Trap1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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392 records found for search term Trap1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
151783360	CV1424533	single nucleotide variant	NM_016292.3(TRAP1):c.88+1G>A	not provided [RCV001865168]	uncertain significance	16	3717420	3717420	Human		name
15117702	CV744850	single nucleotide variant	NM_016292.3(TRAP1):c.89-5T>C	not provided [RCV000895423]	benign	16	3690990	3690990	Human		name
150547428	CV1292022	single nucleotide variant	NM_016292.3(TRAP1):c.543+7G>A	not provided [RCV005057557]\|not specified [RCV001733688]	likely benign	16	3679712	3679712	Human		name
156392809	CV1869721	single nucleotide variant	NM_016292.3(TRAP1):c.814+1G>A	not provided [RCV003051512]	uncertain significance	16	3676035	3676035	Human		name
156416177	CV1976435	single nucleotide variant	NM_016292.3(TRAP1):c.331-1G>A	not provided [RCV002589566]	uncertain significance	16	3686137	3686137	Human		name
156023219	CV2111209	single nucleotide variant	NM_016292.3(TRAP1):c.889-9C>T	TRAP1-related disorder [RCV003916619]\|not provided [RCV002909713]	benign	16	3674503	3674503	Human		name , trait , alternate_id
156382693	CV2118158	single nucleotide variant	NM_016292.3(TRAP1):c.472-3C>T	TRAP1-related disorder [RCV003973576]\|not provided [RCV002943263]	likely benign\|uncertain significance	16	3679793	3679793	Human		name , trait , alternate_id
156295437	CV2119206	single nucleotide variant	NM_016292.3(TRAP1):c.814+6C>T	not provided [RCV002961901]	benign	16	3676030	3676030	Human		name
156206948	CV2131320	single nucleotide variant	NM_016292.3(TRAP1):c.888+8C>G	not provided [RCV002985435]	benign	16	3675316	3675316	Human		name
156097544	CV2132121	single nucleotide variant	NM_016292.3(TRAP1):c.889-8G>A	not provided [RCV003002085]	likely benign	16	3674502	3674502	Human		name
155970586	CV2158043	single nucleotide variant	NM_016292.3(TRAP1):c.705-2A>G	not provided [RCV003033416]	uncertain significance	16	3676147	3676147	Human		name
402497007	CV2875432	single nucleotide variant	NM_016292.3(TRAP1):c.814+7G>A	not provided [RCV003545519]	likely benign	16	3676029	3676029	Human		name
402501791	CV2923219	single nucleotide variant	NM_016292.3(TRAP1):c.889-4C>T	not provided [RCV003574006]	likely benign	16	3674498	3674498	Human		name
405121013	CV2952410	single nucleotide variant	NM_016292.3(TRAP1):c.704+5G>C	not provided [RCV003671473]	uncertain significance	16	3677493	3677493	Human		name
405191430	CV3069965	single nucleotide variant	NM_016292.3(TRAP1):c.704+9C>T	not provided [RCV003729755]	likely benign	16	3677489	3677489	Human		name
405212658	CV3127533	single nucleotide variant	NM_016292.3(TRAP1):c.89-14A>G	not provided [RCV003823581]	benign	16	3690999	3690999	Human		name
405287184	CV3193127	single nucleotide variant	NM_016292.3(TRAP1):c.472-6C>T	TRAP1-related disorder [RCV003981776]	likely benign	16	3679796	3679796	Human		name , trait , alternate_id
405280214	CV3200246	single nucleotide variant	NM_016292.3(TRAP1):c.330+4C>T	TRAP1-related disorder [RCV003977162]	likely benign	16	3689051	3689051	Human		name , trait , alternate_id
597914436	CV3740633	single nucleotide variant	NM_016292.3(TRAP1):c.815-1G>C	not provided [RCV005073970]	uncertain significance	16	3675398	3675398	Human		name
597853773	CV3743544	single nucleotide variant	NM_016292.3(TRAP1):c.330+8C>T	not provided [RCV005060894]	likely benign	16	3689047	3689047	Human		name
597944161	CV3782769	single nucleotide variant	NM_016292.3(TRAP1):c.888+6C>A	not provided [RCV005134309]	uncertain significance	16	3675318	3675318	Human		name
597967692	CV3824306	single nucleotide variant	NM_016292.3(TRAP1):c.472-7T>G	not provided [RCV005165529]	likely benign	16	3679797	3679797	Human		name
597889688	CV3839563	single nucleotide variant	NM_016292.3(TRAP1):c.815-7C>T	not provided [RCV005179455]	likely benign	16	3675404	3675404	Human		name
13788324	CV550049	single nucleotide variant	NM_016292.3(TRAP1):c.543+6C>T	not provided [RCV000676246]	benign	16	3679713	3679713	Human		name
15178221	CV776190	single nucleotide variant	NM_016292.3(TRAP1):c.248-6T>C	not provided [RCV000929346]	likely benign	16	3689143	3689143	Human		name
152176315	CV1541488	single nucleotide variant	NM_016292.3(TRAP1):c.704+17G>A	not provided [RCV002164460]	likely benign	16	3677481	3677481	Human		name
152138678	CV1574508	single nucleotide variant	NM_016292.3(TRAP1):c.1045-6C>T	not provided [RCV002177758]	benign	16	3672826	3672826	Human		name
152132690	CV1588109	single nucleotide variant	NM_016292.3(TRAP1):c.471+18C>T	not provided [RCV002199530]	benign	16	3685978	3685978	Human		name
152117942	CV1619966	single nucleotide variant	NM_016292.3(TRAP1):c.889-19C>T	not provided [RCV002216391]	benign	16	3674513	3674513	Human		name
152146343	CV1631614	single nucleotide variant	NM_016292.3(TRAP1):c.704+16C>T	not provided [RCV002157494]	likely benign	16	3677482	3677482	Human		name
152091942	CV1631713	single nucleotide variant	NM_016292.3(TRAP1):c.1235+9C>G	TRAP1-related disorder [RCV003951107]\|not provided [RCV002132152]	benign	16	3671713	3671713	Human		name , trait , alternate_id
152054697	CV1665480	single nucleotide variant	NM_016292.3(TRAP1):c.247+12T>G	not provided [RCV002089563]	likely benign	16	3690815	3690815	Human		name
156281234	CV1877089	single nucleotide variant	NM_016292.3(TRAP1):c.1165+4C>T	not provided [RCV003061072]	benign	16	3672696	3672696	Human		name
156419710	CV1974186	single nucleotide variant	NM_016292.3(TRAP1):c.704+18C>T	not provided [RCV002612950]	likely benign	16	3677480	3677480	Human		name
156125297	CV1995333	single nucleotide variant	NM_016292.3(TRAP1):c.889-18G>T	not provided [RCV002663013]	likely benign	16	3674512	3674512	Human		name
155952821	CV2043819	single nucleotide variant	NM_016292.3(TRAP1):c.889-15G>A	not provided [RCV002775863]	benign	16	3674509	3674509	Human		name
156331891	CV2075823	single nucleotide variant	NM_016292.3(TRAP1):c.889-10C>G	not provided [RCV002835344]	likely benign	16	3674504	3674504	Human		name
11543428	CV255738	single nucleotide variant	NM_016292.3(TRAP1):c.705-14T>C	not provided [RCV001711719]\|not specified [RCV000242441]	benign	16	3676159	3676159	Human		name
401938487	CV2811009	single nucleotide variant	NM_016292.3(TRAP1):c.1165+5G>A	not provided [RCV003417608]	likely benign\|conflicting interpretations of pathogenicity	16	3672695	3672695	Human		name
404987780	CV2849486	single nucleotide variant	NM_016292.3(TRAP1):c.330+95A>C	not specified [RCV003490343]	benign	16	3688960	3688960	Human		name
405022014	CV2877473	single nucleotide variant	NM_016292.3(TRAP1):c.704+10G>A	not provided [RCV003577686]	likely benign	16	3677488	3677488	Human		name
402509837	CV2881479	single nucleotide variant	NM_016292.3(TRAP1):c.1708+3C>T	not provided [RCV003561386]	uncertain significance	16	3663421	3663421	Human		name
405142570	CV2958837	single nucleotide variant	NM_016292.3(TRAP1):c.1045-3C>G	not provided [RCV003673364]	uncertain significance	16	3672823	3672823	Human		name
405181973	CV3120017	single nucleotide variant	NM_016292.3(TRAP1):c.2014-8C>T	not provided [RCV003820110]	likely benign	16	3658238	3658238	Human		name
405163877	CV3125283	single nucleotide variant	NM_016292.3(TRAP1):c.814+15G>A	not provided [RCV003818555]	benign	16	3676021	3676021	Human		name
405280087	CV3197352	single nucleotide variant	NM_016292.3(TRAP1):c.1940+8C>T	TRAP1-related disorder [RCV003982448]	likely benign	16	3661979	3661979	Human		name , trait , alternate_id
408374440	CV3516192	single nucleotide variant	NM_016292.3(TRAP1):c.1166-4C>T	TRAP1-related disorder [RCV004746743]	likely benign	16	3671795	3671795	Human		name , trait , alternate_id
597864728	CV3814266	single nucleotide variant	NM_016292.3(TRAP1):c.331-12C>T	not provided [RCV005147335]	likely benign	16	3686148	3686148	Human		name
597851981	CV3814848	single nucleotide variant	NM_016292.3(TRAP1):c.1941-1G>A	not provided [RCV005162973]	uncertain significance	16	3658866	3658866	Human		name
597854369	CV3847478	single nucleotide variant	NM_016292.3(TRAP1):c.1709-5C>T	not provided [RCV005190460]	likely benign	16	3662972	3662972	Human		name
15101731	CV778259	single nucleotide variant	NM_016292.3(TRAP1):c.331-10A>G	not provided [RCV000959150]	benign	16	3686146	3686146	Human		name
21075330	CV797325	single nucleotide variant	NM_016292.3(TRAP1):c.2014-7C>T	TRAP1-related disorder [RCV003906135]\|not provided [RCV000996192]	benign\|likely benign	16	3658237	3658237	Human		name , trait , alternate_id
150481139	CV1222105	single nucleotide variant	NM_016292.3(TRAP1):c.705-308A>C	not provided [RCV001616903]	benign	16	3676453	3676453	Human		name
150508641	CV1244882	single nucleotide variant	NM_016292.3(TRAP1):c.330+169G>A	not provided [RCV001659133]	benign	16	3688886	3688886	Human	2	name
150508641	CV1244882	single nucleotide variant	NM_016292.3(TRAP1):c.330+169G>A	not provided [RCV001659133]	benign	16	3688886	3688887	Human	2	name
150442517	CV1249130	deletion	NM_016292.3(TRAP1):c.2014-52del	not provided [RCV001666562]\|not specified [RCV003487644]	benign	16	3658282	3658282	Human		name
151716202	CV1401231	single nucleotide variant	NM_016292.3(TRAP1):c.1795-16C>A	not provided [RCV002022865]	uncertain significance	16	3662148	3662148	Human		name
152144047	CV1543075	single nucleotide variant	NM_016292.3(TRAP1):c.1235+16C>T	not provided [RCV002178449]	benign	16	3671706	3671706	Human		name
152061839	CV1603911	single nucleotide variant	NM_016292.3(TRAP1):c.1708+12C>T	not provided [RCV002220625]	benign	16	3663412	3663412	Human		name
152049652	CV1609712	single nucleotide variant	NM_016292.3(TRAP1):c.1940+11G>A	not provided [RCV002116041]	benign	16	3661976	3661976	Human		name
152033351	CV1610334	single nucleotide variant	NM_016292.3(TRAP1):c.1166-11G>C	not provided [RCV002124916]	benign	16	3671802	3671802	Human		name
152063200	CV1612041	single nucleotide variant	NM_016292.3(TRAP1):c.1166-11G>A	not provided [RCV002128602]	likely benign	16	3671802	3671802	Human		name
152050860	CV1644094	single nucleotide variant	NM_016292.3(TRAP1):c.1795-16C>T	not provided [RCV002125979]	likely benign	16	3662148	3662148	Human		name
156208485	CV1959480	single nucleotide variant	NM_016292.3(TRAP1):c.1709-11C>A	not provided [RCV002575059]	benign	16	3662978	3662978	Human		name
156346249	CV1970544	single nucleotide variant	NM_016292.3(TRAP1):c.1794+13C>T	not provided [RCV002601539]	likely benign	16	3662869	3662869	Human		name
156321391	CV1976111	single nucleotide variant	NM_016292.3(TRAP1):c.1165+19G>A	not provided [RCV002600254]	likely benign	16	3672681	3672681	Human		name
156114713	CV2018710	single nucleotide variant	NM_016292.3(TRAP1):c.1235+20G>A	not provided [RCV002695805]	likely benign	16	3671702	3671702	Human		name
156219433	CV2047824	single nucleotide variant	NM_016292.3(TRAP1):c.1383+17C>G	not provided [RCV002790573]	benign	16	3665954	3665954	Human		name
156160820	CV2147364	single nucleotide variant	NM_016292.3(TRAP1):c.2014-15C>T	not provided [RCV003023188]	likely benign	16	3658245	3658245	Human		name
156101665	CV2153124	single nucleotide variant	NM_016292.3(TRAP1):c.1570-12G>C	not provided [RCV003021071]	likely benign	16	3663574	3663574	Human		name
155985523	CV2159663	single nucleotide variant	NM_016292.3(TRAP1):c.1383+20G>A	not provided [RCV003034076]	likely benign	16	3665951	3665951	Human		name
156361349	CV2180382	single nucleotide variant	NM_016292.3(TRAP1):c.1795-12C>A	not provided [RCV003049044]	likely benign	16	3662144	3662144	Human		name
404988418	CV2849578	single nucleotide variant	NM_016292.3(TRAP1):c.88+7086T>C	not specified [RCV003490435]	benign	16	3710335	3710335	Human		name
405216176	CV3124675	single nucleotide variant	NM_016292.3(TRAP1):c.1235+15G>A	not provided [RCV003824038]	benign	16	3671707	3671707	Human		name
402470736	CV3175251	single nucleotide variant	NM_016292.3(TRAP1):c.1045-10T>A	not provided [RCV003874183]	likely benign	16	3672830	3672830	Human		name
597935449	CV3759425	single nucleotide variant	NM_016292.3(TRAP1):c.1236-19A>C	not provided [RCV005076545]	likely benign	16	3666137	3666137	Human		name
15110674	CV731068	single nucleotide variant	NM_016292.3(TRAP1):c.1044+10T>C	not provided [RCV000894115]	benign	16	3674329	3674329	Human		name
15145390	CV745226	single nucleotide variant	NM_016292.3(TRAP1):c.1569+10C>T	not provided [RCV000900154]	likely benign	16	3664264	3664264	Human		name
150501372	CV1223688	deletion	NM_016292.3(TRAP1):c.1236-248del	not provided [RCV001620809]	benign	16	3666366	3666366	Human		name
150441055	CV1265500	single nucleotide variant	NM_016292.3(TRAP1):c.1045-225G>C	not provided [RCV001679203]	benign	16	3673045	3673045	Human		name
150515214	CV1285466	single nucleotide variant	NM_016292.3(TRAP1):c.2013+227C>T	not provided [RCV001722919]	benign	16	3658566	3658566	Human		name
151750506	CV1508272	single nucleotide variant	NM_016292.3(TRAP1):c.9C>T (p.Arg3=)	not provided [RCV001986236]	likely benign\|uncertain significance	16	3717500	3717500	Human		name
152090208	CV1624293	single nucleotide variant	NM_016292.3(TRAP1):c.6G>C (p.Ala2=)	not provided [RCV002150493]	likely benign	16	3717503	3717503	Human		name
408379800	CV3510822	duplication	NM_016292.3(TRAP1):c.1938_1940+8dup	TRAP1-related disorder [RCV004747896]\|not provided [RCV005103746]	uncertain significance	16	3661978	3661979	Human		name , trait , alternate_id
150516090	CV1216437	microsatellite	NM_016292.3(TRAP1):c.2013+103GTTT[5]	not provided [RCV001608628]	benign	16	3658674	3658675	Human		name
151733122	CV1512383	single nucleotide variant	NM_016292.3(TRAP1):c.4G>T (p.Ala2Ser)	not provided [RCV002021507]\|not specified [RCV004046911]	uncertain significance	16	3717505	3717505	Human		name
152084715	CV1525530	single nucleotide variant	NM_016292.3(TRAP1):c.28C>T (p.Leu10=)	not provided [RCV002131280]	likely benign	16	3717481	3717481	Human		name
405178207	CV3123538	single nucleotide variant	NM_016292.3(TRAP1):c.55C>T (p.Leu19=)	not provided [RCV003819747]	likely benign	16	3717454	3717454	Human		name
405166027	CV3125645	single nucleotide variant	NM_016292.3(TRAP1):c.48G>A (p.Arg16=)	not provided [RCV003818728]	likely benign	16	3717461	3717461	Human		name
405169597	CV3149937	single nucleotide variant	NM_016292.3(TRAP1):c.3G>A (p.Met1Ile)	not provided [RCV003841408]	uncertain significance	16	3717506	3717506	Human		name
405259412	CV3194777	single nucleotide variant	NM_016292.3(TRAP1):c.90A>G (p.Gly30=)	TRAP1-related disorder [RCV003894166]	likely benign	16	3690984	3690984	Human		name , trait , alternate_id
13788332	CV550052	single nucleotide variant	NM_016292.3(TRAP1):c.1A>G (p.Met1Val)	not provided [RCV000676249]	uncertain significance	16	3717508	3717508	Human		name
156324770	CV1972616	single nucleotide variant	NM_016292.3(TRAP1):c.20C>T (p.Ala7Val)	not provided [RCV002600460]\|not specified [RCV004064600]	uncertain significance	16	3717489	3717489	Human		name
156022252	CV2141389	single nucleotide variant	NM_016292.3(TRAP1):c.219G>A (p.Ser73=)	not provided [RCV002976211]	likely benign	16	3690855	3690855	Human		name
329398470	CV2464616	single nucleotide variant	NM_016292.3(TRAP1):c.16C>T (p.Arg6Trp)	not specified [RCV004278303]	uncertain significance	16	3717493	3717493	Human		name
405274019	CV3194941	single nucleotide variant	NM_016292.3(TRAP1):c.189C>T (p.Thr63=)	TRAP1-related disorder [RCV003902183]	likely benign	16	3690885	3690885	Human		name , trait , alternate_id
405291697	CV3205975	single nucleotide variant	NM_016292.3(TRAP1):c.252C>A (p.Ser84=)	TRAP1-related disorder [RCV003964073]	likely benign	16	3689133	3689133	Human		name , trait , alternate_id
597858005	CV3748221	single nucleotide variant	NM_016292.3(TRAP1):c.100C>T (p.Leu34=)	not provided [RCV005067043]	likely benign	16	3690974	3690974	Human		name
597871629	CV3849353	single nucleotide variant	NM_016292.3(TRAP1):c.174G>A (p.Leu58=)	not provided [RCV005197534]	likely benign	16	3690900	3690900	Human		name
150507594	CV1229128	deletion	NM_016292.3(TRAP1):c.705-234_705-220del	not provided [RCV001635999]	benign	16	3676365	3676379	Human		name
152049214	CV1560819	deletion	NM_016292.3(TRAP1):c.2013+15_2013+27del	not provided [RCV002112304]	benign	16	3658766	3658778	Human		name
152033069	CV1610274	single nucleotide variant	NM_016292.3(TRAP1):c.402C>T (p.Asp134=)	not provided [RCV002124866]	benign	16	3686065	3686065	Human		name
156091056	CV1963194	single nucleotide variant	NM_016292.3(TRAP1):c.65C>G (p.Pro22Arg)	not provided [RCV002570224]\|not specified [RCV004064376]	uncertain significance	16	3717444	3717444	Human		name
155915314	CV1980780	single nucleotide variant	NM_016292.3(TRAP1):c.360C>T (p.Ala120=)	not provided [RCV002614278]	likely benign	16	3686107	3686107	Human		name
156416103	CV1983967	single nucleotide variant	NM_016292.3(TRAP1):c.97A>G (p.Ile33Val)	not provided [RCV002609997]	uncertain significance	16	3690977	3690977	Human		name
156177739	CV2072120	single nucleotide variant	NM_016292.3(TRAP1):c.843C>T (p.Val281=)	not provided [RCV002851737]	likely benign	16	3675369	3675369	Human		name
156023927	CV2105963	single nucleotide variant	NM_016292.3(TRAP1):c.537G>T (p.Gly179=)	not provided [RCV002923202]	likely benign	16	3679725	3679725	Human		name
156206978	CV2131321	single nucleotide variant	NM_016292.3(TRAP1):c.825G>A (p.Thr275=)	not provided [RCV002985436]	benign	16	3675387	3675387	Human		name
156037898	CV2143297	single nucleotide variant	NM_016292.3(TRAP1):c.777C>T (p.Ser259=)	not provided [RCV002999404]	likely benign	16	3676073	3676073	Human		name
155944227	CV2271638	single nucleotide variant	NM_016292.3(TRAP1):c.50C>T (p.Pro17Leu)	not specified [RCV004130496]	uncertain significance	16	3717459	3717459	Human		name
401726896	CV2691889	single nucleotide variant	NM_016292.3(TRAP1):c.34G>A (p.Gly12Ser)	not specified [RCV004299628]	uncertain significance	16	3717475	3717475	Human		name
402477396	CV2914171	single nucleotide variant	NM_016292.3(TRAP1):c.663G>T (p.Ser221=)	not provided [RCV003571581]	likely benign	16	3677539	3677539	Human		name
402478210	CV2914560	single nucleotide variant	NM_016292.3(TRAP1):c.786G>A (p.Lys262=)	not provided [RCV003571774]	likely benign	16	3676064	3676064	Human		name
405160806	CV2950304	single nucleotide variant	NM_016292.3(TRAP1):c.363C>T (p.Ser121=)	not provided [RCV003674669]	likely benign	16	3686104	3686104	Human		name
405241949	CV2970892	single nucleotide variant	NM_016292.3(TRAP1):c.351C>A (p.Ile117=)	not provided [RCV003684207]	likely benign	16	3686116	3686116	Human		name
405228972	CV2973843	single nucleotide variant	NM_016292.3(TRAP1):c.777C>G (p.Ser259=)	not provided [RCV003681926]	benign	16	3676073	3676073	Human		name
405086729	CV3047831	single nucleotide variant	NM_016292.3(TRAP1):c.309G>A (p.Arg103=)	not provided [RCV003717525]	likely benign	16	3689076	3689076	Human		name
405079535	CV3050341	single nucleotide variant	NM_016292.3(TRAP1):c.981C>T (p.Tyr327=)	not provided [RCV003717030]	likely benign	16	3674402	3674402	Human		name
405235683	CV3079505	single nucleotide variant	NM_016292.3(TRAP1):c.726C>T (p.Ala242=)	not provided [RCV003735857]	likely benign	16	3676124	3676124	Human		name
405085362	CV3137712	single nucleotide variant	NM_016292.3(TRAP1):c.621A>G (p.Ser207=)	not provided [RCV003834421]	likely benign	16	3677581	3677581	Human		name
405247826	CV3159135	single nucleotide variant	NM_016292.3(TRAP1):c.789G>A (p.Glu263=)	not provided [RCV003869280]	likely benign	16	3676061	3676061	Human		name
405196520	CV3168160	single nucleotide variant	NM_016292.3(TRAP1):c.948C>T (p.Arg316=)	not provided [RCV003860292]	likely benign	16	3674435	3674435	Human		name
405287483	CV3205704	single nucleotide variant	NM_016292.3(TRAP1):c.966C>T (p.His322=)	TRAP1-related disorder [RCV003959824]	likely benign	16	3674417	3674417	Human		name , trait , alternate_id
597963313	CV3791913	single nucleotide variant	NM_016292.3(TRAP1):c.747C>T (p.Thr249=)	not provided [RCV005139469]	likely benign	16	3676103	3676103	Human		name
597921354	CV3808036	single nucleotide variant	NM_016292.3(TRAP1):c.960G>A (p.Gln320=)	not provided [RCV005155744]	likely benign	16	3674423	3674423	Human		name
13788312	CV550046	single nucleotide variant	NM_016292.3(TRAP1):c.933T>C (p.His311=)	not provided [RCV000676242]	benign\|likely benign	16	3674450	3674450	Human		name
13788326	CV550050	single nucleotide variant	NM_016292.3(TRAP1):c.312C>T (p.Ser104=)	not provided [RCV000676247]	likely benign	16	3689073	3689073	Human		name
13788329	CV550051	single nucleotide variant	NM_016292.3(TRAP1):c.37C>T (p.Arg13Cys)	not provided [RCV000676248]\|not specified [RCV003489801]	benign	16	3717472	3717472	Human		name
15161427	CV703678	single nucleotide variant	NM_016292.3(TRAP1):c.594C>T (p.Ile198=)	not provided [RCV000947671]	benign	16	3677608	3677608	Human		name
15104973	CV726630	single nucleotide variant	NM_016292.3(TRAP1):c.666A>G (p.Ala222=)	not provided [RCV000892990]	benign	16	3677536	3677536	Human		name
151891880	CV1460718	single nucleotide variant	NM_016292.3(TRAP1):c.109C>T (p.Arg37Trp)	not provided [RCV001888884]\|not specified [RCV004877715]	likely benign\|uncertain significance	16	3690965	3690965	Human		name
152148722	CV1569110	single nucleotide variant	NM_016292.3(TRAP1):c.1368C>T (p.Thr456=)	not provided [RCV002220457]	likely benign	16	3665986	3665986	Human		name
152046622	CV1582190	single nucleotide variant	NM_016292.3(TRAP1):c.1524A>C (p.Ala508=)	not provided [RCV002089682]	likely benign	16	3664319	3664319	Human		name
152050295	CV1598335	single nucleotide variant	NM_016292.3(TRAP1):c.1974C>T (p.Arg658=)	TRAP1-related disorder [RCV003916282]\|not provided [RCV002121836]	likely benign	16	3658832	3658832	Human		name , trait , alternate_id
152059586	CV1635676	single nucleotide variant	NM_016292.3(TRAP1):c.1665C>T (p.Val555=)	not provided [RCV002203602]	benign\|likely benign	16	3663467	3663467	Human		name
152056798	CV1651820	single nucleotide variant	NM_016292.3(TRAP1):c.1458C>T (p.Tyr486=)	not provided [RCV002180786]	likely benign	16	3664385	3664385	Human		name
156250736	CV1887079	single nucleotide variant	NM_016292.3(TRAP1):c.1050G>A (p.Pro350=)	not provided [RCV003086092]	likely benign	16	3672815	3672815	Human		name
156014534	CV1912668	single nucleotide variant	NM_016292.3(TRAP1):c.1002C>T (p.Asp334=)	not provided [RCV002619077]	likely benign	16	3674381	3674381	Human		name
156369211	CV1926772	single nucleotide variant	NM_016292.3(TRAP1):c.164C>T (p.Ala55Val)	not provided [RCV002633239]	uncertain significance	16	3690910	3690910	Human		name
155964241	CV1931825	single nucleotide variant	NM_016292.3(TRAP1):c.1923G>A (p.Thr641=)	not provided [RCV002616879]	likely benign	16	3662004	3662004	Human		name
156374517	CV1933027	single nucleotide variant	NM_016292.3(TRAP1):c.1713C>T (p.Ala571=)	not provided [RCV002633711]	likely benign	16	3662963	3662963	Human		name
156437394	CV1937537	single nucleotide variant	NM_016292.3(TRAP1):c.1038C>T (p.Pro346=)	not provided [RCV003106929]	likely benign	16	3674345	3674345	Human		name
156407841	CV1957624	single nucleotide variant	NM_016292.3(TRAP1):c.1656G>A (p.Thr552=)	not provided [RCV002586341]	likely benign	16	3663476	3663476	Human		name
156230677	CV2048664	single nucleotide variant	NM_016292.3(TRAP1):c.144C>G (p.Asn48Lys)	not provided [RCV002790986]	uncertain significance	16	3690930	3690930	Human		name
156240305	CV2109138	single nucleotide variant	NM_016292.3(TRAP1):c.2040T>C (p.Ala680=)	not provided [RCV002933176]	likely benign	16	3658204	3658204	Human		name
156016308	CV2121411	single nucleotide variant	NM_016292.3(TRAP1):c.251C>G (p.Ser84Cys)	not provided [RCV002948550]	uncertain significance	16	3689134	3689134	Human		name
156128246	CV2223896	single nucleotide variant	NM_016292.3(TRAP1):c.177C>G (p.Phe59Leu)	not specified [RCV004093895]	likely benign	16	3690897	3690897	Human		name
156031831	CV2259406	single nucleotide variant	NM_016292.3(TRAP1):c.223A>G (p.Ile75Val)	not specified [RCV004122630]	uncertain significance	16	3690851	3690851	Human		name
156105332	CV2387012	single nucleotide variant	NM_016292.3(TRAP1):c.241G>A (p.Val81Met)	not provided [RCV005099156]\|not specified [RCV004226762]	uncertain significance	16	3690833	3690833	Human		name
401933432	CV2801977	single nucleotide variant	NM_016292.3(TRAP1):c.283A>G (p.Lys95Glu)	TRAP1-related disorder [RCV003392936]\|not specified [RCV004877797]	uncertain significance	16	3689102	3689102	Human		name , trait , alternate_id
401903279	CV2811008	single nucleotide variant	NM_016292.3(TRAP1):c.1431C>T (p.Ser477=)	not provided [RCV003411250]	likely benign	16	3664412	3664412	Human		name
402507838	CV2872182	single nucleotide variant	NM_016292.3(TRAP1):c.1833C>T (p.Thr611=)	not provided [RCV003550552]	likely benign	16	3662094	3662094	Human		name
402509747	CV2905193	single nucleotide variant	NM_016292.3(TRAP1):c.1944C>T (p.His648=)	not provided [RCV003560019]	likely benign	16	3658862	3658862	Human		name
405192094	CV2984948	single nucleotide variant	NM_016292.3(TRAP1):c.197A>G (p.Asp66Gly)	not provided [RCV003706559]	uncertain significance	16	3690877	3690877	Human		name
402476744	CV3048893	single nucleotide variant	NM_016292.3(TRAP1):c.1914G>A (p.Leu638=)	not provided [RCV003732857]	likely benign	16	3662013	3662013	Human		name
402476106	CV3065077	single nucleotide variant	NM_016292.3(TRAP1):c.1404G>A (p.Leu468=)	not provided [RCV003726844]	likely benign	16	3664439	3664439	Human		name
402477314	CV3078391	single nucleotide variant	NM_016292.3(TRAP1):c.1710C>T (p.Ala570=)	not provided [RCV003732412]	likely benign	16	3662966	3662966	Human		name
404977045	CV3127072	single nucleotide variant	NM_016292.3(TRAP1):c.1398G>A (p.Lys466=)	not provided [RCV003825295]	likely benign	16	3664445	3664445	Human		name
404978103	CV3127331	single nucleotide variant	NM_016292.3(TRAP1):c.1125G>A (p.Lys375=)	not provided [RCV003825555]	likely benign	16	3672740	3672740	Human		name
405046800	CV3141693	single nucleotide variant	NM_016292.3(TRAP1):c.1518C>T (p.His506=)	not provided [RCV003831794]	likely benign	16	3664325	3664325	Human		name
405238221	CV3169591	single nucleotide variant	NM_016292.3(TRAP1):c.1617T>C (p.Leu539=)	not provided [RCV003866679]	likely benign	16	3663515	3663515	Human		name
405270765	CV3219735	single nucleotide variant	NM_016292.3(TRAP1):c.1233C>T (p.Ile411=)	TRAP1-related disorder [RCV003971483]	likely benign	16	3671724	3671724	Human		name , trait , alternate_id
405267127	CV3220195	single nucleotide variant	NM_016292.3(TRAP1):c.1242C>G (p.Leu414=)	TRAP1-related disorder [RCV003969452]	likely benign	16	3666112	3666112	Human		name , trait , alternate_id
405776934	CV3340295	single nucleotide variant	NM_016292.3(TRAP1):c.214C>T (p.His72Tyr)	not specified [RCV004471273]	uncertain significance	16	3690860	3690860	Human		name
405776940	CV3340296	single nucleotide variant	NM_016292.3(TRAP1):c.215A>C (p.His72Pro)	not specified [RCV004471274]	uncertain significance	16	3690859	3690859	Human		name
405776946	CV3340297	single nucleotide variant	NM_016292.3(TRAP1):c.266A>T (p.Glu89Val)	not specified [RCV004471275]	uncertain significance	16	3689119	3689119	Human		name
407521958	CV3492588	single nucleotide variant	NM_016292.3(TRAP1):c.140G>A (p.Arg47Gln)	not specified [RCV004677491]	likely benign	16	3690934	3690934	Human		name
407521969	CV3492593	single nucleotide variant	NM_016292.3(TRAP1):c.148G>T (p.Ala50Ser)	not specified [RCV004677495]	uncertain significance	16	3690926	3690926	Human		name
407521971	CV3492594	single nucleotide variant	NM_016292.3(TRAP1):c.190G>A (p.Ala64Thr)	not provided [RCV005059742]\|not specified [RCV004677496]	uncertain significance	16	3690884	3690884	Human		name
407521974	CV3492595	single nucleotide variant	NM_016292.3(TRAP1):c.277G>C (p.Glu93Gln)	not specified [RCV004677497]	uncertain significance	16	3689108	3689108	Human		name
408373764	CV3511589	single nucleotide variant	NM_016292.3(TRAP1):c.1086C>T (p.Ser362=)	TRAP1-related disorder [RCV004745632]	likely benign	16	3672779	3672779	Human		name , trait , alternate_id
597796433	CV3621176	single nucleotide variant	NM_016292.3(TRAP1):c.226A>T (p.Ser76Cys)	not specified [RCV004878492]	uncertain significance	16	3690848	3690848	Human		name
597796441	CV3621182	single nucleotide variant	NM_016292.3(TRAP1):c.127T>G (p.Leu43Val)	not specified [RCV004878498]	uncertain significance	16	3690947	3690947	Human		name
597846631	CV3767039	single nucleotide variant	NM_016292.3(TRAP1):c.2025C>T (p.Asn675=)	not provided [RCV005106561]	likely benign	16	3658219	3658219	Human		name
597850267	CV3796019	single nucleotide variant	NM_016292.3(TRAP1):c.1476C>T (p.Ala492=)	not provided [RCV005144850]	likely benign	16	3664367	3664367	Human		name
597893959	CV3810012	single nucleotide variant	NM_016292.3(TRAP1):c.1098C>T (p.Tyr366=)	not provided [RCV005151733]	likely benign	16	3672767	3672767	Human		name
597854206	CV3847830	single nucleotide variant	NM_016292.3(TRAP1):c.1599G>A (p.Glu533=)	not provided [RCV005188559]	likely benign	16	3663533	3663533	Human		name
13788286	CV550038	single nucleotide variant	NM_016292.3(TRAP1):c.2052C>T (p.Asp684=)	not provided [RCV000676234]	benign	16	3658192	3658192	Human		name
13788302	CV550043	insertion	NM_016292.3(TRAP1):c.1166-11_1166-10insC	not provided [RCV000676239]	benign	16	3671801	3671802	Human		name
13788305	CV550044	single nucleotide variant	NM_016292.3(TRAP1):c.1032C>T (p.Tyr344=)	not provided [RCV000676240]	benign	16	3674351	3674351	Human		name
15199246	CV726629	single nucleotide variant	NM_016292.3(TRAP1):c.1461C>T (p.Ala487=)	not provided [RCV000890583]	likely benign	16	3664382	3664382	Human		name
15103561	CV785275	single nucleotide variant	NM_016292.3(TRAP1):c.1338G>A (p.Leu446=)	not provided [RCV000976042]	likely benign	16	3666016	3666016	Human		name
150555840	CV1305329	single nucleotide variant	NM_016292.3(TRAP1):c.340C>T (p.Arg114Trp)	not provided [RCV001773262]	uncertain significance	16	3686127	3686127	Human		name
151806915	CV1370962	single nucleotide variant	NM_016292.3(TRAP1):c.847T>C (p.Phe283Leu)	not provided [RCV001877888]\|not specified [RCV004039070]	uncertain significance	16	3675365	3675365	Human		name
151836465	CV1389411	single nucleotide variant	NM_016292.3(TRAP1):c.671C>T (p.Pro224Leu)	not provided [RCV001902348]\|not specified [RCV004039850]	uncertain significance	16	3677531	3677531	Human		name
151833065	CV1396272	single nucleotide variant	NM_016292.3(TRAP1):c.688C>T (p.Gln230Ter)	not provided [RCV001902002]	uncertain significance	16	3677514	3677514	Human		name
151716206	CV1448537	single nucleotide variant	NM_016292.3(TRAP1):c.824C>T (p.Thr275Met)	TRAP1-related disorder [RCV003892986]\|not provided [RCV001965263]	uncertain significance	16	3675388	3675388	Human		name , trait , alternate_id
151726092	CV1488137	single nucleotide variant	NM_016292.3(TRAP1):c.430C>G (p.His144Asp)	not provided [RCV001966606]	uncertain significance	16	3686037	3686037	Human		name
151885310	CV1506921	single nucleotide variant	NM_016292.3(TRAP1):c.446C>G (p.Ala149Gly)	not provided [RCV001962516]	uncertain significance	16	3686021	3686021	Human		name
152088725	CV1541413	single nucleotide variant	NM_016292.3(TRAP1):c.574G>A (p.Glu192Lys)	TRAP1-related disorder [RCV003978884]\|not provided [RCV002171545]	benign	16	3677628	3677628	Human		name , trait , alternate_id
156205619	CV1905887	single nucleotide variant	NM_016292.3(TRAP1):c.629T>C (p.Met210Thr)	not provided [RCV003084390]	benign	16	3677573	3677573	Human		name
156418139	CV1914471	single nucleotide variant	NM_016292.3(TRAP1):c.341G>A (p.Arg114Gln)	not provided [RCV002611314]	uncertain significance	16	3686126	3686126	Human		name
156274050	CV1915515	single nucleotide variant	NM_016292.3(TRAP1):c.841G>A (p.Val281Ile)	not provided [RCV002628201]\|not specified [RCV004676162]	uncertain significance	16	3675371	3675371	Human		name
156310605	CV1925135	single nucleotide variant	NM_016292.3(TRAP1):c.778G>A (p.Asp260Asn)	not provided [RCV002629742]\|not specified [RCV004072088]	uncertain significance	16	3676072	3676072	Human		name
156289490	CV1926436	single nucleotide variant	NM_016292.3(TRAP1):c.727G>A (p.Glu243Lys)	not provided [RCV002628753]\|not specified [RCV004070724]	uncertain significance	16	3676123	3676123	Human		name
156342966	CV1957976	single nucleotide variant	NM_016292.3(TRAP1):c.936G>C (p.Glu312Asp)	not provided [RCV002580607]	uncertain significance	16	3674447	3674447	Human		name
156413586	CV1979066	single nucleotide variant	NM_016292.3(TRAP1):c.812G>C (p.Arg271Pro)	not provided [RCV002608887]	uncertain significance	16	3676038	3676038	Human		name
156007797	CV2042507	single nucleotide variant	NM_016292.3(TRAP1):c.448G>A (p.Glu150Lys)	not provided [RCV002794932]	uncertain significance	16	3686019	3686019	Human		name
156111214	CV2042652	single nucleotide variant	NM_016292.3(TRAP1):c.872G>A (p.Arg291Gln)	not provided [RCV002785406]	uncertain significance	16	3675340	3675340	Human		name
156081086	CV2050116	single nucleotide variant	NM_016292.3(TRAP1):c.330G>C (p.Glu110Asp)	not provided [RCV002823857]	uncertain significance	16	3689055	3689055	Human		name
156124275	CV2112253	single nucleotide variant	NM_016292.3(TRAP1):c.937G>C (p.Glu313Gln)	not provided [RCV002927944]\|not specified [RCV004067037]	uncertain significance	16	3674446	3674446	Human		name
156372813	CV2127674	single nucleotide variant	NM_016292.3(TRAP1):c.493C>G (p.Gln165Glu)	not provided [RCV002942471]	uncertain significance	16	3679769	3679769	Human		name
156016781	CV2177554	single nucleotide variant	NM_016292.3(TRAP1):c.505G>C (p.Val169Leu)	not provided [RCV003035525]	uncertain significance	16	3679757	3679757	Human		name
156193259	CV2217884	single nucleotide variant	NM_016292.3(TRAP1):c.658C>T (p.Arg220Cys)	not specified [RCV004084053]	uncertain significance	16	3677544	3677544	Human		name
156279463	CV2297680	single nucleotide variant	NM_016292.3(TRAP1):c.764T>C (p.Ile255Thr)	not specified [RCV004155364]	uncertain significance	16	3676086	3676086	Human		name
156178251	CV2374579	single nucleotide variant	NM_016292.3(TRAP1):c.308G>A (p.Arg103Gln)	not specified [RCV004225205]	uncertain significance	16	3689077	3689077	Human		name
243051452	CV2415847	single nucleotide variant	NM_016292.3(TRAP1):c.472G>C (p.Asp158His)	VATER association [RCV005414676]	uncertain significance	16	3679790	3679790	Human	1	name
329396063	CV2451861	single nucleotide variant	NM_016292.3(TRAP1):c.556G>A (p.Ala186Thr)	not specified [RCV004276542]	likely benign	16	3677646	3677646	Human		name
11547030	CV255737	single nucleotide variant	NM_016292.3(TRAP1):c.919C>G (p.Arg307Gly)	not provided [RCV000676243]\|not specified [RCV000247229]	benign	16	3674464	3674464	Human		name
401757647	CV2675436	single nucleotide variant	NM_016292.3(TRAP1):c.298A>G (p.Ile100Val)	not specified [RCV004292236]	likely benign	16	3689087	3689087	Human		name
401736169	CV2703061	single nucleotide variant	NM_016292.3(TRAP1):c.555T>G (p.Asp185Glu)	not specified [RCV004321363]	likely benign	16	3677647	3677647	Human		name
401883765	CV2754977	single nucleotide variant	NM_016292.3(TRAP1):c.319T>G (p.Ser107Ala)	not specified [RCV004341442]	uncertain significance	16	3689066	3689066	Human		name
401934640	CV2800419	single nucleotide variant	NM_016292.3(TRAP1):c.353C>G (p.Ser118Cys)	TRAP1-related disorder [RCV003411975]	uncertain significance	16	3686114	3686114	Human		name , trait , alternate_id
405018606	CV2856124	single nucleotide variant	NM_016292.3(TRAP1):c.812G>A (p.Arg271Gln)	not provided [RCV003577335]	uncertain significance	16	3676038	3676038	Human		name
405211065	CV2921058	single nucleotide variant	NM_016292.3(TRAP1):c.404G>A (p.Gly135Asp)	not provided [RCV003567174]	uncertain significance	16	3686063	3686063	Human		name
405245402	CV2968996	single nucleotide variant	NM_016292.3(TRAP1):c.410C>T (p.Ala137Val)	not provided [RCV003685066]	uncertain significance	16	3686057	3686057	Human		name
405125276	CV3043562	single nucleotide variant	NM_016292.3(TRAP1):c.713T>C (p.Val238Ala)	not provided [RCV003724309]	uncertain significance	16	3676137	3676137	Human		name
405177438	CV3049338	single nucleotide variant	NM_016292.3(TRAP1):c.748G>A (p.Gly250Arg)	not provided [RCV003728330]	uncertain significance	16	3676102	3676102	Human		name
405242003	CV3078573	single nucleotide variant	NM_016292.3(TRAP1):c.799G>A (p.Glu267Lys)	not provided [RCV003737481]	uncertain significance	16	3676051	3676051	Human		name
402516473	CV3135847	single nucleotide variant	NM_016292.3(TRAP1):c.952G>A (p.Val318Ile)	not provided [RCV003824473]	uncertain significance	16	3674431	3674431	Human		name
405105945	CV3139883	single nucleotide variant	NM_016292.3(TRAP1):c.734C>T (p.Ser245Leu)	not provided [RCV003835294]	uncertain significance	16	3676116	3676116	Human		name
405106435	CV3139991	single nucleotide variant	NM_016292.3(TRAP1):c.391C>G (p.Leu131Val)	not provided [RCV003835402]	uncertain significance	16	3686076	3686076	Human		name
405776950	CV3340298	single nucleotide variant	NM_016292.3(TRAP1):c.356A>G (p.Asn119Ser)	not specified [RCV004471276]	uncertain significance	16	3686111	3686111	Human		name
405776955	CV3340299	single nucleotide variant	NM_016292.3(TRAP1):c.382C>T (p.Arg128Cys)	not specified [RCV004471277]	uncertain significance	16	3686085	3686085	Human		name
405776961	CV3340300	single nucleotide variant	NM_016292.3(TRAP1):c.475A>G (p.Thr159Ala)	not specified [RCV004471278]	uncertain significance	16	3679787	3679787	Human		name
405776968	CV3340301	single nucleotide variant	NM_016292.3(TRAP1):c.481A>G (p.Ile161Val)	not specified [RCV004471279]	uncertain significance	16	3679781	3679781	Human		name
405776982	CV3340303	single nucleotide variant	NM_016292.3(TRAP1):c.760A>G (p.Ile254Val)	not provided [RCV005104756]\|not specified [RCV004471281]	uncertain significance	16	3676090	3676090	Human		name
405776988	CV3340304	single nucleotide variant	NM_016292.3(TRAP1):c.875T>C (p.Met292Thr)	not specified [RCV004471282]	uncertain significance	16	3675337	3675337	Human		name
407521955	CV3492587	single nucleotide variant	NM_016292.3(TRAP1):c.766C>A (p.His256Asn)	not specified [RCV004677490]	uncertain significance	16	3676084	3676084	Human		name
407521960	CV3492589	single nucleotide variant	NM_016292.3(TRAP1):c.521C>T (p.Thr174Met)	not specified [RCV004677492]	uncertain significance	16	3679741	3679741	Human		name
407521963	CV3492590	single nucleotide variant	NM_016292.3(TRAP1):c.594C>G (p.Ile198Met)	not specified [RCV004677493]	uncertain significance	16	3677608	3677608	Human		name
407461322	CV3492592	single nucleotide variant	NM_016292.3(TRAP1):c.724G>A (p.Ala242Thr)	not specified [RCV004687624]	uncertain significance	16	3676126	3676126	Human		name
407461326	CV3492602	single nucleotide variant	NM_016292.3(TRAP1):c.678C>G (p.Ser226Arg)	not specified [RCV004687625]	uncertain significance	16	3677524	3677524	Human		name
597796429	CV3621174	single nucleotide variant	NM_016292.3(TRAP1):c.818T>G (p.Val273Gly)	not specified [RCV004878490]	uncertain significance	16	3675394	3675394	Human		name
597796435	CV3621180	single nucleotide variant	NM_016292.3(TRAP1):c.815A>G (p.Asp272Gly)	not specified [RCV004878496]	uncertain significance	16	3675397	3675397	Human		name
597796439	CV3621181	single nucleotide variant	NM_016292.3(TRAP1):c.585C>G (p.Ser195Arg)	not specified [RCV004878497]	uncertain significance	16	3677617	3677617	Human		name
597882376	CV3745046	single nucleotide variant	NM_016292.3(TRAP1):c.576G>T (p.Glu192Asp)	not provided [RCV005070071]	uncertain significance	16	3677626	3677626	Human		name
597958176	CV3755272	single nucleotide variant	NM_016292.3(TRAP1):c.836A>G (p.Asn279Ser)	not provided [RCV005080942]	uncertain significance	16	3675376	3675376	Human		name
597939008	CV3756749	single nucleotide variant	NM_016292.3(TRAP1):c.754A>G (p.Lys252Glu)	not provided [RCV005077130]	uncertain significance	16	3676096	3676096	Human		name
597831329	CV3830741	single nucleotide variant	NM_016292.3(TRAP1):c.995A>G (p.Lys332Arg)	not provided [RCV005170139]	uncertain significance	16	3674388	3674388	Human		name
598273776	CV3924723	single nucleotide variant	NM_016292.3(TRAP1):c.436C>G (p.Gln146Glu)	not specified [RCV005303573]	uncertain significance	16	3686031	3686031	Human		name
598273777	CV3924724	single nucleotide variant	NM_016292.3(TRAP1):c.803C>G (p.Ala268Gly)	not specified [RCV005303574]	uncertain significance	16	3676047	3676047	Human		name
598201906	CV3924726	single nucleotide variant	NM_016292.3(TRAP1):c.943T>C (p.Tyr315His)	not specified [RCV005290271]	uncertain significance	16	3674440	3674440	Human		name
12913094	CV422094	single nucleotide variant	NM_016292.3(TRAP1):c.956C>T (p.Ala319Val)	not provided [RCV000493380]\|not specified [RCV004023297]	uncertain significance	16	3674427	3674427	Human		name
13788321	CV550048	single nucleotide variant	NM_016292.3(TRAP1):c.757A>G (p.Ile253Val)	TRAP1-related disorder [RCV003980299]\|not provided [RCV000676245]	benign\|likely benign\|conflicting interpretations of pathogenicity	16	3676093	3676093	Human		name , trait , alternate_id
13832135	CV582626	single nucleotide variant	NM_016292.3(TRAP1):c.320C>G (p.Ser107Ter)	not provided [RCV000722818]	uncertain significance	16	3689065	3689065	Human		name
13832340	CV582834	single nucleotide variant	NM_016292.3(TRAP1):c.499G>A (p.Glu167Lys)	not provided [RCV000723027]	uncertain significance	16	3679763	3679763	Human		name
13832550	CV583045	single nucleotide variant	NM_016292.3(TRAP1):c.691T>C (p.Trp231Arg)	not provided [RCV000723242]	uncertain significance	16	3677511	3677511	Human		name
21075331	CV797326	single nucleotide variant	NM_016292.3(TRAP1):c.383G>A (p.Arg128His)	not provided [RCV000996193]	benign\|likely benign	16	3686084	3686084	Human		name
150547425	CV1292021	single nucleotide variant	NM_016292.3(TRAP1):c.1204C>T (p.Arg402Trp)	not provided [RCV004692717]\|not specified [RCV001733687]	uncertain significance	16	3671753	3671753	Human		name
150556319	CV1296887	single nucleotide variant	NM_016292.3(TRAP1):c.1484G>A (p.Arg495His)	not provided [RCV001774177]\|not specified [RCV004040175]	uncertain significance	16	3664359	3664359	Human		name
151717946	CV1347471	single nucleotide variant	NM_016292.3(TRAP1):c.1618C>T (p.Arg540Cys)	not provided [RCV002027922]	uncertain significance	16	3663514	3663514	Human		name
151711887	CV1351183	single nucleotide variant	NM_016292.3(TRAP1):c.1721T>C (p.Leu574Pro)	not provided [RCV002004908]	uncertain significance	16	3662955	3662955	Human		name
151814928	CV1368402	single nucleotide variant	NM_016292.3(TRAP1):c.1405C>T (p.Arg469Cys)	not provided [RCV001950289]	uncertain significance	16	3664438	3664438	Human		name
151811308	CV1398788	single nucleotide variant	NM_016292.3(TRAP1):c.1427C>T (p.Pro476Leu)	not provided [RCV001942787]	uncertain significance	16	3664416	3664416	Human		name
151855781	CV1421636	single nucleotide variant	NM_016292.3(TRAP1):c.1163G>A (p.Arg388Gln)	not provided [RCV001937929]	uncertain significance	16	3672702	3672702	Human		name
151793850	CV1422609	single nucleotide variant	NM_016292.3(TRAP1):c.1090G>A (p.Ala364Thr)	not provided [RCV001898435]	uncertain significance	16	3672775	3672775	Human		name
151832916	CV1439264	single nucleotide variant	NM_016292.3(TRAP1):c.1324G>A (p.Glu442Lys)	not provided [RCV001976824]	uncertain significance	16	3666030	3666030	Human		name
151815802	CV1467500	single nucleotide variant	NM_016292.3(TRAP1):c.2020G>C (p.Glu674Gln)	not provided [RCV001952544]	uncertain significance	16	3658224	3658224	Human		name
151769282	CV1473661	single nucleotide variant	NM_016292.3(TRAP1):c.1855C>T (p.Arg619Cys)	not provided [RCV001864798]\|not specified [RCV004039703]	uncertain significance	16	3662072	3662072	Human		name
151814746	CV1485512	single nucleotide variant	NM_016292.3(TRAP1):c.1186A>G (p.Ile396Val)	not provided [RCV002029317]\|not specified [RCV004046810]	uncertain significance	16	3671771	3671771	Human		name
156099256	CV1896695	single nucleotide variant	NM_016292.3(TRAP1):c.1225G>A (p.Ala409Thr)	not provided [RCV003080537]	uncertain significance	16	3671732	3671732	Human		name
156403749	CV1901766	single nucleotide variant	NM_016292.3(TRAP1):c.1390A>G (p.Ile464Val)	not provided [RCV002585275]	uncertain significance	16	3664453	3664453	Human		name
156309845	CV1913394	single nucleotide variant	NM_016292.3(TRAP1):c.1346G>A (p.Arg449Gln)	not provided [RCV002599589]\|not specified [RCV004068992]	uncertain significance	16	3666008	3666008	Human		name
156414159	CV1915766	single nucleotide variant	NM_016292.3(TRAP1):c.1753T>C (p.Trp585Arg)	not provided [RCV002588445]	uncertain significance	16	3662923	3662923	Human		name
156025950	CV1918734	single nucleotide variant	NM_016292.3(TRAP1):c.1070G>A (p.Arg357Gln)	not provided [RCV002636943]	uncertain significance	16	3672795	3672795	Human		name
156374499	CV1933026	single nucleotide variant	NM_016292.3(TRAP1):c.1822G>T (p.Ala608Ser)	not provided [RCV002633710]\|not specified [RCV004070760]	uncertain significance	16	3662105	3662105	Human		name
156300750	CV1933464	single nucleotide variant	NM_016292.3(TRAP1):c.1007C>A (p.Pro336Gln)	not provided [RCV002629232]	uncertain significance	16	3674376	3674376	Human		name
156147989	CV1970782	single nucleotide variant	NM_016292.3(TRAP1):c.1748T>C (p.Met583Thr)	not provided [RCV002594054]	uncertain significance	16	3662928	3662928	Human		name
156247510	CV1988952	single nucleotide variant	NM_016292.3(TRAP1):c.1049C>T (p.Pro350Leu)	not provided [RCV002627341]	uncertain significance	16	3672816	3672816	Human		name
156243988	CV1996479	single nucleotide variant	NM_016292.3(TRAP1):c.1619G>C (p.Arg540Pro)	not provided [RCV002668023]\|not specified [RCV004066849]	uncertain significance	16	3663513	3663513	Human		name
156291320	CV1998093	single nucleotide variant	NM_016292.3(TRAP1):c.1619G>A (p.Arg540His)	not provided [RCV002670777]\|not specified [RCV004066769]	uncertain significance	16	3663513	3663513	Human		name
156143982	CV2002893	single nucleotide variant	NM_016292.3(TRAP1):c.1511A>G (p.Asn504Ser)	not provided [RCV002663671]	uncertain significance	16	3664332	3664332	Human		name
156091233	CV2016388	single nucleotide variant	NM_016292.3(TRAP1):c.1778G>A (p.Arg593His)	not provided [RCV002715332]\|not specified [RCV004067663]	uncertain significance	16	3662898	3662898	Human		name
156208699	CV2040480	indel	NM_016292.3(TRAP1):c.331-18_331-17delinsAT	not provided [RCV002790157]	uncertain significance	16	3686153	3686154	Human		name
156108548	CV2096592	single nucleotide variant	NM_016292.3(TRAP1):c.1504G>A (p.Ala502Thr)	not provided [RCV002913684]	uncertain significance	16	3664339	3664339	Human		name
156099511	CV2103084	single nucleotide variant	NM_016292.3(TRAP1):c.1386G>T (p.Glu462Asp)	not provided [RCV002913349]	likely benign	16	3664457	3664457	Human		name
156351348	CV2122368	single nucleotide variant	NM_016292.3(TRAP1):c.1912C>A (p.Leu638Met)	not provided [RCV002966319]\|not specified [RCV004068116]	uncertain significance	16	3662015	3662015	Human		name
156386674	CV2125579	single nucleotide variant	NM_016292.3(TRAP1):c.1744C>T (p.Leu582Phe)	not provided [RCV002943535]	uncertain significance	16	3662932	3662932	Human		name
155937065	CV2125781	single nucleotide variant	NM_016292.3(TRAP1):c.1636A>C (p.Lys546Gln)	not provided [RCV002971026]	uncertain significance	16	3663496	3663496	Human		name
156006158	CV2126581	single nucleotide variant	NM_016292.3(TRAP1):c.1111C>G (p.Leu371Val)	not provided [RCV002975411]	likely benign	16	3672754	3672754	Human		name
155959885	CV2131734	single nucleotide variant	NM_016292.3(TRAP1):c.1012A>G (p.Asn338Asp)	not provided [RCV002995102]\|not specified [RCV004065212]	uncertain significance	16	3674371	3674371	Human		name
156218180	CV2132598	single nucleotide variant	NM_016292.3(TRAP1):c.1459G>A (p.Ala487Thr)	TRAP1-related disorder [RCV004747174]\|not provided [RCV003007269]	uncertain significance	16	3664384	3664384	Human		name , trait , alternate_id
156033679	CV2132767	single nucleotide variant	NM_016292.3(TRAP1):c.2108G>A (p.Arg703Gln)	not provided [RCV002999247]	uncertain significance	16	3658136	3658136	Human		name
155951455	CV2133232	single nucleotide variant	NM_016292.3(TRAP1):c.1847G>T (p.Gly616Val)	not provided [RCV002994654]	uncertain significance	16	3662080	3662080	Human		name
156201766	CV2134704	single nucleotide variant	NM_016292.3(TRAP1):c.1007C>T (p.Pro336Leu)	not provided [RCV002985241]	uncertain significance	16	3674376	3674376	Human		name
155964690	CV2142461	single nucleotide variant	NM_016292.3(TRAP1):c.1471C>T (p.Arg491Trp)	not provided [RCV002995325]\|not specified [RCV004686754]	uncertain significance	16	3664372	3664372	Human		name
156039424	CV2143374	single nucleotide variant	NM_016292.3(TRAP1):c.1333G>A (p.Gly445Ser)	not provided [RCV002999459]\|not specified [RCV004068375]	uncertain significance	16	3666021	3666021	Human		name
156262783	CV2143437	single nucleotide variant	NM_016292.3(TRAP1):c.1418C>T (p.Ser473Leu)	not provided [RCV003008985]\|not specified [RCV004068385]	uncertain significance	16	3664425	3664425	Human		name
156143954	CV2208685	single nucleotide variant	NM_016292.3(TRAP1):c.1139T>C (p.Leu380Pro)	not specified [RCV004091195]	uncertain significance	16	3672726	3672726	Human		name
156238679	CV2235830	single nucleotide variant	NM_016292.3(TRAP1):c.1237A>C (p.Lys413Gln)	not specified [RCV004111948]	uncertain significance	16	3666117	3666117	Human		name
156273756	CV2277823	single nucleotide variant	NM_016292.3(TRAP1):c.1574T>C (p.Leu525Pro)	not specified [RCV004147244]	uncertain significance	16	3663558	3663558	Human		name
156135291	CV2284725	single nucleotide variant	NM_016292.3(TRAP1):c.1363G>A (p.Ala455Thr)	not specified [RCV004140872]	likely benign	16	3665991	3665991	Human		name
156241182	CV2286101	single nucleotide variant	NM_016292.3(TRAP1):c.1559A>C (p.Lys520Thr)	not specified [RCV004143987]	uncertain significance	16	3664284	3664284	Human		name
155954600	CV2302181	single nucleotide variant	NM_016292.3(TRAP1):c.2027C>T (p.Ala676Val)	not specified [RCV004159185]	uncertain significance	16	3658217	3658217	Human		name
156041073	CV2310861	single nucleotide variant	NM_016292.3(TRAP1):c.1036C>G (p.Pro346Ala)	not provided [RCV005099831]\|not specified [RCV004163904]	uncertain significance	16	3674347	3674347	Human		name
156062509	CV2321005	single nucleotide variant	NM_016292.3(TRAP1):c.1717T>G (p.Cys573Gly)	not specified [RCV004172799]	uncertain significance	16	3662959	3662959	Human		name
155905308	CV2349731	single nucleotide variant	NM_016292.3(TRAP1):c.1411G>A (p.Glu471Lys)	TRAP1-related disorder [RCV003434655]\|not specified [RCV004204145]	uncertain significance	16	3664432	3664432	Human		name , trait , alternate_id
156224450	CV2355660	single nucleotide variant	NM_016292.3(TRAP1):c.1883C>T (p.Ala628Val)	not specified [RCV004198618]	uncertain significance	16	3662044	3662044	Human		name
156012891	CV2358982	single nucleotide variant	NM_016292.3(TRAP1):c.1153C>T (p.Arg385Cys)	not specified [RCV004212311]	uncertain significance	16	3672712	3672712	Human		name
156044747	CV2381653	single nucleotide variant	NM_016292.3(TRAP1):c.1069C>T (p.Arg357Trp)	not specified [RCV004232124]	uncertain significance	16	3672796	3672796	Human		name
156391635	CV2382460	single nucleotide variant	NM_016292.3(TRAP1):c.1973G>A (p.Arg658His)	not specified [RCV004230795]	uncertain significance	16	3658833	3658833	Human		name
156083973	CV2395099	single nucleotide variant	NM_016292.3(TRAP1):c.1945G>A (p.Ala649Thr)	TRAP1-related disorder [RCV003420529]\|not specified [RCV004236781]	likely benign\|uncertain significance	16	3658861	3658861	Human		name , trait , alternate_id
329376040	CV2431708	single nucleotide variant	NM_016292.3(TRAP1):c.1006C>A (p.Pro336Thr)	not specified [RCV004248872]	uncertain significance	16	3674377	3674377	Human		name
329954015	CV2671376	single nucleotide variant	NM_016292.3(TRAP1):c.1915C>T (p.Gln639Ter)	Congenital anomalies of kidney and urinary tract 1 [RCV003235001]	pathogenic	16	3662012	3662012	Human	1	name
401736057	CV2689246	single nucleotide variant	NM_016292.3(TRAP1):c.1294A>G (p.Lys432Glu)	not specified [RCV004306089]	uncertain significance	16	3666060	3666060	Human		name
401759333	CV2701495	single nucleotide variant	NM_016292.3(TRAP1):c.1187T>C (p.Ile396Thr)	not specified [RCV004312158]	uncertain significance	16	3671770	3671770	Human		name
401777702	CV2704285	single nucleotide variant	NM_016292.3(TRAP1):c.1130C>T (p.Thr377Met)	not specified [RCV004311273]	uncertain significance	16	3672735	3672735	Human		name
401718807	CV2704810	single nucleotide variant	NM_016292.3(TRAP1):c.1342A>G (p.Met448Val)	not specified [RCV004307398]	uncertain significance	16	3666012	3666012	Human		name
401747977	CV2719509	single nucleotide variant	NM_016292.3(TRAP1):c.1834G>A (p.Val612Met)	not specified [RCV004326901]	uncertain significance	16	3662093	3662093	Human		name
401769553	CV2731402	single nucleotide variant	NM_016292.3(TRAP1):c.1243C>T (p.Arg415Trp)	not specified [RCV004330765]	uncertain significance	16	3666111	3666111	Human		name
401871096	CV2766799	single nucleotide variant	NM_016292.3(TRAP1):c.1087G>A (p.Val363Ile)	not provided [RCV003738440]\|not specified [RCV004349185]	likely benign\|uncertain significance	16	3672778	3672778	Human		name
401857544	CV2771518	single nucleotide variant	NM_016292.3(TRAP1):c.1789G>C (p.Val597Leu)	not specified [RCV004348550]	uncertain significance	16	3662887	3662887	Human		name
401902592	CV2804797	single nucleotide variant	NM_016292.3(TRAP1):c.2057C>G (p.Pro686Arg)	TRAP1-related disorder [RCV003394329]	uncertain significance	16	3658187	3658187	Human		name , trait , alternate_id
401903512	CV2811007	single nucleotide variant	NM_016292.3(TRAP1):c.1631A>G (p.Lys544Arg)	not provided [RCV003411249]	uncertain significance	16	3663501	3663501	Human		name
402508149	CV2861594	single nucleotide variant	NM_016292.3(TRAP1):c.1922C>T (p.Thr641Met)	not provided [RCV003551569]	benign	16	3662005	3662005	Human		name
402507952	CV2865444	single nucleotide variant	NM_016292.3(TRAP1):c.1530C>G (p.His510Gln)	not provided [RCV003544563]	uncertain significance	16	3664313	3664313	Human		name
402508339	CV2872482	single nucleotide variant	NM_016292.3(TRAP1):c.2074C>T (p.Arg692Cys)	not provided [RCV003553257]	uncertain significance	16	3658170	3658170	Human		name
402507494	CV2875467	single nucleotide variant	NM_016292.3(TRAP1):c.1946C>T (p.Ala649Val)	not provided [RCV003548289]	uncertain significance	16	3658860	3658860	Human		name
405156514	CV2890841	single nucleotide variant	NM_016292.3(TRAP1):c.1271A>C (p.Lys424Thr)	not provided [RCV003562091]	uncertain significance	16	3666083	3666083	Human		name
402509236	CV2891394	single nucleotide variant	NM_016292.3(TRAP1):c.1655C>T (p.Thr552Met)	not provided [RCV003556857]\|not specified [RCV004369159]	uncertain significance	16	3663477	3663477	Human		name
402472228	CV2951502	single nucleotide variant	NM_016292.3(TRAP1):c.1462A>C (p.Ser488Arg)	not provided [RCV003670856]	uncertain significance	16	3664381	3664381	Human		name
405138252	CV3048700	single nucleotide variant	NM_016292.3(TRAP1):c.1106A>G (p.Lys369Arg)	not provided [RCV003725423]	uncertain significance	16	3672759	3672759	Human		name
402476367	CV3057645	single nucleotide variant	NM_016292.3(TRAP1):c.1799C>T (p.Thr600Ile)	not provided [RCV003728919]	uncertain significance	16	3662128	3662128	Human		name
402477377	CV3061075	single nucleotide variant	NM_016292.3(TRAP1):c.1778G>C (p.Arg593Pro)	not provided [RCV003731574]\|not specified [RCV004877824]	uncertain significance	16	3662898	3662898	Human		name
405156199	CV3064938	single nucleotide variant	NM_016292.3(TRAP1):c.1345C>T (p.Arg449Trp)	not provided [RCV003726769]	uncertain significance	16	3666009	3666009	Human		name
405049362	CV3080116	single nucleotide variant	NM_016292.3(TRAP1):c.1018C>T (p.Arg340Cys)	not provided [RCV003740481]	uncertain significance	16	3674365	3674365	Human		name
405139365	CV3130873	single nucleotide variant	NM_016292.3(TRAP1):c.2113T>C (p.Ter705Arg)	not provided [RCV003839107]	uncertain significance	16	3658131	3658131	Human		name
405142038	CV3131299	single nucleotide variant	NM_016292.3(TRAP1):c.1901G>A (p.Arg634His)	not provided [RCV003839339]\|not specified [RCV005291059]	uncertain significance	16	3662026	3662026	Human		name
405052789	CV3138052	single nucleotide variant	NM_016292.3(TRAP1):c.2099C>T (p.Ala700Val)	not provided [RCV003832090]	uncertain significance	16	3658145	3658145	Human		name
405249355	CV3170056	single nucleotide variant	NM_016292.3(TRAP1):c.1916A>T (p.Gln639Leu)	not provided [RCV003869685]	uncertain significance	16	3662011	3662011	Human		name
405273565	CV3202855	single nucleotide variant	NM_016292.3(TRAP1):c.1394C>A (p.Ala465Glu)	TRAP1-related disorder [RCV003913918]	likely benign	16	3664449	3664449	Human		name , trait , alternate_id
405276805	CV3215857	single nucleotide variant	NM_016292.3(TRAP1):c.1775C>T (p.Ser592Leu)	TRAP1-related disorder [RCV003947002]\|not provided [RCV005101866]	uncertain significance	16	3662901	3662901	Human		name , trait , alternate_id
405776879	CV3340286	single nucleotide variant	NM_016292.3(TRAP1):c.1207G>A (p.Glu403Lys)	not specified [RCV004471264]	uncertain significance	16	3671750	3671750	Human		name
405776885	CV3340287	single nucleotide variant	NM_016292.3(TRAP1):c.1334G>A (p.Gly445Asp)	not specified [RCV004471265]	uncertain significance	16	3666020	3666020	Human		name
405776891	CV3340288	single nucleotide variant	NM_016292.3(TRAP1):c.1394C>G (p.Ala465Gly)	not provided [RCV005104755]\|not specified [RCV004471266]	uncertain significance	16	3664449	3664449	Human		name
405776902	CV3340290	single nucleotide variant	NM_016292.3(TRAP1):c.1783A>G (p.Thr595Ala)	not specified [RCV004471268]	uncertain significance	16	3662893	3662893	Human		name
405776908	CV3340291	single nucleotide variant	NM_016292.3(TRAP1):c.1795G>A (p.Val599Met)	not specified [RCV004471269]	uncertain significance	16	3662132	3662132	Human		name
405776915	CV3340292	single nucleotide variant	NM_016292.3(TRAP1):c.1871T>C (p.Met624Thr)	not specified [RCV004471270]	uncertain significance	16	3662056	3662056	Human		name
405776922	CV3340293	single nucleotide variant	NM_016292.3(TRAP1):c.1894G>C (p.Glu632Gln)	not specified [RCV004471271]	uncertain significance	16	3662033	3662033	Human		name
405776928	CV3340294	single nucleotide variant	NM_016292.3(TRAP1):c.2005G>C (p.Val669Leu)	not specified [RCV004471272]	uncertain significance	16	3658801	3658801	Human		name
407451524	CV3492596	single nucleotide variant	NM_016292.3(TRAP1):c.1612C>G (p.His538Asp)	not specified [RCV004677498]	uncertain significance	16	3663520	3663520	Human		name
407451529	CV3492597	single nucleotide variant	NM_016292.3(TRAP1):c.1493A>G (p.Tyr498Cys)	not specified [RCV004677499]	uncertain significance	16	3664350	3664350	Human		name
407451533	CV3492598	single nucleotide variant	NM_016292.3(TRAP1):c.2041G>A (p.Gly681Arg)	not specified [RCV004677500]	uncertain significance	16	3658203	3658203	Human		name
407451536	CV3492599	single nucleotide variant	NM_016292.3(TRAP1):c.1715A>T (p.Glu572Val)	not specified [RCV004677501]	uncertain significance	16	3662961	3662961	Human		name
407451539	CV3492601	single nucleotide variant	NM_016292.3(TRAP1):c.1703C>T (p.Ser568Phe)	not specified [RCV004677503]	uncertain significance	16	3663429	3663429	Human		name
408379745	CV3507941	single nucleotide variant	NM_016292.3(TRAP1):c.1483C>T (p.Arg495Cys)	TRAP1-related disorder [RCV004747533]	uncertain significance	16	3664360	3664360	Human		name , trait , alternate_id
597689792	CV3621173	single nucleotide variant	NM_016292.3(TRAP1):c.2083G>A (p.Glu695Lys)	not specified [RCV004878489]	uncertain significance	16	3658161	3658161	Human		name
597689801	CV3621175	single nucleotide variant	NM_016292.3(TRAP1):c.1648G>T (p.Val550Leu)	not specified [RCV004878491]	uncertain significance	16	3663484	3663484	Human		name
597689813	CV3621177	single nucleotide variant	NM_016292.3(TRAP1):c.1976C>T (p.Ala659Val)	not specified [RCV004878493]	uncertain significance	16	3658830	3658830	Human		name
597689825	CV3621178	single nucleotide variant	NM_016292.3(TRAP1):c.1879C>G (p.Leu627Val)	not specified [RCV004878494]	uncertain significance	16	3662048	3662048	Human		name
597689834	CV3621179	single nucleotide variant	NM_016292.3(TRAP1):c.1712C>T (p.Ala571Val)	not specified [RCV004878495]	uncertain significance	16	3662964	3662964	Human		name
597689845	CV3621183	single nucleotide variant	NM_016292.3(TRAP1):c.1868G>A (p.Arg623His)	not specified [RCV004878499]	uncertain significance	16	3662059	3662059	Human		name
597842552	CV3743275	single nucleotide variant	NM_016292.3(TRAP1):c.1514G>A (p.Arg505His)	not provided [RCV005062283]	uncertain significance	16	3664329	3664329	Human		name
597911955	CV3745676	single nucleotide variant	NM_016292.3(TRAP1):c.1223G>T (p.Ser408Ile)	not provided [RCV005073677]	uncertain significance	16	3671734	3671734	Human		name
597850039	CV3746836	single nucleotide variant	NM_016292.3(TRAP1):c.1369G>A (p.Glu457Lys)	not provided [RCV005060463]	uncertain significance	16	3665985	3665985	Human		name
597844321	CV3753103	single nucleotide variant	NM_016292.3(TRAP1):c.1459G>T (p.Ala487Ser)	not provided [RCV005087328]	uncertain significance	16	3664384	3664384	Human		name
597844308	CV3760760	single nucleotide variant	NM_016292.3(TRAP1):c.1975G>A (p.Ala659Thr)	not provided [RCV005085311]\|not specified [RCV005303487]	uncertain significance	16	3658831	3658831	Human		name
597850513	CV3802851	single nucleotide variant	NM_016292.3(TRAP1):c.2065A>G (p.Met689Val)	not provided [RCV005147638]	uncertain significance	16	3658179	3658179	Human		name
597850826	CV3803817	single nucleotide variant	NM_016292.3(TRAP1):c.2036C>T (p.Ala679Val)	not provided [RCV005151378]	uncertain significance	16	3658208	3658208	Human		name
597850746	CV3804300	single nucleotide variant	NM_016292.3(TRAP1):c.1421C>T (p.Ala474Val)	not provided [RCV005150751]	uncertain significance	16	3664422	3664422	Human		name
597850965	CV3804609	single nucleotide variant	NM_016292.3(TRAP1):c.1477G>A (p.Gly493Ser)	not provided [RCV005153044]	uncertain significance	16	3664366	3664366	Human		name
597850397	CV3816674	single nucleotide variant	NM_016292.3(TRAP1):c.1405C>G (p.Arg469Gly)	not provided [RCV005146247]	uncertain significance	16	3664438	3664438	Human		name
597853040	CV3823110	single nucleotide variant	NM_016292.3(TRAP1):c.1940G>C (p.Arg647Thr)	not provided [RCV005175460]	uncertain significance	16	3661987	3661987	Human		name
597853876	CV3833754	single nucleotide variant	NM_016292.3(TRAP1):c.1714G>T (p.Glu572Ter)	not provided [RCV005183114]	uncertain significance	16	3662962	3662962	Human		name
597854554	CV3843488	single nucleotide variant	NM_016292.3(TRAP1):c.1972C>T (p.Arg658Cys)	not provided [RCV005192525]	uncertain significance	16	3658834	3658834	Human		name
597935948	CV3845338	single nucleotide variant	NM_016292.3(TRAP1):c.1172T>C (p.Val391Ala)	not provided [RCV005186651]	uncertain significance	16	3671785	3671785	Human		name
598201895	CV3924722	single nucleotide variant	NM_016292.3(TRAP1):c.1154G>A (p.Arg385His)	not specified [RCV005290269]	uncertain significance	16	3672711	3672711	Human		name
598201901	CV3924725	single nucleotide variant	NM_016292.3(TRAP1):c.1189C>T (p.Pro397Ser)	not specified [RCV005290270]	uncertain significance	16	3671768	3671768	Human		name
598273778	CV3924727	single nucleotide variant	NM_016292.3(TRAP1):c.1623G>C (p.Glu541Asp)	not specified [RCV005303575]	uncertain significance	16	3663509	3663509	Human		name
12902082	CV409624	single nucleotide variant	NM_016292.3(TRAP1):c.2053G>A (p.Asp685Asn)	HER2 positive breast carcinoma [RCV002466514]\|TRAP1-related disorder [RCV003925399]\|not provided [RCV000676233]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	16	3658191	3658191	Human	1	name , trait , alternate_id
13509800	CV482099	single nucleotide variant	NM_016292.3(TRAP1):c.2107C>T (p.Arg703Ter)	not provided [RCV000578836]	uncertain significance	16	3658137	3658137	Human		name
13795997	CV488239	single nucleotide variant	NM_016292.3(TRAP1):c.1604C>G (p.Thr535Ser)	Hereditary renal cell carcinoma [RCV000678680]\|not provided [RCV002061993]	benign\|uncertain significance	16	3663528	3663528	Human	1	name
13788281	CV550037	single nucleotide variant	NM_016292.3(TRAP1):c.2075G>A (p.Arg692His)	not provided [RCV000676232]	benign\|likely benign	16	3658169	3658169	Human		name
13788290	CV550039	single nucleotide variant	NM_016292.3(TRAP1):c.1714G>A (p.Glu572Lys)	not provided [RCV000676235]\|not specified [RCV004026142]	uncertain significance	16	3662962	3662962	Human		name
13788293	CV550040	single nucleotide variant	NM_016292.3(TRAP1):c.1406G>A (p.Arg469His)	Congenital anomaly of kidney and urinary tract [RCV001849425]\|TRAP1-related disorder [RCV003938025]\|not provided [RCV000676236]	pathogenic\|benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	16	3664437	3664437	Human	1	name , trait , alternate_id
13788296	CV550041	single nucleotide variant	NM_016292.3(TRAP1):c.1330T>A (p.Tyr444Asn)	TRAP1-related disorder [RCV003918111]\|not provided [RCV000676237]	benign\|likely benign\|uncertain significance	16	3666024	3666024	Human		name , trait , alternate_id
13788299	CV550042	single nucleotide variant	NM_016292.3(TRAP1):c.1185C>G (p.Asp395Glu)	not provided [RCV000676238]\|not specified [RCV003489800]	benign	16	3671772	3671772	Human		name
13788309	CV550045	single nucleotide variant	NM_016292.3(TRAP1):c.1019G>A (p.Arg340His)	not provided [RCV000676241]\|not specified [RCV004026143]	uncertain significance	16	3674364	3674364	Human		name
15169057	CV726627	single nucleotide variant	NM_016292.3(TRAP1):c.2115A>C (p.Ter705Cys)	not provided [RCV000894114]	benign	16	3658129	3658129	Human		name
15104970	CV726628	single nucleotide variant	NM_016292.3(TRAP1):c.1472G>A (p.Arg491Gln)	not provided [RCV000892989]	benign	16	3664371	3664371	Human		name
15191630	CV740177	single nucleotide variant	NM_016292.3(TRAP1):c.1805G>A (p.Arg602Gln)	TRAP1-related disorder [RCV003913001]\|not provided [RCV000910302]	likely benign	16	3662122	3662122	Human		name , trait , alternate_id
41405822	CV982013	single nucleotide variant	NM_016292.3(TRAP1):c.1512C>G (p.Asn504Lys)	not provided [RCV001810588]	uncertain significance	16	3664331	3664331	Human		name
597860405	CV3832918	duplication	NM_016292.3(TRAP1):c.187_190dup (p.Ala64fs)	not provided [RCV005174831]	uncertain significance	16	3690883	3690884	Human		name
156097433	CV1981045	deletion	NM_016292.3(TRAP1):c.2101_*5del (p.Leu701fs)	not provided [RCV002622086]	uncertain significance	16	3658124	3658143	Human		name
156133879	CV2109341	microsatellite	NM_016292.3(TRAP1):c.934GAG[1] (p.Glu313del)	not provided [RCV002914654]	benign	16	3674444	3674446	Human		name
156091648	CV2135577	microsatellite	NM_016292.3(TRAP1):c.1681GAG[1] (p.Glu562del)	TRAP1-related disorder [RCV003963544]\|not provided [RCV003001854]	likely benign\|uncertain significance	16	3663446	3663448	Human		name , trait , alternate_id
597855122	CV3837366	microsatellite	NM_016292.3(TRAP1):c.1990_1994del (p.Leu664fs)	not provided [RCV005185524]	uncertain significance	16	3658812	3658816	Human		name
13832280	CV582773	microsatellite	NM_016292.3(TRAP1):c.1728_1729del (p.Lys577fs)	not provided [RCV000722966]	uncertain significance	16	3662947	3662948	Human		name
13788318	CV550047	indel	NM_016292.3(TRAP1):c.776_777delinsTG (p.Ser259Leu)	not provided [RCV000676244]	benign	16	3676073	3676074	Human		name
13831518	CV582016	duplication	NM_016292.3(TRAP1):c.572dup (p.Ala191_Glu192insTer)	not provided [RCV000722198]	uncertain significance	16	3677629	3677630	Human		name
15149541	CV714907	duplication	NM_016292.3(TRAP1):c.1430_1432dup (p.Ser477_Gly478insAla)	not provided [RCV000967773]	benign	16	3664410	3664411	Human		name

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