (p.Val1041Ile)	not specified [RCV004477394]	uncertain significance	4	143220448	143220448	Human		name
598275301	CV3932833	single nucleotide variant	NM_032557.6(USP38):c.3054C>G (p.Asp1018Glu)	not specified [RCV005304435]	uncertain significance	4	143220381	143220381	Human		name

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