Usp42 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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229 records found for search term Usp42

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401925581	CV2828294	single nucleotide variant	NM_032172.3(USP42):c.153A>G (p.Thr51=)	not provided [RCV003436633]	likely benign	7	6111286	6111286	Human		name
597724130	CV3623085	single nucleotide variant	NM_032172.3(USP42):c.22T>G (p.Ser8Ala)	not specified [RCV004888143]	uncertain significance	7	6111155	6111155	Human		name
156390130	CV2373100	single nucleotide variant	NM_032172.3(USP42):c.65G>A (p.Ser22Asn)	not specified [RCV004217794]	uncertain significance	7	6111198	6111198	Human		name
597798986	CV3623090	single nucleotide variant	NM_032172.3(USP42):c.74C>G (p.Ala25Gly)	not specified [RCV004879453]	uncertain significance	7	6111207	6111207	Human		name
597799005	CV3623100	single nucleotide variant	NM_032172.3(USP42):c.70G>C (p.Glu24Gln)	not specified [RCV004879462]	uncertain significance	7	6111203	6111203	Human		name
597799242	CV3623107	single nucleotide variant	NM_032172.3(USP42):c.29C>A (p.Ser10Tyr)	not specified [RCV004879466]	uncertain significance	7	6111162	6111162	Human		name
405800781	CV3338276	single nucleotide variant	NM_032172.3(USP42):c.259G>A (p.Ala87Thr)	not specified [RCV004477475]	uncertain significance	7	6115340	6115340	Human		name
405800789	CV3338280	single nucleotide variant	NM_032172.3(USP42):c.2763C>T (p.Gly921=)	not specified [RCV004477479]	likely benign	7	6154317	6154317	Human		name
598204375	CV3932885	single nucleotide variant	NM_032172.3(USP42):c.223T>C (p.Ser75Pro)	not specified [RCV005290681]	uncertain significance	7	6111356	6111356	Human		name
598238769	CV3932898	single nucleotide variant	NM_032172.3(USP42):c.124T>C (p.Ser42Pro)	not specified [RCV005296471]	uncertain significance	7	6111257	6111257	Human		name
15199021	CV700166	single nucleotide variant	NM_032172.3(USP42):c.1884T>A (p.Ile628=)	not provided [RCV000956923]	benign	7	6150080	6150080	Human		name
156320366	CV2197287	single nucleotide variant	NM_032172.3(USP42):c.572G>A (p.Arg191His)	not specified [RCV004079059]	uncertain significance	7	6139110	6139110	Human		name
156046902	CV2304306	single nucleotide variant	NM_032172.3(USP42):c.534T>G (p.Phe178Leu)	not specified [RCV004164427]	uncertain significance	7	6135932	6135932	Human		name
156084021	CV2330797	single nucleotide variant	NM_032172.3(USP42):c.326T>C (p.Val109Ala)	not specified [RCV004185857]	uncertain significance	7	6115407	6115407	Human		name
329353730	CV2439609	single nucleotide variant	NM_032172.3(USP42):c.529A>G (p.Met177Val)	not specified [RCV004255627]	uncertain significance	7	6135927	6135927	Human		name
329374296	CV2443825	single nucleotide variant	NM_032172.3(USP42):c.299G>A (p.Cys100Tyr)	not specified [RCV004258166]	uncertain significance	7	6115380	6115380	Human		name
401925582	CV2828295	single nucleotide variant	NM_032172.3(USP42):c.3045C>T (p.Gly1015=)	not provided [RCV003436634]	likely benign	7	6154599	6154599	Human		name
405800826	CV3338299	single nucleotide variant	NM_032172.3(USP42):c.542A>G (p.Asn181Ser)	not specified [RCV004477498]	uncertain significance	7	6135940	6135940	Human		name
405800828	CV3338300	single nucleotide variant	NM_032172.3(USP42):c.566A>T (p.His189Leu)	not specified [RCV004477499]	uncertain significance	7	6139104	6139104	Human		name
597696636	CV3623117	single nucleotide variant	NM_032172.3(USP42):c.571C>T (p.Arg191Cys)	not specified [RCV004885177]	uncertain significance	7	6139109	6139109	Human		name
598238703	CV3932873	single nucleotide variant	NM_032172.3(USP42):c.373G>A (p.Ala125Thr)	not specified [RCV005296459]	uncertain significance	7	6115454	6115454	Human		name
598204389	CV3932887	single nucleotide variant	NM_032172.3(USP42):c.909G>T (p.Arg303Ser)	not specified [RCV005290683]	uncertain significance	7	6144115	6144115	Human		name
156096944	CV2206702	single nucleotide variant	NM_032172.3(USP42):c.2746G>A (p.Ala916Thr)	not specified [RCV004083394]	uncertain significance	7	6154300	6154300	Human		name
156256445	CV2219765	single nucleotide variant	NM_032172.3(USP42):c.1420A>C (p.Lys474Gln)	not specified [RCV004095458]	uncertain significance	7	6149616	6149616	Human		name
156167307	CV2237221	single nucleotide variant	NM_032172.3(USP42):c.1456G>A (p.Gly486Arg)	not specified [RCV004114955]	uncertain significance	7	6149652	6149652	Human		name
156303100	CV2258780	single nucleotide variant	NM_032172.3(USP42):c.2837G>C (p.Arg946Thr)	not specified [RCV004118009]	uncertain significance	7	6154391	6154391	Human		name
155999168	CV2261061	single nucleotide variant	NM_032172.3(USP42):c.1018A>G (p.Ile340Val)	not specified [RCV004127711]	uncertain significance	7	6145543	6145543	Human		name
155946678	CV2262394	single nucleotide variant	NM_032172.3(USP42):c.2860C>T (p.Arg954Cys)	not specified [RCV004128842]	uncertain significance	7	6154414	6154414	Human		name
156367816	CV2266883	single nucleotide variant	NM_032172.3(USP42):c.1644C>A (p.Asn548Lys)	not specified [RCV004131549]	uncertain significance	7	6149840	6149840	Human		name
155944750	CV2269314	single nucleotide variant	NM_032172.3(USP42):c.2756G>T (p.Ser919Ile)	not specified [RCV004130718]	uncertain significance	7	6154310	6154310	Human		name
155903508	CV2274891	single nucleotide variant	NM_032172.3(USP42):c.1667C>G (p.Ser556Cys)	not specified [RCV004133078]	uncertain significance	7	6149863	6149863	Human		name
156251317	CV2286833	single nucleotide variant	NM_032172.3(USP42):c.2525G>A (p.Gly842Asp)	not specified [RCV004142635]	uncertain significance	7	6154079	6154079	Human		name
155901451	CV2294488	single nucleotide variant	NM_032172.3(USP42):c.2957G>A (p.Arg986Gln)	not specified [RCV004159981]	uncertain significance	7	6154511	6154511	Human		name
156099502	CV2294643	single nucleotide variant	NM_032172.3(USP42):c.2892G>C (p.Glu964Asp)	not specified [RCV004161896]	uncertain significance	7	6154446	6154446	Human		name
156070402	CV2295811	single nucleotide variant	NM_032172.3(USP42):c.1562A>G (p.Lys521Arg)	not specified [RCV004151733]	uncertain significance	7	6149758	6149758	Human		name
156197573	CV2306809	single nucleotide variant	NM_032172.3(USP42):c.2089A>G (p.Asn697Asp)	not specified [RCV004159378]	uncertain significance	7	6150285	6150285	Human		name
155961612	CV2311932	single nucleotide variant	NM_032172.3(USP42):c.2635C>G (p.His879Asp)	not specified [RCV004170755]	uncertain significance	7	6154189	6154189	Human		name
155962321	CV2312022	single nucleotide variant	NM_032172.3(USP42):c.2692C>T (p.Arg898Trp)	not specified [RCV004164651]	uncertain significance	7	6154246	6154246	Human		name
156255343	CV2325742	single nucleotide variant	NM_032172.3(USP42):c.2977C>A (p.Arg993Ser)	not specified [RCV004173636]	uncertain significance	7	6154531	6154531	Human		name
155966706	CV2329829	single nucleotide variant	NM_032172.3(USP42):c.2255C>G (p.Pro752Arg)	not specified [RCV004183290]	uncertain significance	7	6153809	6153809	Human		name
155970992	CV2334166	single nucleotide variant	NM_032172.3(USP42):c.1637T>C (p.Leu546Ser)	not specified [RCV004186156]	uncertain significance	7	6149833	6149833	Human		name
156087747	CV2337798	single nucleotide variant	NM_032172.3(USP42):c.2026C>T (p.Pro676Ser)	not specified [RCV004183813]	uncertain significance	7	6150222	6150222	Human		name
156191581	CV2339847	single nucleotide variant	NM_032172.3(USP42):c.2638G>C (p.Ala880Pro)	not specified [RCV004196530]	uncertain significance	7	6154192	6154192	Human		name
155974496	CV2341441	single nucleotide variant	NM_032172.3(USP42):c.1379T>C (p.Met460Thr)	not specified [RCV004188838]	uncertain significance	7	6147885	6147885	Human		name
156116011	CV2349345	single nucleotide variant	NM_032172.3(USP42):c.2189C>T (p.Thr730Met)	not specified [RCV004199284]	uncertain significance	7	6150494	6150494	Human		name
156336968	CV2360853	single nucleotide variant	NM_032172.3(USP42):c.1742C>T (p.Pro581Leu)	not specified [RCV004213624]	uncertain significance	7	6149938	6149938	Human		name
156050507	CV2378451	single nucleotide variant	NM_032172.3(USP42):c.2716A>T (p.Met906Leu)	not specified [RCV004226462]	uncertain significance	7	6154270	6154270	Human		name
156227304	CV2388204	single nucleotide variant	NM_032172.3(USP42):c.1807G>A (p.Val603Met)	not specified [RCV004234664]	uncertain significance	7	6150003	6150003	Human		name
156160837	CV2398224	single nucleotide variant	NM_032172.3(USP42):c.2761G>A (p.Gly921Ser)	not specified [RCV004235138]	uncertain significance	7	6154315	6154315	Human		name
156096461	CV2399081	single nucleotide variant	NM_032172.3(USP42):c.1889C>T (p.Thr630Met)	not specified [RCV004246524]	uncertain significance	7	6150085	6150085	Human		name
329354192	CV2437641	single nucleotide variant	NM_032172.3(USP42):c.2701G>A (p.Ala901Thr)	not specified [RCV004260959]	uncertain significance	7	6154255	6154255	Human		name
329353711	CV2439571	single nucleotide variant	NM_032172.3(USP42):c.2645A>T (p.Asp882Val)	not specified [RCV004255594]	uncertain significance	7	6154199	6154199	Human		name
329392245	CV2441348	single nucleotide variant	NM_032172.3(USP42):c.1712C>T (p.Thr571Met)	not specified [RCV004257157]	likely benign	7	6149908	6149908	Human		name
329391808	CV2453145	single nucleotide variant	NM_032172.3(USP42):c.2745C>A (p.Asp915Glu)	not specified [RCV004279529]	uncertain significance	7	6154299	6154299	Human		name
329356378	CV2460290	single nucleotide variant	NM_032172.3(USP42):c.1849G>A (p.Glu617Lys)	not specified [RCV004266837]	uncertain significance	7	6150045	6150045	Human		name
401727890	CV2678555	single nucleotide variant	NM_032172.3(USP42):c.1186A>G (p.Ile396Val)	not specified [RCV004292565]	uncertain significance	7	6146202	6146202	Human		name
401727465	CV2681040	single nucleotide variant	NM_032172.3(USP42):c.2956C>T (p.Arg986Trp)	not specified [RCV004296104]	uncertain significance	7	6154510	6154510	Human		name
401725219	CV2697318	single nucleotide variant	NM_032172.3(USP42):c.2273A>C (p.Glu758Ala)	not specified [RCV004304076]	uncertain significance	7	6153827	6153827	Human		name
401740786	CV2702632	single nucleotide variant	NM_032172.3(USP42):c.2876G>C (p.Arg959Pro)	not specified [RCV004318901]	uncertain significance	7	6154430	6154430	Human		name
401759704	CV2705686	single nucleotide variant	NM_032172.3(USP42):c.2807C>G (p.Ser936Cys)	not specified [RCV004318539]	uncertain significance	7	6154361	6154361	Human		name
401778469	CV2709160	single nucleotide variant	NM_032172.3(USP42):c.2779G>A (p.Ala927Thr)	not specified [RCV004316345]	uncertain significance	7	6154333	6154333	Human		name
401763126	CV2710449	single nucleotide variant	NM_032172.3(USP42):c.2269G>A (p.Ala757Thr)	not specified [RCV004317602]	uncertain significance	7	6153823	6153823	Human		name
401771103	CV2726365	single nucleotide variant	NM_032172.3(USP42):c.2969G>A (p.Arg990His)	not specified [RCV004326798]	uncertain significance	7	6154523	6154523	Human		name
401857011	CV2759923	single nucleotide variant	NM_032172.3(USP42):c.1597C>G (p.Arg533Gly)	not specified [RCV004345348]	uncertain significance	7	6149793	6149793	Human		name
401889823	CV2763428	single nucleotide variant	NM_032172.3(USP42):c.1657G>A (p.Val553Ile)	not specified [RCV004349317]	uncertain significance	7	6149853	6149853	Human		name
401894037	CV2774390	single nucleotide variant	NM_032172.3(USP42):c.2006C>T (p.Pro669Leu)	not specified [RCV004347732]	likely benign	7	6150202	6150202	Human		name
401885743	CV2774496	single nucleotide variant	NM_032172.3(USP42):c.2309G>A (p.Ser770Asn)	not specified [RCV004349985]	uncertain significance	7	6153863	6153863	Human		name
401880838	CV2787659	single nucleotide variant	NM_032172.3(USP42):c.2446C>T (p.Pro816Ser)	not specified [RCV004356585]	likely benign	7	6154000	6154000	Human		name
405800745	CV3338257	single nucleotide variant	NM_032172.3(USP42):c.1144C>T (p.Leu382Phe)	not specified [RCV004477456]	uncertain significance	7	6146160	6146160	Human		name
405800747	CV3338258	single nucleotide variant	NM_032172.3(USP42):c.1487T>C (p.Val496Ala)	not specified [RCV004477457]	uncertain significance	7	6149683	6149683	Human		name
405800749	CV3338259	single nucleotide variant	NM_032172.3(USP42):c.1598G>T (p.Arg533Leu)	not specified [RCV004477458]	uncertain significance	7	6149794	6149794	Human		name
405800751	CV3338260	single nucleotide variant	NM_032172.3(USP42):c.1615C>T (p.Pro539Ser)	not specified [RCV004477459]	uncertain significance	7	6149811	6149811	Human		name
405800753	CV3338261	single nucleotide variant	NM_032172.3(USP42):c.1625A>G (p.His542Arg)	not specified [RCV004477460]	uncertain significance	7	6149821	6149821	Human		name
405800755	CV3338262	single nucleotide variant	NM_032172.3(USP42):c.1649C>G (p.Thr550Ser)	not specified [RCV004477461]	likely benign	7	6149845	6149845	Human		name
405800757	CV3338263	single nucleotide variant	NM_032172.3(USP42):c.1666T>C (p.Ser556Pro)	not specified [RCV004477462]	uncertain significance	7	6149862	6149862	Human		name
405800759	CV3338264	single nucleotide variant	NM_032172.3(USP42):c.1723T>A (p.Ser575Thr)	not specified [RCV004477463]	uncertain significance	7	6149919	6149919	Human		name
405800761	CV3338265	single nucleotide variant	NM_032172.3(USP42):c.1750C>T (p.Arg584Cys)	not specified [RCV004477464]	uncertain significance	7	6149946	6149946	Human		name
405800762	CV3338266	single nucleotide variant	NM_032172.3(USP42):c.1943C>T (p.Pro648Leu)	not specified [RCV004477465]	uncertain significance	7	6150139	6150139	Human		name
405800766	CV3338268	single nucleotide variant	NM_032172.3(USP42):c.2063A>C (p.His688Pro)	not specified [RCV004477467]	uncertain significance	7	6150259	6150259	Human		name
405800974	CV3338269	single nucleotide variant	NM_032172.3(USP42):c.2065T>G (p.Ser689Ala)	not specified [RCV004477468]	uncertain significance	7	6150261	6150261	Human		name
405800770	CV3338270	single nucleotide variant	NM_032172.3(USP42):c.2395G>A (p.Glu799Lys)	not specified [RCV004477469]	uncertain significance	7	6153949	6153949	Human		name
405800772	CV3338271	single nucleotide variant	NM_032172.3(USP42):c.2474C>T (p.Thr825Ile)	not specified [RCV004477470]	uncertain significance	7	6154028	6154028	Human		name
405800774	CV3338272	single nucleotide variant	NM_032172.3(USP42):c.2489C>T (p.Pro830Leu)	not specified [RCV004477471]	uncertain significance	7	6154043	6154043	Human		name
405800776	CV3338273	single nucleotide variant	NM_032172.3(USP42):c.2546C>T (p.Ala849Val)	not specified [RCV004477472]	likely benign	7	6154100	6154100	Human		name
405800777	CV3338274	single nucleotide variant	NM_032172.3(USP42):c.2554C>T (p.Pro852Ser)	not specified [RCV004477473]	uncertain significance	7	6154108	6154108	Human		name
405800779	CV3338275	single nucleotide variant	NM_032172.3(USP42):c.2572G>A (p.Ala858Thr)	not specified [RCV004477474]	uncertain significance	7	6154126	6154126	Human		name
405800783	CV3338277	single nucleotide variant	NM_032172.3(USP42):c.2632G>T (p.Asp878Tyr)	not specified [RCV004477476]	uncertain significance	7	6154186	6154186	Human		name
405800785	CV3338278	single nucleotide variant	NM_032172.3(USP42):c.2702C>T (p.Ala901Val)	not specified [RCV004477477]	uncertain significance	7	6154256	6154256	Human		name
405800787	CV3338279	single nucleotide variant	NM_032172.3(USP42):c.2755A>G (p.Ser919Gly)	not specified [RCV004477478]	uncertain significance	7	6154309	6154309	Human		name
405800791	CV3338281	single nucleotide variant	NM_032172.3(USP42):c.2795C>T (p.Ala932Val)	not specified [RCV004477480]	likely benign	7	6154349	6154349	Human		name
405800793	CV3338282	single nucleotide variant	NM_032172.3(USP42):c.2849G>A (p.Arg950Gln)	not specified [RCV004477481]	uncertain significance	7	6154403	6154403	Human		name
405800794	CV3338283	single nucleotide variant	NM_032172.3(USP42):c.2918C>T (p.Thr973Ile)	not specified [RCV004477482]	uncertain significance	7	6154472	6154472	Human		name
405800796	CV3338284	single nucleotide variant	NM_032172.3(USP42):c.2936G>A (p.Arg979Gln)	not specified [RCV004477483]	uncertain significance	7	6154490	6154490	Human		name
407528881	CV3487645	single nucleotide variant	NM_032172.3(USP42):c.1472A>G (p.Asn491Ser)	not specified [RCV004680613]	likely benign	7	6149668	6149668	Human		name
407528888	CV3487649	single nucleotide variant	NM_032172.3(USP42):c.1277A>G (p.His426Arg)	not specified [RCV004680617]	uncertain significance	7	6147783	6147783	Human		name
407528890	CV3487650	single nucleotide variant	NM_032172.3(USP42):c.2851G>A (p.Gly951Ser)	not specified [RCV004680618]	uncertain significance	7	6154405	6154405	Human		name
407528892	CV3487651	single nucleotide variant	NM_032172.3(USP42):c.1912G>A (p.Gly638Ser)	not specified [RCV004680619]	uncertain significance	7	6150108	6150108	Human		name
407528894	CV3487652	single nucleotide variant	NM_032172.3(USP42):c.1748C>G (p.Pro583Arg)	not specified [RCV004680620]	uncertain significance	7	6149944	6149944	Human		name
407528898	CV3487654	single nucleotide variant	NM_032172.3(USP42):c.2675C>T (p.Ala892Val)	not specified [RCV004680622]	likely benign	7	6154229	6154229	Human		name
407528900	CV3487655	single nucleotide variant	NM_032172.3(USP42):c.2907C>A (p.Ser969Arg)	not specified [RCV004680623]	uncertain significance	7	6154461	6154461	Human		name
407528902	CV3487656	single nucleotide variant	NM_032172.3(USP42):c.2528C>T (p.Pro843Leu)	not specified [RCV004680624]	uncertain significance	7	6154082	6154082	Human		name
407528906	CV3487658	single nucleotide variant	NM_032172.3(USP42):c.2632G>A (p.Asp878Asn)	not specified [RCV004680626]	uncertain significance	7	6154186	6154186	Human		name
407528908	CV3487659	single nucleotide variant	NM_032172.3(USP42):c.2812G>A (p.Ala938Thr)	not specified [RCV004680627]	uncertain significance	7	6154366	6154366	Human		name
407528911	CV3487660	single nucleotide variant	NM_032172.3(USP42):c.2595G>T (p.Glu865Asp)	not specified [RCV004680628]	likely benign	7	6154149	6154149	Human		name
407528913	CV3487661	single nucleotide variant	NM_032172.3(USP42):c.2722C>A (p.Pro908Thr)	not specified [RCV004680629]	likely benign	7	6154276	6154276	Human		name
407528914	CV3487662	single nucleotide variant	NM_032172.3(USP42):c.2519C>T (p.Ala840Val)	not specified [RCV004680630]	uncertain significance	7	6154073	6154073	Human		name
407528916	CV3487663	single nucleotide variant	NM_032172.3(USP42):c.1628G>A (p.Ser543Asn)	not specified [RCV004680631]	likely benign	7	6149824	6149824	Human		name
407528922	CV3487666	single nucleotide variant	NM_032172.3(USP42):c.2984C>G (p.Ala995Gly)	not specified [RCV004680634]	uncertain significance	7	6154538	6154538	Human		name
407528924	CV3487667	single nucleotide variant	NM_032172.3(USP42):c.1828G>A (p.Glu610Lys)	not specified [RCV004680635]	uncertain significance	7	6150024	6150024	Human		name
597798975	CV3623084	single nucleotide variant	NM_032172.3(USP42):c.1928A>G (p.Asp643Gly)	not specified [RCV004879448]	uncertain significance	7	6150124	6150124	Human		name
597798979	CV3623087	single nucleotide variant	NM_032172.3(USP42):c.1645C>G (p.Pro549Ala)	not specified [RCV004879450]	likely benign	7	6149841	6149841	Human		name
597798981	CV3623088	single nucleotide variant	NM_032172.3(USP42):c.2294C>G (p.Ala765Gly)	not specified [RCV004879451]	uncertain significance	7	6153848	6153848	Human		name
597798988	CV3623091	single nucleotide variant	NM_032172.3(USP42):c.2804C>T (p.Pro935Leu)	not specified [RCV004879454]	uncertain significance	7	6154358	6154358	Human		name
597798994	CV3623094	single nucleotide variant	NM_032172.3(USP42):c.2686G>A (p.Ala896Thr)	not specified [RCV004879457]	uncertain significance	7	6154240	6154240	Human		name
597798997	CV3623095	single nucleotide variant	NM_032172.3(USP42):c.1974C>G (p.Asn658Lys)	not specified [RCV004879458]	uncertain significance	7	6150170	6150170	Human		name
597724141	CV3623099	single nucleotide variant	NM_032172.3(USP42):c.2523G>C (p.Glu841Asp)	not specified [RCV004888144]	uncertain significance	7	6154077	6154077	Human		name
597799007	CV3623101	single nucleotide variant	NM_032172.3(USP42):c.2569C>G (p.Pro857Ala)	not specified [RCV004879463]	uncertain significance	7	6154123	6154123	Human		name
597724152	CV3623102	single nucleotide variant	NM_032172.3(USP42):c.1285G>A (p.Gly429Ser)	not specified [RCV004888145]	uncertain significance	7	6147791	6147791	Human		name
597724172	CV3623104	single nucleotide variant	NM_032172.3(USP42):c.2483C>T (p.Ala828Val)	not specified [RCV004888147]	uncertain significance	7	6154037	6154037	Human		name
597799244	CV3623106	single nucleotide variant	NM_032172.3(USP42):c.2036C>T (p.Ala679Val)	not specified [RCV004879465]	uncertain significance	7	6150232	6150232	Human		name
597799239	CV3623109	single nucleotide variant	NM_032172.3(USP42):c.1918G>C (p.Asp640His)	not specified [RCV004879467]	uncertain significance	7	6150114	6150114	Human		name
597799237	CV3623110	single nucleotide variant	NM_032172.3(USP42):c.2638G>A (p.Ala880Thr)	not specified [RCV004879468]	uncertain significance	7	6154192	6154192	Human		name
597799235	CV3623111	single nucleotide variant	NM_032172.3(USP42):c.1391C>A (p.Pro464Gln)	not specified [RCV004879469]	uncertain significance	7	6149587	6149587	Human		name
597799234	CV3623114	single nucleotide variant	NM_032172.3(USP42):c.2041T>C (p.Cys681Arg)	not specified [RCV004879470]	uncertain significance	7	6150237	6150237	Human		name
597696620	CV3623115	single nucleotide variant	NM_032172.3(USP42):c.1010A>G (p.Tyr337Cys)	not specified [RCV004885175]	uncertain significance	7	6145535	6145535	Human		name
597799231	CV3623119	single nucleotide variant	NM_032172.3(USP42):c.1653G>C (p.Lys551Asn)	not specified [RCV004879471]	uncertain significance	7	6149849	6149849	Human		name
598275319	CV3932867	single nucleotide variant	NM_032172.3(USP42):c.2440G>A (p.Ala814Thr)	not specified [RCV005304453]	uncertain significance	7	6153994	6153994	Human		name
598275320	CV3932868	single nucleotide variant	NM_032172.3(USP42):c.1876A>C (p.Asn626His)	not specified [RCV005304454]	uncertain significance	7	6150072	6150072	Human		name
598238700	CV3932872	single nucleotide variant	NM_032172.3(USP42):c.2546C>A (p.Ala849Glu)	not specified [RCV005296458]	uncertain significance	7	6154100	6154100	Human		name
598238708	CV3932874	single nucleotide variant	NM_032172.3(USP42):c.2441C>T (p.Ala814Val)	not specified [RCV005296460]	uncertain significance	7	6153995	6153995	Human		name
598204366	CV3932880	single nucleotide variant	NM_032172.3(USP42):c.2575C>G (p.Pro859Ala)	not specified [RCV005290680]	uncertain significance	7	6154129	6154129	Human		name
598238723	CV3932881	single nucleotide variant	NM_032172.3(USP42):c.2701G>C (p.Ala901Pro)	not specified [RCV005296463]	uncertain significance	7	6154255	6154255	Human		name
598238729	CV3932882	single nucleotide variant	NM_032172.3(USP42):c.2365G>C (p.Gly789Arg)	not specified [RCV005296464]	uncertain significance	7	6153919	6153919	Human		name
598238735	CV3932883	single nucleotide variant	NM_032172.3(USP42):c.2582C>T (p.Ala861Val)	not specified [RCV005296465]	likely benign	7	6154136	6154136	Human		name
598238741	CV3932884	single nucleotide variant	NM_032172.3(USP42):c.2863A>C (p.Ser955Arg)	not specified [RCV005296466]	uncertain significance	7	6154417	6154417	Human		name
598204411	CV3932892	single nucleotide variant	NM_032172.3(USP42):c.2257G>T (p.Gly753Cys)	not specified [RCV005290686]	uncertain significance	7	6153811	6153811	Human		name
598238756	CV3932896	single nucleotide variant	NM_032172.3(USP42):c.1378A>G (p.Met460Val)	not specified [RCV005296469]	likely benign	7	6147884	6147884	Human		name
598204440	CV3932900	single nucleotide variant	NM_032172.3(USP42):c.1262T>A (p.Leu421His)	not specified [RCV005290691]	uncertain significance	7	6147768	6147768	Human		name
598204452	CV3932902	single nucleotide variant	NM_032172.3(USP42):c.2351C>T (p.Pro784Leu)	not specified [RCV005290693]	uncertain significance	7	6153905	6153905	Human		name
156274077	CV2202568	single nucleotide variant	NM_032172.3(USP42):c.3439C>T (p.Leu1147Phe)	not specified [RCV004080851]	uncertain significance	7	6154993	6154993	Human		name
155979721	CV2215249	single nucleotide variant	NM_032172.3(USP42):c.3896G>A (p.Arg1299Gln)	not specified [RCV004086952]	uncertain significance	7	6157008	6157008	Human		name
156386496	CV2228231	single nucleotide variant	NM_032172.3(USP42):c.3133G>C (p.Gly1045Arg)	not specified [RCV004097965]	uncertain significance	7	6154687	6154687	Human		name
156063041	CV2232118	single nucleotide variant	NM_032172.3(USP42):c.3505A>G (p.Asn1169Asp)	not specified [RCV004093153]	uncertain significance	7	6155059	6155059	Human		name
156180379	CV2246015	single nucleotide variant	NM_032172.3(USP42):c.3386C>G (p.Pro1129Arg)	not specified [RCV004113933]	uncertain significance	7	6154940	6154940	Human		name
156212088	CV2259926	single nucleotide variant	NM_032172.3(USP42):c.3370G>T (p.Ala1124Ser)	not specified [RCV004118955]	uncertain significance	7	6154924	6154924	Human		name
156212105	CV2259927	single nucleotide variant	NM_032172.3(USP42):c.3371C>T (p.Ala1124Val)	not specified [RCV004118956]	uncertain significance	7	6154925	6154925	Human		name
156158237	CV2262464	single nucleotide variant	NM_032172.3(USP42):c.3894A>T (p.Leu1298Phe)	not specified [RCV004128902]	uncertain significance	7	6157006	6157006	Human		name
155917066	CV2278527	single nucleotide variant	NM_032172.3(USP42):c.3631C>A (p.Arg1211Ser)	not specified [RCV004132963]	uncertain significance	7	6155185	6155185	Human		name
156198084	CV2306847	single nucleotide variant	NM_032172.3(USP42):c.3812G>A (p.Arg1271Gln)	not specified [RCV004159412]	uncertain significance	7	6156924	6156924	Human		name
155964153	CV2308355	single nucleotide variant	NM_032172.3(USP42):c.3776C>G (p.Pro1259Arg)	not specified [RCV004164835]	uncertain significance	7	6156888	6156888	Human		name
156288754	CV2309609	single nucleotide variant	NM_032172.3(USP42):c.3887A>T (p.Lys1296Ile)	not specified [RCV004158983]	uncertain significance	7	6156999	6156999	Human		name
156066519	CV2317852	single nucleotide variant	NM_032172.3(USP42):c.3810C>A (p.Phe1270Leu)	not specified [RCV004175090]	uncertain significance	7	6156922	6156922	Human		name
156273065	CV2323495	single nucleotide variant	NM_032172.3(USP42):c.3151C>G (p.Pro1051Ala)	not specified [RCV004165703]	likely benign	7	6154705	6154705	Human		name
156360945	CV2329716	single nucleotide variant	NM_032172.3(USP42):c.3740C>T (p.Ser1247Leu)	not specified [RCV004180820]	uncertain significance	7	6156852	6156852	Human		name
155967505	CV2329927	single nucleotide variant	NM_032172.3(USP42):c.3037T>G (p.Ser1013Ala)	not specified [RCV004183382]	uncertain significance	7	6154591	6154591	Human		name
155972275	CV2334318	single nucleotide variant	NM_032172.3(USP42):c.3733A>G (p.Arg1245Gly)	not specified [RCV004188298]	uncertain significance	7	6156845	6156845	Human		name
155973091	CV2334401	single nucleotide variant	NM_032172.3(USP42):c.3526A>G (p.Lys1176Glu)	not specified [RCV004188377]	uncertain significance	7	6155080	6155080	Human		name
156283250	CV2334654	single nucleotide variant	NM_032172.3(USP42):c.3038C>T (p.Ser1013Phe)	not specified [RCV004188639]	uncertain significance	7	6154592	6154592	Human		name
156065096	CV2346452	single nucleotide variant	NM_032172.3(USP42):c.3316G>A (p.Ala1106Thr)	not specified [RCV004206378]	uncertain significance	7	6154870	6154870	Human		name
156065448	CV2346520	single nucleotide variant	NM_032172.3(USP42):c.3448C>G (p.Arg1150Gly)	not specified [RCV004206440]	uncertain significance	7	6155002	6155002	Human		name
156002328	CV2347671	single nucleotide variant	NM_032172.3(USP42):c.3895C>G (p.Arg1299Gly)	not specified [RCV004200603]	uncertain significance	7	6157007	6157007	Human		name
156071131	CV2353089	single nucleotide variant	NM_032172.3(USP42):c.3492C>G (p.His1164Gln)	not specified [RCV004203571]	uncertain significance	7	6155046	6155046	Human		name
156052244	CV2363374	single nucleotide variant	NM_032172.3(USP42):c.3811C>T (p.Arg1271Trp)	not specified [RCV004213912]	uncertain significance	7	6156923	6156923	Human		name
156101156	CV2367620	single nucleotide variant	NM_032172.3(USP42):c.3390C>G (p.Asp1130Glu)	not specified [RCV004211545]	likely benign	7	6154944	6154944	Human		name
156347403	CV2382890	single nucleotide variant	NM_032172.3(USP42):c.3383A>C (p.His1128Pro)	not specified [RCV004217488]	uncertain significance	7	6154937	6154937	Human		name
156091264	CV2384657	single nucleotide variant	NM_032172.3(USP42):c.3143A>T (p.Lys1048Met)	not specified [RCV004232435]	uncertain significance	7	6154697	6154697	Human		name
156109711	CV2390402	single nucleotide variant	NM_032172.3(USP42):c.3271C>T (p.Arg1091Trp)	not specified [RCV004234102]	uncertain significance	7	6154825	6154825	Human		name
329392153	CV2441271	single nucleotide variant	NM_032172.3(USP42):c.3518A>G (p.His1173Arg)	not specified [RCV004264002]	uncertain significance	7	6155072	6155072	Human		name
329357253	CV2453502	single nucleotide variant	NM_032172.3(USP42):c.3465A>C (p.Glu1155Asp)	not specified [RCV004269192]	uncertain significance	7	6155019	6155019	Human		name
329362888	CV2464821	single nucleotide variant	NM_032172.3(USP42):c.3285C>G (p.Asp1095Glu)	not specified [RCV004284770]	uncertain significance	7	6154839	6154839	Human		name
329392879	CV2469031	single nucleotide variant	NM_032172.3(USP42):c.3376G>T (p.Ala1126Ser)	not specified [RCV004274279]	uncertain significance	7	6154930	6154930	Human		name
401731653	CV2693924	single nucleotide variant	NM_032172.3(USP42):c.3802G>A (p.Ala1268Thr)	not specified [RCV004300222]	uncertain significance	7	6156914	6156914	Human		name
401735559	CV2702808	single nucleotide variant	NM_032172.3(USP42):c.3242G>T (p.Arg1081Leu)	not specified [RCV004319371]	uncertain significance	7	6154796	6154796	Human		name
401722394	CV2706500	single nucleotide variant	NM_032172.3(USP42):c.3493G>A (p.Asp1165Asn)	not specified [RCV004317314]	uncertain significance	7	6155047	6155047	Human		name
401774510	CV2713520	single nucleotide variant	NM_032172.3(USP42):c.3873C>G (p.Phe1291Leu)	not specified [RCV004319118]	uncertain significance	7	6156985	6156985	Human		name
401783055	CV2716108	single nucleotide variant	NM_032172.3(USP42):c.3568C>G (p.Pro1190Ala)	not specified [RCV004323351]	uncertain significance	7	6155122	6155122	Human		name
401760132	CV2718725	single nucleotide variant	NM_032172.3(USP42):c.3415C>G (p.Leu1139Val)	not specified [RCV004328481]	uncertain significance	7	6154969	6154969	Human		name
401762070	CV2722627	single nucleotide variant	NM_032172.3(USP42):c.3353G>A (p.Arg1118His)	not specified [RCV004325084]	uncertain significance	7	6154907	6154907	Human		name
401752057	CV2723103	single nucleotide variant	NM_032172.3(USP42):c.3511G>C (p.Asp1171His)	not specified [RCV004327574]	uncertain significance	7	6155065	6155065	Human		name
401751472	CV2727006	single nucleotide variant	NM_032172.3(USP42):c.3065C>T (p.Ser1022Phe)	not specified [RCV004325388]	uncertain significance	7	6154619	6154619	Human		name
401893149	CV2755883	single nucleotide variant	NM_032172.3(USP42):c.3142A>G (p.Lys1048Glu)	not specified [RCV004335976]	uncertain significance	7	6154696	6154696	Human		name
401882486	CV2767969	single nucleotide variant	NM_032172.3(USP42):c.3178C>G (p.Arg1060Gly)	not specified [RCV004348216]	uncertain significance	7	6154732	6154732	Human		name
401885406	CV2783286	single nucleotide variant	NM_032172.3(USP42):c.3326G>C (p.Arg1109Thr)	not specified [RCV004363894]	uncertain significance	7	6154880	6154880	Human		name
405800799	CV3338285	single nucleotide variant	NM_032172.3(USP42):c.2998C>T (p.Pro1000Ser)	not specified [RCV004477484]	uncertain significance	7	6154552	6154552	Human		name
405800800	CV3338286	single nucleotide variant	NM_032172.3(USP42):c.3070C>T (p.His1024Tyr)	not specified [RCV004477485]	uncertain significance	7	6154624	6154624	Human		name
405800802	CV3338287	single nucleotide variant	NM_032172.3(USP42):c.3199G>A (p.Ala1067Thr)	not specified [RCV004477486]	uncertain significance	7	6154753	6154753	Human		name
405800804	CV3338288	single nucleotide variant	NM_032172.3(USP42):c.3208G>A (p.Ala1070Thr)	not specified [RCV004477487]	likely benign	7	6154762	6154762	Human		name
405800806	CV3338289	single nucleotide variant	NM_032172.3(USP42):c.3226C>G (p.Pro1076Ala)	not specified [RCV004477488]	uncertain significance	7	6154780	6154780	Human		name
405800808	CV3338290	single nucleotide variant	NM_032172.3(USP42):c.3278A>C (p.His1093Pro)	not specified [RCV004477489]	uncertain significance	7	6154832	6154832	Human		name
405800810	CV3338291	single nucleotide variant	NM_032172.3(USP42):c.3344G>C (p.Ser1115Thr)	not specified [RCV004477490]	uncertain significance	7	6154898	6154898	Human		name
405800812	CV3338292	single nucleotide variant	NM_032172.3(USP42):c.3355G>A (p.Ala1119Thr)	not specified [RCV004477491]	uncertain significance	7	6154909	6154909	Human		name
405800816	CV3338294	single nucleotide variant	NM_032172.3(USP42):c.3422C>T (p.Ala1141Val)	not specified [RCV004477493]	uncertain significance	7	6154976	6154976	Human		name
405800820	CV3338296	single nucleotide variant	NM_032172.3(USP42):c.3796A>G (p.Thr1266Ala)	not specified [RCV004477495]	uncertain significance	7	6156908	6156908	Human		name
405800822	CV3338297	single nucleotide variant	NM_032172.3(USP42):c.3862G>A (p.Val1288Ile)	not specified [RCV004477496]	uncertain significance	7	6156974	6156974	Human		name
405800824	CV3338298	single nucleotide variant	NM_032172.3(USP42):c.3922C>T (p.Arg1308Cys)	not specified [RCV004477497]	uncertain significance	7	6157034	6157034	Human		name
407528882	CV3487646	single nucleotide variant	NM_032172.3(USP42):c.3404A>G (p.Asp1135Gly)	not specified [RCV004680614]	uncertain significance	7	6154958	6154958	Human		name
407528885	CV3487647	single nucleotide variant	NM_032172.3(USP42):c.3152C>G (p.Pro1051Arg)	not specified [RCV004680615]	uncertain significance	7	6154706	6154706	Human		name
407528896	CV3487653	single nucleotide variant	NM_032172.3(USP42):c.3510T>G (p.Ser1170Arg)	not specified [RCV004680621]	uncertain significance	7	6155064	6155064	Human		name
407528904	CV3487657	single nucleotide variant	NM_032172.3(USP42):c.3299G>A (p.Arg1100His)	not specified [RCV004680625]	uncertain significance	7	6154853	6154853	Human		name
407528918	CV3487664	single nucleotide variant	NM_032172.3(USP42):c.3346A>G (p.Ser1116Gly)	not specified [RCV004680632]	uncertain significance	7	6154900	6154900	Human		name
407528920	CV3487665	single nucleotide variant	NM_032172.3(USP42):c.3319C>T (p.Arg1107Trp)	not specified [RCV004680633]	uncertain significance	7	6154873	6154873	Human		name
597798973	CV3623083	single nucleotide variant	NM_032172.3(USP42):c.3536G>A (p.Arg1179Gln)	not specified [RCV004879447]	likely benign	7	6155090	6155090	Human		name
597798984	CV3623089	single nucleotide variant	NM_032172.3(USP42):c.3377C>A (p.Ala1126Asp)	not specified [RCV004879452]	uncertain significance	7	6154931	6154931	Human		name
597798990	CV3623092	single nucleotide variant	NM_032172.3(USP42):c.3181T>C (p.Tyr1061His)	not specified [RCV004879455]	uncertain significance	7	6154735	6154735	Human		name
597798992	CV3623093	single nucleotide variant	NM_032172.3(USP42):c.3249C>G (p.His1083Gln)	not specified [RCV004879456]	uncertain significance	7	6154803	6154803	Human		name
597799001	CV3623097	single nucleotide variant	NM_032172.3(USP42):c.3272G>A (p.Arg1091Gln)	not specified [RCV004879460]	uncertain significance	7	6154826	6154826	Human		name
597799003	CV3623098	single nucleotide variant	NM_032172.3(USP42):c.3374T>G (p.Leu1125Arg)	not specified [RCV004879461]	uncertain significance	7	6154928	6154928	Human		name
597724159	CV3623103	single nucleotide variant	NM_032172.3(USP42):c.3694A>G (p.Arg1232Gly)	not specified [RCV004888146]	uncertain significance	7	6156806	6156806	Human		name
597724184	CV3623108	single nucleotide variant	NM_032172.3(USP42):c.3127G>C (p.Gly1043Arg)	not specified [RCV004888148]	uncertain significance	7	6154681	6154681	Human		name
597724196	CV3623112	single nucleotide variant	NM_032172.3(USP42):c.3560T>C (p.Leu1187Pro)	not specified [RCV004888149]	uncertain significance	7	6155114	6155114	Human		name
597724206	CV3623113	single nucleotide variant	NM_032172.3(USP42):c.3295G>A (p.Gly1099Ser)	not specified [RCV004888150]	likely benign	7	6154849	6154849	Human		name
597696645	CV3623118	single nucleotide variant	NM_032172.3(USP42):c.3073C>G (p.Arg1025Gly)	not specified [RCV004885178]	uncertain significance	7	6154627	6154627	Human		name
598275318	CV3932866	single nucleotide variant	NM_032172.3(USP42):c.3865G>A (p.Gly1289Arg)	not specified [RCV005304452]	uncertain significance	7	6156977	6156977	Human		name
598204341	CV3932869	single nucleotide variant	NM_032172.3(USP42):c.3506A>G (p.Asn1169Ser)	not specified [RCV005290676]	uncertain significance	7	6155060	6155060	Human		name
598238694	CV3932871	single nucleotide variant	NM_032172.3(USP42):c.3557C>T (p.Pro1186Leu)	not specified [RCV005296457]	uncertain significance	7	6155111	6155111	Human		name
598238713	CV3932875	single nucleotide variant	NM_032172.3(USP42):c.3722A>G (p.Lys1241Arg)	not specified [RCV005296461]	uncertain significance	7	6156834	6156834	Human		name
598204347	CV3932876	single nucleotide variant	NM_032172.3(USP42):c.3299G>T (p.Arg1100Leu)	not specified [RCV005290677]	uncertain significance	7	6154853	6154853	Human		name
598238718	CV3932877	single nucleotide variant	NM_032172.3(USP42):c.3013A>T (p.Arg1005Trp)	not specified [RCV005296462]	uncertain significance	7	6154567	6154567	Human		name
598204353	CV3932878	single nucleotide variant	NM_032172.3(USP42):c.3263T>C (p.Leu1088Pro)	not specified [RCV005290678]	uncertain significance	7	6154817	6154817	Human		name
598204360	CV3932879	single nucleotide variant	NM_032172.3(USP42):c.3752T>A (p.Val1251Asp)	not specified [RCV005290679]	uncertain significance	7	6156864	6156864	Human		name
598204382	CV3932886	single nucleotide variant	NM_032172.3(USP42):c.3309C>G (p.Cys1103Trp)	not specified [RCV005290682]	uncertain significance	7	6154863	6154863	Human		name
598204396	CV3932888	single nucleotide variant	NM_032172.3(USP42):c.3200C>T (p.Ala1067Val)	not specified [RCV005290684]	uncertain significance	7	6154754	6154754	Human		name
598204404	CV3932889	single nucleotide variant	NM_032172.3(USP42):c.3548A>G (p.Gln1183Arg)	not specified [RCV005290685]	uncertain significance	7	6155102	6155102	Human		name
598238751	CV3932891	single nucleotide variant	NM_032172.3(USP42):c.3164G>C (p.Arg1055Pro)	not specified [RCV005296468]	uncertain significance	7	6154718	6154718	Human		name
598204417	CV3932893	single nucleotide variant	NM_032172.3(USP42):c.3788G>A (p.Ser1263Asn)	not specified [RCV005290687]	uncertain significance	7	6156900	6156900	Human		name
598204422	CV3932894	single nucleotide variant	NM_032172.3(USP42):c.3298C>G (p.Arg1100Gly)	not specified [RCV005290688]	uncertain significance	7	6154852	6154852	Human		name
598204428	CV3932895	single nucleotide variant	NM_032172.3(USP42):c.3857A>C (p.Glu1286Ala)	not specified [RCV005290689]	uncertain significance	7	6156969	6156969	Human		name
598238763	CV3932897	single nucleotide variant	NM_032172.3(USP42):c.3617A>G (p.Asp1206Gly)	not specified [RCV005296470]	uncertain significance	7	6155171	6155171	Human		name
598204434	CV3932899	single nucleotide variant	NM_032172.3(USP42):c.3349C>T (p.Pro1117Ser)	not specified [RCV005290690]	uncertain significance	7	6154903	6154903	Human		name

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