Trpv1 Variant Search Result - Rat Genome Database

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110 records found for search term Trpv1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15165194	CV779925	single nucleotide variant	NM_080704.4(TRPV1):c.284+9G>A	not provided [RCV000970898]	benign	17	3592058	3592058	Human		name
15149474	CV744961	single nucleotide variant	NM_080704.4(TRPV1):c.2347+8G>A	not provided [RCV000900941]	likely benign	17	3571516	3571516	Human		name
10042006	CV186968	single nucleotide variant	NM_080704.4(TRPV1):c.-34+7395T>C	Nephropathic cystinosis [RCV000169540]	benign	17	3601032	3601032	Human	1	name
156204824	CV2297825	single nucleotide variant	NM_080704.4(TRPV1):c.23A>C (p.Asp8Ala)	not specified [RCV004157771]	uncertain significance	17	3592328	3592328	Human		name
15181451	CV715392	single nucleotide variant	NM_080704.4(TRPV1):c.180G>A (p.Pro60=)	not provided [RCV000974396]	benign	17	3592171	3592171	Human		name
15191238	CV771447	single nucleotide variant	NM_080704.4(TRPV1):c.261A>G (p.Pro87=)	not provided [RCV000932745]	likely benign	17	3592090	3592090	Human		name
156219680	CV2344925	single nucleotide variant	NM_080704.4(TRPV1):c.42C>A (p.Asp14Glu)	not specified [RCV004191054]	uncertain significance	17	3592309	3592309	Human		name
401868545	CV2767269	single nucleotide variant	NM_080704.4(TRPV1):c.70C>T (p.Pro24Ser)	not specified [RCV004349440]	uncertain significance	17	3592281	3592281	Human		name
405777284	CV3344487	single nucleotide variant	NM_080704.4(TRPV1):c.58A>G (p.Thr20Ala)	not specified [RCV004471332]	likely benign	17	3592293	3592293	Human		name
405777290	CV3344488	single nucleotide variant	NM_080704.4(TRPV1):c.67G>C (p.Asp23His)	not specified [RCV004471333]	uncertain significance	17	3592284	3592284	Human		name
597681007	CV3621309	single nucleotide variant	NM_080704.4(TRPV1):c.74T>C (p.Leu25Pro)	not specified [RCV004883597]	likely benign	17	3592277	3592277	Human		name
13827443	CV578539	single nucleotide variant	NM_080704.4(TRPV1):c.63C>A (p.Cys21Ter)	not provided [RCV000714771]	uncertain significance	17	3592288	3592288	Human		name
15152989	CV740698	single nucleotide variant	NM_080704.4(TRPV1):c.576C>T (p.Asn192=)	not provided [RCV000901676]	likely benign	17	3590992	3590992	Human		name
15134708	CV755791	single nucleotide variant	NM_080704.4(TRPV1):c.897G>A (p.Thr299=)	not provided [RCV000920732]	likely benign	17	3589954	3589954	Human		name
15202920	CV755793	single nucleotide variant	NM_080704.4(TRPV1):c.624C>T (p.Ile208=)	not provided [RCV000913615]	likely benign	17	3590373	3590373	Human		name
156261221	CV2204880	single nucleotide variant	NM_080704.4(TRPV1):c.277G>A (p.Gly93Ser)	not specified [RCV004075122]	uncertain significance	17	3592074	3592074	Human		name
155934318	CV2225251	single nucleotide variant	NM_080704.4(TRPV1):c.229A>T (p.Thr77Ser)	not specified [RCV004098900]	uncertain significance	17	3592122	3592122	Human		name
156133580	CV2350366	single nucleotide variant	NM_080704.4(TRPV1):c.244A>G (p.Ile82Val)	not specified [RCV004202311]	likely benign	17	3592107	3592107	Human		name
156034216	CV2376656	single nucleotide variant	NM_080704.4(TRPV1):c.112C>A (p.Pro38Thr)	not specified [RCV004222854]	uncertain significance	17	3592239	3592239	Human		name
401743847	CV2688040	single nucleotide variant	NM_080704.4(TRPV1):c.152G>A (p.Gly51Glu)	not specified [RCV004305112]	uncertain significance	17	3592199	3592199	Human		name
405762318	CV3344476	single nucleotide variant	NM_080704.4(TRPV1):c.116A>G (p.Gln39Arg)	not specified [RCV004468841]	uncertain significance	17	3592235	3592235	Human		name
405762350	CV3344482	single nucleotide variant	NM_080704.4(TRPV1):c.215C>A (p.Ser72Tyr)	not specified [RCV004468847]	uncertain significance	17	3592136	3592136	Human		name
597680988	CV3621306	single nucleotide variant	NM_080704.4(TRPV1):c.258G>C (p.Arg86Ser)	not specified [RCV004883594]	uncertain significance	17	3592093	3592093	Human		name
597680993	CV3621307	single nucleotide variant	NM_080704.4(TRPV1):c.125C>T (p.Thr42Met)	not specified [RCV004883595]	uncertain significance	17	3592226	3592226	Human		name
597681308	CV3621325	single nucleotide variant	NM_080704.4(TRPV1):c.177C>A (p.Phe59Leu)	not specified [RCV004883611]	uncertain significance	17	3592174	3592174	Human		name
598215466	CV3932273	single nucleotide variant	NM_080704.4(TRPV1):c.251T>C (p.Ile84Thr)	not specified [RCV005292731]	uncertain significance	17	3592100	3592100	Human		name
15102714	CV704099	single nucleotide variant	NM_080704.4(TRPV1):c.1836G>A (p.Thr612=)	not provided [RCV000959339]	benign	17	3573900	3573900	Human		name
15127777	CV740694	single nucleotide variant	NM_080704.4(TRPV1):c.1857T>G (p.Pro619=)	not provided [RCV000897166]	benign	17	3573879	3573879	Human		name
15126622	CV755789	single nucleotide variant	NM_080704.4(TRPV1):c.1420C>A (p.Arg474=)	not provided [RCV000919357]	likely benign	17	3583394	3583394	Human		name
155795034	CV1292133	single nucleotide variant	NM_080704.4(TRPV1):c.993C>G (p.Asn331Lys)	See cases [RCV002463813]	likely pathogenic	17	3589858	3589858	Human		name
155980075	CV2211880	single nucleotide variant	NM_080704.4(TRPV1):c.593G>A (p.Ser198Asn)	not specified [RCV004087014]	uncertain significance	17	3590975	3590975	Human		name
155929016	CV2224482	single nucleotide variant	NM_080704.4(TRPV1):c.691G>A (p.Ala231Thr)	not specified [RCV004098074]	uncertain significance	17	3590306	3590306	Human		name
156253147	CV2264554	single nucleotide variant	NM_080704.4(TRPV1):c.848C>T (p.Ser283Leu)	not specified [RCV004132569]	uncertain significance	17	3590003	3590003	Human		name
155976777	CV2266337	single nucleotide variant	NM_080704.4(TRPV1):c.871G>A (p.Ala291Thr)	not specified [RCV004129156]	uncertain significance	17	3589980	3589980	Human		name
156243730	CV2267287	single nucleotide variant	NM_080704.4(TRPV1):c.965C>T (p.Pro322Leu)	not specified [RCV004133961]	uncertain significance	17	3589886	3589886	Human		name
156034504	CV2282899	single nucleotide variant	NM_080704.4(TRPV1):c.673G>A (p.Gly225Arg)	not specified [RCV004143542]	uncertain significance	17	3590324	3590324	Human		name
156276623	CV2330769	single nucleotide variant	NM_080704.4(TRPV1):c.319G>A (p.Glu107Lys)	not specified [RCV004185831]	uncertain significance	17	3591319	3591319	Human		name
156345642	CV2377684	single nucleotide variant	NM_080704.4(TRPV1):c.587C>T (p.Thr196Met)	not specified [RCV004228230]	uncertain significance	17	3590981	3590981	Human		name
155961387	CV2388028	single nucleotide variant	NM_080704.4(TRPV1):c.307G>A (p.Ala103Thr)	not specified [RCV004241159]	likely benign	17	3591331	3591331	Human		name
156266248	CV2389146	single nucleotide variant	NM_080704.4(TRPV1):c.908C>T (p.Thr303Met)	not specified [RCV004235476]	uncertain significance	17	3589943	3589943	Human		name
329371979	CV2442970	single nucleotide variant	NM_080704.4(TRPV1):c.782A>G (p.Gln261Arg)	not specified [RCV004253564]	uncertain significance	17	3590069	3590069	Human		name
401720595	CV2673391	single nucleotide variant	NM_080704.4(TRPV1):c.967A>T (p.Thr323Ser)	not specified [RCV004288369]	uncertain significance	17	3589884	3589884	Human		name
401728624	CV2693681	single nucleotide variant	NM_080704.4(TRPV1):c.920C>T (p.Thr307Met)	not specified [RCV004298015]	uncertain significance	17	3589931	3589931	Human		name
401779257	CV2709602	single nucleotide variant	NM_080704.4(TRPV1):c.728G>T (p.Arg243Leu)	not specified [RCV004318827]	uncertain significance	17	3590269	3590269	Human		name
401739472	CV2722136	single nucleotide variant	NM_080704.4(TRPV1):c.500A>G (p.His167Arg)	not specified [RCV004328393]	uncertain significance	17	3591068	3591068	Human		name
401761628	CV2726843	single nucleotide variant	NM_080704.4(TRPV1):c.520A>T (p.Ile174Phe)	not specified [RCV004323146]	uncertain significance	17	3591048	3591048	Human		name
401877281	CV2790113	single nucleotide variant	NM_080704.4(TRPV1):c.567G>C (p.Glu189Asp)	not specified [RCV004364054]	uncertain significance	17	3591001	3591001	Human		name
405777272	CV3344485	single nucleotide variant	NM_080704.4(TRPV1):c.352A>T (p.Ile118Phe)	not specified [RCV004471330]	uncertain significance	17	3591286	3591286	Human		name
405777279	CV3344486	single nucleotide variant	NM_080704.4(TRPV1):c.364G>A (p.Val122Ile)	not specified [RCV004471331]	uncertain significance	17	3591274	3591274	Human		name
405777296	CV3344489	single nucleotide variant	NM_080704.4(TRPV1):c.925A>G (p.Met309Val)	not specified [RCV004471334]	uncertain significance	17	3589926	3589926	Human		name
407527887	CV3488923	single nucleotide variant	NM_080704.4(TRPV1):c.889G>A (p.Asp297Asn)	not specified [RCV004680187]	uncertain significance	17	3589962	3589962	Human		name
407527890	CV3488924	single nucleotide variant	NM_080704.4(TRPV1):c.985C>T (p.Leu329Phe)	not specified [RCV004680188]	uncertain significance	17	3589866	3589866	Human		name
597680975	CV3621303	single nucleotide variant	NM_080704.4(TRPV1):c.860C>T (p.Thr287Met)	not specified [RCV004883592]	uncertain significance	17	3589991	3589991	Human		name
597680980	CV3621305	single nucleotide variant	NM_080704.4(TRPV1):c.901G>A (p.Asp301Asn)	not specified [RCV004883593]	uncertain significance	17	3589950	3589950	Human		name
597681021	CV3621311	single nucleotide variant	NM_080704.4(TRPV1):c.628A>T (p.Ile210Phe)	not specified [RCV004883599]	uncertain significance	17	3590369	3590369	Human		name
597681272	CV3621320	single nucleotide variant	NM_080704.4(TRPV1):c.988A>G (p.Thr330Ala)	not specified [RCV004883607]	uncertain significance	17	3589863	3589863	Human		name
597681282	CV3621321	single nucleotide variant	NM_080704.4(TRPV1):c.626C>T (p.Ala209Val)	not specified [RCV004883608]	uncertain significance	17	3590371	3590371	Human		name
597681300	CV3621323	single nucleotide variant	NM_080704.4(TRPV1):c.935A>C (p.Glu312Ala)	not specified [RCV004883610]	uncertain significance	17	3589916	3589916	Human		name
598237038	CV3932268	single nucleotide variant	NM_080704.4(TRPV1):c.746G>A (p.Gly249Asp)	not specified [RCV005296164]	uncertain significance	17	3590105	3590105	Human		name
598215451	CV3932270	single nucleotide variant	NM_080704.4(TRPV1):c.551C>T (p.Thr184Met)	not specified [RCV005292728]	uncertain significance	17	3591017	3591017	Human		name
15165188	CV715391	single nucleotide variant	NM_080704.4(TRPV1):c.655A>G (p.Thr219Ala)	not provided [RCV000970897]	benign	17	3590342	3590342	Human		name
15155555	CV755792	single nucleotide variant	NM_080704.4(TRPV1):c.863T>G (p.Val288Gly)	not provided [RCV000924488]\|not specified [RCV004029500]	likely benign\|uncertain significance	17	3589988	3589988	Human		name
152046115	CV1670387	single nucleotide variant	NM_080704.4(TRPV1):c.2165G>A (p.Arg722His)	Malignant hyperthermia of anesthesia [RCV002225239]	uncertain significance	17	3572188	3572188	Human	2	name
156173087	CV2247568	single nucleotide variant	NM_080704.4(TRPV1):c.1300A>G (p.Ile434Val)	not specified [RCV004108871]	uncertain significance	17	3585851	3585851	Human		name
156004586	CV2295978	single nucleotide variant	NM_080704.4(TRPV1):c.2017A>C (p.Ile673Leu)	not specified [RCV004151868]	uncertain significance	17	3573719	3573719	Human		name
156088837	CV2344296	single nucleotide variant	NM_080704.4(TRPV1):c.1643G>A (p.Gly548Asp)	not specified [RCV004195057]	uncertain significance	17	3577668	3577668	Human		name
156280153	CV2348420	single nucleotide variant	NM_080704.4(TRPV1):c.1846T>C (p.Trp616Arg)	not specified [RCV004193610]	uncertain significance	17	3573890	3573890	Human		name
156005070	CV2357623	single nucleotide variant	NM_080704.4(TRPV1):c.1084G>A (p.Glu362Lys)	not specified [RCV004202885]	uncertain significance	17	3588328	3588328	Human		name
155928780	CV2388982	single nucleotide variant	NM_080704.4(TRPV1):c.1290C>A (p.Phe430Leu)	not specified [RCV004241977]	uncertain significance	17	3585861	3585861	Human		name
155959008	CV2390460	single nucleotide variant	NM_080704.4(TRPV1):c.2503G>A (p.Ala835Thr)	not specified [RCV004239002]	uncertain significance	17	3566832	3566832	Human		name
329357274	CV2431313	single nucleotide variant	NM_080704.4(TRPV1):c.1165G>C (p.Asp389His)	not specified [RCV004252435]	uncertain significance	17	3588247	3588247	Human		name
329382267	CV2438661	single nucleotide variant	NM_080704.4(TRPV1):c.2509G>A (p.Gly837Arg)	not specified [RCV004261823]	uncertain significance	17	3566826	3566826	Human		name
329372417	CV2443029	single nucleotide variant	NM_080704.4(TRPV1):c.2357G>A (p.Arg786Lys)	not specified [RCV004253619]	uncertain significance	17	3566978	3566978	Human		name
329395935	CV2451790	single nucleotide variant	NM_080704.4(TRPV1):c.1400A>C (p.Glu467Ala)	not specified [RCV004276474]	uncertain significance	17	3583414	3583414	Human		name
329364084	CV2469715	single nucleotide variant	NM_080704.4(TRPV1):c.1209C>G (p.Ser403Arg)	not specified [RCV004283125]	uncertain significance	17	3588203	3588203	Human		name
401738231	CV2676173	single nucleotide variant	NM_080704.4(TRPV1):c.1865G>A (p.Arg622Lys)	not specified [RCV004284391]	uncertain significance	17	3573871	3573871	Human		name
401721999	CV2680778	single nucleotide variant	NM_080704.4(TRPV1):c.1229G>A (p.Arg410His)	not specified [RCV004293428]	uncertain significance	17	3585922	3585922	Human		name
401740387	CV2683344	single nucleotide variant	NM_080704.4(TRPV1):c.1033G>A (p.Gly345Arg)	not specified [RCV004288119]	uncertain significance	17	3589818	3589818	Human		name
401771964	CV2689673	single nucleotide variant	NM_080704.4(TRPV1):c.1237A>G (p.Met413Val)	not specified [RCV004297597]	uncertain significance	17	3585914	3585914	Human		name
401777087	CV2707706	single nucleotide variant	NM_080704.4(TRPV1):c.2282A>C (p.Asn761Thr)	not specified [RCV004306961]	uncertain significance	17	3571589	3571589	Human		name
405762313	CV3344475	single nucleotide variant	NM_080704.4(TRPV1):c.1019T>C (p.Leu340Pro)	not specified [RCV004468840]	uncertain significance	17	3589832	3589832	Human		name
405762324	CV3344477	single nucleotide variant	NM_080704.4(TRPV1):c.1667C>A (p.Thr556Asn)	not specified [RCV004468842]	uncertain significance	17	3577644	3577644	Human		name
405762329	CV3344478	single nucleotide variant	NM_080704.4(TRPV1):c.1699G>A (p.Val567Ile)	not specified [RCV004468843]	uncertain significance	17	3577612	3577612	Human		name
405762334	CV3344479	single nucleotide variant	NM_080704.4(TRPV1):c.1736G>A (p.Arg579His)	not specified [RCV004468844]	uncertain significance	17	3577170	3577170	Human		name
405762340	CV3344480	single nucleotide variant	NM_080704.4(TRPV1):c.1838C>T (p.Ser613Leu)	not specified [RCV004468845]	uncertain significance	17	3573898	3573898	Human		name
405762344	CV3344481	single nucleotide variant	NM_080704.4(TRPV1):c.2122G>T (p.Asp708Tyr)	not specified [RCV004468846]	uncertain significance	17	3572231	3572231	Human		name
405762356	CV3344483	single nucleotide variant	NM_080704.4(TRPV1):c.2171G>A (p.Gly724Asp)	not specified [RCV004468848]	uncertain significance	17	3572182	3572182	Human		name
405762360	CV3344484	single nucleotide variant	NM_080704.4(TRPV1):c.2477A>G (p.Asp826Gly)	not specified [RCV004468849]	uncertain significance	17	3566858	3566858	Human		name
407527881	CV3488921	single nucleotide variant	NM_080704.4(TRPV1):c.2308G>A (p.Val770Ile)	not specified [RCV004680185]	likely benign	17	3571563	3571563	Human		name
407527884	CV3488922	single nucleotide variant	NM_080704.4(TRPV1):c.1472G>A (p.Arg491Gln)	not specified [RCV004680186]	uncertain significance	17	3583342	3583342	Human		name
407527893	CV3488925	single nucleotide variant	NM_080704.4(TRPV1):c.2479G>T (p.Ala827Ser)	not specified [RCV004680189]	uncertain significance	17	3566856	3566856	Human		name
407527896	CV3488926	single nucleotide variant	NM_080704.4(TRPV1):c.2366A>G (p.Lys789Arg)	not specified [RCV004680190]	uncertain significance	17	3566969	3566969	Human		name
597681000	CV3621308	single nucleotide variant	NM_080704.4(TRPV1):c.1823C>T (p.Pro608Leu)	not specified [RCV004883596]	uncertain significance	17	3573913	3573913	Human		name
597681014	CV3621310	single nucleotide variant	NM_080704.4(TRPV1):c.1544T>G (p.Leu515Arg)	not specified [RCV004883598]	uncertain significance	17	3580460	3580460	Human		name
597681029	CV3621312	single nucleotide variant	NM_080704.4(TRPV1):c.2221T>G (p.Trp741Gly)	not specified [RCV004883600]	uncertain significance	17	3572132	3572132	Human		name
597681037	CV3621314	single nucleotide variant	NM_080704.4(TRPV1):c.1696G>A (p.Ala566Thr)	not specified [RCV004883601]	uncertain significance	17	3577615	3577615	Human		name
597681045	CV3621315	single nucleotide variant	NM_080704.4(TRPV1):c.1609T>C (p.Tyr537His)	not specified [RCV004883602]	uncertain significance	17	3577702	3577702	Human		name
597681054	CV3621316	single nucleotide variant	NM_080704.4(TRPV1):c.1918A>G (p.Lys640Glu)	not specified [RCV004883603]	uncertain significance	17	3573818	3573818	Human		name
597681063	CV3621317	single nucleotide variant	NM_080704.4(TRPV1):c.2408G>A (p.Arg803Gln)	not specified [RCV004883604]	uncertain significance	17	3566927	3566927	Human		name
597681069	CV3621318	single nucleotide variant	NM_080704.4(TRPV1):c.2268C>G (p.Asn756Lys)	not specified [RCV004883605]	uncertain significance	17	3571603	3571603	Human		name
597681264	CV3621319	single nucleotide variant	NM_080704.4(TRPV1):c.2118C>G (p.Ile706Met)	not specified [RCV004883606]	uncertain significance	17	3572235	3572235	Human		name
597681289	CV3621322	single nucleotide variant	NM_080704.4(TRPV1):c.2381T>C (p.Val794Ala)	not specified [RCV004883609]	uncertain significance	17	3566954	3566954	Human		name
598215457	CV3932271	single nucleotide variant	NM_080704.4(TRPV1):c.2447G>A (p.Arg816Gln)	not specified [RCV005292729]	uncertain significance	17	3566888	3566888	Human		name
598215462	CV3932272	single nucleotide variant	NM_080704.4(TRPV1):c.1460A>C (p.Tyr487Ser)	not specified [RCV005292730]	uncertain significance	17	3583354	3583354	Human		name
598237043	CV3932274	single nucleotide variant	NM_080704.4(TRPV1):c.1514C>T (p.Thr505Ile)	not specified [RCV005296165]	uncertain significance	17	3580490	3580490	Human		name
15186708	CV704100	single nucleotide variant	NM_080704.4(TRPV1):c.1767C>G (p.Phe589Leu)	not provided [RCV000953365]	likely benign	17	3577139	3577139	Human		name
15189853	CV704101	single nucleotide variant	NM_080704.4(TRPV1):c.1513A>G (p.Thr505Ala)	not provided [RCV000954302]	benign	17	3580491	3580491	Human		name
15198796	CV727116	single nucleotide variant	NM_080704.4(TRPV1):c.1835C>T (p.Thr612Met)	not provided [RCV000890459]	likely benign	17	3573901	3573901	Human		name
15194610	CV727119	single nucleotide variant	NM_080704.4(TRPV1):c.1372G>A (p.Val458Met)	not provided [RCV000889269]	likely benign	17	3585779	3585779	Human		name
15159209	CV740693	single nucleotide variant	NM_080704.4(TRPV1):c.1873G>A (p.Asp625Asn)	not provided [RCV000902889]	likely benign	17	3573863	3573863	Human		name

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