Ubxn6 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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68 records found for search term Ubxn6

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155955109	CV2389876	single nucleotide variant	NM_025241.3(UBXN6):c.58G>A (p.Gly20Ser)	not specified [RCV004236090]	uncertain significance	19	4457640	4457640	Human		name
401908246	CV2815203	single nucleotide variant	NM_025241.3(UBXN6):c.645C>T (p.His215=)	not provided [RCV003423212]	likely benign	19	4446891	4446891	Human		name
597685185	CV3622774	single nucleotide variant	NM_025241.3(UBXN6):c.88A>G (p.Lys30Glu)	not specified [RCV004884020]	uncertain significance	19	4454089	4454089	Human		name
598190099	CV3929133	single nucleotide variant	NM_025241.3(UBXN6):c.94C>T (p.His32Tyr)	not specified [RCV005288163]	uncertain significance	19	4454083	4454083	Human		name
156165756	CV2315190	single nucleotide variant	NM_025241.3(UBXN6):c.205C>T (p.Arg69Trp)	not specified [RCV004165362]	uncertain significance	19	4453972	4453972	Human		name
156011682	CV2358763	single nucleotide variant	NM_025241.3(UBXN6):c.119C>T (p.Ala40Val)	not specified [RCV004210071]	uncertain significance	19	4454058	4454058	Human		name
156041928	CV2381409	single nucleotide variant	NM_025241.3(UBXN6):c.283G>A (p.Gly95Arg)	not specified [RCV004229898]	uncertain significance	19	4453487	4453487	Human		name
329387318	CV2436380	single nucleotide variant	NM_025241.3(UBXN6):c.224C>T (p.Ser75Leu)	not specified [RCV004251774]	uncertain significance	19	4453953	4453953	Human		name
401889550	CV2756626	single nucleotide variant	NM_025241.3(UBXN6):c.134G>A (p.Arg45His)	not specified [RCV004345147]	uncertain significance	19	4454043	4454043	Human		name
401897879	CV2773086	single nucleotide variant	NM_025241.3(UBXN6):c.259C>T (p.Leu87Phe)	not specified [RCV004351519]	uncertain significance	19	4453511	4453511	Human		name
401896575	CV2782268	single nucleotide variant	NM_025241.3(UBXN6):c.172G>A (p.Ala58Thr)	not specified [RCV004359234]	uncertain significance	19	4454005	4454005	Human		name
597685195	CV3622775	single nucleotide variant	NM_025241.3(UBXN6):c.248T>C (p.Val83Ala)	not specified [RCV004884021]	uncertain significance	19	4453522	4453522	Human		name
598190093	CV3929129	single nucleotide variant	NM_025241.3(UBXN6):c.284G>T (p.Gly95Val)	not specified [RCV005288162]	uncertain significance	19	4453486	4453486	Human		name
598265883	CV3929131	single nucleotide variant	NM_025241.3(UBXN6):c.190G>A (p.Glu64Lys)	not specified [RCV005301815]	uncertain significance	19	4453987	4453987	Human		name
598265889	CV3929132	single nucleotide variant	NM_025241.3(UBXN6):c.122C>A (p.Pro41His)	not specified [RCV005301816]	uncertain significance	19	4454055	4454055	Human		name
156096414	CV2210435	single nucleotide variant	NM_025241.3(UBXN6):c.320A>G (p.Glu107Gly)	not specified [RCV004089577]	uncertain significance	19	4452485	4452485	Human		name
156341874	CV2225944	single nucleotide variant	NM_025241.3(UBXN6):c.769A>G (p.Lys257Glu)	not specified [RCV004105114]	uncertain significance	19	4446651	4446651	Human		name
156157756	CV2262426	single nucleotide variant	NM_025241.3(UBXN6):c.953G>A (p.Arg318Gln)	not specified [RCV004128871]	uncertain significance	19	4446381	4446381	Human		name
156337029	CV2271018	single nucleotide variant	NM_025241.3(UBXN6):c.946G>C (p.Val316Leu)	not specified [RCV004133829]	uncertain significance	19	4446388	4446388	Human		name
156266887	CV2296498	single nucleotide variant	NM_025241.3(UBXN6):c.734C>G (p.Thr245Ser)	not specified [RCV004154579]	uncertain significance	19	4446686	4446686	Human		name
156296896	CV2297618	single nucleotide variant	NM_025241.3(UBXN6):c.619C>T (p.Arg207Cys)	not specified [RCV004155315]	uncertain significance	19	4446917	4446917	Human		name
156061453	CV2320913	single nucleotide variant	NM_025241.3(UBXN6):c.881A>G (p.Asn294Ser)	not specified [RCV004172725]	uncertain significance	19	4446539	4446539	Human		name
155966026	CV2329752	single nucleotide variant	NM_025241.3(UBXN6):c.361G>A (p.Val121Met)	not specified [RCV004183225]	uncertain significance	19	4452444	4452444	Human		name
156073827	CV2331612	single nucleotide variant	NM_025241.3(UBXN6):c.973A>G (p.Lys325Glu)	not specified [RCV004184248]	uncertain significance	19	4446361	4446361	Human		name
156186197	CV2332508	single nucleotide variant	NM_025241.3(UBXN6):c.305C>G (p.Thr102Ser)	not specified [RCV004196229]	uncertain significance	19	4453465	4453465	Human		name
155976036	CV2342731	single nucleotide variant	NM_025241.3(UBXN6):c.559C>G (p.Leu187Val)	not specified [RCV004196803]	uncertain significance	19	4447606	4447606	Human		name
156119860	CV2354115	single nucleotide variant	NM_025241.3(UBXN6):c.938G>T (p.Arg313Leu)	not provided [RCV004695658]\|not specified [RCV004206552]	uncertain significance	19	4446396	4446396	Human		name
156153009	CV2369340	single nucleotide variant	NM_025241.3(UBXN6):c.662T>C (p.Ile221Thr)	not specified [RCV004208244]	uncertain significance	19	4446874	4446874	Human		name
155995194	CV2374909	single nucleotide variant	NM_025241.3(UBXN6):c.488C>T (p.Thr163Met)	not specified [RCV004227931]	uncertain significance	19	4448369	4448369	Human		name
156104244	CV2386953	single nucleotide variant	NM_025241.3(UBXN6):c.574G>A (p.Glu192Lys)	not specified [RCV004233578]	uncertain significance	19	4447591	4447591	Human		name
329372674	CV2424174	single nucleotide variant	NM_025241.3(UBXN6):c.568G>A (p.Glu190Lys)	not specified [RCV004249860]	uncertain significance	19	4447597	4447597	Human		name
329361586	CV2437662	single nucleotide variant	NM_025241.3(UBXN6):c.737C>G (p.Thr246Ser)	not specified [RCV004260978]	uncertain significance	19	4446683	4446683	Human		name
401742247	CV2673737	single nucleotide variant	NM_025241.3(UBXN6):c.799C>T (p.Arg267Cys)	not specified [RCV004291085]	uncertain significance	19	4446621	4446621	Human		name
401756855	CV2681623	single nucleotide variant	NM_025241.3(UBXN6):c.564C>A (p.His188Gln)	not specified [RCV004294183]	uncertain significance	19	4447601	4447601	Human		name
401862692	CV2768645	single nucleotide variant	NM_025241.3(UBXN6):c.938G>A (p.Arg313Gln)	not specified [RCV004344495]	uncertain significance	19	4446396	4446396	Human		name
405800405	CV3337865	single nucleotide variant	NM_025241.3(UBXN6):c.617A>G (p.Glu206Gly)	not specified [RCV004477252]	uncertain significance	19	4446919	4446919	Human		name
405800407	CV3337866	single nucleotide variant	NM_025241.3(UBXN6):c.788C>T (p.Ala263Val)	not specified [RCV004477253]	uncertain significance	19	4446632	4446632	Human		name
405800408	CV3337867	single nucleotide variant	NM_025241.3(UBXN6):c.802G>A (p.Ala268Thr)	not specified [RCV004477254]	uncertain significance	19	4446618	4446618	Human		name
405800410	CV3337868	single nucleotide variant	NM_025241.3(UBXN6):c.853C>A (p.Gln285Lys)	not specified [RCV004477255]	uncertain significance	19	4446567	4446567	Human		name
405800412	CV3337869	single nucleotide variant	NM_025241.3(UBXN6):c.879C>A (p.Phe293Leu)	not specified [RCV004477256]	uncertain significance	19	4446541	4446541	Human		name
405800416	CV3337871	single nucleotide variant	NM_025241.3(UBXN6):c.937C>T (p.Arg313Trp)	not specified [RCV004477258]	uncertain significance	19	4446397	4446397	Human		name
405800418	CV3337872	single nucleotide variant	NM_025241.3(UBXN6):c.950T>C (p.Leu317Pro)	not specified [RCV004477259]	uncertain significance	19	4446384	4446384	Human		name
407523156	CV3491225	single nucleotide variant	NM_025241.3(UBXN6):c.419G>A (p.Cys140Tyr)	not specified [RCV004677946]	uncertain significance	19	4452386	4452386	Human		name
407523162	CV3491227	single nucleotide variant	NM_025241.3(UBXN6):c.883C>T (p.Leu295Phe)	not specified [RCV004677948]	uncertain significance	19	4446537	4446537	Human		name
407523164	CV3491228	single nucleotide variant	NM_025241.3(UBXN6):c.547G>A (p.Asp183Asn)	not specified [RCV004677949]	uncertain significance	19	4447618	4447618	Human		name
597685117	CV3622766	single nucleotide variant	NM_025241.3(UBXN6):c.562C>G (p.His188Asp)	not specified [RCV004884013]	uncertain significance	19	4447603	4447603	Human		name
597685137	CV3622768	single nucleotide variant	NM_025241.3(UBXN6):c.839C>T (p.Ser280Leu)	not specified [RCV004884015]	uncertain significance	19	4446581	4446581	Human		name
597685147	CV3622769	single nucleotide variant	NM_025241.3(UBXN6):c.623T>C (p.Ile208Thr)	not specified [RCV004884016]	uncertain significance	19	4446913	4446913	Human		name
597685157	CV3622770	single nucleotide variant	NM_025241.3(UBXN6):c.409C>T (p.Arg137Trp)	not specified [RCV004884017]	uncertain significance	19	4452396	4452396	Human		name
597685175	CV3622773	single nucleotide variant	NM_025241.3(UBXN6):c.739T>G (p.Leu247Val)	not specified [RCV004884019]	uncertain significance	19	4446681	4446681	Human		name
597685204	CV3622776	single nucleotide variant	NM_025241.3(UBXN6):c.784G>A (p.Ala262Thr)	not specified [RCV004884022]	uncertain significance	19	4446636	4446636	Human		name
598190085	CV3929126	single nucleotide variant	NM_025241.3(UBXN6):c.756C>A (p.Ser252Arg)	not specified [RCV005288161]	uncertain significance	19	4446664	4446664	Human		name
598265871	CV3929128	single nucleotide variant	NM_025241.3(UBXN6):c.583C>T (p.Arg195Trp)	not specified [RCV005301813]	uncertain significance	19	4447582	4447582	Human		name
598265877	CV3929130	single nucleotide variant	NM_025241.3(UBXN6):c.374G>A (p.Cys125Tyr)	not specified [RCV005301814]	uncertain significance	19	4452431	4452431	Human		name
156237168	CV2224189	single nucleotide variant	NM_025241.3(UBXN6):c.1270G>A (p.Glu424Lys)	not specified [RCV004096034]	uncertain significance	19	4445554	4445554	Human		name
156277883	CV2252038	single nucleotide variant	NM_025241.3(UBXN6):c.1262C>T (p.Ala421Val)	not specified [RCV004122073]	uncertain significance	19	4445562	4445562	Human		name
155944702	CV2291803	single nucleotide variant	NM_025241.3(UBXN6):c.1294G>A (p.Glu432Lys)	not specified [RCV004158339]	uncertain significance	19	4445530	4445530	Human		name
156068474	CV2356858	single nucleotide variant	NM_025241.3(UBXN6):c.1240G>A (p.Val414Met)	not specified [RCV004204235]	uncertain significance	19	4445584	4445584	Human		name
401898285	CV2791174	single nucleotide variant	NM_025241.3(UBXN6):c.1090G>T (p.Gly364Trp)	not specified [RCV004356529]	uncertain significance	19	4446159	4446159	Human		name
405800399	CV3337862	single nucleotide variant	NM_025241.3(UBXN6):c.1237G>A (p.Ala413Thr)	not specified [RCV004477249]	uncertain significance	19	4445587	4445587	Human		name
405800401	CV3337863	single nucleotide variant	NM_025241.3(UBXN6):c.1272G>C (p.Glu424Asp)	not specified [RCV004477250]	uncertain significance	19	4445552	4445552	Human		name
407523150	CV3491223	single nucleotide variant	NM_025241.3(UBXN6):c.1252A>G (p.Ile418Val)	not specified [RCV004677944]	uncertain significance	19	4445572	4445572	Human		name
407523153	CV3491224	single nucleotide variant	NM_025241.3(UBXN6):c.1307C>G (p.Ala436Gly)	not specified [RCV004677945]	uncertain significance	19	4445517	4445517	Human		name
407523159	CV3491226	single nucleotide variant	NM_025241.3(UBXN6):c.1033G>T (p.Asp345Tyr)	not specified [RCV004677947]	uncertain significance	19	4446301	4446301	Human		name
597685124	CV3622767	single nucleotide variant	NM_025241.3(UBXN6):c.1282A>C (p.Ile428Leu)	not specified [RCV004884014]	uncertain significance	19	4445542	4445542	Human		name
598265866	CV3929127	single nucleotide variant	NM_025241.3(UBXN6):c.1117G>T (p.Asp373Tyr)	not specified [RCV005301812]	uncertain significance	19	4446132	4446132	Human		name
8636808	CV92033	single nucleotide variant	NM_001171091.1(UBXN6):c.810G>A (p.Arg270=)	Malignant melanoma [RCV000072131]	not provided	19	4446365	4446365	Human		name
8636809	CV92034	single nucleotide variant	NM_001171091.1(UBXN6):c.809G>A (p.Arg270Gln)	Malignant melanoma [RCV000072132]	not provided	19	4446366	4446366	Human		name

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