Trim47 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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78 records found for search term Trim47

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155916690	CV2282213	single nucleotide variant	NM_033452.3(TRIM47):c.6C>G (p.Asp2Glu)	not specified [RCV004132795]	uncertain significance	17	75878543	75878543	Human		name
401935879	CV2808391	single nucleotide variant	NM_033452.3(TRIM47):c.867C>T (p.Ile289=)	not provided [RCV003413342]	likely benign	17	75876397	75876397	Human		name
155969042	CV2213262	single nucleotide variant	NM_033452.3(TRIM47):c.151G>A (p.Ala51Thr)	not specified [RCV004085481]	uncertain significance	17	75878398	75878398	Human		name
401752481	CV2723250	single nucleotide variant	NM_033452.3(TRIM47):c.244G>T (p.Gly82Cys)	not specified [RCV004329482]	uncertain significance	17	75878305	75878305	Human		name
401892074	CV2777211	single nucleotide variant	NM_033452.3(TRIM47):c.278C>T (p.Pro93Leu)	not specified [RCV004354245]	uncertain significance	17	75878271	75878271	Human		name
597801915	CV3617811	single nucleotide variant	NM_033452.3(TRIM47):c.122G>C (p.Gly41Ala)	not specified [RCV004880968]	uncertain significance	17	75878427	75878427	Human		name
597801928	CV3617819	single nucleotide variant	NM_033452.3(TRIM47):c.154G>A (p.Ala52Thr)	not specified [RCV004880975]	uncertain significance	17	75878395	75878395	Human		name
598274206	CV3935501	single nucleotide variant	NM_033452.3(TRIM47):c.271C>T (p.Pro91Ser)	not specified [RCV005303808]	uncertain significance	17	75878278	75878278	Human		name
155926523	CV2208215	single nucleotide variant	NM_033452.3(TRIM47):c.539G>C (p.Ser180Thr)	not specified [RCV004088673]	uncertain significance	17	75878010	75878010	Human		name
156111592	CV2261779	single nucleotide variant	NM_033452.3(TRIM47):c.925G>C (p.Glu309Gln)	not specified [RCV004126066]	uncertain significance	17	75876339	75876339	Human		name
156238791	CV2268993	single nucleotide variant	NM_033452.3(TRIM47):c.916C>G (p.Arg306Gly)	not specified [RCV004128391]	uncertain significance	17	75876348	75876348	Human		name
156066933	CV2270807	single nucleotide variant	NM_033452.3(TRIM47):c.383G>T (p.Arg128Leu)	not specified [RCV004131857]	uncertain significance	17	75878166	75878166	Human		name
156169845	CV2276838	single nucleotide variant	NM_033452.3(TRIM47):c.382C>T (p.Arg128Cys)	not specified [RCV004140187]	uncertain significance	17	75878167	75878167	Human		name
156273367	CV2283831	single nucleotide variant	NM_033452.3(TRIM47):c.781G>A (p.Val261Ile)	not specified [RCV004142345]	uncertain significance	17	75876483	75876483	Human		name
156056928	CV2308965	single nucleotide variant	NM_033452.3(TRIM47):c.676G>T (p.Ala226Ser)	not specified [RCV004169247]	uncertain significance	17	75876813	75876813	Human		name
156167329	CV2330188	single nucleotide variant	NM_033452.3(TRIM47):c.806G>A (p.Arg269Gln)	not specified [RCV004185673]	likely benign	17	75876458	75876458	Human		name
155983815	CV2367829	single nucleotide variant	NM_033452.3(TRIM47):c.776C>T (p.Ala259Val)	not specified [RCV004222941]	uncertain significance	17	75876488	75876488	Human		name
156152467	CV2369272	single nucleotide variant	NM_033452.3(TRIM47):c.380T>A (p.Val127Glu)	not specified [RCV004208185]	uncertain significance	17	75878169	75878169	Human		name
156144683	CV2383945	single nucleotide variant	NM_033452.3(TRIM47):c.473C>T (p.Pro158Leu)	not specified [RCV004231797]	uncertain significance	17	75878076	75878076	Human		name
155929984	CV2389281	single nucleotide variant	NM_033452.3(TRIM47):c.892G>C (p.Gly298Arg)	not specified [RCV004235598]	uncertain significance	17	75876372	75876372	Human		name
156159411	CV2398109	single nucleotide variant	NM_033452.3(TRIM47):c.433C>T (p.Leu145Phe)	not specified [RCV004241693]	uncertain significance	17	75878116	75878116	Human		name
329364157	CV2460337	single nucleotide variant	NM_033452.3(TRIM47):c.853G>C (p.Val285Leu)	not specified [RCV004268664]	uncertain significance	17	75876411	75876411	Human		name
401742273	CV2677549	single nucleotide variant	NM_033452.3(TRIM47):c.524G>T (p.Arg175Leu)	not specified [RCV004291653]	uncertain significance	17	75878025	75878025	Human		name
405796563	CV3337040	single nucleotide variant	NM_033452.3(TRIM47):c.449C>A (p.Ser150Tyr)	not specified [RCV004475901]	uncertain significance	17	75878100	75878100	Human		name
405796566	CV3337041	single nucleotide variant	NM_033452.3(TRIM47):c.506G>A (p.Arg169His)	not specified [RCV004475902]	uncertain significance	17	75878043	75878043	Human		name
405796569	CV3337042	single nucleotide variant	NM_033452.3(TRIM47):c.581G>T (p.Arg194Leu)	not specified [RCV004475903]	uncertain significance	17	75877968	75877968	Human		name
405796572	CV3337043	single nucleotide variant	NM_033452.3(TRIM47):c.590G>T (p.Arg197Leu)	not specified [RCV004475904]	uncertain significance	17	75877959	75877959	Human		name
405796575	CV3337044	single nucleotide variant	NM_033452.3(TRIM47):c.681G>C (p.Glu227Asp)	not specified [RCV004475905]	uncertain significance	17	75876808	75876808	Human		name
405796946	CV3337045	single nucleotide variant	NM_033452.3(TRIM47):c.722A>G (p.Glu241Gly)	not specified [RCV004475906]	uncertain significance	17	75876767	75876767	Human		name
405796943	CV3337046	single nucleotide variant	NM_033452.3(TRIM47):c.821C>G (p.Ala274Gly)	not specified [RCV004475907]	uncertain significance	17	75876443	75876443	Human		name
405796940	CV3337047	single nucleotide variant	NM_033452.3(TRIM47):c.913C>T (p.Arg305Trp)	not specified [RCV004475908]	uncertain significance	17	75876351	75876351	Human		name
405796937	CV3337048	single nucleotide variant	NM_033452.3(TRIM47):c.928C>G (p.Gln310Glu)	not specified [RCV004475909]	uncertain significance	17	75876336	75876336	Human		name
405796934	CV3337049	single nucleotide variant	NM_033452.3(TRIM47):c.938G>A (p.Arg313His)	not specified [RCV004475910]	uncertain significance	17	75876326	75876326	Human		name
405796927	CV3337051	single nucleotide variant	NM_033452.3(TRIM47):c.995T>G (p.Phe332Cys)	not specified [RCV004475912]	uncertain significance	17	75876269	75876269	Human		name
407453913	CV3490557	single nucleotide variant	NM_033452.3(TRIM47):c.703G>A (p.Val235Met)	not specified [RCV004684710]	uncertain significance	17	75876786	75876786	Human		name
407453917	CV3490558	single nucleotide variant	NM_033452.3(TRIM47):c.895C>A (p.Arg299Ser)	not specified [RCV004684711]	uncertain significance	17	75876369	75876369	Human		name
407453920	CV3490559	single nucleotide variant	NM_033452.3(TRIM47):c.571C>A (p.Arg191Ser)	not specified [RCV004684712]	uncertain significance	17	75877978	75877978	Human		name
407453922	CV3490561	single nucleotide variant	NM_033452.3(TRIM47):c.526C>G (p.Arg176Gly)	not specified [RCV004684713]	uncertain significance	17	75878023	75878023	Human		name
407461471	CV3490562	single nucleotide variant	NM_033452.3(TRIM47):c.389A>G (p.Asp130Gly)	not specified [RCV004687661]	uncertain significance	17	75878160	75878160	Human		name
407453925	CV3490563	single nucleotide variant	NM_033452.3(TRIM47):c.710A>C (p.Asp237Ala)	not specified [RCV004684714]	uncertain significance	17	75876779	75876779	Human		name
597801934	CV3614365	single nucleotide variant	NM_033452.3(TRIM47):c.706G>A (p.Glu236Lys)	not specified [RCV004880978]	uncertain significance	17	75876783	75876783	Human		name
597801917	CV3617813	single nucleotide variant	NM_033452.3(TRIM47):c.712C>T (p.Arg238Cys)	not specified [RCV004880969]	uncertain significance	17	75876777	75876777	Human		name
597801918	CV3617814	single nucleotide variant	NM_033452.3(TRIM47):c.835C>G (p.Gln279Glu)	not specified [RCV004880970]	uncertain significance	17	75876429	75876429	Human		name
597801926	CV3617818	single nucleotide variant	NM_033452.3(TRIM47):c.992G>A (p.Ser331Asn)	not specified [RCV004880974]	uncertain significance	17	75876272	75876272	Human		name
598274203	CV3935499	single nucleotide variant	NM_033452.3(TRIM47):c.895C>T (p.Arg299Cys)	not specified [RCV005303807]	uncertain significance	17	75876369	75876369	Human		name
598202845	CV3935500	single nucleotide variant	NM_033452.3(TRIM47):c.391G>A (p.Ala131Thr)	not specified [RCV005290442]	uncertain significance	17	75878158	75878158	Human		name
598274215	CV3935506	single nucleotide variant	NM_033452.3(TRIM47):c.577T>C (p.Cys193Arg)	not specified [RCV005303812]	uncertain significance	17	75877972	75877972	Human		name
156111673	CV2217913	single nucleotide variant	NM_033452.3(TRIM47):c.1253C>T (p.Ala418Val)	not specified [RCV004086372]	uncertain significance	17	75875423	75875423	Human		name
156052285	CV2329011	single nucleotide variant	NM_033452.3(TRIM47):c.1544G>A (p.Arg515His)	not specified [RCV004180299]	uncertain significance	17	75874856	75874856	Human		name
156057721	CV2343568	single nucleotide variant	NM_033452.3(TRIM47):c.1742G>A (p.Arg581His)	not specified [RCV004190600]	uncertain significance	17	75874658	75874658	Human		name
155904235	CV2353796	single nucleotide variant	NM_033452.3(TRIM47):c.1562G>A (p.Cys521Tyr)	not specified [RCV004201801]	uncertain significance	17	75874838	75874838	Human		name
155982806	CV2371166	single nucleotide variant	NM_033452.3(TRIM47):c.1012G>T (p.Ala338Ser)	not specified [RCV004220913]	uncertain significance	17	75876090	75876090	Human		name
156169347	CV2400467	single nucleotide variant	NM_033452.3(TRIM47):c.1105G>A (p.Val369Met)	not specified [RCV004246669]	uncertain significance	17	75875997	75875997	Human		name
329388724	CV2447803	single nucleotide variant	NM_033452.3(TRIM47):c.1498G>A (p.Glu500Lys)	not specified [RCV004258579]	uncertain significance	17	75874902	75874902	Human		name
329369918	CV2461275	single nucleotide variant	NM_033452.3(TRIM47):c.1699G>C (p.Gly567Arg)	not specified [RCV004267452]	uncertain significance	17	75874701	75874701	Human		name
401781846	CV2678340	single nucleotide variant	NM_033452.3(TRIM47):c.1123G>A (p.Val375Met)	not specified [RCV004290327]	uncertain significance	17	75875979	75875979	Human		name
401752827	CV2682950	single nucleotide variant	NM_033452.3(TRIM47):c.1303G>A (p.Asp435Asn)	not specified [RCV004283741]	uncertain significance	17	75875097	75875097	Human		name
401734944	CV2690722	single nucleotide variant	NM_033452.3(TRIM47):c.1663G>A (p.Ala555Thr)	not specified [RCV004298447]	uncertain significance	17	75874737	75874737	Human		name
401891470	CV2779147	single nucleotide variant	NM_033452.3(TRIM47):c.1575T>A (p.Asn525Lys)	not specified [RCV004349063]	uncertain significance	17	75874825	75874825	Human		name
401884081	CV2782342	single nucleotide variant	NM_033452.3(TRIM47):c.1736G>A (p.Arg579Gln)	not specified [RCV004365089]	uncertain significance	17	75874664	75874664	Human		name
405796543	CV3337034	single nucleotide variant	NM_033452.3(TRIM47):c.1225G>A (p.Glu409Lys)	not specified [RCV004475895]	uncertain significance	17	75875451	75875451	Human		name
405796546	CV3337035	single nucleotide variant	NM_033452.3(TRIM47):c.1390C>T (p.Arg464Cys)	not specified [RCV004475896]	uncertain significance	17	75875010	75875010	Human		name
405796553	CV3337037	single nucleotide variant	NM_033452.3(TRIM47):c.1579C>T (p.Arg527Cys)	not specified [RCV004475898]	uncertain significance	17	75874821	75874821	Human		name
405796557	CV3337038	single nucleotide variant	NM_033452.3(TRIM47):c.1696G>A (p.Asp566Asn)	not specified [RCV004475899]	uncertain significance	17	75874704	75874704	Human		name
405796560	CV3337039	single nucleotide variant	NM_033452.3(TRIM47):c.1717C>T (p.Arg573Trp)	not specified [RCV004475900]	uncertain significance	17	75874683	75874683	Human		name
407453911	CV3490556	single nucleotide variant	NM_033452.3(TRIM47):c.1160C>T (p.Pro387Leu)	not specified [RCV004684709]	likely benign	17	75875942	75875942	Human		name
407461467	CV3490560	single nucleotide variant	NM_033452.3(TRIM47):c.1857C>A (p.Asp619Glu)	not specified [RCV004687660]	uncertain significance	17	75874543	75874543	Human		name
597801920	CV3617815	single nucleotide variant	NM_033452.3(TRIM47):c.1640C>T (p.Thr547Met)	not specified [RCV004880971]	uncertain significance	17	75874760	75874760	Human		name
597801922	CV3617816	single nucleotide variant	NM_033452.3(TRIM47):c.1898C>A (p.Ser633Tyr)	not specified [RCV004880972]	uncertain significance	17	75874502	75874502	Human		name
597801924	CV3617817	single nucleotide variant	NM_033452.3(TRIM47):c.1385C>T (p.Pro462Leu)	not specified [RCV004880973]	uncertain significance	17	75875015	75875015	Human		name
597801930	CV3617820	single nucleotide variant	NM_033452.3(TRIM47):c.1139A>G (p.Gln380Arg)	not specified [RCV004880976]	uncertain significance	17	75875963	75875963	Human		name
597801932	CV3617821	single nucleotide variant	NM_033452.3(TRIM47):c.1360T>C (p.Cys454Arg)	not specified [RCV004880977]	uncertain significance	17	75875040	75875040	Human		name
598274210	CV3935503	single nucleotide variant	NM_033452.3(TRIM47):c.1525G>A (p.Asp509Asn)	not specified [RCV005303810]	uncertain significance	17	75874875	75874875	Human		name
598274212	CV3935504	single nucleotide variant	NM_033452.3(TRIM47):c.1531G>A (p.Gly511Ser)	not specified [RCV005303811]	uncertain significance	17	75874869	75874869	Human		name
598202851	CV3935505	single nucleotide variant	NM_033452.3(TRIM47):c.1612G>A (p.Ala538Thr)	not specified [RCV005290443]	uncertain significance	17	75874788	75874788	Human		name
598274217	CV3935507	single nucleotide variant	NM_033452.3(TRIM47):c.1639A>G (p.Thr547Ala)	not specified [RCV005303813]	uncertain significance	17	75874761	75874761	Human		name
598274219	CV3935508	single nucleotide variant	NM_033452.3(TRIM47):c.1006C>A (p.Leu336Met)	not specified [RCV005303814]	uncertain significance	17	75876096	75876096	Human		name
598202856	CV3935509	single nucleotide variant	NM_033452.3(TRIM47):c.1735C>T (p.Arg579Trp)	not specified [RCV005290444]	uncertain significance	17	75874665	75874665	Human		name

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