Trim50 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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84 records found for search term Trim50

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405796688	CV3337103	single nucleotide variant	NM_178125.3(TRIM50):c.25G>A (p.Glu9Lys)	not specified [RCV004475964]	uncertain significance	7	73324763	73324763	Human		name
407454002	CV3490596	single nucleotide variant	NM_178125.3(TRIM50):c.13G>A (p.Val5Met)	not specified [RCV004684740]	uncertain significance	7	73324775	73324775	Human		name
597802027	CV3614416	single nucleotide variant	NM_178125.3(TRIM50):c.10C>A (p.Gln4Lys)	not specified [RCV004881027]	uncertain significance	7	73324778	73324778	Human		name
156294725	CV2243773	single nucleotide variant	NM_178125.3(TRIM50):c.56G>A (p.Cys19Tyr)	not specified [RCV004114464]	uncertain significance	7	73324732	73324732	Human		name
156280518	CV2315983	single nucleotide variant	NM_178125.3(TRIM50):c.50C>T (p.Pro17Leu)	not specified [RCV004172047]	uncertain significance	7	73324738	73324738	Human		name
401735113	CV2690781	single nucleotide variant	NM_178125.3(TRIM50):c.92G>T (p.Cys31Phe)	not specified [RCV004298498]	uncertain significance	7	73324696	73324696	Human		name
597802021	CV3614413	single nucleotide variant	NM_178125.3(TRIM50):c.58C>A (p.Leu20Met)	not specified [RCV004881024]	uncertain significance	7	73324730	73324730	Human		name
15188440	CV736231	single nucleotide variant	NM_178125.3(TRIM50):c.363G>A (p.Pro121=)	not provided [RCV000909370]	benign	7	73324425	73324425	Human		name
8626451	CV81595	single nucleotide variant	NM_178125.3(TRIM50):c.858C>T (p.Phe286=)	Malignant melanoma [RCV000061673]	not provided	7	73316581	73316581	Human		name
156119154	CV2275775	single nucleotide variant	NM_178125.3(TRIM50):c.128T>C (p.Leu43Pro)	not specified [RCV004139455]	uncertain significance	7	73324660	73324660	Human		name
156273768	CV2277826	single nucleotide variant	NM_178125.3(TRIM50):c.272A>G (p.His91Arg)	not specified [RCV004147247]	uncertain significance	7	73324516	73324516	Human		name
156330202	CV2339442	single nucleotide variant	NM_178125.3(TRIM50):c.169C>T (p.Arg57Trp)	not specified [RCV004194112]	uncertain significance	7	73324619	73324619	Human		name
329385212	CV2432054	single nucleotide variant	NM_178125.3(TRIM50):c.226G>A (p.Glu76Lys)	not specified [RCV004249205]	uncertain significance	7	73324562	73324562	Human		name
329387159	CV2436302	single nucleotide variant	NM_178125.3(TRIM50):c.154C>T (p.Arg52Cys)	not specified [RCV004251707]	uncertain significance	7	73324634	73324634	Human		name
329359628	CV2446358	single nucleotide variant	NM_178125.3(TRIM50):c.268G>C (p.Val90Leu)	not specified [RCV004249483]	uncertain significance	7	73324520	73324520	Human		name
329392520	CV2468206	single nucleotide variant	NM_178125.3(TRIM50):c.107G>T (p.Cys36Phe)	not specified [RCV004275787]	uncertain significance	7	73324681	73324681	Human		name
401729768	CV2686941	single nucleotide variant	NM_178125.3(TRIM50):c.268G>A (p.Val90Met)	not specified [RCV004304275]	uncertain significance	7	73324520	73324520	Human		name
401895834	CV2768818	single nucleotide variant	NM_178125.3(TRIM50):c.194C>T (p.Ser65Phe)	not specified [RCV004346945]	uncertain significance	7	73324594	73324594	Human		name
401922537	CV2825739	single nucleotide variant	NM_178125.3(TRIM50):c.1419C>A (p.Pro473=)	not provided [RCV003433858]	likely benign	7	73312966	73312966	Human		name
401922512	CV2825740	single nucleotide variant	NM_178125.3(TRIM50):c.1224C>T (p.Ala408=)	not provided [RCV003433859]	likely benign	7	73313161	73313161	Human		name
405796685	CV3337102	single nucleotide variant	NM_178125.3(TRIM50):c.256C>G (p.Pro86Ala)	not specified [RCV004475963]	uncertain significance	7	73324532	73324532	Human		name
407453999	CV3490595	single nucleotide variant	NM_178125.3(TRIM50):c.205G>A (p.Val69Ile)	not specified [RCV004684739]	uncertain significance	7	73324583	73324583	Human		name
597802019	CV3614412	single nucleotide variant	NM_178125.3(TRIM50):c.278G>A (p.Arg93Gln)	not specified [RCV004881023]	uncertain significance	7	73324510	73324510	Human		name
597802023	CV3614414	single nucleotide variant	NM_178125.3(TRIM50):c.111G>T (p.Lys37Asn)	not specified [RCV004881025]	uncertain significance	7	73324677	73324677	Human		name
156343018	CV2222597	single nucleotide variant	NM_178125.3(TRIM50):c.784G>A (p.Ala262Thr)	not specified [RCV004099425]	likely benign	7	73316655	73316655	Human		name
156073035	CV2240617	single nucleotide variant	NM_178125.3(TRIM50):c.525C>G (p.Ile175Met)	not specified [RCV004119259]	uncertain significance	7	73319023	73319023	Human		name
155955570	CV2274474	single nucleotide variant	NM_178125.3(TRIM50):c.605G>A (p.Arg202His)	not specified [RCV004136831]	uncertain significance	7	73318943	73318943	Human		name
155909488	CV2303400	single nucleotide variant	NM_178125.3(TRIM50):c.488G>A (p.Arg163Gln)	not specified [RCV004159742]	uncertain significance	7	73320154	73320154	Human		name
156074637	CV2321704	single nucleotide variant	NM_178125.3(TRIM50):c.460A>G (p.Ile154Val)	not specified [RCV004179705]	uncertain significance	7	73320182	73320182	Human		name
156359919	CV2328334	single nucleotide variant	NM_178125.3(TRIM50):c.389G>A (p.Ser130Asn)	not specified [RCV004175451]	uncertain significance	7	73324399	73324399	Human		name
156338589	CV2351446	single nucleotide variant	NM_178125.3(TRIM50):c.592G>C (p.Gly198Arg)	not specified [RCV004193132]	uncertain significance	7	73318956	73318956	Human		name
155904511	CV2353892	single nucleotide variant	NM_178125.3(TRIM50):c.947T>G (p.Val316Gly)	not specified [RCV004201890]	uncertain significance	7	73313438	73313438	Human		name
155902190	CV2356409	single nucleotide variant	NM_178125.3(TRIM50):c.368C>T (p.Thr123Met)	not specified [RCV004206210]	uncertain significance	7	73324420	73324420	Human		name
156102978	CV2363272	single nucleotide variant	NM_178125.3(TRIM50):c.527G>A (p.Arg176His)	not specified [RCV004213827]	uncertain significance	7	73319021	73319021	Human		name
156019280	CV2366912	single nucleotide variant	NM_178125.3(TRIM50):c.470T>C (p.Leu157Pro)	not specified [RCV004213324]	uncertain significance	7	73320172	73320172	Human		name
156156015	CV2367925	single nucleotide variant	NM_178125.3(TRIM50):c.368C>A (p.Thr123Lys)	not specified [RCV004223022]	uncertain significance	7	73324420	73324420	Human		name
156258445	CV2383765	single nucleotide variant	NM_178125.3(TRIM50):c.481C>T (p.Arg161Trp)	not specified [RCV004231643]	uncertain significance	7	73320161	73320161	Human		name
329373080	CV2434098	single nucleotide variant	NM_178125.3(TRIM50):c.440A>G (p.Gln147Arg)	not specified [RCV004249996]	uncertain significance	7	73320202	73320202	Human		name
329358793	CV2450711	single nucleotide variant	NM_178125.3(TRIM50):c.394A>G (p.Met132Val)	not specified [RCV004267656]	uncertain significance	7	73324394	73324394	Human		name
329368478	CV2453260	single nucleotide variant	NM_178125.3(TRIM50):c.859C>T (p.Arg287Trp)	not specified [RCV004266901]	uncertain significance	7	73316580	73316580	Human		name
329385763	CV2462293	single nucleotide variant	NM_178125.3(TRIM50):c.889A>G (p.Lys297Glu)	not specified [RCV004266285]	uncertain significance	7	73313496	73313496	Human		name
401729891	CV2686991	single nucleotide variant	NM_178125.3(TRIM50):c.766G>A (p.Ala256Thr)	not specified [RCV004304321]	uncertain significance	7	73316673	73316673	Human		name
401885320	CV2759683	single nucleotide variant	NM_178125.3(TRIM50):c.955G>C (p.Gly319Arg)	not specified [RCV004340690]	uncertain significance	7	73313430	73313430	Human		name
405796691	CV3337104	single nucleotide variant	NM_178125.3(TRIM50):c.338T>A (p.Leu113Gln)	not specified [RCV004475965]	uncertain significance	7	73324450	73324450	Human		name
405796694	CV3337105	single nucleotide variant	NM_178125.3(TRIM50):c.623T>C (p.Leu208Pro)	not specified [RCV004475966]	uncertain significance	7	73318925	73318925	Human		name
405796700	CV3337107	single nucleotide variant	NM_178125.3(TRIM50):c.770G>A (p.Arg257Gln)	not specified [RCV004475968]	uncertain significance	7	73316669	73316669	Human		name
405796705	CV3337108	single nucleotide variant	NM_178125.3(TRIM50):c.890A>G (p.Lys297Arg)	not specified [RCV004475969]	uncertain significance	7	73313495	73313495	Human		name
407454005	CV3490597	single nucleotide variant	NM_178125.3(TRIM50):c.477C>A (p.Asn159Lys)	not specified [RCV004684741]	uncertain significance	7	73320165	73320165	Human		name
407461512	CV3490598	single nucleotide variant	NM_178125.3(TRIM50):c.656G>A (p.Arg219Gln)	not specified [RCV004687669]	likely benign	7	73318892	73318892	Human		name
407454008	CV3490601	single nucleotide variant	NM_178125.3(TRIM50):c.578G>A (p.Cys193Tyr)	not specified [RCV004684742]	uncertain significance	7	73318970	73318970	Human		name
407461528	CV3490602	single nucleotide variant	NM_178125.3(TRIM50):c.991C>T (p.Arg331Cys)	not specified [RCV004687672]	uncertain significance	7	73313394	73313394	Human		name
597802015	CV3614410	single nucleotide variant	NM_178125.3(TRIM50):c.548A>G (p.His183Arg)	not specified [RCV004881021]	uncertain significance	7	73319000	73319000	Human		name
597802017	CV3614411	single nucleotide variant	NM_178125.3(TRIM50):c.761C>T (p.Pro254Leu)	not specified [RCV004881022]	uncertain significance	7	73316678	73316678	Human		name
597802025	CV3614415	single nucleotide variant	NM_178125.3(TRIM50):c.373G>A (p.Val125Ile)	not specified [RCV004881026]	uncertain significance	7	73324415	73324415	Human		name
597802031	CV3614418	single nucleotide variant	NM_178125.3(TRIM50):c.526C>T (p.Arg176Cys)	not specified [RCV004881029]	uncertain significance	7	73319022	73319022	Human		name
597802033	CV3614419	single nucleotide variant	NM_178125.3(TRIM50):c.709C>A (p.His237Asn)	not specified [RCV004881030]	uncertain significance	7	73318839	73318839	Human		name
598202965	CV3935543	single nucleotide variant	NM_178125.3(TRIM50):c.819C>A (p.His273Gln)	not specified [RCV005290461]	uncertain significance	7	73316620	73316620	Human		name
598274258	CV3935544	single nucleotide variant	NM_178125.3(TRIM50):c.941C>T (p.Thr314Met)	not specified [RCV005303832]	uncertain significance	7	73313444	73313444	Human		name
598274262	CV3935548	single nucleotide variant	NM_178125.3(TRIM50):c.884C>T (p.Pro295Leu)	not specified [RCV005303834]	uncertain significance	7	73313501	73313501	Human		name
8632625	CV87840	single nucleotide variant	NM_178125.3(TRIM50):c.688G>A (p.Glu230Lys)	Malignant melanoma [RCV000067932]	not provided	7	73318860	73318860	Human		name
156383197	CV2223816	single nucleotide variant	NM_178125.3(TRIM50):c.1237C>T (p.Arg413Cys)	not specified [RCV004093872]	uncertain significance	7	73313148	73313148	Human		name
156071595	CV2254913	single nucleotide variant	NM_178125.3(TRIM50):c.1405G>A (p.Val469Met)	not specified [RCV004117152]	uncertain significance	7	73312980	73312980	Human		name
155928369	CV2281090	single nucleotide variant	NM_178125.3(TRIM50):c.1171G>A (p.Glu391Lys)	not specified [RCV004147358]	uncertain significance	7	73313214	73313214	Human		name
155922479	CV2284368	single nucleotide variant	NM_178125.3(TRIM50):c.1125G>C (p.Lys375Asn)	not specified [RCV004146710]	uncertain significance	7	73313260	73313260	Human		name
156083127	CV2292997	single nucleotide variant	NM_178125.3(TRIM50):c.1423G>C (p.Gly475Arg)	not specified [RCV004148473]	uncertain significance	7	73312962	73312962	Human		name
156192868	CV2301921	single nucleotide variant	NM_178125.3(TRIM50):c.1024C>T (p.Arg342Cys)	not specified [RCV004156702]	uncertain significance	7	73313361	73313361	Human		name
156184772	CV2324612	single nucleotide variant	NM_178125.3(TRIM50):c.1084C>T (p.Arg362Cys)	not specified [RCV004172865]	uncertain significance	7	73313301	73313301	Human		name
156162879	CV2368306	single nucleotide variant	NM_178125.3(TRIM50):c.1150G>T (p.Val384Leu)	not specified [RCV004219088]	uncertain significance	7	73313235	73313235	Human		name
329369996	CV2461304	single nucleotide variant	NM_178125.3(TRIM50):c.1238G>A (p.Arg413His)	not specified [RCV004267476]	uncertain significance	7	73313147	73313147	Human		name
401779625	CV2676634	single nucleotide variant	NM_178125.3(TRIM50):c.1177C>T (p.Arg393Trp)	not specified [RCV004282594]	uncertain significance	7	73313208	73313208	Human		name
401746794	CV2691984	single nucleotide variant	NM_178125.3(TRIM50):c.1352A>C (p.Tyr451Ser)	not specified [RCV004301713]	uncertain significance	7	73313033	73313033	Human		name
401728691	CV2729746	single nucleotide variant	NM_178125.3(TRIM50):c.1444G>A (p.Glu482Lys)	not specified [RCV004332767]	uncertain significance	7	73312941	73312941	Human		name
401870843	CV2762930	single nucleotide variant	NM_178125.3(TRIM50):c.1204C>G (p.Arg402Gly)	not specified [RCV004342680]	uncertain significance	7	73313181	73313181	Human		name
405796676	CV3337099	single nucleotide variant	NM_178125.3(TRIM50):c.1042C>T (p.Arg348Cys)	not specified [RCV004475960]	uncertain significance	7	73313343	73313343	Human		name
405796679	CV3337100	single nucleotide variant	NM_178125.3(TRIM50):c.1136C>T (p.Ser379Phe)	not specified [RCV004475961]	uncertain significance	7	73313249	73313249	Human		name
405796682	CV3337101	single nucleotide variant	NM_178125.3(TRIM50):c.1378G>C (p.Glu460Gln)	not specified [RCV004475962]	uncertain significance	7	73313007	73313007	Human		name
407461506	CV3490594	single nucleotide variant	NM_178125.3(TRIM50):c.1085G>A (p.Arg362His)	not specified [RCV004687668]	uncertain significance	7	73313300	73313300	Human		name
407461522	CV3490600	single nucleotide variant	NM_178125.3(TRIM50):c.1162G>A (p.Gly388Ser)	not specified [RCV004687671]	uncertain significance	7	73313223	73313223	Human		name
597802029	CV3614417	single nucleotide variant	NM_178125.3(TRIM50):c.1310G>A (p.Arg437Gln)	not specified [RCV004881028]	uncertain significance	7	73313075	73313075	Human		name
598274254	CV3935541	single nucleotide variant	NM_178125.3(TRIM50):c.1300G>A (p.Asp434Asn)	not specified [RCV005303830]	uncertain significance	7	73313085	73313085	Human		name
598274256	CV3935542	single nucleotide variant	NM_178125.3(TRIM50):c.1025G>T (p.Arg342Leu)	not specified [RCV005303831]	uncertain significance	7	73313360	73313360	Human		name
598202971	CV3935545	single nucleotide variant	NM_178125.3(TRIM50):c.1294C>T (p.Arg432Cys)	not specified [RCV005290462]	uncertain significance	7	73313091	73313091	Human		name
598202977	CV3935546	single nucleotide variant	NM_178125.3(TRIM50):c.1382G>A (p.Arg461Lys)	not specified [RCV005290463]	uncertain significance	7	73313003	73313003	Human		name
598274260	CV3935547	single nucleotide variant	NM_178125.3(TRIM50):c.1108G>A (p.Ala370Thr)	not specified [RCV005303833]	uncertain significance	7	73313277	73313277	Human		name

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