Otud3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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35 records found for search term Otud3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597656186	CV3567917	single nucleotide variant	NM_015207.2(OTUD3):c.20C>T (p.Ala7Val)	not specified [RCV004827486]	uncertain significance	1	19882533	19882533	Human		name
329377192	CV2451920	single nucleotide variant	NM_015207.2(OTUD3):c.34G>A (p.Gly12Ser)	not specified [RCV004276590]	uncertain significance	1	19882547	19882547	Human		name
401773944	CV2727682	single nucleotide variant	NM_015207.2(OTUD3):c.89G>T (p.Arg30Leu)	not specified [RCV004329854]	uncertain significance	1	19882602	19882602	Human		name
401778772	CV2735495	single nucleotide variant	NM_015207.2(OTUD3):c.70C>T (p.Arg24Trp)	not specified [RCV004331053]	uncertain significance	1	19882583	19882583	Human		name
405785527	CV3374514	single nucleotide variant	NM_015207.2(OTUD3):c.57G>T (p.Glu19Asp)	not specified [RCV004504727]	uncertain significance	1	19882570	19882570	Human		name
405785547	CV3374518	single nucleotide variant	NM_015207.2(OTUD3):c.89G>A (p.Arg30His)	not specified [RCV004504731]	uncertain significance	1	19882602	19882602	Human		name
405785552	CV3374519	single nucleotide variant	NM_015207.2(OTUD3):c.97C>G (p.Leu33Val)	not specified [RCV004504732]	uncertain significance	1	19882610	19882610	Human		name
597736657	CV3567920	single nucleotide variant	NM_015207.2(OTUD3):c.32C>T (p.Pro11Leu)	not specified [RCV004843752]	uncertain significance	1	19882545	19882545	Human		name
156044267	CV2340093	single nucleotide variant	NM_015207.2(OTUD3):c.131G>A (p.Gly44Asp)	not specified [RCV004192335]	uncertain significance	1	19882644	19882644	Human		name
597736649	CV3567915	single nucleotide variant	NM_015207.2(OTUD3):c.172A>G (p.Asn58Asp)	not specified [RCV004843750]	uncertain significance	1	19882685	19882685	Human		name
156251837	CV2196607	single nucleotide variant	NM_015207.2(OTUD3):c.309G>C (p.Met103Ile)	not specified [RCV004073880]	uncertain significance	1	19890472	19890472	Human		name
155970475	CV2213484	single nucleotide variant	NM_015207.2(OTUD3):c.808C>T (p.Leu270Phe)	not specified [RCV004087453]	uncertain significance	1	19904960	19904960	Human		name
156262157	CV2216534	single nucleotide variant	NM_015207.2(OTUD3):c.805G>A (p.Val269Met)	not specified [RCV004097323]	likely benign	1	19904957	19904957	Human		name
156040575	CV2342059	single nucleotide variant	NM_015207.2(OTUD3):c.523A>G (p.Ile175Val)	not specified [RCV004189494]	uncertain significance	1	19897579	19897579	Human		name
156131920	CV2349976	single nucleotide variant	NM_015207.2(OTUD3):c.536A>G (p.Tyr179Cys)	not specified [RCV004199904]	uncertain significance	1	19897592	19897592	Human		name
156210088	CV2370195	single nucleotide variant	NM_015207.2(OTUD3):c.569A>G (p.Asn190Ser)	not specified [RCV004211074]	uncertain significance	1	19897625	19897625	Human		name
329362975	CV2449609	single nucleotide variant	NM_015207.2(OTUD3):c.811C>G (p.Arg271Gly)	not specified [RCV004268528]	uncertain significance	1	19904963	19904963	Human		name
405785533	CV3374515	single nucleotide variant	NM_015207.2(OTUD3):c.739G>A (p.Asp247Asn)	not specified [RCV004504728]	uncertain significance	1	19904891	19904891	Human		name
405785538	CV3374516	single nucleotide variant	NM_015207.2(OTUD3):c.751A>G (p.Ile251Val)	not specified [RCV004504729]	uncertain significance	1	19904903	19904903	Human		name
405785543	CV3374517	single nucleotide variant	NM_015207.2(OTUD3):c.887C>G (p.Pro296Arg)	not specified [RCV004504730]	uncertain significance	1	19906483	19906483	Human		name
407517309	CV3459787	single nucleotide variant	NM_015207.2(OTUD3):c.488G>A (p.Arg163His)	not specified [RCV004650557]	uncertain significance	1	19897544	19897544	Human		name
407517306	CV3459788	single nucleotide variant	NM_015207.2(OTUD3):c.569A>C (p.Asn190Thr)	not specified [RCV004650558]	uncertain significance	1	19897625	19897625	Human		name
597656180	CV3567916	single nucleotide variant	NM_015207.2(OTUD3):c.812G>A (p.Arg271Gln)	not specified [RCV004827485]	likely benign	1	19904964	19904964	Human		name
597656194	CV3567918	single nucleotide variant	NM_015207.2(OTUD3):c.808C>A (p.Leu270Ile)	not specified [RCV004827487]	uncertain significance	1	19904960	19904960	Human		name
598162452	CV3995657	single nucleotide variant	NM_015207.2(OTUD3):c.533G>A (p.Arg178Gln)	not specified [RCV005390817]	uncertain significance	1	19897589	19897589	Human		name
598162458	CV3995658	single nucleotide variant	NM_015207.2(OTUD3):c.689A>T (p.Asp230Val)	not specified [RCV005390818]	uncertain significance	1	19904349	19904349	Human		name
598162467	CV3995660	single nucleotide variant	NM_015207.2(OTUD3):c.326A>T (p.Asp109Val)	not specified [RCV005390820]	uncertain significance	1	19890489	19890489	Human		name
598162472	CV3995661	single nucleotide variant	NM_015207.2(OTUD3):c.886C>T (p.Pro296Ser)	not specified [RCV005390821]	uncertain significance	1	19906482	19906482	Human		name
598162478	CV3995662	single nucleotide variant	NM_015207.2(OTUD3):c.535T>G (p.Tyr179Asp)	not specified [RCV005390822]	uncertain significance	1	19897591	19897591	Human		name
155967145	CV2216799	single nucleotide variant	NM_015207.2(OTUD3):c.1157A>C (p.Gln386Pro)	not specified [RCV004083236]	uncertain significance	1	19907706	19907706	Human		name
156124824	CV2350136	single nucleotide variant	NM_015207.2(OTUD3):c.1121G>C (p.Arg374Thr)	not specified [RCV004200056]	uncertain significance	1	19907670	19907670	Human		name
405785517	CV3374512	single nucleotide variant	NM_015207.2(OTUD3):c.1056G>T (p.Met352Ile)	not specified [RCV004504725]	uncertain significance	1	19907605	19907605	Human		name
405785522	CV3374513	single nucleotide variant	NM_015207.2(OTUD3):c.1192A>T (p.Ile398Phe)	not specified [RCV004504726]	uncertain significance	1	19907741	19907741	Human		name
597736644	CV3567914	single nucleotide variant	NM_015207.2(OTUD3):c.1099C>G (p.Leu367Val)	not specified [RCV004843749]	uncertain significance	1	19907648	19907648	Human		name
597736654	CV3567919	single nucleotide variant	NM_015207.2(OTUD3):c.1012C>T (p.Leu338Phe)	not specified [RCV004843751]	uncertain significance	1	19906608	19906608	Human		name

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