Utp3 Variant Search Result - Rat Genome Database

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31 records found for search term Utp3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15174456	CV709440	single nucleotide variant	NM_020368.3(UTP3):c.84T>C (p.Asn28=)	not provided [RCV000972719]	benign	4	70688761	70688761	Human		name
15174453	CV709439	single nucleotide variant	NM_020368.3(UTP3):c.68C>T (p.Thr23Met)	not provided [RCV000972718]	benign	4	70688745	70688745	Human		name
156003208	CV2399637	single nucleotide variant	NM_020368.3(UTP3):c.180A>T (p.Leu60Phe)	not specified [RCV004244153]	uncertain significance	4	70688857	70688857	Human		name
329369724	CV2461198	single nucleotide variant	NM_020368.3(UTP3):c.164G>A (p.Arg55Gln)	not specified [RCV004267395]	uncertain significance	4	70688841	70688841	Human		name
598204965	CV3933117	single nucleotide variant	NM_020368.3(UTP3):c.112C>T (p.Pro38Ser)	not specified [RCV005290776]	uncertain significance	4	70688789	70688789	Human		name
598204971	CV3933118	single nucleotide variant	NM_020368.3(UTP3):c.182C>T (p.Ala61Val)	not specified [RCV005290777]	uncertain significance	4	70688859	70688859	Human		name
156129971	CV2357902	single nucleotide variant	NM_020368.3(UTP3):c.713C>T (p.Thr238Ile)	not specified [RCV004209691]	uncertain significance	4	70689390	70689390	Human		name
156141834	CV2358443	single nucleotide variant	NM_020368.3(UTP3):c.659G>A (p.Arg220Gln)	not specified [RCV004207335]	uncertain significance	4	70689336	70689336	Human		name
156135735	CV2379959	single nucleotide variant	NM_020368.3(UTP3):c.676C>T (p.Leu226Phe)	not specified [RCV004222103]	uncertain significance	4	70689353	70689353	Human		name
401729637	CV2683747	single nucleotide variant	NM_020368.3(UTP3):c.718G>A (p.Val240Ile)	not specified [RCV004284485]	uncertain significance	4	70689395	70689395	Human		name
405801515	CV3348578	single nucleotide variant	NM_020368.3(UTP3):c.360G>C (p.Glu120Asp)	not specified [RCV004477841]	uncertain significance	4	70689037	70689037	Human		name
405801517	CV3348579	single nucleotide variant	NM_020368.3(UTP3):c.844T>C (p.Tyr282His)	not specified [RCV004477842]	uncertain significance	4	70689521	70689521	Human		name
405801519	CV3348580	single nucleotide variant	NM_020368.3(UTP3):c.922A>T (p.Ile308Phe)	not specified [RCV004477843]	uncertain significance	4	70689599	70689599	Human		name
405801521	CV3348581	single nucleotide variant	NM_020368.3(UTP3):c.977T>C (p.Leu326Ser)	not specified [RCV004477844]	uncertain significance	4	70689654	70689654	Human		name
407529223	CV3493218	single nucleotide variant	NM_020368.3(UTP3):c.811C>T (p.Leu271Phe)	not specified [RCV004680790]	uncertain significance	4	70689488	70689488	Human		name
597803459	CV3632986	single nucleotide variant	NM_020368.3(UTP3):c.670C>G (p.Pro224Ala)	not specified [RCV004881746]	uncertain significance	4	70689347	70689347	Human		name
598204958	CV3933116	single nucleotide variant	NM_020368.3(UTP3):c.605G>A (p.Arg202Gln)	not specified [RCV005290775]	uncertain significance	4	70689282	70689282	Human		name
598204979	CV3933119	single nucleotide variant	NM_020368.3(UTP3):c.338G>A (p.Ser113Asn)	not specified [RCV005290778]	uncertain significance	4	70689015	70689015	Human		name
598239515	CV3933120	single nucleotide variant	NM_020368.3(UTP3):c.299A>G (p.Glu100Gly)	not specified [RCV005296604]	uncertain significance	4	70688976	70688976	Human		name
156188447	CV2226767	single nucleotide variant	NM_020368.3(UTP3):c.1067C>G (p.Ala356Gly)	not specified [RCV004101986]	uncertain significance	4	70689744	70689744	Human		name
329353245	CV2469032	single nucleotide variant	NM_020368.3(UTP3):c.1234A>G (p.Thr412Ala)	not specified [RCV004274280]	uncertain significance	4	70689911	70689911	Human		name
401731703	CV2674457	single nucleotide variant	NM_020368.3(UTP3):c.1037C>T (p.Pro346Leu)	not specified [RCV004291361]	uncertain significance	4	70689714	70689714	Human		name
401870477	CV2769268	single nucleotide variant	NM_020368.3(UTP3):c.1360G>T (p.Val454Phe)	not specified [RCV004357278]	uncertain significance	4	70690037	70690037	Human		name
405801507	CV3348574	single nucleotide variant	NM_020368.3(UTP3):c.1280A>C (p.Lys427Thr)	not specified [RCV004477837]	uncertain significance	4	70689957	70689957	Human		name
405801509	CV3348575	single nucleotide variant	NM_020368.3(UTP3):c.1364G>A (p.Arg455His)	not specified [RCV004477838]	uncertain significance	4	70690041	70690041	Human		name
405801511	CV3348576	single nucleotide variant	NM_020368.3(UTP3):c.1406G>A (p.Arg469His)	not specified [RCV004477839]	uncertain significance	4	70690083	70690083	Human		name
407529221	CV3493217	single nucleotide variant	NM_020368.3(UTP3):c.1201G>A (p.Ala401Thr)	not specified [RCV004680789]	uncertain significance	4	70689878	70689878	Human		name
407529226	CV3493219	single nucleotide variant	NM_020368.3(UTP3):c.1421A>G (p.Lys474Arg)	not specified [RCV004680791]	uncertain significance	4	70690098	70690098	Human		name
597803457	CV3632984	single nucleotide variant	NM_020368.3(UTP3):c.1100A>G (p.Asp367Gly)	not specified [RCV004881745]	uncertain significance	4	70689777	70689777	Human		name
597697498	CV3632985	single nucleotide variant	NM_020368.3(UTP3):c.1289G>T (p.Arg430Leu)	not specified [RCV004885273]	uncertain significance	4	70689966	70689966	Human		name
15124540	CV709441	single nucleotide variant	NM_020368.3(UTP3):c.1113T>A (p.Asp371Glu)	not provided [RCV000963434]	benign	4	70689790	70689790	Human		name

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