Trim72 Variant Search Result - Rat Genome Database

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67 records found for search term Trim72

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329393421	CV2466956	single nucleotide variant	NM_001008274.4(TRIM72):c.91C>T (p.His31Tyr)	not specified [RCV004282711]	uncertain significance	16	31214829	31214829	Human		name
405797522	CV3347284	single nucleotide variant	NM_001008274.4(TRIM72):c.73G>A (p.Val25Met)	not specified [RCV004476209]	uncertain significance	16	31214811	31214811	Human		name
15161587	CV703661	single nucleotide variant	NM_001008274.4(TRIM72):c.618C>T (p.Arg206=)	not provided [RCV000947698]	benign	16	31219420	31219420	Human		name
15156761	CV740160	single nucleotide variant	NM_001008274.4(TRIM72):c.807A>C (p.Ser269=)	not provided [RCV000902389]	likely benign	16	31222893	31222893	Human		name
405797481	CV3347269	single nucleotide variant	NM_001008274.4(TRIM72):c.109T>C (p.Cys37Arg)	not specified [RCV004476194]	uncertain significance	16	31214847	31214847	Human		name
405797486	CV3347271	single nucleotide variant	NM_001008274.4(TRIM72):c.118C>A (p.Arg40Ser)	not specified [RCV004476196]	uncertain significance	16	31214856	31214856	Human		name
405797492	CV3347273	single nucleotide variant	NM_001008274.4(TRIM72):c.158G>A (p.Cys53Tyr)	not specified [RCV004476198]	uncertain significance	16	31214896	31214896	Human		name
405797494	CV3347274	single nucleotide variant	NM_001008274.4(TRIM72):c.205C>A (p.Leu69Met)	not specified [RCV004476199]	uncertain significance	16	31214943	31214943	Human		name
407454155	CV3490726	single nucleotide variant	NM_001008274.4(TRIM72):c.224T>A (p.Val75Glu)	not specified [RCV004684849]	uncertain significance	16	31214962	31214962	Human		name
407454156	CV3490727	single nucleotide variant	NM_001008274.4(TRIM72):c.169C>G (p.Gln57Glu)	not specified [RCV004684850]	uncertain significance	16	31214907	31214907	Human		name
597802387	CV3614609	single nucleotide variant	NM_001008274.4(TRIM72):c.103C>T (p.Arg35Cys)	not specified [RCV004881206]	uncertain significance	16	31214841	31214841	Human		name
156272939	CV2195355	single nucleotide variant	NM_001008274.4(TRIM72):c.962C>T (p.Ala321Val)	not specified [RCV004080274]	uncertain significance	16	31224283	31224283	Human		name
156399178	CV2204962	single nucleotide variant	NM_001008274.4(TRIM72):c.500A>T (p.Gln167Leu)	not specified [RCV004077584]	uncertain significance	16	31219302	31219302	Human		name
156171728	CV2247465	single nucleotide variant	NM_001008274.4(TRIM72):c.671A>C (p.Lys224Thr)	not specified [RCV004108789]	uncertain significance	16	31219473	31219473	Human		name
156017056	CV2266603	single nucleotide variant	NM_001008274.4(TRIM72):c.491C>T (p.Thr164Ile)	not specified [RCV004131152]	uncertain significance	16	31219293	31219293	Human		name
155916998	CV2278490	single nucleotide variant	NM_001008274.4(TRIM72):c.506G>T (p.Arg169Leu)	not specified [RCV004132932]	uncertain significance	16	31219308	31219308	Human		name
156249966	CV2311181	single nucleotide variant	NM_001008274.4(TRIM72):c.641C>G (p.Ser214Cys)	not specified [RCV004166278]	uncertain significance	16	31219443	31219443	Human		name
156195974	CV2347623	single nucleotide variant	NM_001008274.4(TRIM72):c.617G>T (p.Arg206Leu)	not specified [RCV004200559]	uncertain significance	16	31219419	31219419	Human		name
156340572	CV2347966	single nucleotide variant	NM_001008274.4(TRIM72):c.385C>T (p.Leu129Phe)	not specified [RCV004197654]	uncertain significance	16	31215123	31215123	Human		name
156109430	CV2355486	single nucleotide variant	NM_001008274.4(TRIM72):c.779G>A (p.Arg260His)	not specified [RCV004205336]	uncertain significance	16	31222865	31222865	Human		name
329368882	CV2424684	single nucleotide variant	NM_001008274.4(TRIM72):c.382C>T (p.Arg128Cys)	not specified [RCV004248581]	uncertain significance	16	31215120	31215120	Human		name
329355628	CV2445552	single nucleotide variant	NM_001008274.4(TRIM72):c.475G>T (p.Val159Leu)	not specified [RCV004257599]	uncertain significance	16	31219179	31219179	Human		name
329393885	CV2449930	single nucleotide variant	NM_001008274.4(TRIM72):c.620G>A (p.Arg207Gln)	not specified [RCV004269002]	uncertain significance	16	31219422	31219422	Human		name
401722073	CV2680809	single nucleotide variant	NM_001008274.4(TRIM72):c.529G>T (p.Gly177Cys)	not specified [RCV004293457]	uncertain significance	16	31219331	31219331	Human		name
401880651	CV2792923	single nucleotide variant	NM_001008274.4(TRIM72):c.512C>A (p.Ala171Asp)	not specified [RCV004365654]	uncertain significance	16	31219314	31219314	Human		name
405797497	CV3347275	single nucleotide variant	NM_001008274.4(TRIM72):c.451G>A (p.Val151Met)	not specified [RCV004476200]	uncertain significance	16	31219155	31219155	Human		name
405797505	CV3347278	single nucleotide variant	NM_001008274.4(TRIM72):c.496C>A (p.Arg166Ser)	not specified [RCV004476203]	uncertain significance	16	31219298	31219298	Human		name
405797508	CV3347279	single nucleotide variant	NM_001008274.4(TRIM72):c.497G>A (p.Arg166His)	not specified [RCV004476204]	uncertain significance	16	31219299	31219299	Human		name
405797511	CV3347280	single nucleotide variant	NM_001008274.4(TRIM72):c.541G>T (p.Val181Leu)	not specified [RCV004476205]	likely benign	16	31219343	31219343	Human		name
405797514	CV3347281	single nucleotide variant	NM_001008274.4(TRIM72):c.551C>T (p.Ala184Val)	not specified [RCV004476206]	uncertain significance	16	31219353	31219353	Human		name
405797517	CV3347282	single nucleotide variant	NM_001008274.4(TRIM72):c.593G>A (p.Arg198Gln)	not specified [RCV004476207]	uncertain significance	16	31219395	31219395	Human		name
405797525	CV3347285	single nucleotide variant	NM_001008274.4(TRIM72):c.778C>T (p.Arg260Cys)	not specified [RCV004476210]	uncertain significance	16	31222864	31222864	Human		name
405797527	CV3347286	single nucleotide variant	NM_001008274.4(TRIM72):c.937T>C (p.Cys313Arg)	not specified [RCV004476211]	uncertain significance	16	31224258	31224258	Human		name
597802383	CV3614607	single nucleotide variant	NM_001008274.4(TRIM72):c.772C>A (p.Pro258Thr)	not specified [RCV004881204]	uncertain significance	16	31222858	31222858	Human		name
597802385	CV3614608	single nucleotide variant	NM_001008274.4(TRIM72):c.505C>T (p.Arg169Trp)	not specified [RCV004881205]	uncertain significance	16	31219307	31219307	Human		name
597677791	CV3614612	single nucleotide variant	NM_001008274.4(TRIM72):c.418C>G (p.Leu140Val)	not specified [RCV004883193]	uncertain significance	16	31219122	31219122	Human		name
597677813	CV3614615	single nucleotide variant	NM_001008274.4(TRIM72):c.514G>A (p.Val172Met)	not specified [RCV004883195]	uncertain significance	16	31219316	31219316	Human		name
597677825	CV3614616	single nucleotide variant	NM_001008274.4(TRIM72):c.884C>G (p.Pro295Arg)	not specified [RCV004883196]	uncertain significance	16	31224205	31224205	Human		name
597677845	CV3614618	single nucleotide variant	NM_001008274.4(TRIM72):c.351T>A (p.His117Gln)	not specified [RCV004883198]	uncertain significance	16	31215089	31215089	Human		name
598274442	CV3935705	single nucleotide variant	NM_001008274.4(TRIM72):c.872T>C (p.Leu291Pro)	not specified [RCV005303929]	uncertain significance	16	31224193	31224193	Human		name
598214360	CV3935706	single nucleotide variant	NM_001008274.4(TRIM72):c.596G>A (p.Gly199Asp)	not specified [RCV005292507]	uncertain significance	16	31219398	31219398	Human		name
598214365	CV3935707	single nucleotide variant	NM_001008274.4(TRIM72):c.737G>C (p.Ser246Thr)	not specified [RCV005292508]	uncertain significance	16	31220915	31220915	Human		name
598274444	CV3935708	single nucleotide variant	NM_001008274.4(TRIM72):c.358C>A (p.Leu120Met)	not specified [RCV005303930]	uncertain significance	16	31215096	31215096	Human		name
598214370	CV3935709	single nucleotide variant	NM_001008274.4(TRIM72):c.925C>A (p.Arg309Ser)	not specified [RCV005292509]	uncertain significance	16	31224246	31224246	Human		name
598274446	CV3935711	single nucleotide variant	NM_001008274.4(TRIM72):c.592C>G (p.Arg198Gly)	not specified [RCV005303931]	uncertain significance	16	31219394	31219394	Human		name
598274448	CV3935713	single nucleotide variant	NM_001008274.4(TRIM72):c.994G>A (p.Val332Met)	not specified [RCV005303932]	uncertain significance	16	31224315	31224315	Human		name
15193941	CV703660	single nucleotide variant	NM_001008274.4(TRIM72):c.574C>T (p.Arg192Cys)	not provided [RCV000955511]	benign	16	31219376	31219376	Human		name
156261378	CV2314721	single nucleotide variant	NM_001008274.4(TRIM72):c.1238T>C (p.Ile413Thr)	not specified [RCV004170866]	uncertain significance	16	31224559	31224559	Human		name
156327759	CV2332145	single nucleotide variant	NM_001008274.4(TRIM72):c.1016A>T (p.Gln339Leu)	not provided [RCV004703303]\|not specified [RCV004189181]	likely benign	16	31224337	31224337	Human		name
155917326	CV2336310	single nucleotide variant	NM_001008274.4(TRIM72):c.1117C>T (p.His373Tyr)	not specified [RCV004192059]	uncertain significance	16	31224438	31224438	Human		name
401730258	CV2680068	single nucleotide variant	NM_001008274.4(TRIM72):c.1397C>T (p.Pro466Leu)	not specified [RCV004286562]	uncertain significance	16	31224718	31224718	Human		name
401750656	CV2689487	single nucleotide variant	NM_001008274.4(TRIM72):c.1310C>T (p.Pro437Leu)	not specified [RCV004308329]	likely benign	16	31224631	31224631	Human		name
401717863	CV2703512	single nucleotide variant	NM_001008274.4(TRIM72):c.1382G>A (p.Gly461Asp)	not specified [RCV004317691]	uncertain significance	16	31224703	31224703	Human		name
401720333	CV2705833	single nucleotide variant	NM_001008274.4(TRIM72):c.1258G>C (p.Gly420Arg)	not specified [RCV004320450]	uncertain significance	16	31224579	31224579	Human		name
401870006	CV2765541	single nucleotide variant	NM_001008274.4(TRIM72):c.1067G>A (p.Arg356His)	not specified [RCV004342245]	uncertain significance	16	31224388	31224388	Human		name
401873939	CV2773604	single nucleotide variant	NM_001008274.4(TRIM72):c.1360G>A (p.Asp454Asn)	not specified [RCV004356300]	uncertain significance	16	31224681	31224681	Human		name
405797484	CV3347270	single nucleotide variant	NM_001008274.4(TRIM72):c.1102C>A (p.Arg368Ser)	not specified [RCV004476195]	uncertain significance	16	31224423	31224423	Human		name
405797489	CV3347272	single nucleotide variant	NM_001008274.4(TRIM72):c.1270C>A (p.Leu424Ile)	not specified [RCV004476197]	uncertain significance	16	31224591	31224591	Human		name
407454157	CV3490728	single nucleotide variant	NM_001008274.4(TRIM72):c.1154T>C (p.Leu385Pro)	not specified [RCV004684851]	uncertain significance	16	31224475	31224475	Human		name
597677772	CV3614610	single nucleotide variant	NM_001008274.4(TRIM72):c.1087G>T (p.Ala363Ser)	not specified [RCV004883191]	likely benign	16	31224408	31224408	Human		name
597677781	CV3614611	single nucleotide variant	NM_001008274.4(TRIM72):c.1175A>C (p.Glu392Ala)	not specified [RCV004883192]	uncertain significance	16	31224496	31224496	Human		name
597677803	CV3614614	single nucleotide variant	NM_001008274.4(TRIM72):c.1204G>A (p.Ala402Thr)	not specified [RCV004883194]	uncertain significance	16	31224525	31224525	Human		name
597677836	CV3614617	single nucleotide variant	NM_001008274.4(TRIM72):c.1012C>G (p.Gln338Glu)	not specified [RCV004883197]	uncertain significance	16	31224333	31224333	Human		name
597677854	CV3614619	single nucleotide variant	NM_001008274.4(TRIM72):c.1327G>A (p.Glu443Lys)	not specified [RCV004883199]	uncertain significance	16	31224648	31224648	Human		name
598214354	CV3935703	single nucleotide variant	NM_001008274.4(TRIM72):c.1295C>A (p.Ala432Asp)	not specified [RCV005292506]	uncertain significance	16	31224616	31224616	Human		name
598214376	CV3935710	single nucleotide variant	NM_001008274.4(TRIM72):c.1121C>G (p.Ala374Gly)	not specified [RCV005292510]	uncertain significance	16	31224442	31224442	Human		name
598214381	CV3935712	single nucleotide variant	NM_001008274.4(TRIM72):c.1363G>A (p.Val455Met)	not specified [RCV005292511]	uncertain significance	16	31224684	31224684	Human		name

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