Ltk Variant Search Result - Rat Genome Database

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113 records found for search term Ltk

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156263362	CV2201164	single nucleotide variant	NM_002344.6(LTK):c.30G>C (p.Trp10Cys)	not specified [RCV004077315]	uncertain significance	15	41513680	41513680	Human		name
156076838	CV2331836	single nucleotide variant	NM_002344.6(LTK):c.62G>A (p.Ser21Asn)	not specified [RCV004184450]	uncertain significance	15	41513102	41513102	Human		name
156203303	CV2399681	single nucleotide variant	NM_002344.6(LTK):c.40G>T (p.Ala14Ser)	not specified [RCV004245500]	uncertain significance	15	41513670	41513670	Human		name
405815963	CV3284624	single nucleotide variant	NM_002344.6(LTK):c.49A>G (p.Ile17Val)	not specified [RCV004410829]	uncertain significance	15	41513115	41513115	Human		name
597644399	CV3699766	single nucleotide variant	NM_002344.6(LTK):c.37G>A (p.Ala13Thr)	not specified [RCV004942129]	uncertain significance	15	41513673	41513673	Human		name
155901689	CV2294611	single nucleotide variant	NM_002344.6(LTK):c.233G>A (p.Arg78Gln)	not specified [RCV004161869]	uncertain significance	15	41512833	41512833	Human		name
156013802	CV2300476	single nucleotide variant	NM_002344.6(LTK):c.254A>C (p.Gln85Pro)	not specified [RCV004153664]	uncertain significance	15	41512812	41512812	Human		name
156334541	CV2333402	single nucleotide variant	NM_002344.6(LTK):c.143C>T (p.Ala48Val)	not specified [RCV004190109]	uncertain significance	15	41513021	41513021	Human		name
156402621	CV2361836	single nucleotide variant	NM_002344.6(LTK):c.121C>T (p.Pro41Ser)	not specified [RCV004223305]	uncertain significance	15	41513043	41513043	Human		name
405811152	CV3284613	single nucleotide variant	NM_002344.6(LTK):c.129C>G (p.Asp43Glu)	not specified [RCV004408341]	uncertain significance	15	41513035	41513035	Human		name
405811156	CV3284615	single nucleotide variant	NM_002344.6(LTK):c.1509C>G (p.Thr503=)	not specified [RCV004408343]	likely benign	15	41507127	41507127	Human		name
405811158	CV3284616	single nucleotide variant	NM_002344.6(LTK):c.152G>T (p.Ser51Ile)	not specified [RCV004408344]	uncertain significance	15	41513012	41513012	Human		name
597643975	CV3699761	single nucleotide variant	NM_002344.6(LTK):c.197G>A (p.Gly66Glu)	not specified [RCV004942124]	uncertain significance	15	41512869	41512869	Human		name
597644405	CV3699765	single nucleotide variant	NM_002344.6(LTK):c.283G>A (p.Val95Met)	not specified [RCV004942128]	uncertain significance	15	41512783	41512783	Human		name
597644342	CV3699776	single nucleotide variant	NM_002344.6(LTK):c.296T>G (p.Val99Gly)	not specified [RCV004942138]	uncertain significance	15	41512770	41512770	Human		name
598251757	CV3981273	single nucleotide variant	NM_002344.6(LTK):c.235C>T (p.His79Tyr)	not specified [RCV005366842]	uncertain significance	15	41512831	41512831	Human		name
14396846	CV613008	single nucleotide variant	NM_002344.6(LTK):c.203G>T (p.Trp68Leu)	not provided [RCV000761905]	uncertain significance	15	41512863	41512863	Human		name
15149238	CV739599	single nucleotide variant	NM_002344.6(LTK):c.1170A>G (p.Gln390=)	not provided [RCV000900892]	benign	15	41508148	41508148	Human		name
155945572	CV2238003	single nucleotide variant	NM_002344.6(LTK):c.550C>G (p.Arg184Gly)	not specified [RCV004111036]	uncertain significance	15	41511924	41511924	Human		name
155973357	CV2238961	single nucleotide variant	NM_002344.6(LTK):c.508G>A (p.Gly170Arg)	not specified [RCV004109855]	uncertain significance	15	41512117	41512117	Human		name
156183271	CV2243257	single nucleotide variant	NM_002344.6(LTK):c.415G>A (p.Ala139Thr)	not specified [RCV004110142]	uncertain significance	15	41512210	41512210	Human		name
155960510	CV2314038	single nucleotide variant	NM_002344.6(LTK):c.334C>T (p.Arg112Cys)	not specified [RCV004164321]	uncertain significance	15	41512732	41512732	Human		name
155903140	CV2386439	single nucleotide variant	NM_002344.6(LTK):c.607C>T (p.Arg203Cys)	not specified [RCV004228763]	uncertain significance	15	41511867	41511867	Human		name
156190888	CV2391206	single nucleotide variant	NM_002344.6(LTK):c.652T>A (p.Phe218Ile)	not specified [RCV004237222]	uncertain significance	15	41511822	41511822	Human		name
156193606	CV2398050	single nucleotide variant	NM_002344.6(LTK):c.958G>A (p.Gly320Arg)	not specified [RCV004241640]	uncertain significance	15	41511203	41511203	Human		name
329369077	CV2450520	single nucleotide variant	NM_002344.6(LTK):c.413G>A (p.Arg138Gln)	not specified [RCV004265433]	uncertain significance	15	41512212	41512212	Human		name
329396514	CV2462586	single nucleotide variant	NM_002344.6(LTK):c.662G>C (p.Arg221Pro)	not specified [RCV004278535]	uncertain significance	15	41511574	41511574	Human		name
401733511	CV2682134	single nucleotide variant	NM_002344.6(LTK):c.895G>A (p.Gly299Ser)	not specified [RCV004290186]	uncertain significance	15	41511266	41511266	Human		name
401750570	CV2689457	single nucleotide variant	NM_002344.6(LTK):c.718C>G (p.Leu240Val)	not specified [RCV004308304]	uncertain significance	15	41511518	41511518	Human		name
401757406	CV2735000	single nucleotide variant	NM_002344.6(LTK):c.755C>G (p.Pro252Arg)	not specified [RCV004333704]	uncertain significance	15	41511481	41511481	Human		name
401858147	CV2756709	single nucleotide variant	NM_002344.6(LTK):c.482G>T (p.Gly161Val)	not specified [RCV004345216]	uncertain significance	15	41512143	41512143	Human		name
401863191	CV2765578	single nucleotide variant	NM_002344.6(LTK):c.710G>C (p.Arg237Pro)	not specified [RCV004335595]	uncertain significance	15	41511526	41511526	Human		name
405811170	CV3284622	single nucleotide variant	NM_002344.6(LTK):c.308G>A (p.Gly103Glu)	not specified [RCV004408350]	uncertain significance	15	41512758	41512758	Human		name
405811172	CV3284623	single nucleotide variant	NM_002344.6(LTK):c.322G>T (p.Val108Leu)	not specified [RCV004408351]	uncertain significance	15	41512744	41512744	Human		name
405815962	CV3284625	single nucleotide variant	NM_002344.6(LTK):c.548C>T (p.Ser183Phe)	not specified [RCV004410830]	uncertain significance	15	41511926	41511926	Human		name
405815960	CV3284627	single nucleotide variant	NM_002344.6(LTK):c.608G>T (p.Arg203Leu)	not specified [RCV004410832]	uncertain significance	15	41511866	41511866	Human		name
405815959	CV3284628	single nucleotide variant	NM_002344.6(LTK):c.914C>T (p.Ala305Val)	not specified [RCV004410833]	uncertain significance	15	41511247	41511247	Human		name
407482957	CV3453202	single nucleotide variant	NM_002344.6(LTK):c.844C>G (p.Pro282Ala)	not specified [RCV004640257]	uncertain significance	15	41511317	41511317	Human		name
407468535	CV3453206	single nucleotide variant	NM_002344.6(LTK):c.749C>T (p.Ala250Val)	not specified [RCV004636321]	uncertain significance	15	41511487	41511487	Human		name
597643952	CV3699757	single nucleotide variant	NM_002344.6(LTK):c.943T>C (p.Phe315Leu)	not specified [RCV004942120]	uncertain significance	15	41511218	41511218	Human		name
597643964	CV3699759	single nucleotide variant	NM_002344.6(LTK):c.567C>G (p.His189Gln)	not specified [RCV004942122]	uncertain significance	15	41511907	41511907	Human		name
597643970	CV3699760	single nucleotide variant	NM_002344.6(LTK):c.676G>A (p.Glu226Lys)	not specified [RCV004942123]	uncertain significance	15	41511560	41511560	Human		name
597644410	CV3699764	single nucleotide variant	NM_002344.6(LTK):c.585C>A (p.Ser195Arg)	not specified [RCV004942127]	uncertain significance	15	41511889	41511889	Human		name
597644386	CV3699768	single nucleotide variant	NM_002344.6(LTK):c.493G>C (p.Glu165Gln)	not specified [RCV004942131]	uncertain significance	15	41512132	41512132	Human		name
597644372	CV3699770	single nucleotide variant	NM_002344.6(LTK):c.398A>G (p.Lys133Arg)	not specified [RCV004942133]	uncertain significance	15	41512227	41512227	Human		name
597644363	CV3699773	single nucleotide variant	NM_002344.6(LTK):c.410C>T (p.Ser137Leu)	not specified [RCV004942135]	uncertain significance	15	41512215	41512215	Human		name
597644325	CV3699778	single nucleotide variant	NM_002344.6(LTK):c.962C>T (p.Ala321Val)	not specified [RCV004942140]	uncertain significance	15	41511199	41511199	Human		name
598224210	CV3981278	single nucleotide variant	NM_002344.6(LTK):c.820G>A (p.Gly274Arg)	not specified [RCV005380172]	uncertain significance	15	41511341	41511341	Human		name
598163453	CV3981280	single nucleotide variant	NM_002344.6(LTK):c.737G>T (p.Gly246Val)	not specified [RCV005368830]	uncertain significance	15	41511499	41511499	Human		name
598224235	CV3981284	single nucleotide variant	NM_002344.6(LTK):c.776C>G (p.Ser259Trp)	not specified [RCV005380175]	uncertain significance	15	41511460	41511460	Human		name
8635432	CV90653	single nucleotide variant	NM_002344.6(LTK):c.457G>A (p.Gly153Arg)	not specified [RCV004942141]	uncertain significance\|not provided	15	41512168	41512168	Human		name
156373254	CV2204899	single nucleotide variant	NM_002344.6(LTK):c.1556G>A (p.Gly519Asp)	not specified [RCV004075141]	uncertain significance	15	41505991	41505991	Human		name
156081851	CV2205390	single nucleotide variant	NM_002344.6(LTK):c.1958G>A (p.Cys653Tyr)	not specified [RCV004082338]	uncertain significance	15	41505032	41505032	Human		name
156251391	CV2232296	single nucleotide variant	NM_002344.6(LTK):c.2111C>T (p.Thr704Ile)	not specified [RCV004105073]	uncertain significance	15	41504782	41504782	Human		name
156071034	CV2251387	single nucleotide variant	NM_002344.6(LTK):c.1594C>G (p.Leu532Val)	not specified [RCV004117374]	uncertain significance	15	41505953	41505953	Human		name
156039318	CV2261200	single nucleotide variant	NM_002344.6(LTK):c.1562T>C (p.Phe521Ser)	not specified [RCV004128082]	uncertain significance	15	41505985	41505985	Human		name
156153529	CV2303835	single nucleotide variant	NM_002344.6(LTK):c.1936G>A (p.Ala646Thr)	not specified [RCV004168131]	uncertain significance	15	41505054	41505054	Human		name
156363875	CV2330100	single nucleotide variant	NM_002344.6(LTK):c.2180G>A (p.Arg727His)	not specified [RCV004185590]	uncertain significance	15	41504581	41504581	Human		name
155963265	CV2330309	single nucleotide variant	NM_002344.6(LTK):c.1111G>A (p.Gly371Arg)	not specified [RCV004180893]	uncertain significance	15	41508207	41508207	Human		name
155969583	CV2335484	single nucleotide variant	NM_002344.6(LTK):c.2206G>A (p.Val736Ile)	not specified [RCV004191654]	uncertain significance	15	41504555	41504555	Human		name
155975876	CV2342713	single nucleotide variant	NM_002344.6(LTK):c.2221C>T (p.Arg741Trp)	not specified [RCV004196790]	uncertain significance	15	41504540	41504540	Human		name
156221209	CV2345127	single nucleotide variant	NM_002344.6(LTK):c.1654C>T (p.Pro552Ser)	not specified [RCV004193397]	uncertain significance	15	41505756	41505756	Human		name
156123666	CV2350042	single nucleotide variant	NM_002344.6(LTK):c.2045G>A (p.Arg682Gln)	not specified [RCV004199968]	uncertain significance	15	41504848	41504848	Human		name
156264632	CV2388966	single nucleotide variant	NM_002344.6(LTK):c.1756C>G (p.Arg586Gly)	not specified [RCV004241965]	uncertain significance	15	41505472	41505472	Human		name
156038860	CV2390257	single nucleotide variant	NM_002344.6(LTK):c.2153C>T (p.Ser718Leu)	not specified [RCV004240630]	uncertain significance	15	41504608	41504608	Human		name
156248397	CV2393942	single nucleotide variant	NM_002344.6(LTK):c.1967C>T (p.Pro656Leu)	not specified [RCV004236173]	uncertain significance	15	41505023	41505023	Human		name
155964634	CV2395862	single nucleotide variant	NM_002344.6(LTK):c.2351C>T (p.Pro784Leu)	not specified [RCV004235376]	uncertain significance	15	41504240	41504240	Human		name
329356156	CV2430608	single nucleotide variant	NM_002344.6(LTK):c.2326C>T (p.Arg776Cys)	not specified [RCV004253802]	uncertain significance	15	41504362	41504362	Human		name
329375270	CV2440872	single nucleotide variant	NM_002344.6(LTK):c.2261G>A (p.Arg754His)	not specified [RCV004261267]	uncertain significance	15	41504427	41504427	Human		name
329399719	CV2443394	single nucleotide variant	NM_002344.6(LTK):c.1723C>T (p.Arg575Trp)	not specified [RCV004262237]	uncertain significance	15	41505505	41505505	Human		name
329377447	CV2453307	single nucleotide variant	NM_002344.6(LTK):c.2044C>G (p.Arg682Gly)	not specified [RCV004266937]	uncertain significance	15	41504849	41504849	Human		name
401730189	CV2700487	single nucleotide variant	NM_002344.6(LTK):c.2333A>G (p.Gln778Arg)	not specified [RCV004311119]	uncertain significance	15	41504355	41504355	Human		name
401718630	CV2704712	single nucleotide variant	NM_002344.6(LTK):c.2330T>C (p.Leu777Pro)	not specified [RCV004307317]	uncertain significance	15	41504358	41504358	Human		name
401724846	CV2714995	single nucleotide variant	NM_002344.6(LTK):c.1751C>A (p.Thr584Asn)	not specified [RCV004322312]	uncertain significance	15	41505477	41505477	Human		name
401723605	CV2724962	single nucleotide variant	NM_002344.6(LTK):c.2053C>T (p.Leu685Phe)	not specified [RCV004319726]	uncertain significance	15	41504840	41504840	Human		name
401857831	CV2777786	single nucleotide variant	NM_002344.6(LTK):c.1127G>C (p.Arg376Pro)	not specified [RCV004345614]	uncertain significance	15	41508191	41508191	Human		name
401878977	CV2778049	single nucleotide variant	NM_002344.6(LTK):c.2360T>C (p.Leu787Pro)	not specified [RCV004348000]	uncertain significance	15	41504231	41504231	Human		name
405811154	CV3284614	single nucleotide variant	NM_002344.6(LTK):c.1468C>T (p.Leu490Phe)	not specified [RCV004408342]	uncertain significance	15	41507168	41507168	Human		name
405811160	CV3284617	single nucleotide variant	NM_002344.6(LTK):c.1757G>A (p.Arg586His)	not specified [RCV004408345]	uncertain significance	15	41505471	41505471	Human		name
405811162	CV3284618	single nucleotide variant	NM_002344.6(LTK):c.1852C>T (p.Arg618Trp)	not specified [RCV004408346]	uncertain significance	15	41505281	41505281	Human		name
405811164	CV3284619	single nucleotide variant	NM_002344.6(LTK):c.1916T>A (p.Phe639Tyr)	not specified [RCV004408347]	uncertain significance	15	41505217	41505217	Human		name
405811166	CV3284620	single nucleotide variant	NM_002344.6(LTK):c.1973G>C (p.Arg658Pro)	not specified [RCV004408348]	uncertain significance	15	41505017	41505017	Human		name
405811168	CV3284621	single nucleotide variant	NM_002344.6(LTK):c.2222G>A (p.Arg741Gln)	not specified [RCV004408349]	uncertain significance	15	41504539	41504539	Human		name
407482962	CV3453203	single nucleotide variant	NM_002344.6(LTK):c.1843C>G (p.Leu615Val)	not specified [RCV004640258]	uncertain significance	15	41505290	41505290	Human		name
407482971	CV3453204	single nucleotide variant	NM_002344.6(LTK):c.1393C>A (p.Pro465Thr)	not specified [RCV004640259]	uncertain significance	15	41507243	41507243	Human		name
407482976	CV3453205	single nucleotide variant	NM_002344.6(LTK):c.2245C>T (p.Pro749Ser)	not specified [RCV004640260]	uncertain significance	15	41504516	41504516	Human		name
407468538	CV3453207	single nucleotide variant	NM_002344.6(LTK):c.1652C>G (p.Ser551Trp)	not specified [RCV004636322]	uncertain significance	15	41505758	41505758	Human		name
597643957	CV3699758	single nucleotide variant	NM_002344.6(LTK):c.1985T>C (p.Ile662Thr)	not specified [RCV004942121]	uncertain significance	15	41505005	41505005	Human		name
597644421	CV3699762	single nucleotide variant	NM_002344.6(LTK):c.1126C>G (p.Arg376Gly)	not specified [RCV004942125]	uncertain significance	15	41508192	41508192	Human		name
597644416	CV3699763	single nucleotide variant	NM_002344.6(LTK):c.1241C>T (p.Thr414Ile)	not specified [RCV004942126]	uncertain significance	15	41508077	41508077	Human		name
597644392	CV3699767	single nucleotide variant	NM_002344.6(LTK):c.1895A>G (p.His632Arg)	not specified [RCV004942130]	uncertain significance	15	41505238	41505238	Human		name
597644380	CV3699769	single nucleotide variant	NM_002344.6(LTK):c.1149C>G (p.His383Gln)	not specified [RCV004942132]	uncertain significance	15	41508169	41508169	Human		name
597644366	CV3699772	single nucleotide variant	NM_002344.6(LTK):c.1526A>G (p.Asn509Ser)	not specified [RCV004942134]	uncertain significance	15	41507110	41507110	Human		name
597644358	CV3699774	single nucleotide variant	NM_002344.6(LTK):c.1850T>C (p.Met617Thr)	not specified [RCV004942136]	uncertain significance	15	41505283	41505283	Human		name
597644350	CV3699775	single nucleotide variant	NM_002344.6(LTK):c.1000G>T (p.Gly334Cys)	not specified [RCV004942137]	uncertain significance	15	41509127	41509127	Human		name
597644334	CV3699777	single nucleotide variant	NM_002344.6(LTK):c.2339G>A (p.Cys780Tyr)	not specified [RCV004942139]	uncertain significance	15	41504349	41504349	Human		name
597644317	CV3699779	single nucleotide variant	NM_002344.6(LTK):c.1934C>T (p.Ala645Val)	not specified [RCV004942142]	uncertain significance	15	41505056	41505056	Human		name
597644313	CV3699780	single nucleotide variant	NM_002344.6(LTK):c.1037G>A (p.Gly346Glu)	not specified [RCV004942143]	uncertain significance	15	41509090	41509090	Human		name
597644306	CV3699782	single nucleotide variant	NM_002344.6(LTK):c.2035A>G (p.Arg679Gly)	not specified [RCV004942144]	uncertain significance	15	41504858	41504858	Human		name
597644300	CV3699783	single nucleotide variant	NM_002344.6(LTK):c.1763T>G (p.Ile588Ser)	not specified [RCV004942145]	uncertain significance	15	41505465	41505465	Human		name
598163436	CV3981274	single nucleotide variant	NM_002344.6(LTK):c.1237G>A (p.Val413Ile)	not specified [RCV005368827]	likely benign	15	41508081	41508081	Human		name
598224203	CV3981275	single nucleotide variant	NM_002344.6(LTK):c.1537C>T (p.Leu513Phe)	not specified [RCV005380171]	uncertain significance	15	41507099	41507099	Human		name
598163441	CV3981276	single nucleotide variant	NM_002344.6(LTK):c.1838C>T (p.Ser613Leu)	not specified [RCV005368828]	uncertain significance	15	41505295	41505295	Human		name
598163447	CV3981277	single nucleotide variant	NM_002344.6(LTK):c.1645C>T (p.Leu549Phe)	not specified [RCV005368829]	uncertain significance	15	41505765	41505765	Human		name
598224220	CV3981279	single nucleotide variant	NM_002344.6(LTK):c.2330T>G (p.Leu777Arg)	not specified [RCV005380173]	uncertain significance	15	41504358	41504358	Human		name
598163459	CV3981281	single nucleotide variant	NM_002344.6(LTK):c.2577T>G (p.Asn859Lys)	not specified [RCV005368831]	uncertain significance	15	41504014	41504014	Human		name
598224227	CV3981282	single nucleotide variant	NM_002344.6(LTK):c.1824C>G (p.His608Gln)	not specified [RCV005380174]	uncertain significance	15	41505404	41505404	Human		name
598163465	CV3981283	single nucleotide variant	NM_002344.6(LTK):c.1694T>C (p.Ile565Thr)	not specified [RCV005368832]	uncertain significance	15	41505716	41505716	Human		name
617151539	CV4021851	single nucleotide variant	NM_002344.6(LTK):c.1131G>C (p.Arg377Ser)	not provided [RCV005426812]	uncertain significance	15	41508187	41508187	Human		name
14396845	CV613007	single nucleotide variant	NM_002344.6(LTK):c.2447G>C (p.Arg816Thr)	not provided [RCV000761904]	uncertain significance	15	41504144	41504144	Human		name
15171320	CV714419	single nucleotide variant	NM_002344.6(LTK):c.2437G>T (p.Glu813Ter)	not provided [RCV000972175]	likely benign	15	41504154	41504154	Human		name
15141621	CV714420	single nucleotide variant	NM_002344.6(LTK):c.1705C>A (p.Arg569Ser)	not provided [RCV000966335]	benign	15	41505523	41505523	Human		name
8635433	CV90654	single nucleotide variant	NM_001135685.1(LTK):c.429C>T (p.Phe143=)	Malignant melanoma [RCV000070752]	not provided	15	41512196	41512196	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

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