Rpusd4 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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42 records found for search term Rpusd4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156331136	CV2218116	single nucleotide variant	NM_032795.3(RPUSD4):c.11C>T (p.Pro4Leu)	not specified [RCV004086545]	uncertain significance	11	126211628	126211628	Human		name
401743754	CV2726159	single nucleotide variant	NM_032795.3(RPUSD4):c.40C>T (p.Arg14Trp)	not specified [RCV004326638]	uncertain significance	11	126211599	126211599	Human		name
405740031	CV3316525	single nucleotide variant	NM_032795.3(RPUSD4):c.31C>A (p.Pro11Thr)	not specified [RCV004452236]	uncertain significance	11	126211608	126211608	Human		name
405740057	CV3316528	single nucleotide variant	NM_032795.3(RPUSD4):c.73A>T (p.Thr25Ser)	not specified [RCV004452239]	likely benign	11	126211566	126211566	Human		name
597786463	CV3604450	single nucleotide variant	NM_032795.3(RPUSD4):c.34T>C (p.Trp12Arg)	not specified [RCV004854986]	uncertain significance	11	126211605	126211605	Human		name
156003122	CV2396694	single nucleotide variant	NM_032795.3(RPUSD4):c.134G>A (p.Arg45Lys)	not specified [RCV004233850]	uncertain significance	11	126211505	126211505	Human		name
405740018	CV3316523	single nucleotide variant	NM_032795.3(RPUSD4):c.228A>G (p.Ile76Met)	not specified [RCV004452234]	uncertain significance	11	126211017	126211017	Human		name
155942132	CV2229471	single nucleotide variant	NM_032795.3(RPUSD4):c.329A>G (p.Asn110Ser)	not specified [RCV004101236]	uncertain significance	11	126210916	126210916	Human		name
156062141	CV2277141	single nucleotide variant	NM_032795.3(RPUSD4):c.790A>G (p.Ile264Val)	not specified [RCV004142787]	likely benign	11	126205474	126205474	Human		name
156126569	CV2350302	single nucleotide variant	NM_032795.3(RPUSD4):c.901T>C (p.Ser301Pro)	not specified [RCV004202255]	likely benign	11	126203651	126203651	Human		name
156200643	CV2362966	single nucleotide variant	NM_032795.3(RPUSD4):c.682G>A (p.Asp228Asn)	not specified [RCV004211112]	likely benign	11	126205582	126205582	Human		name
156050744	CV2367601	single nucleotide variant	NM_032795.3(RPUSD4):c.661T>C (p.Ser221Pro)	not specified [RCV004211527]	uncertain significance	11	126205603	126205603	Human		name
156384314	CV2371378	single nucleotide variant	NM_032795.3(RPUSD4):c.581T>C (p.Met194Thr)	not specified [RCV004223379]	uncertain significance	11	126205758	126205758	Human		name
156102937	CV2386872	single nucleotide variant	NM_032795.3(RPUSD4):c.598G>A (p.Val200Met)	not specified [RCV004233508]	uncertain significance	11	126205741	126205741	Human		name
156097468	CV2392702	single nucleotide variant	NM_032795.3(RPUSD4):c.794C>T (p.Thr265Ile)	not specified [RCV004247077]	uncertain significance	11	126205470	126205470	Human		name
329375565	CV2431566	single nucleotide variant	NM_032795.3(RPUSD4):c.707G>A (p.Arg236His)	not specified [RCV004254717]	likely benign	11	126205557	126205557	Human		name
329399274	CV2436531	single nucleotide variant	NM_032795.3(RPUSD4):c.694G>A (p.Val232Met)	not specified [RCV004253692]	uncertain significance	11	126205570	126205570	Human		name
329354164	CV2447243	single nucleotide variant	NM_032795.3(RPUSD4):c.853G>A (p.Gly285Ser)	not specified [RCV004262537]	uncertain significance	11	126204272	126204272	Human		name
401757572	CV2707855	single nucleotide variant	NM_032795.3(RPUSD4):c.439C>A (p.His147Asn)	not specified [RCV004309134]	uncertain significance	11	126209639	126209639	Human		name
401741676	CV2710020	single nucleotide variant	NM_032795.3(RPUSD4):c.905T>G (p.Val302Gly)	not specified [RCV004315082]	uncertain significance	11	126203647	126203647	Human		name
405740023	CV3316524	single nucleotide variant	NM_032795.3(RPUSD4):c.317T>C (p.Leu106Pro)	not specified [RCV004452235]	uncertain significance	11	126210928	126210928	Human		name
405740050	CV3316527	single nucleotide variant	NM_032795.3(RPUSD4):c.451C>T (p.Arg151Trp)	not specified [RCV004452238]	uncertain significance	11	126209627	126209627	Human		name
407488381	CV3476289	single nucleotide variant	NM_032795.3(RPUSD4):c.964C>G (p.Leu322Val)	not specified [RCV004665857]	uncertain significance	11	126203588	126203588	Human		name
407488389	CV3476290	single nucleotide variant	NM_032795.3(RPUSD4):c.760C>G (p.Leu254Val)	not specified [RCV004665858]	uncertain significance	11	126205504	126205504	Human		name
407488394	CV3476292	single nucleotide variant	NM_032795.3(RPUSD4):c.851T>C (p.Leu284Pro)	not specified [RCV004665859]	uncertain significance	11	126204274	126204274	Human		name
407488399	CV3476293	single nucleotide variant	NM_032795.3(RPUSD4):c.769G>A (p.Ala257Thr)	not specified [RCV004665860]	uncertain significance	11	126205495	126205495	Human		name
597786460	CV3604446	single nucleotide variant	NM_032795.3(RPUSD4):c.674G>A (p.Arg225His)	not specified [RCV004854985]	uncertain significance	11	126205590	126205590	Human		name
597710385	CV3604447	single nucleotide variant	NM_032795.3(RPUSD4):c.713G>A (p.Arg238Gln)	not specified [RCV004860951]	uncertain significance	11	126205551	126205551	Human		name
597710394	CV3604448	single nucleotide variant	NM_032795.3(RPUSD4):c.719C>T (p.Ala240Val)	not specified [RCV004860952]	uncertain significance	11	126205545	126205545	Human		name
597710403	CV3604449	single nucleotide variant	NM_032795.3(RPUSD4):c.529A>G (p.Arg177Gly)	not specified [RCV004860953]	uncertain significance	11	126209549	126209549	Human		name
597786467	CV3604451	single nucleotide variant	NM_032795.3(RPUSD4):c.949T>A (p.Tyr317Asn)	not specified [RCV004854987]	uncertain significance	11	126203603	126203603	Human		name
598221828	CV3903115	single nucleotide variant	NM_032795.3(RPUSD4):c.660G>T (p.Leu220Phe)	not specified [RCV005272554]	uncertain significance	11	126205604	126205604	Human		name
598221817	CV3903117	single nucleotide variant	NM_032795.3(RPUSD4):c.314A>G (p.Asn105Ser)	not specified [RCV005272556]	uncertain significance	11	126210931	126210931	Human		name
598221808	CV3903119	single nucleotide variant	NM_032795.3(RPUSD4):c.991G>T (p.Ala331Ser)	not specified [RCV005272558]	uncertain significance	11	126203561	126203561	Human		name
598221803	CV3903120	single nucleotide variant	NM_032795.3(RPUSD4):c.938C>G (p.Ser313Trp)	not specified [RCV005272559]	uncertain significance	11	126203614	126203614	Human		name
156233282	CV2245244	single nucleotide variant	NM_032795.3(RPUSD4):c.1070G>A (p.Arg357His)	not specified [RCV004107014]	uncertain significance	11	126203482	126203482	Human		name
401899703	CV2755424	single nucleotide variant	NM_032795.3(RPUSD4):c.1039C>T (p.Arg347Cys)	not specified [RCV004337582]	uncertain significance	11	126203513	126203513	Human		name
405740003	CV3316521	single nucleotide variant	NM_032795.3(RPUSD4):c.1014A>C (p.Glu338Asp)	not specified [RCV004452232]	likely benign	11	126203538	126203538	Human		name
405740010	CV3316522	single nucleotide variant	NM_032795.3(RPUSD4):c.1064G>A (p.Arg355His)	not specified [RCV004452233]	uncertain significance	11	126203488	126203488	Human		name
407488374	CV3476288	single nucleotide variant	NM_032795.3(RPUSD4):c.1040G>A (p.Arg347His)	not specified [RCV004665856]	likely benign	11	126203512	126203512	Human		name
598221823	CV3903116	single nucleotide variant	NM_032795.3(RPUSD4):c.1063C>T (p.Arg355Cys)	not specified [RCV005272555]	uncertain significance	11	126203489	126203489	Human		name
598221812	CV3903118	single nucleotide variant	NM_032795.3(RPUSD4):c.1097A>G (p.Asn366Ser)	not specified [RCV005272557]	uncertain significance	11	126203455	126203455	Human		name

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