Uspl1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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107 records found for search term Uspl1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405801462	CV3338509	single nucleotide variant	NM_005800.5(USPL1):c.8A>T (p.Asp3Val)	not specified [RCV004477708]	uncertain significance	13	30621148	30621148	Human		name
156066117	CV2376148	single nucleotide variant	NM_005800.5(USPL1):c.76C>T (p.His26Tyr)	not specified [RCV004220378]	uncertain significance	13	30621216	30621216	Human		name
329398473	CV2464619	single nucleotide variant	NM_005800.5(USPL1):c.97A>G (p.Lys33Glu)	not specified [RCV004278305]	uncertain significance	13	30621237	30621237	Human		name
156398117	CV2204262	single nucleotide variant	NM_005800.5(USPL1):c.185G>A (p.Arg62Gln)	not specified [RCV004079096]	uncertain significance	13	30621849	30621849	Human		name
156351506	CV2323771	single nucleotide variant	NM_005800.5(USPL1):c.257T>G (p.Leu86Arg)	not specified [RCV004176319]	uncertain significance	13	30630863	30630863	Human		name
156120115	CV2354141	single nucleotide variant	NM_005800.5(USPL1):c.264C>A (p.Asn88Lys)	not specified [RCV004206577]	uncertain significance	13	30630870	30630870	Human		name
155919534	CV2360297	single nucleotide variant	NM_005800.5(USPL1):c.261T>A (p.Asn87Lys)	not specified [RCV004208638]	uncertain significance	13	30630867	30630867	Human		name
329356339	CV2430700	single nucleotide variant	NM_005800.5(USPL1):c.288A>C (p.Glu96Asp)	not specified [RCV004253886]	likely benign	13	30630894	30630894	Human		name
329380980	CV2464425	single nucleotide variant	NM_005800.5(USPL1):c.274C>G (p.Pro92Ala)	not specified [RCV004276353]	uncertain significance	13	30630880	30630880	Human		name
405801256	CV3338502	single nucleotide variant	NM_005800.5(USPL1):c.239C>G (p.Pro80Arg)	not specified [RCV004477701]	uncertain significance	13	30630845	30630845	Human		name
407529095	CV3487768	single nucleotide variant	NM_005800.5(USPL1):c.118G>A (p.Val40Ile)	not specified [RCV004680720]	uncertain significance	13	30621782	30621782	Human		name
598239194	CV3933027	single nucleotide variant	NM_005800.5(USPL1):c.148A>G (p.Arg50Gly)	not specified [RCV005296547]	uncertain significance	13	30621812	30621812	Human		name
156314201	CV2196610	single nucleotide variant	NM_005800.5(USPL1):c.661T>C (p.Phe221Leu)	not specified [RCV004073882]	uncertain significance	13	30631267	30631267	Human		name
156041136	CV2219537	single nucleotide variant	NM_005800.5(USPL1):c.428G>A (p.Gly143Glu)	not specified [RCV004095275]	uncertain significance	13	30631034	30631034	Human		name
156231445	CV2264402	single nucleotide variant	NM_005800.5(USPL1):c.878G>C (p.Cys293Ser)	not specified [RCV004138302]	uncertain significance	13	30637753	30637753	Human		name
156007137	CV2299666	single nucleotide variant	NM_005800.5(USPL1):c.413A>G (p.Asn138Ser)	not specified [RCV004154981]	uncertain significance	13	30631019	30631019	Human		name
156164496	CV2315094	single nucleotide variant	NM_005800.5(USPL1):c.593G>A (p.Arg198Lys)	not specified [RCV004165280]	uncertain significance	13	30631199	30631199	Human		name
156046190	CV2319080	single nucleotide variant	NM_005800.5(USPL1):c.391A>G (p.Ile131Val)	not specified [RCV004178160]	uncertain significance	13	30630997	30630997	Human		name
156269449	CV2398580	single nucleotide variant	NM_005800.5(USPL1):c.793A>C (p.Ile265Leu)	not specified [RCV004237893]	uncertain significance	13	30631399	30631399	Human		name
401739330	CV2673267	single nucleotide variant	NM_005800.5(USPL1):c.743C>T (p.Ser248Leu)	not specified [RCV004286070]	likely benign	13	30631349	30631349	Human		name
401770407	CV2678662	single nucleotide variant	NM_005800.5(USPL1):c.770G>A (p.Gly257Glu)	not specified [RCV004294702]	likely benign	13	30631376	30631376	Human		name
401721035	CV2702237	single nucleotide variant	NM_005800.5(USPL1):c.701C>T (p.Ala234Val)	not specified [RCV004314577]	uncertain significance	13	30631307	30631307	Human		name
401748405	CV2711186	single nucleotide variant	NM_005800.5(USPL1):c.595C>A (p.Pro199Thr)	not specified [RCV004312985]	likely benign	13	30631201	30631201	Human		name
401780189	CV2725920	single nucleotide variant	NM_005800.5(USPL1):c.793A>G (p.Ile265Val)	not specified [RCV004324293]	likely benign	13	30631399	30631399	Human		name
401886224	CV2771110	single nucleotide variant	NM_005800.5(USPL1):c.890C>G (p.Thr297Ser)	not specified [RCV004346114]	uncertain significance	13	30637765	30637765	Human		name
405801464	CV3338508	single nucleotide variant	NM_005800.5(USPL1):c.511C>T (p.Arg171Trp)	not specified [RCV004477707]	uncertain significance	13	30631117	30631117	Human		name
407529092	CV3487767	single nucleotide variant	NM_005800.5(USPL1):c.433G>A (p.Val145Ile)	not specified [RCV004680719]	uncertain significance	13	30631039	30631039	Human		name
407529106	CV3487776	single nucleotide variant	NM_005800.5(USPL1):c.988A>G (p.Met330Val)	not specified [RCV004680726]	uncertain significance	13	30642633	30642633	Human		name
597799266	CV3623343	single nucleotide variant	NM_005800.5(USPL1):c.506T>C (p.Leu169Ser)	not specified [RCV004879591]	uncertain significance	13	30631112	30631112	Human		name
597697192	CV3623350	single nucleotide variant	NM_005800.5(USPL1):c.403A>C (p.Lys135Gln)	not specified [RCV004885239]	likely benign	13	30631009	30631009	Human		name
597799274	CV3623351	single nucleotide variant	NM_005800.5(USPL1):c.875A>G (p.Asp292Gly)	not specified [RCV004879595]	uncertain significance	13	30637750	30637750	Human		name
597697200	CV3623354	single nucleotide variant	NM_005800.5(USPL1):c.425A>G (p.Asn142Ser)	not specified [RCV004885240]	uncertain significance	13	30631031	30631031	Human		name
597799284	CV3623357	single nucleotide variant	NM_005800.5(USPL1):c.383A>G (p.Tyr128Cys)	not specified [RCV004879600]	uncertain significance	13	30630989	30630989	Human		name
598204739	CV3933025	single nucleotide variant	NM_005800.5(USPL1):c.803G>A (p.Arg268Gln)	not specified [RCV005290742]	likely benign	13	30631409	30631409	Human		name
598204747	CV3933029	single nucleotide variant	NM_005800.5(USPL1):c.338A>C (p.Tyr113Ser)	not specified [RCV005290743]	uncertain significance	13	30630944	30630944	Human		name
598239211	CV3933031	single nucleotide variant	NM_005800.5(USPL1):c.892T>C (p.Ser298Pro)	not specified [RCV005296550]	uncertain significance	13	30637767	30637767	Human		name
156233732	CV2197141	single nucleotide variant	NM_005800.5(USPL1):c.2567G>C (p.Ser856Thr)	not specified [RCV004071565]	uncertain significance	13	30658644	30658644	Human		name
156400647	CV2199323	single nucleotide variant	NM_005800.5(USPL1):c.1174G>T (p.Ala392Ser)	not specified [RCV004082669]	uncertain significance	13	30646993	30646993	Human		name
156400649	CV2199324	single nucleotide variant	NM_005800.5(USPL1):c.1195A>C (p.Asn399His)	not specified [RCV004082670]	uncertain significance	13	30647014	30647014	Human		name
156401760	CV2217679	single nucleotide variant	NM_005800.5(USPL1):c.1648C>T (p.Pro550Ser)	not specified [RCV004083871]	uncertain significance	13	30657725	30657725	Human		name
156379553	CV2217908	single nucleotide variant	NM_005800.5(USPL1):c.1922A>G (p.Asn641Ser)	not specified [RCV004086367]	uncertain significance	13	30657999	30657999	Human		name
156224681	CV2219427	single nucleotide variant	NM_005800.5(USPL1):c.2872C>G (p.Pro958Ala)	not specified [RCV004095221]	likely benign	13	30658949	30658949	Human		name
155976395	CV2245973	single nucleotide variant	NM_005800.5(USPL1):c.2344A>G (p.Thr782Ala)	not specified [RCV004113900]	uncertain significance	13	30658421	30658421	Human		name
155994353	CV2249152	single nucleotide variant	NM_005800.5(USPL1):c.2900C>G (p.Thr967Ser)	not specified [RCV004118202]	uncertain significance	13	30658977	30658977	Human		name
155952992	CV2264294	single nucleotide variant	NM_005800.5(USPL1):c.2960A>G (p.Glu987Gly)	not specified [RCV004138217]	uncertain significance	13	30659037	30659037	Human		name
155945312	CV2269562	single nucleotide variant	NM_005800.5(USPL1):c.2767G>C (p.Val923Leu)	not specified [RCV004124664]	uncertain significance	13	30658844	30658844	Human		name
155960836	CV2285447	single nucleotide variant	NM_005800.5(USPL1):c.2150G>A (p.Arg717His)	not specified [RCV004139301]	likely benign	13	30658227	30658227	Human		name
156197929	CV2293624	single nucleotide variant	NM_005800.5(USPL1):c.2941G>T (p.Val981Phe)	not specified [RCV004153137]	uncertain significance	13	30659018	30659018	Human		name
156050799	CV2323301	single nucleotide variant	NM_005800.5(USPL1):c.2577T>G (p.Cys859Trp)	not specified [RCV004171715]	uncertain significance	13	30658654	30658654	Human		name
156192207	CV2336000	single nucleotide variant	NM_005800.5(USPL1):c.1745A>G (p.Asn582Ser)	not specified [RCV004189606]	uncertain significance	13	30657822	30657822	Human		name
155977979	CV2339878	single nucleotide variant	NM_005800.5(USPL1):c.1762C>G (p.Leu588Val)	not specified [RCV004189984]	uncertain significance	13	30657839	30657839	Human		name
156103821	CV2352405	single nucleotide variant	NM_005800.5(USPL1):c.1672C>T (p.Arg558Cys)	not specified [RCV004200872]	uncertain significance	13	30657749	30657749	Human		name
155927849	CV2391553	single nucleotide variant	NM_005800.5(USPL1):c.2799A>C (p.Glu933Asp)	not specified [RCV004239934]	uncertain significance	13	30658876	30658876	Human		name
329400724	CV2438706	single nucleotide variant	NM_005800.5(USPL1):c.2737A>G (p.Arg913Gly)	not specified [RCV004261859]	likely benign	13	30658814	30658814	Human		name
329389583	CV2445069	single nucleotide variant	NM_005800.5(USPL1):c.2447G>A (p.Arg816His)	not specified [RCV004261674]	likely benign	13	30658524	30658524	Human		name
329391939	CV2445199	single nucleotide variant	NM_005800.5(USPL1):c.2747G>A (p.Arg916Gln)	not specified [RCV004263834]	uncertain significance	13	30658824	30658824	Human		name
329390588	CV2455323	single nucleotide variant	NM_005800.5(USPL1):c.2438A>G (p.Lys813Arg)	not specified [RCV004274831]	likely benign	13	30658515	30658515	Human		name
329370128	CV2461623	single nucleotide variant	NM_005800.5(USPL1):c.2113T>C (p.Phe705Leu)	not specified [RCV004269798]	uncertain significance	13	30658190	30658190	Human		name
329381597	CV2471308	single nucleotide variant	NM_005800.5(USPL1):c.1276T>G (p.Leu426Val)	not specified [RCV004280323]	uncertain significance	13	30653185	30653185	Human		name
401753691	CV2685027	single nucleotide variant	NM_005800.5(USPL1):c.2777A>T (p.Asp926Val)	not specified [RCV004289610]	uncertain significance	13	30658854	30658854	Human		name
401781879	CV2689977	single nucleotide variant	NM_005800.5(USPL1):c.1098C>A (p.His366Gln)	not specified [RCV004297860]	uncertain significance	13	30642743	30642743	Human		name
401732133	CV2690308	single nucleotide variant	NM_005800.5(USPL1):c.2522A>G (p.His841Arg)	not specified [RCV004302304]	uncertain significance	13	30658599	30658599	Human		name
401771800	CV2693517	single nucleotide variant	NM_005800.5(USPL1):c.2710G>C (p.Ala904Pro)	not specified [RCV004297503]	uncertain significance	13	30658787	30658787	Human		name
401743374	CV2715465	single nucleotide variant	NM_005800.5(USPL1):c.1480A>G (p.Ile494Val)	not specified [RCV004326567]	uncertain significance	13	30657557	30657557	Human		name
401867010	CV2792580	single nucleotide variant	NM_005800.5(USPL1):c.1126C>G (p.Leu376Val)	not specified [RCV004363612]	uncertain significance	13	30646945	30646945	Human		name
401895152	CV2792821	single nucleotide variant	NM_005800.5(USPL1):c.1516G>C (p.Asp506His)	not specified [RCV004365571]	uncertain significance	13	30657593	30657593	Human		name
405801247	CV3338497	single nucleotide variant	NM_005800.5(USPL1):c.1907T>A (p.Val636Glu)	not specified [RCV004477696]	uncertain significance	13	30657984	30657984	Human		name
405801249	CV3338498	single nucleotide variant	NM_005800.5(USPL1):c.1907T>G (p.Val636Gly)	not specified [RCV004477697]	uncertain significance	13	30657984	30657984	Human		name
405801251	CV3338499	single nucleotide variant	NM_005800.5(USPL1):c.2080G>A (p.Val694Ile)	not specified [RCV004477698]	uncertain significance	13	30658157	30658157	Human		name
405801252	CV3338500	single nucleotide variant	NM_005800.5(USPL1):c.2375G>C (p.Gly792Ala)	not specified [RCV004477699]	uncertain significance	13	30658452	30658452	Human		name
405801254	CV3338501	single nucleotide variant	NM_005800.5(USPL1):c.2389G>T (p.Gly797Cys)	not specified [RCV004477700]	uncertain significance	13	30658466	30658466	Human		name
405801258	CV3338503	single nucleotide variant	NM_005800.5(USPL1):c.2551T>G (p.Leu851Val)	not specified [RCV004477702]	uncertain significance	13	30658628	30658628	Human		name
405801260	CV3338504	single nucleotide variant	NM_005800.5(USPL1):c.2716C>T (p.Leu906Phe)	not specified [RCV004477703]	uncertain significance	13	30658793	30658793	Human		name
405801262	CV3338505	single nucleotide variant	NM_005800.5(USPL1):c.2918C>T (p.Ala973Val)	not specified [RCV004477704]	uncertain significance	13	30658995	30658995	Human		name
407529090	CV3487765	single nucleotide variant	NM_005800.5(USPL1):c.1982C>T (p.Thr661Ile)	not specified [RCV004680718]	uncertain significance	13	30658059	30658059	Human		name
407464689	CV3487766	single nucleotide variant	NM_005800.5(USPL1):c.2431G>A (p.Val811Ile)	not specified [RCV004688570]	uncertain significance	13	30658508	30658508	Human		name
407529098	CV3487770	single nucleotide variant	NM_005800.5(USPL1):c.2051C>A (p.Ala684Asp)	not specified [RCV004680722]	uncertain significance	13	30658128	30658128	Human		name
407464692	CV3487771	single nucleotide variant	NM_005800.5(USPL1):c.1018C>G (p.Leu340Val)	not specified [RCV004688571]	uncertain significance	13	30642663	30642663	Human		name
407529100	CV3487772	single nucleotide variant	NM_005800.5(USPL1):c.1768G>C (p.Glu590Gln)	not specified [RCV004680723]	uncertain significance	13	30657845	30657845	Human		name
407464696	CV3487773	single nucleotide variant	NM_005800.5(USPL1):c.2407G>A (p.Gly803Ser)	not specified [RCV004688572]	uncertain significance	13	30658484	30658484	Human		name
407529102	CV3487774	single nucleotide variant	NM_005800.5(USPL1):c.2533C>T (p.His845Tyr)	not specified [RCV004680724]	uncertain significance	13	30658610	30658610	Human		name
407529104	CV3487775	single nucleotide variant	NM_005800.5(USPL1):c.1708G>A (p.Asp570Asn)	not specified [RCV004680725]	uncertain significance	13	30657785	30657785	Human		name
407529108	CV3487777	single nucleotide variant	NM_005800.5(USPL1):c.1966T>C (p.Ser656Pro)	not specified [RCV004680727]	uncertain significance	13	30658043	30658043	Human		name
407529110	CV3487778	single nucleotide variant	NM_005800.5(USPL1):c.2879T>C (p.Val960Ala)	not specified [RCV004680728]	uncertain significance	13	30658956	30658956	Human		name
407529111	CV3487779	single nucleotide variant	NM_005800.5(USPL1):c.2968G>A (p.Glu990Lys)	not specified [RCV004680729]	uncertain significance	13	30659045	30659045	Human		name
407529115	CV3487781	single nucleotide variant	NM_005800.5(USPL1):c.2608A>C (p.Asn870His)	not specified [RCV004680731]	uncertain significance	13	30658685	30658685	Human		name
407529117	CV3487782	single nucleotide variant	NM_005800.5(USPL1):c.1433G>A (p.Cys478Tyr)	not specified [RCV004680732]	uncertain significance	13	30657510	30657510	Human		name
597799264	CV3623342	single nucleotide variant	NM_005800.5(USPL1):c.2855C>G (p.Ser952Cys)	not specified [RCV004879590]	uncertain significance	13	30658932	30658932	Human		name
597799268	CV3623344	single nucleotide variant	NM_005800.5(USPL1):c.2149C>T (p.Arg717Cys)	not specified [RCV004879592]	uncertain significance	13	30658226	30658226	Human		name
597697165	CV3623345	single nucleotide variant	NM_005800.5(USPL1):c.2152G>A (p.Val718Ile)	not specified [RCV004885236]	uncertain significance	13	30658229	30658229	Human		name
597799272	CV3623348	single nucleotide variant	NM_005800.5(USPL1):c.1897G>C (p.Ala633Pro)	not specified [RCV004879594]	uncertain significance	13	30657974	30657974	Human		name
597697182	CV3623349	single nucleotide variant	NM_005800.5(USPL1):c.1586T>A (p.Val529Glu)	not specified [RCV004885238]	uncertain significance	13	30657663	30657663	Human		name
597799278	CV3623353	single nucleotide variant	NM_005800.5(USPL1):c.1503A>G (p.Ile501Met)	not specified [RCV004879597]	uncertain significance	13	30657580	30657580	Human		name
597799280	CV3623355	single nucleotide variant	NM_005800.5(USPL1):c.1443G>T (p.Arg481Ser)	not specified [RCV004879598]	uncertain significance	13	30657520	30657520	Human		name
597799282	CV3623356	single nucleotide variant	NM_005800.5(USPL1):c.1814C>T (p.Ala605Val)	not specified [RCV004879599]	uncertain significance	13	30657891	30657891	Human		name
598239180	CV3933024	single nucleotide variant	NM_005800.5(USPL1):c.2027C>A (p.Thr676Asn)	not specified [RCV005296545]	uncertain significance	13	30658104	30658104	Human		name
598239188	CV3933026	single nucleotide variant	NM_005800.5(USPL1):c.2300G>T (p.Gly767Val)	not specified [RCV005296546]	uncertain significance	13	30658377	30658377	Human		name
598239199	CV3933028	single nucleotide variant	NM_005800.5(USPL1):c.2383A>T (p.Asn795Tyr)	not specified [RCV005296548]	uncertain significance	13	30658460	30658460	Human		name
156150510	CV2197728	single nucleotide variant	NM_005800.5(USPL1):c.3001A>G (p.Ser1001Gly)	not specified [RCV004074931]	likely benign	13	30659078	30659078	Human		name
156216374	CV2253763	single nucleotide variant	NM_005800.5(USPL1):c.3244C>T (p.Pro1082Ser)	not specified [RCV004127470]	uncertain significance	13	30659321	30659321	Human		name
156246461	CV2347315	single nucleotide variant	NM_005800.5(USPL1):c.3119A>T (p.Asp1040Val)	not specified [RCV004206794]	uncertain significance	13	30659196	30659196	Human		name
329379270	CV2443354	single nucleotide variant	NM_005800.5(USPL1):c.3187G>A (p.Asp1063Asn)	not specified [RCV004260153]	uncertain significance	13	30659264	30659264	Human		name
405801264	CV3338506	single nucleotide variant	NM_005800.5(USPL1):c.3062G>A (p.Arg1021Lys)	not specified [RCV004477705]	uncertain significance	13	30659139	30659139	Human		name
405801466	CV3338507	single nucleotide variant	NM_005800.5(USPL1):c.3253G>A (p.Asp1085Asn)	not specified [RCV004477706]	uncertain significance	13	30659330	30659330	Human		name
597799270	CV3623346	single nucleotide variant	NM_005800.5(USPL1):c.3092A>C (p.Lys1031Thr)	not specified [RCV004879593]	uncertain significance	13	30659169	30659169	Human		name
597697175	CV3623347	single nucleotide variant	NM_005800.5(USPL1):c.3056A>G (p.His1019Arg)	not specified [RCV004885237]	uncertain significance	13	30659133	30659133	Human		name
8627436	CV82580	single nucleotide variant	NM_005800.4(USPL1):c.3100C>T (p.Pro1034Ser)	Malignant melanoma [RCV000062659]	not provided	13	30659177	30659177	Human		name

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Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

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