Ubxn6 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

68 records found for search term Ubxn6

Refine Term:

Sort By:

Export

CSV

TAB

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

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
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)

Create Name:

Description:

Send us a Message