Trim66 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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132 records found for search term Trim66

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15146625	CV779480	single nucleotide variant	NM_001388022.1(TRIM66):c.842+7C>T	not provided [RCV000967192]	benign	11	8647963	8647963	Human		name
405854054	CV3393747	single nucleotide variant	NM_001388022.1(TRIM66):c.2712T>C (p.Pro904=)	not provided [RCV004546973]	likely benign	11	8624827	8624827	Human		name
15198964	CV702017	single nucleotide variant	NM_001388022.1(TRIM66):c.2481C>T (p.Ser827=)	not provided [RCV000956908]	benign	11	8625058	8625058	Human		name
156380592	CV2208279	single nucleotide variant	NM_001388022.1(TRIM66):c.620C>T (p.Thr207Ile)	not specified [RCV004088722]	uncertain significance	11	8648521	8648521	Human		name
156231387	CV2227597	single nucleotide variant	NM_001388022.1(TRIM66):c.523A>G (p.Thr175Ala)	not specified [RCV004094019]	uncertain significance	11	8649809	8649809	Human		name
156037126	CV2313421	single nucleotide variant	NM_001388022.1(TRIM66):c.446A>G (p.Asn149Ser)	not specified [RCV004163742]	uncertain significance	11	8649886	8649886	Human		name
156050467	CV2319377	single nucleotide variant	NM_001388022.1(TRIM66):c.911T>C (p.Met304Thr)	not specified [RCV004180197]	uncertain significance	11	8646493	8646493	Human		name
156266310	CV2329594	single nucleotide variant	NM_001388022.1(TRIM66):c.632C>T (p.Pro211Leu)	not specified [RCV004180714]	uncertain significance	11	8648509	8648509	Human		name
156362861	CV2330404	single nucleotide variant	NM_001388022.1(TRIM66):c.797A>C (p.His266Pro)	not specified [RCV004180978]	uncertain significance	11	8648015	8648015	Human		name
401732731	CV2691092	single nucleotide variant	NM_001388022.1(TRIM66):c.944T>C (p.Ile315Thr)	not specified [RCV004301090]	uncertain significance	11	8646460	8646460	Human		name
401759571	CV2701615	single nucleotide variant	NM_001388022.1(TRIM66):c.572G>C (p.Arg191Pro)	not specified [RCV004314035]	uncertain significance	11	8649760	8649760	Human		name
401736173	CV2703062	single nucleotide variant	NM_001388022.1(TRIM66):c.610G>A (p.Gly204Arg)	not specified [RCV004321364]	uncertain significance	11	8648531	8648531	Human		name
405797258	CV3347191	single nucleotide variant	NM_001388022.1(TRIM66):c.466A>G (p.Lys156Glu)	not specified [RCV004476116]	uncertain significance	11	8649866	8649866	Human		name
407454131	CV3490698	single nucleotide variant	NM_001388022.1(TRIM66):c.857A>C (p.Lys286Thr)	not specified [RCV004684825]	uncertain significance	11	8646547	8646547	Human		name
597802230	CV3614527	single nucleotide variant	NM_001388022.1(TRIM66):c.677A>G (p.Asp226Gly)	not specified [RCV004881127]	uncertain significance	11	8648464	8648464	Human		name
597802233	CV3614528	single nucleotide variant	NM_001388022.1(TRIM66):c.776G>T (p.Gly259Val)	not specified [RCV004881128]	uncertain significance	11	8648036	8648036	Human		name
597802234	CV3614529	single nucleotide variant	NM_001388022.1(TRIM66):c.706G>A (p.Val236Met)	not specified [RCV004881129]	uncertain significance	11	8648435	8648435	Human		name
597802240	CV3614532	single nucleotide variant	NM_001388022.1(TRIM66):c.692A>G (p.His231Arg)	not specified [RCV004881132]	uncertain significance	11	8648449	8648449	Human		name
597802242	CV3614534	single nucleotide variant	NM_001388022.1(TRIM66):c.934A>G (p.Asn312Asp)	not specified [RCV004881133]	uncertain significance	11	8646470	8646470	Human		name
597802258	CV3614542	single nucleotide variant	NM_001388022.1(TRIM66):c.623T>C (p.Leu208Ser)	not specified [RCV004881141]	uncertain significance	11	8648518	8648518	Human		name
597802264	CV3614546	single nucleotide variant	NM_001388022.1(TRIM66):c.490A>G (p.Thr164Ala)	not specified [RCV004881144]	uncertain significance	11	8649842	8649842	Human		name
598274369	CV3935649	single nucleotide variant	NM_001388022.1(TRIM66):c.862C>G (p.Gln288Glu)	not specified [RCV005303891]	uncertain significance	11	8646542	8646542	Human		name
15162152	CV713229	single nucleotide variant	NM_001388022.1(TRIM66):c.935A>C (p.Asn312Thr)	not provided [RCV000970219]	benign	11	8646469	8646469	Human		name
156065188	CV2196863	single nucleotide variant	NM_001388022.1(TRIM66):c.1621G>A (p.Glu541Lys)	not specified [RCV004069867]	uncertain significance	11	8640754	8640754	Human		name
156077292	CV2198222	single nucleotide variant	NM_001388022.1(TRIM66):c.1421C>T (p.Ser474Leu)	not provided [RCV003404142]\|not specified [RCV004079805]	likely benign\|uncertain significance	11	8640954	8640954	Human		name
156118743	CV2219201	single nucleotide variant	NM_001388022.1(TRIM66):c.1052A>G (p.Asn351Ser)	not specified [RCV004093470]	uncertain significance	11	8645793	8645793	Human		name
155985830	CV2233926	single nucleotide variant	NM_001388022.1(TRIM66):c.2551C>T (p.Leu851Phe)	not specified [RCV004104278]	uncertain significance	11	8624988	8624988	Human		name
156025573	CV2242251	single nucleotide variant	NM_001388022.1(TRIM66):c.2686G>A (p.Ala896Thr)	not specified [RCV004111275]	uncertain significance	11	8624853	8624853	Human		name
156180341	CV2246013	single nucleotide variant	NM_001388022.1(TRIM66):c.1663C>G (p.Pro555Ala)	not specified [RCV004113931]	uncertain significance	11	8640712	8640712	Human		name
156095528	CV2253039	single nucleotide variant	NM_001388022.1(TRIM66):c.2968G>A (p.Ala990Thr)	not specified [RCV004120832]	uncertain significance	11	8624410	8624410	Human		name
156107913	CV2254353	single nucleotide variant	NM_001388022.1(TRIM66):c.1325T>G (p.Val442Gly)	not specified [RCV004123750]	uncertain significance	11	8641050	8641050	Human		name
156318946	CV2260761	single nucleotide variant	NM_001388022.1(TRIM66):c.2678C>A (p.Pro893Gln)	not specified [RCV004125681]	uncertain significance	11	8624861	8624861	Human		name
156271808	CV2286473	single nucleotide variant	NM_001388022.1(TRIM66):c.1831C>T (p.His611Tyr)	not specified [RCV004139980]	uncertain significance	11	8640544	8640544	Human		name
156179774	CV2288041	single nucleotide variant	NM_001388022.1(TRIM66):c.1948A>G (p.Met650Val)	not specified [RCV004147797]	likely benign	11	8640427	8640427	Human		name
156283671	CV2288918	single nucleotide variant	NM_001388022.1(TRIM66):c.1895A>C (p.His632Pro)	not specified [RCV004149888]	uncertain significance	11	8640480	8640480	Human		name
155932184	CV2290515	single nucleotide variant	NM_001388022.1(TRIM66):c.2972C>T (p.Pro991Leu)	not specified [RCV004155204]	uncertain significance	11	8624406	8624406	Human		name
156069848	CV2292841	single nucleotide variant	NM_001388022.1(TRIM66):c.2959C>T (p.Pro987Ser)	not specified [RCV004148356]	uncertain significance	11	8624419	8624419	Human		name
155901282	CV2294406	single nucleotide variant	NM_001388022.1(TRIM66):c.1450C>G (p.Pro484Ala)	not specified [RCV004159916]	uncertain significance	11	8640925	8640925	Human		name
156178895	CV2298334	single nucleotide variant	NM_001388022.1(TRIM66):c.1816C>G (p.Pro606Ala)	not specified [RCV004160231]	uncertain significance	11	8640559	8640559	Human		name
156048366	CV2304420	single nucleotide variant	NM_001388022.1(TRIM66):c.2659G>A (p.Gly887Ser)	not specified [RCV004164520]	uncertain significance	11	8624880	8624880	Human		name
156169303	CV2315449	single nucleotide variant	NM_001388022.1(TRIM66):c.1051A>C (p.Asn351His)	not specified [RCV004167403]	uncertain significance	11	8645794	8645794	Human		name
156273512	CV2320191	single nucleotide variant	NM_001388022.1(TRIM66):c.1540A>G (p.Arg514Gly)	not specified [RCV004169814]	uncertain significance	11	8640835	8640835	Human		name
156065231	CV2348764	single nucleotide variant	NM_001388022.1(TRIM66):c.1810C>G (p.Pro604Ala)	not specified [RCV004203214]	uncertain significance	11	8640565	8640565	Human		name
156137180	CV2357345	single nucleotide variant	NM_001388022.1(TRIM66):c.2566T>C (p.Phe856Leu)	not specified [RCV004200234]	uncertain significance	11	8624973	8624973	Human		name
329386066	CV2428185	single nucleotide variant	NM_001388022.1(TRIM66):c.1376C>T (p.Ala459Val)	not specified [RCV004251222]	uncertain significance	11	8640999	8640999	Human		name
329361628	CV2437712	single nucleotide variant	NM_001388022.1(TRIM66):c.1612G>T (p.Val538Leu)	not specified [RCV004261023]	uncertain significance	11	8640763	8640763	Human		name
329379635	CV2443493	single nucleotide variant	NM_001388022.1(TRIM66):c.1609C>G (p.Pro537Ala)	not specified [RCV004262328]	uncertain significance	11	8640766	8640766	Human		name
329354409	CV2448123	single nucleotide variant	NM_001388022.1(TRIM66):c.1019A>C (p.Asn340Thr)	not specified [RCV004263344]	uncertain significance	11	8645826	8645826	Human		name
329390051	CV2457552	single nucleotide variant	NM_001388022.1(TRIM66):c.1823C>T (p.Pro608Leu)	not specified [RCV004267356]	uncertain significance	11	8640552	8640552	Human		name
401735551	CV2702805	single nucleotide variant	NM_001388022.1(TRIM66):c.2194C>A (p.Pro732Thr)	not specified [RCV004319368]	uncertain significance	11	8638770	8638770	Human		name
401770234	CV2711005	single nucleotide variant	NM_001388022.1(TRIM66):c.1448C>T (p.Pro483Leu)	not specified [RCV004310708]	uncertain significance	11	8640927	8640927	Human		name
401860191	CV2765490	single nucleotide variant	NM_001388022.1(TRIM66):c.1274A>G (p.Tyr425Cys)	not specified [RCV004341802]	uncertain significance	11	8641101	8641101	Human		name
401898516	CV2787975	single nucleotide variant	NM_001388022.1(TRIM66):c.2984C>T (p.Thr995Met)	not specified [RCV004358631]	uncertain significance	11	8624394	8624394	Human		name
401869817	CV2792190	single nucleotide variant	NM_001388022.1(TRIM66):c.1010T>C (p.Met337Thr)	not specified [RCV004361396]	uncertain significance	11	8645835	8645835	Human		name
405797202	CV3347173	single nucleotide variant	NM_001388022.1(TRIM66):c.1448C>A (p.Pro483Gln)	not specified [RCV004476098]	uncertain significance	11	8640927	8640927	Human		name
405797205	CV3347174	single nucleotide variant	NM_001388022.1(TRIM66):c.1474T>C (p.Phe492Leu)	not specified [RCV004476099]	uncertain significance	11	8640901	8640901	Human		name
405797209	CV3347175	single nucleotide variant	NM_001388022.1(TRIM66):c.1562G>T (p.Ser521Ile)	not specified [RCV004476100]	uncertain significance	11	8640813	8640813	Human		name
405797215	CV3347177	single nucleotide variant	NM_001388022.1(TRIM66):c.2459G>A (p.Ser820Asn)	not specified [RCV004476102]	uncertain significance	11	8625080	8625080	Human		name
405797218	CV3347178	single nucleotide variant	NM_001388022.1(TRIM66):c.2477T>C (p.Val826Ala)	not specified [RCV004476103]	uncertain significance	11	8625062	8625062	Human		name
405797221	CV3347179	single nucleotide variant	NM_001388022.1(TRIM66):c.2762G>A (p.Arg921Gln)	not specified [RCV004476104]	uncertain significance	11	8624777	8624777	Human		name
405797224	CV3347180	single nucleotide variant	NM_001388022.1(TRIM66):c.2789A>G (p.Asp930Gly)	not specified [RCV004476105]	uncertain significance	11	8624750	8624750	Human		name
405797227	CV3347181	single nucleotide variant	NM_001388022.1(TRIM66):c.2926C>G (p.Leu976Val)	not specified [RCV004476106]	uncertain significance	11	8624452	8624452	Human		name
405797231	CV3347182	single nucleotide variant	NM_001388022.1(TRIM66):c.2969C>T (p.Ala990Val)	not specified [RCV004476107]	likely benign	11	8624409	8624409	Human		name
405797270	CV3347195	single nucleotide variant	NM_001388022.1(TRIM66):c.1181C>G (p.Thr394Ser)	not specified [RCV004476120]	uncertain significance	11	8643050	8643050	Human		name
405797273	CV3347196	single nucleotide variant	NM_001388022.1(TRIM66):c.1396T>C (p.Cys466Arg)	not specified [RCV004476121]	uncertain significance	11	8640979	8640979	Human		name
405797276	CV3347197	single nucleotide variant	NM_001388022.1(TRIM66):c.1408T>C (p.Cys470Arg)	not specified [RCV004476122]	uncertain significance	11	8640967	8640967	Human		name
407454128	CV3490694	single nucleotide variant	NM_001388022.1(TRIM66):c.2505G>C (p.Gln835His)	not specified [RCV004684822]	uncertain significance	11	8625034	8625034	Human		name
407454129	CV3490695	single nucleotide variant	NM_001388022.1(TRIM66):c.1208A>G (p.Gln403Arg)	not specified [RCV004684823]	uncertain significance	11	8643023	8643023	Human		name
597802237	CV3614530	single nucleotide variant	NM_001388022.1(TRIM66):c.1369T>G (p.Ser457Ala)	not specified [RCV004881130]	uncertain significance	11	8641006	8641006	Human		name
597802238	CV3614531	single nucleotide variant	NM_001388022.1(TRIM66):c.2299G>A (p.Val767Met)	not specified [RCV004881131]	uncertain significance	11	8638665	8638665	Human		name
597802244	CV3614535	single nucleotide variant	NM_001388022.1(TRIM66):c.2269G>A (p.Asp757Asn)	not specified [RCV004881134]	uncertain significance	11	8638695	8638695	Human		name
597802250	CV3614538	single nucleotide variant	NM_001388022.1(TRIM66):c.1484C>A (p.Pro495His)	not specified [RCV004881137]	uncertain significance	11	8640891	8640891	Human		name
597802254	CV3614540	single nucleotide variant	NM_001388022.1(TRIM66):c.1517T>A (p.Leu506Gln)	not specified [RCV004881139]	uncertain significance	11	8640858	8640858	Human		name
597802256	CV3614541	single nucleotide variant	NM_001388022.1(TRIM66):c.1061T>C (p.Val354Ala)	not specified [RCV004881140]	uncertain significance	11	8645784	8645784	Human		name
597802266	CV3614547	single nucleotide variant	NM_001388022.1(TRIM66):c.2335G>T (p.Gly779Cys)	not specified [RCV004881145]	uncertain significance	11	8625204	8625204	Human		name
597802270	CV3614549	single nucleotide variant	NM_001388022.1(TRIM66):c.2027G>A (p.Ser676Asn)	not specified [RCV004881147]	uncertain significance	11	8640348	8640348	Human		name
597802272	CV3614550	single nucleotide variant	NM_001388022.1(TRIM66):c.2117T>G (p.Val706Gly)	not specified [RCV004881148]	uncertain significance	11	8640258	8640258	Human		name
597802276	CV3614552	single nucleotide variant	NM_001388022.1(TRIM66):c.1636C>T (p.Arg546Trp)	not specified [RCV004881150]	uncertain significance	11	8640739	8640739	Human		name
598274360	CV3935641	single nucleotide variant	NM_001388022.1(TRIM66):c.1648C>A (p.Gln550Lys)	not specified [RCV005303886]	uncertain significance	11	8640727	8640727	Human		name
598203266	CV3935644	single nucleotide variant	NM_001388022.1(TRIM66):c.1970T>A (p.Phe657Tyr)	not specified [RCV005290505]	uncertain significance	11	8640405	8640405	Human		name
598203273	CV3935645	single nucleotide variant	NM_001388022.1(TRIM66):c.1609C>A (p.Pro537Thr)	not specified [RCV005290506]	uncertain significance	11	8640766	8640766	Human		name
598274367	CV3935648	single nucleotide variant	NM_001388022.1(TRIM66):c.2525C>A (p.Thr842Asn)	not specified [RCV005303890]	uncertain significance	11	8625014	8625014	Human		name
598274376	CV3935655	single nucleotide variant	NM_001388022.1(TRIM66):c.1298C>T (p.Pro433Leu)	not specified [RCV005303895]	uncertain significance	11	8641077	8641077	Human		name
598274378	CV3935656	single nucleotide variant	NM_001388022.1(TRIM66):c.2471A>G (p.Lys824Arg)	not specified [RCV005303896]	uncertain significance	11	8625068	8625068	Human		name
598214272	CV3935657	single nucleotide variant	NM_001388022.1(TRIM66):c.2332A>G (p.Met778Val)	not specified [RCV005292491]	uncertain significance	11	8625207	8625207	Human		name
15198960	CV702016	single nucleotide variant	NM_001388022.1(TRIM66):c.2549G>A (p.Ser850Asn)	not provided [RCV000956907]	benign	11	8624990	8624990	Human		name
156274426	CV2202612	single nucleotide variant	NM_001388022.1(TRIM66):c.4064C>T (p.Pro1355Leu)	not specified [RCV004082869]	uncertain significance	11	8618805	8618805	Human		name
156108278	CV2214373	single nucleotide variant	NM_001388022.1(TRIM66):c.3193C>G (p.Gln1065Glu)	not specified [RCV004088146]	uncertain significance	11	8621707	8621707	Human		name
155942335	CV2225677	single nucleotide variant	NM_001388022.1(TRIM66):c.3906C>G (p.Asp1302Glu)	not specified [RCV004103100]	uncertain significance	11	8618963	8618963	Human		name
156251305	CV2286830	single nucleotide variant	NM_001388022.1(TRIM66):c.3385A>G (p.Ile1129Val)	not specified [RCV004142632]	uncertain significance	11	8621192	8621192	Human		name
156262874	CV2329324	single nucleotide variant	NM_001388022.1(TRIM66):c.3005A>G (p.Tyr1002Cys)	not specified [RCV004187343]	uncertain significance	11	8624373	8624373	Human		name
156219800	CV2344939	single nucleotide variant	NM_001388022.1(TRIM66):c.3751C>T (p.Arg1251Trp)	not specified [RCV004193234]	uncertain significance	11	8619532	8619532	Human		name
155906465	CV2357327	single nucleotide variant	NM_001388022.1(TRIM66):c.3110A>G (p.Tyr1037Cys)	not specified [RCV004200217]	uncertain significance	11	8621790	8621790	Human		name
156253906	CV2366336	single nucleotide variant	NM_001388022.1(TRIM66):c.3742C>T (p.Pro1248Ser)	not specified [RCV004212392]	uncertain significance	11	8620055	8620055	Human		name
155909206	CV2369492	single nucleotide variant	NM_001388022.1(TRIM66):c.3488G>A (p.Arg1163His)	not specified [RCV004210429]	likely benign	11	8621089	8621089	Human		name
329358247	CV2425167	single nucleotide variant	NM_001388022.1(TRIM66):c.3550G>C (p.Glu1184Gln)	not specified [RCV004249054]	uncertain significance	11	8620568	8620568	Human		name
329377724	CV2449982	single nucleotide variant	NM_001388022.1(TRIM66):c.3734C>T (p.Pro1245Leu)	not specified [RCV004269045]	uncertain significance	11	8620063	8620063	Human		name
401730095	CV2683946	single nucleotide variant	NM_001388022.1(TRIM66):c.3392G>A (p.Arg1131Gln)	not specified [RCV004286497]	uncertain significance	11	8621185	8621185	Human		name
401864250	CV2767576	single nucleotide variant	NM_001388022.1(TRIM66):c.4049C>T (p.Thr1350Ile)	not specified [RCV004343726]	uncertain significance	11	8618820	8618820	Human		name
401933180	CV2816426	single nucleotide variant	NM_001388022.1(TRIM66):c.3637C>T (p.Arg1213Trp)	not provided [RCV003409258]	likely benign	11	8620481	8620481	Human		name
405797233	CV3347183	single nucleotide variant	NM_001388022.1(TRIM66):c.3116G>A (p.Arg1039Gln)	not specified [RCV004476108]	uncertain significance	11	8621784	8621784	Human		name
405797236	CV3347184	single nucleotide variant	NM_001388022.1(TRIM66):c.3125G>A (p.Arg1042Gln)	not specified [RCV004476109]	uncertain significance	11	8621775	8621775	Human		name
405797239	CV3347185	single nucleotide variant	NM_001388022.1(TRIM66):c.3131A>G (p.Lys1044Arg)	not specified [RCV004476110]	uncertain significance	11	8621769	8621769	Human		name
405797242	CV3347186	single nucleotide variant	NM_001388022.1(TRIM66):c.3161C>G (p.Pro1054Arg)	not specified [RCV004476111]	uncertain significance	11	8621739	8621739	Human		name
405797248	CV3347188	single nucleotide variant	NM_001388022.1(TRIM66):c.3415C>G (p.Pro1139Ala)	not specified [RCV004476113]	uncertain significance	11	8621162	8621162	Human		name
405797251	CV3347189	single nucleotide variant	NM_001388022.1(TRIM66):c.3461A>G (p.Asn1154Ser)	not specified [RCV004476114]	uncertain significance	11	8621116	8621116	Human		name
405797254	CV3347190	single nucleotide variant	NM_001388022.1(TRIM66):c.3707A>G (p.Asn1236Ser)	not specified [RCV004476115]	uncertain significance	11	8620090	8620090	Human		name
405797261	CV3347192	single nucleotide variant	NM_001388022.1(TRIM66):c.3773A>G (p.Lys1258Arg)	not specified [RCV004476117]	uncertain significance	11	8619510	8619510	Human		name
405797264	CV3347193	single nucleotide variant	NM_001388022.1(TRIM66):c.3829C>T (p.His1277Tyr)	not specified [RCV004476118]	uncertain significance	11	8619454	8619454	Human		name
405797267	CV3347194	single nucleotide variant	NM_001388022.1(TRIM66):c.3992A>G (p.Gln1331Arg)	not specified [RCV004476119]	uncertain significance	11	8618877	8618877	Human		name
407454122	CV3490688	single nucleotide variant	NM_001388022.1(TRIM66):c.3293C>T (p.Pro1098Leu)	not specified [RCV004684816]	uncertain significance	11	8621284	8621284	Human		name
407454123	CV3490689	single nucleotide variant	NM_001388022.1(TRIM66):c.3982C>T (p.Arg1328Trp)	not specified [RCV004684817]	uncertain significance	11	8618887	8618887	Human		name
407454124	CV3490690	single nucleotide variant	NM_001388022.1(TRIM66):c.3974C>T (p.Pro1325Leu)	not specified [RCV004684818]	uncertain significance	11	8618895	8618895	Human		name
407454125	CV3490691	single nucleotide variant	NM_001388022.1(TRIM66):c.3246G>C (p.Met1082Ile)	not specified [RCV004684819]	uncertain significance	11	8621654	8621654	Human		name
407454130	CV3490696	single nucleotide variant	NM_001388022.1(TRIM66):c.3929G>T (p.Arg1310Leu)	not specified [RCV004684824]	uncertain significance	11	8618940	8618940	Human		name
407461591	CV3490697	single nucleotide variant	NM_001388022.1(TRIM66):c.3313G>T (p.Val1105Phe)	not specified [RCV004687685]	uncertain significance	11	8621264	8621264	Human		name
597802246	CV3614536	single nucleotide variant	NM_001388022.1(TRIM66):c.3089A>G (p.Asn1030Ser)	not specified [RCV004881135]	likely benign	11	8621811	8621811	Human		name
597802248	CV3614537	single nucleotide variant	NM_001388022.1(TRIM66):c.3683A>G (p.Lys1228Arg)	not specified [RCV004881136]	uncertain significance	11	8620114	8620114	Human		name
597802252	CV3614539	single nucleotide variant	NM_001388022.1(TRIM66):c.3730G>A (p.Glu1244Lys)	not specified [RCV004881138]	uncertain significance	11	8620067	8620067	Human		name
597802260	CV3614543	single nucleotide variant	NM_001388022.1(TRIM66):c.3319G>A (p.Val1107Ile)	not specified [RCV004881142]	uncertain significance	11	8621258	8621258	Human		name
597802262	CV3614545	single nucleotide variant	NM_001388022.1(TRIM66):c.3822C>G (p.Asp1274Glu)	not specified [RCV004881143]	uncertain significance	11	8619461	8619461	Human		name
597802268	CV3614548	single nucleotide variant	NM_001388022.1(TRIM66):c.3967A>G (p.Ile1323Val)	not specified [RCV004881146]	uncertain significance	11	8618902	8618902	Human		name
597802274	CV3614551	single nucleotide variant	NM_001388022.1(TRIM66):c.3728A>G (p.His1243Arg)	not specified [RCV004881149]	uncertain significance	11	8620069	8620069	Human		name
598274361	CV3935642	single nucleotide variant	NM_001388022.1(TRIM66):c.3220G>A (p.Glu1074Lys)	not specified [RCV005303887]	uncertain significance	11	8621680	8621680	Human		name
598274365	CV3935646	single nucleotide variant	NM_001388022.1(TRIM66):c.3131A>T (p.Lys1044Met)	not specified [RCV005303889]	uncertain significance	11	8621769	8621769	Human		name
598203280	CV3935647	single nucleotide variant	NM_001388022.1(TRIM66):c.3866G>A (p.Arg1289His)	not specified [RCV005290507]	uncertain significance	11	8619417	8619417	Human		name
598274371	CV3935650	single nucleotide variant	NM_001388022.1(TRIM66):c.3702C>G (p.Cys1234Trp)	not specified [RCV005303892]	uncertain significance	11	8620095	8620095	Human		name
598203288	CV3935651	single nucleotide variant	NM_001388022.1(TRIM66):c.3989C>T (p.Ala1330Val)	not specified [RCV005290508]	uncertain significance	11	8618880	8618880	Human		name
598274372	CV3935652	single nucleotide variant	NM_001388022.1(TRIM66):c.3439G>A (p.Asp1147Asn)	not specified [RCV005303893]	uncertain significance	11	8621138	8621138	Human		name
598274374	CV3935653	single nucleotide variant	NM_001388022.1(TRIM66):c.3800G>A (p.Arg1267Gln)	not specified [RCV005303894]	uncertain significance	11	8619483	8619483	Human		name
598274380	CV3935658	single nucleotide variant	NM_001388022.1(TRIM66):c.3911A>G (p.Glu1304Gly)	not specified [RCV005303897]	uncertain significance	11	8618958	8618958	Human		name
15168752	CV724779	single nucleotide variant	NM_001388022.1(TRIM66):c.3662A>G (p.Tyr1221Cys)	not provided [RCV000883129]	likely benign	11	8620456	8620456	Human		name

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