Llgl2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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169 records found for search term Llgl2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15201547	CV778294	single nucleotide variant	NM_001031803.2(LLGL2):c.1875-5C>G	not provided [RCV000957653]	benign	17	75570343	75570343	Human		name
401766402	CV2725519	single nucleotide variant	NM_001031803.2(LLGL2):c.5G>C (p.Arg2Thr)	not specified [RCV004320138]	uncertain significance	17	75543431	75543431	Human		name
401764295	CV2725520	single nucleotide variant	NM_001031803.2(LLGL2):c.6G>T (p.Arg2Ser)	not specified [RCV004320139]	uncertain significance	17	75543432	75543432	Human		name
598237775	CV3980963	single nucleotide variant	NM_001031803.2(LLGL2):c.7C>T (p.Arg3Trp)	not specified [RCV005364138]	uncertain significance	17	75543433	75543433	Human		name
155925894	CV2208062	single nucleotide variant	NM_001031803.2(LLGL2):c.98A>G (p.His33Arg)	not specified [RCV004086754]	uncertain significance	17	75556068	75556068	Human		name
156290274	CV2342567	single nucleotide variant	NM_001031803.2(LLGL2):c.52C>T (p.Arg18Trp)	not specified [RCV004196661]	uncertain significance	17	75543478	75543478	Human		name
401898599	CV2782528	single nucleotide variant	NM_001031803.2(LLGL2):c.37C>T (p.Arg13Trp)	not specified [RCV004359567]	uncertain significance	17	75543463	75543463	Human		name
407461032	CV3449149	single nucleotide variant	NM_001031803.2(LLGL2):c.53G>A (p.Arg18Gln)	not specified [RCV004634021]	uncertain significance	17	75543479	75543479	Human		name
15120599	CV741021	single nucleotide variant	NM_001031803.2(LLGL2):c.735C>T (p.Leu245=)	not provided [RCV000895921]	benign	17	75563372	75563372	Human		name
155924990	CV2220417	single nucleotide variant	NM_001031803.2(LLGL2):c.113T>C (p.Leu38Pro)	not specified [RCV004095820]	uncertain significance	17	75556083	75556083	Human		name
156061525	CV2263142	single nucleotide variant	NM_001031803.2(LLGL2):c.188G>T (p.Gly63Val)	not specified [RCV004131379]	uncertain significance	17	75558169	75558169	Human		name
155977608	CV2338799	single nucleotide variant	NM_001031803.2(LLGL2):c.125C>T (p.Pro42Leu)	not specified [RCV004182357]	uncertain significance	17	75556095	75556095	Human		name
329367280	CV2456750	single nucleotide variant	NM_001031803.2(LLGL2):c.218A>G (p.Asn73Ser)	not specified [RCV004270727]	uncertain significance	17	75558199	75558199	Human		name
329393152	CV2466730	single nucleotide variant	NM_001031803.2(LLGL2):c.121A>G (p.Ser41Gly)	not specified [RCV004280688]	uncertain significance	17	75556091	75556091	Human		name
405809403	CV3287543	single nucleotide variant	NM_001031803.2(LLGL2):c.133C>T (p.Arg45Cys)	not specified [RCV004407505]	uncertain significance	17	75556103	75556103	Human		name
405809405	CV3287544	single nucleotide variant	NM_001031803.2(LLGL2):c.155G>A (p.Arg52His)	not specified [RCV004407506]	uncertain significance	17	75556125	75556125	Human		name
405809426	CV3287554	single nucleotide variant	NM_001031803.2(LLGL2):c.2325G>A (p.Pro775=)	not specified [RCV004407516]	likely benign	17	75571929	75571929	Human		name
405809437	CV3287559	single nucleotide variant	NM_001031803.2(LLGL2):c.269C>T (p.Thr90Ile)	not specified [RCV004407521]	uncertain significance	17	75558525	75558525	Human		name
407461044	CV3449156	single nucleotide variant	NM_001031803.2(LLGL2):c.226G>A (p.Val76Met)	not specified [RCV004634024]	uncertain significance	17	75558207	75558207	Human		name
597623135	CV3693230	single nucleotide variant	NM_001031803.2(LLGL2):c.230C>A (p.Thr77Lys)	not specified [RCV004936168]	uncertain significance	17	75558211	75558211	Human		name
597623136	CV3693232	single nucleotide variant	NM_001031803.2(LLGL2):c.154C>T (p.Arg52Cys)	not specified [RCV004936169]	uncertain significance	17	75556124	75556124	Human		name
598237785	CV3980965	single nucleotide variant	NM_001031803.2(LLGL2):c.274C>G (p.Leu92Val)	not specified [RCV005364140]	uncertain significance	17	75558530	75558530	Human		name
598260998	CV3980974	single nucleotide variant	NM_001031803.2(LLGL2):c.250G>C (p.Gly84Arg)	not specified [RCV005347742]	uncertain significance	17	75558231	75558231	Human		name
598261009	CV3980980	single nucleotide variant	NM_001031803.2(LLGL2):c.223G>A (p.Ala75Thr)	not specified [RCV005347744]	uncertain significance	17	75558204	75558204	Human		name
15148061	CV715704	single nucleotide variant	NM_001031803.2(LLGL2):c.1464C>T (p.Pro488=)	not provided [RCV000967468]	benign	17	75569119	75569119	Human		name
15196446	CV756116	single nucleotide variant	NM_001031803.2(LLGL2):c.2745C>T (p.Pro915=)	not provided [RCV000911698]	benign	17	75573500	75573500	Human		name
156065806	CV2225412	single nucleotide variant	NM_001031803.2(LLGL2):c.856A>G (p.Ile286Val)	not specified [RCV004100817]	uncertain significance	17	75563781	75563781	Human		name
155923892	CV2248636	single nucleotide variant	NM_001031803.2(LLGL2):c.500G>A (p.Arg167Gln)	not specified [RCV004121819]	uncertain significance	17	75559380	75559380	Human		name
156154535	CV2266082	single nucleotide variant	NM_001031803.2(LLGL2):c.686G>A (p.Ser229Asn)	not specified [RCV004126892]	uncertain significance	17	75563171	75563171	Human		name
156061701	CV2280487	single nucleotide variant	NM_001031803.2(LLGL2):c.989C>T (p.Ser330Phe)	not specified [RCV004142692]	uncertain significance	17	75564460	75564460	Human		name
156208158	CV2298099	single nucleotide variant	NM_001031803.2(LLGL2):c.721G>A (p.Asp241Asn)	not specified [RCV004157984]	uncertain significance	17	75563358	75563358	Human		name
155965002	CV2330520	single nucleotide variant	NM_001031803.2(LLGL2):c.499C>T (p.Arg167Trp)	not specified [RCV004181084]	uncertain significance	17	75559379	75559379	Human		name
156383318	CV2361499	single nucleotide variant	NM_001031803.2(LLGL2):c.557G>A (p.Arg186His)	not specified [RCV004221137]	uncertain significance	17	75563042	75563042	Human		name
156258019	CV2395322	single nucleotide variant	NM_001031803.2(LLGL2):c.560T>G (p.Val187Gly)	not specified [RCV004239418]	uncertain significance	17	75563045	75563045	Human		name
156170572	CV2400591	single nucleotide variant	NM_001031803.2(LLGL2):c.457G>A (p.Val153Met)	not specified [RCV004246771]	uncertain significance	17	75559337	75559337	Human		name
329372872	CV2433988	single nucleotide variant	NM_001031803.2(LLGL2):c.958G>A (p.Asp320Asn)	not specified [RCV004249894]	likely benign	17	75564429	75564429	Human		name
329365284	CV2440223	single nucleotide variant	NM_001031803.2(LLGL2):c.874A>G (p.Arg292Gly)	not specified [RCV004260669]	uncertain significance	17	75563799	75563799	Human		name
329352237	CV2452124	single nucleotide variant	NM_001031803.2(LLGL2):c.796C>A (p.Pro266Thr)	not specified [RCV004278841]	uncertain significance	17	75563433	75563433	Human		name
401739057	CV2708299	single nucleotide variant	NM_001031803.2(LLGL2):c.319G>A (p.Gly107Arg)	not specified [RCV004311636]	uncertain significance	17	75558575	75558575	Human		name
401750658	CV2715719	single nucleotide variant	NM_001031803.2(LLGL2):c.934C>T (p.Arg312Cys)	not specified [RCV004328864]	uncertain significance	17	75564405	75564405	Human		name
405809444	CV3287562	single nucleotide variant	NM_001031803.2(LLGL2):c.3000C>T (p.Ser1000=)	not specified [RCV004407524]	likely benign	17	75574613	75574613	Human		name
405809448	CV3287564	single nucleotide variant	NM_001031803.2(LLGL2):c.3027C>T (p.Ala1009=)	not specified [RCV004407526]	likely benign	17	75574640	75574640	Human		name
405809454	CV3287567	single nucleotide variant	NM_001031803.2(LLGL2):c.310G>T (p.Val104Phe)	not specified [RCV004407529]	uncertain significance	17	75558566	75558566	Human		name
405809456	CV3287568	single nucleotide variant	NM_001031803.2(LLGL2):c.326C>T (p.Ser109Leu)	not specified [RCV004407530]	uncertain significance	17	75558582	75558582	Human		name
405809458	CV3287569	single nucleotide variant	NM_001031803.2(LLGL2):c.443C>T (p.Thr148Ile)	not specified [RCV004407531]	uncertain significance	17	75559323	75559323	Human		name
405809463	CV3287571	single nucleotide variant	NM_001031803.2(LLGL2):c.445G>A (p.Glu149Lys)	not specified [RCV004407533]	uncertain significance	17	75559325	75559325	Human		name
405809465	CV3287572	single nucleotide variant	NM_001031803.2(LLGL2):c.751G>A (p.Asp251Asn)	not specified [RCV004407534]	uncertain significance	17	75563388	75563388	Human		name
405809467	CV3287573	single nucleotide variant	NM_001031803.2(LLGL2):c.784G>A (p.Glu262Lys)	not specified [RCV004407535]	uncertain significance	17	75563421	75563421	Human		name
405809469	CV3287574	single nucleotide variant	NM_001031803.2(LLGL2):c.841A>C (p.Lys281Gln)	not specified [RCV004407536]	uncertain significance	17	75563766	75563766	Human		name
407470706	CV3449154	single nucleotide variant	NM_001031803.2(LLGL2):c.724G>A (p.Gly242Ser)	not specified [RCV004637173]	uncertain significance	17	75563361	75563361	Human		name
407470725	CV3449161	single nucleotide variant	NM_001031803.2(LLGL2):c.475C>A (p.Pro159Thr)	not specified [RCV004637178]	uncertain significance	17	75559355	75559355	Human		name
597623116	CV3693214	single nucleotide variant	NM_001031803.2(LLGL2):c.727C>T (p.Arg243Cys)	not specified [RCV004936153]	uncertain significance	17	75563364	75563364	Human		name
597623124	CV3693219	single nucleotide variant	NM_001031803.2(LLGL2):c.505A>T (p.Ile169Phe)	not specified [RCV004936158]	uncertain significance	17	75559385	75559385	Human		name
597623130	CV3693225	single nucleotide variant	NM_001031803.2(LLGL2):c.808C>T (p.Arg270Cys)	not specified [RCV004936163]	uncertain significance	17	75563445	75563445	Human		name
598260974	CV3980966	single nucleotide variant	NM_001031803.2(LLGL2):c.994G>A (p.Val332Ile)	not specified [RCV005347737]	uncertain significance	17	75564465	75564465	Human		name
598237791	CV3980968	single nucleotide variant	NM_001031803.2(LLGL2):c.512C>T (p.Ser171Leu)	not specified [RCV005364141]	uncertain significance	17	75559392	75559392	Human		name
598260994	CV3980971	single nucleotide variant	NM_001031803.2(LLGL2):c.928G>A (p.Gly310Arg)	not specified [RCV005347741]	uncertain significance	17	75564399	75564399	Human		name
598237845	CV3980983	single nucleotide variant	NM_001031803.2(LLGL2):c.740G>C (p.Ser247Thr)	not specified [RCV005364150]	uncertain significance	17	75563377	75563377	Human		name
155962622	CV2197609	single nucleotide variant	NM_001031803.2(LLGL2):c.2213A>C (p.Asn738Thr)	not specified [RCV004074826]	uncertain significance	17	75571703	75571703	Human		name
156074062	CV2201450	single nucleotide variant	NM_001031803.2(LLGL2):c.2581G>A (p.Glu861Lys)	not specified [RCV004079603]	uncertain significance	17	75573134	75573134	Human		name
156192884	CV2202434	single nucleotide variant	NM_001031803.2(LLGL2):c.2902G>A (p.Glu968Lys)	not specified [RCV004080742]	uncertain significance	17	75573977	75573977	Human		name
156093548	CV2217013	single nucleotide variant	NM_001031803.2(LLGL2):c.2237C>T (p.Ser746Phe)	not specified [RCV004085371]	uncertain significance	17	75571727	75571727	Human		name
156400778	CV2217162	single nucleotide variant	NM_001031803.2(LLGL2):c.1280G>C (p.Ser427Thr)	not specified [RCV004087621]	uncertain significance	17	75568797	75568797	Human		name
156245327	CV2218966	single nucleotide variant	NM_001031803.2(LLGL2):c.1387C>T (p.Leu463Phe)	not specified [RCV004087148]	uncertain significance	17	75569042	75569042	Human		name
156382014	CV2227150	single nucleotide variant	NM_001031803.2(LLGL2):c.2675G>A (p.Arg892Gln)	not specified [RCV004091764]	uncertain significance	17	75573228	75573228	Human		name
156384703	CV2231163	single nucleotide variant	NM_001031803.2(LLGL2):c.2155G>A (p.Ala719Thr)	not specified [RCV004094371]	uncertain significance	17	75571079	75571079	Human		name
156017257	CV2266690	single nucleotide variant	NM_001031803.2(LLGL2):c.1447G>A (p.Gly483Ser)	not specified [RCV004131221]	uncertain significance	17	75569102	75569102	Human		name
156341286	CV2268244	single nucleotide variant	NM_001031803.2(LLGL2):c.2183G>A (p.Arg728Gln)	not specified [RCV004138546]	uncertain significance	17	75571673	75571673	Human		name
155929269	CV2278035	single nucleotide variant	NM_001031803.2(LLGL2):c.2507C>T (p.Thr836Met)	not specified [RCV004141262]	uncertain significance	17	75573060	75573060	Human		name
155906687	CV2279371	single nucleotide variant	NM_001031803.2(LLGL2):c.1450G>A (p.Glu484Lys)	not specified [RCV004141925]	uncertain significance	17	75569105	75569105	Human		name
156130045	CV2279760	single nucleotide variant	NM_001031803.2(LLGL2):c.2606A>C (p.Asn869Thr)	not specified [RCV004144374]	uncertain significance	17	75573159	75573159	Human		name
156171711	CV2293197	single nucleotide variant	NM_001031803.2(LLGL2):c.2933G>A (p.Arg978His)	not specified [RCV004150708]	likely benign	17	75574240	75574240	Human		name
156200475	CV2313075	single nucleotide variant	NM_001031803.2(LLGL2):c.2846C>T (p.Ala949Val)	not specified [RCV004161349]	uncertain significance	17	75573601	75573601	Human		name
156274042	CV2319930	single nucleotide variant	NM_001031803.2(LLGL2):c.2882C>T (p.Ser961Leu)	not specified [RCV004167808]	uncertain significance	17	75573957	75573957	Human		name
155975550	CV2327816	single nucleotide variant	NM_001031803.2(LLGL2):c.2648C>T (p.Pro883Leu)	not specified [RCV004179156]	uncertain significance	17	75573201	75573201	Human		name
156074121	CV2331634	single nucleotide variant	NM_001031803.2(LLGL2):c.1966C>T (p.Arg656Trp)	not specified [RCV004184268]	uncertain significance	17	75570439	75570439	Human		name
156193040	CV2344169	single nucleotide variant	NM_001031803.2(LLGL2):c.2936C>T (p.Ala979Val)	not specified [RCV004195766]	uncertain significance	17	75574243	75574243	Human		name
155937224	CV2379981	single nucleotide variant	NM_001031803.2(LLGL2):c.2842G>A (p.Gly948Ser)	not specified [RCV004222123]	uncertain significance	17	75573597	75573597	Human		name
156081512	CV2384757	single nucleotide variant	NM_001031803.2(LLGL2):c.2657G>A (p.Arg886His)	not specified [RCV004232523]	uncertain significance	17	75573210	75573210	Human		name
155959388	CV2390522	single nucleotide variant	NM_001031803.2(LLGL2):c.2992C>T (p.Arg998Cys)	not specified [RCV004239058]	uncertain significance	17	75574491	75574491	Human		name
156190965	CV2391224	single nucleotide variant	NM_001031803.2(LLGL2):c.1427A>G (p.Asn476Ser)	not specified [RCV004237239]	likely benign	17	75569082	75569082	Human		name
329356691	CV2430859	single nucleotide variant	NM_001031803.2(LLGL2):c.1976G>A (p.Arg659Gln)	not specified [RCV004254031]	uncertain significance	17	75570449	75570449	Human		name
329383950	CV2434925	single nucleotide variant	NM_001031803.2(LLGL2):c.1412C>T (p.Thr471Ile)	not specified [RCV004250796]	uncertain significance	17	75569067	75569067	Human		name
329387075	CV2436249	single nucleotide variant	NM_001031803.2(LLGL2):c.1219G>A (p.Ala407Thr)	not specified [RCV004251664]	uncertain significance	17	75568658	75568658	Human		name
329375849	CV2441163	single nucleotide variant	NM_001031803.2(LLGL2):c.1009G>C (p.Val337Leu)	not specified [RCV004263561]	uncertain significance	17	75564480	75564480	Human		name
329388682	CV2447764	single nucleotide variant	NM_001031803.2(LLGL2):c.2252C>T (p.Pro751Leu)	not specified [RCV004258545]	uncertain significance	17	75571742	75571742	Human		name
329389231	CV2448818	single nucleotide variant	NM_001031803.2(LLGL2):c.1686G>C (p.Glu562Asp)	not specified [RCV004261506]	uncertain significance	17	75570067	75570067	Human		name
329387383	CV2464171	single nucleotide variant	NM_001031803.2(LLGL2):c.2561G>A (p.Arg854His)	not specified [RCV004273853]	uncertain significance	17	75573114	75573114	Human		name
329376006	CV2467431	single nucleotide variant	NM_001031803.2(LLGL2):c.1306G>T (p.Asp436Tyr)	not specified [RCV004287046]	uncertain significance	17	75568823	75568823	Human		name
401721455	CV2673721	single nucleotide variant	NM_001031803.2(LLGL2):c.1249A>G (p.Thr417Ala)	not specified [RCV004282448]	uncertain significance	17	75568688	75568688	Human		name
401741869	CV2676544	single nucleotide variant	NM_001031803.2(LLGL2):c.1118C>T (p.Pro373Leu)	not specified [RCV004288732]	uncertain significance	17	75568557	75568557	Human		name
401729292	CV2683632	single nucleotide variant	NM_001031803.2(LLGL2):c.1964G>A (p.Arg655His)	not specified [RCV004282551]	uncertain significance	17	75570437	75570437	Human		name
401731586	CV2693883	single nucleotide variant	NM_001031803.2(LLGL2):c.1414G>A (p.Asp472Asn)	not specified [RCV004300183]	uncertain significance	17	75569069	75569069	Human		name
401776987	CV2711580	single nucleotide variant	NM_001031803.2(LLGL2):c.1963C>T (p.Arg655Cys)	not specified [RCV004306887]	uncertain significance	17	75570436	75570436	Human		name
401784315	CV2721261	single nucleotide variant	NM_001031803.2(LLGL2):c.2569G>A (p.Glu857Lys)	not specified [RCV004330185]	uncertain significance	17	75573122	75573122	Human		name
401764126	CV2725445	single nucleotide variant	NM_001031803.2(LLGL2):c.1549G>A (p.Gly517Ser)	not specified [RCV004320080]	uncertain significance	17	75569293	75569293	Human		name
401864760	CV2761035	single nucleotide variant	NM_001031803.2(LLGL2):c.1715G>A (p.Arg572His)	not specified [RCV004338702]	likely benign	17	75570096	75570096	Human		name
401876540	CV2761097	single nucleotide variant	NM_001031803.2(LLGL2):c.1856G>T (p.Arg619Leu)	not specified [RCV004338756]	uncertain significance	17	75570237	75570237	Human		name
401893494	CV2765335	single nucleotide variant	NM_001031803.2(LLGL2):c.2531G>A (p.Arg844Gln)	not specified [RCV004339846]	uncertain significance	17	75573084	75573084	Human		name
401890895	CV2768793	single nucleotide variant	NM_001031803.2(LLGL2):c.2332G>A (p.Gly778Ser)	not specified [RCV004346925]	uncertain significance	17	75571936	75571936	Human		name
401897659	CV2776636	single nucleotide variant	NM_001031803.2(LLGL2):c.2872G>A (p.Ala958Thr)	not specified [RCV004357507]	uncertain significance	17	75573627	75573627	Human		name
401894208	CV2780446	single nucleotide variant	NM_001031803.2(LLGL2):c.2321C>T (p.Ala774Val)	not specified [RCV004358148]	uncertain significance	17	75571925	75571925	Human		name
401888212	CV2788140	single nucleotide variant	NM_001031803.2(LLGL2):c.1973G>A (p.Arg658His)	not specified [RCV004352759]	uncertain significance	17	75570446	75570446	Human		name
401877059	CV2793333	single nucleotide variant	NM_001031803.2(LLGL2):c.2579G>C (p.Gly860Ala)	not specified [RCV004362146]	uncertain significance	17	75573132	75573132	Human		name
405809401	CV3287542	single nucleotide variant	NM_001031803.2(LLGL2):c.1337C>T (p.Thr446Met)	not specified [RCV004407504]	uncertain significance	17	75568992	75568992	Human		name
405809407	CV3287545	single nucleotide variant	NM_001031803.2(LLGL2):c.1655A>G (p.Asp552Gly)	not specified [RCV004407507]	uncertain significance	17	75570036	75570036	Human		name
405809409	CV3287546	single nucleotide variant	NM_001031803.2(LLGL2):c.1763C>T (p.Pro588Leu)	not specified [RCV004407508]	uncertain significance	17	75570144	75570144	Human		name
405809412	CV3287547	single nucleotide variant	NM_001031803.2(LLGL2):c.1769T>C (p.Val590Ala)	not specified [RCV004407509]	uncertain significance	17	75570150	75570150	Human		name
405809414	CV3287548	single nucleotide variant	NM_001031803.2(LLGL2):c.1802G>A (p.Arg601Gln)	not specified [RCV004407510]	uncertain significance	17	75570183	75570183	Human		name
405809416	CV3287549	single nucleotide variant	NM_001031803.2(LLGL2):c.1859G>A (p.Arg620Gln)	not specified [RCV004407511]	uncertain significance	17	75570240	75570240	Human		name
405809420	CV3287551	single nucleotide variant	NM_001031803.2(LLGL2):c.2006C>T (p.Pro669Leu)	not specified [RCV004407513]	uncertain significance	17	75570479	75570479	Human		name
405809422	CV3287552	single nucleotide variant	NM_001031803.2(LLGL2):c.2054G>A (p.Arg685Gln)	not specified [RCV004407514]	uncertain significance	17	75570978	75570978	Human		name
405809424	CV3287553	single nucleotide variant	NM_001031803.2(LLGL2):c.2281C>T (p.Arg761Trp)	not specified [RCV004407515]	uncertain significance	17	75571771	75571771	Human		name
405809428	CV3287555	single nucleotide variant	NM_001031803.2(LLGL2):c.2440G>A (p.Val814Ile)	not specified [RCV004407517]	uncertain significance	17	75572044	75572044	Human		name
405809431	CV3287556	single nucleotide variant	NM_001031803.2(LLGL2):c.2564G>A (p.Arg855Gln)	not specified [RCV004407518]	uncertain significance	17	75573117	75573117	Human		name
405809433	CV3287557	single nucleotide variant	NM_001031803.2(LLGL2):c.2579G>T (p.Gly860Val)	not specified [RCV004407519]	uncertain significance	17	75573132	75573132	Human		name
405809435	CV3287558	single nucleotide variant	NM_001031803.2(LLGL2):c.2690G>C (p.Gly897Ala)	not specified [RCV004407520]	uncertain significance	17	75573243	75573243	Human		name
405809439	CV3287560	single nucleotide variant	NM_001031803.2(LLGL2):c.2945G>C (p.Ser982Thr)	not specified [RCV004407522]	uncertain significance	17	75574252	75574252	Human		name
405809441	CV3287561	single nucleotide variant	NM_001031803.2(LLGL2):c.2947G>A (p.Asp983Asn)	not specified [RCV004407523]	uncertain significance	17	75574254	75574254	Human		name
407470682	CV3449146	single nucleotide variant	NM_001031803.2(LLGL2):c.1456G>A (p.Glu486Lys)	not specified [RCV004637167]	uncertain significance	17	75569111	75569111	Human		name
407470686	CV3449147	single nucleotide variant	NM_001031803.2(LLGL2):c.2732A>T (p.Tyr911Phe)	not specified [RCV004637168]	uncertain significance	17	75573487	75573487	Human		name
407470690	CV3449148	single nucleotide variant	NM_001031803.2(LLGL2):c.1025A>G (p.Asp342Gly)	not specified [RCV004637169]	uncertain significance	17	75564496	75564496	Human		name
407461037	CV3449150	single nucleotide variant	NM_001031803.2(LLGL2):c.1542G>T (p.Lys514Asn)	not specified [RCV004634022]	uncertain significance	17	75569286	75569286	Human		name
407470694	CV3449151	single nucleotide variant	NM_001031803.2(LLGL2):c.1994G>A (p.Arg665Gln)	not specified [RCV004637170]	uncertain significance	17	75570467	75570467	Human		name
407470697	CV3449152	single nucleotide variant	NM_001031803.2(LLGL2):c.2653G>C (p.Val885Leu)	not specified [RCV004637171]	uncertain significance	17	75573206	75573206	Human		name
407470701	CV3449153	single nucleotide variant	NM_001031803.2(LLGL2):c.1925G>A (p.Arg642His)	not specified [RCV004637172]	uncertain significance	17	75570398	75570398	Human		name
407461041	CV3449155	single nucleotide variant	NM_001031803.2(LLGL2):c.2892G>C (p.Gln964His)	not specified [RCV004634023]	uncertain significance	17	75573967	75573967	Human		name
407470710	CV3449157	single nucleotide variant	NM_001031803.2(LLGL2):c.2574C>G (p.Asp858Glu)	not specified [RCV004637174]	uncertain significance	17	75573127	75573127	Human		name
407470717	CV3449159	single nucleotide variant	NM_001031803.2(LLGL2):c.2036G>A (p.Gly679Glu)	not specified [RCV004637176]	uncertain significance	17	75570960	75570960	Human		name
407470721	CV3449160	single nucleotide variant	NM_001031803.2(LLGL2):c.2944A>T (p.Ser982Cys)	not specified [RCV004637177]	uncertain significance	17	75574251	75574251	Human		name
597623120	CV3693216	single nucleotide variant	NM_001031803.2(LLGL2):c.1445A>G (p.Gln482Arg)	not specified [RCV004936155]	uncertain significance	17	75569100	75569100	Human		name
597623121	CV3693217	single nucleotide variant	NM_001031803.2(LLGL2):c.2261G>A (p.Arg754Gln)	not specified [RCV004936156]	uncertain significance	17	75571751	75571751	Human		name
597623123	CV3693218	single nucleotide variant	NM_001031803.2(LLGL2):c.1429G>A (p.Glu477Lys)	not specified [RCV004936157]	uncertain significance	17	75569084	75569084	Human		name
597623126	CV3693220	single nucleotide variant	NM_001031803.2(LLGL2):c.2683G>A (p.Val895Ile)	not specified [RCV004936159]	uncertain significance	17	75573236	75573236	Human		name
597623127	CV3693221	single nucleotide variant	NM_001031803.2(LLGL2):c.1517G>A (p.Gly506Asp)	not specified [RCV004936160]	uncertain significance	17	75569261	75569261	Human		name
597623128	CV3693222	single nucleotide variant	NM_001031803.2(LLGL2):c.2365C>T (p.Leu789Phe)	not specified [RCV004936161]	uncertain significance	17	75571969	75571969	Human		name
597623129	CV3693224	single nucleotide variant	NM_001031803.2(LLGL2):c.2258A>T (p.Glu753Val)	not specified [RCV004936162]	uncertain significance	17	75571748	75571748	Human		name
597623131	CV3693226	single nucleotide variant	NM_001031803.2(LLGL2):c.1175A>T (p.His392Leu)	not specified [RCV004936164]	uncertain significance	17	75568614	75568614	Human		name
597623132	CV3693227	single nucleotide variant	NM_001031803.2(LLGL2):c.2726G>T (p.Gly909Val)	not specified [RCV004936165]	uncertain significance	17	75573481	75573481	Human		name
597623133	CV3693228	single nucleotide variant	NM_001031803.2(LLGL2):c.1135C>G (p.Leu379Val)	not specified [RCV004936166]	uncertain significance	17	75568574	75568574	Human		name
597623134	CV3693229	single nucleotide variant	NM_001031803.2(LLGL2):c.1333G>A (p.Gly445Ser)	not specified [RCV004936167]	uncertain significance	17	75568988	75568988	Human		name
597795890	CV3693231	single nucleotide variant	NM_001031803.2(LLGL2):c.1154C>T (p.Ser385Phe)	not specified [RCV004935029]	uncertain significance	17	75568593	75568593	Human		name
598260969	CV3980959	single nucleotide variant	NM_001031803.2(LLGL2):c.1237G>A (p.Ala413Thr)	not specified [RCV005347736]	likely benign	17	75568676	75568676	Human		name
598237758	CV3980960	single nucleotide variant	NM_001031803.2(LLGL2):c.2671C>T (p.Arg891Cys)	not specified [RCV005364135]	uncertain significance	17	75573224	75573224	Human		name
598237763	CV3980961	single nucleotide variant	NM_001031803.2(LLGL2):c.1177G>A (p.Val393Ile)	not specified [RCV005364136]	uncertain significance	17	75568616	75568616	Human		name
598237781	CV3980964	single nucleotide variant	NM_001031803.2(LLGL2):c.2554G>A (p.Gly852Ser)	not specified [RCV005364139]	uncertain significance	17	75573107	75573107	Human		name
598260979	CV3980967	single nucleotide variant	NM_001031803.2(LLGL2):c.2993G>A (p.Arg998His)	not specified [RCV005347738]	uncertain significance	17	75574492	75574492	Human		name
598260984	CV3980969	single nucleotide variant	NM_001031803.2(LLGL2):c.1571C>T (p.Thr524Met)	not specified [RCV005347739]	uncertain significance	17	75569315	75569315	Human		name
598260989	CV3980970	single nucleotide variant	NM_001031803.2(LLGL2):c.1019A>G (p.Glu340Gly)	not specified [RCV005347740]	uncertain significance	17	75564490	75564490	Human		name
598237803	CV3980973	single nucleotide variant	NM_001031803.2(LLGL2):c.1952G>A (p.Arg651His)	not specified [RCV005364143]	uncertain significance	17	75570425	75570425	Human		name
598237808	CV3980975	single nucleotide variant	NM_001031803.2(LLGL2):c.1684G>A (p.Glu562Lys)	not specified [RCV005364144]	uncertain significance	17	75570065	75570065	Human		name
598237814	CV3980976	single nucleotide variant	NM_001031803.2(LLGL2):c.1601A>G (p.Asn534Ser)	not specified [RCV005364145]	uncertain significance	17	75569982	75569982	Human		name
598237821	CV3980977	single nucleotide variant	NM_001031803.2(LLGL2):c.1123C>A (p.Gln375Lys)	not specified [RCV005364146]	uncertain significance	17	75568562	75568562	Human		name
598261003	CV3980979	single nucleotide variant	NM_001031803.2(LLGL2):c.2078T>C (p.Leu693Pro)	not specified [RCV005347743]	uncertain significance	17	75571002	75571002	Human		name
598237840	CV3980982	single nucleotide variant	NM_001031803.2(LLGL2):c.2113G>T (p.Ala705Ser)	not specified [RCV005364149]	uncertain significance	17	75571037	75571037	Human		name
598230428	CV3980984	single nucleotide variant	NM_001031803.2(LLGL2):c.2356A>G (p.Ser786Gly)	not specified [RCV005362703]	uncertain significance	17	75571960	75571960	Human		name
15201542	CV704373	single nucleotide variant	NM_001031803.2(LLGL2):c.1632G>C (p.Gln544His)	not provided [RCV000957652]	benign	17	75570013	75570013	Human		name
15201550	CV704374	single nucleotide variant	NM_001031803.2(LLGL2):c.1915C>T (p.Pro639Ser)	not provided [RCV000957654]	benign	17	75570388	75570388	Human		name
15164882	CV704375	single nucleotide variant	NM_001031803.2(LLGL2):c.2230G>A (p.Ala744Thr)	not provided [RCV000948455]	benign\|likely benign	17	75571720	75571720	Human		name
15196441	CV756115	single nucleotide variant	NM_001031803.2(LLGL2):c.2243G>A (p.Arg748His)	not provided [RCV000911697]	benign	17	75571733	75571733	Human		name
155919755	CV2202772	single nucleotide variant	NM_001031803.2(LLGL2):c.3020G>C (p.Arg1007Pro)	not specified [RCV004083011]	uncertain significance	17	75574633	75574633	Human		name
155964268	CV2261601	single nucleotide variant	NM_001031803.2(LLGL2):c.3047A>G (p.Asn1016Ser)	not specified [RCV004125930]	uncertain significance	17	75574660	75574660	Human		name
156047033	CV2304314	single nucleotide variant	NM_001031803.2(LLGL2):c.3025G>A (p.Ala1009Thr)	not specified [RCV004164434]	uncertain significance	17	75574638	75574638	Human		name
329382296	CV2438704	single nucleotide variant	NM_001031803.2(LLGL2):c.3020G>A (p.Arg1007Gln)	not specified [RCV004261858]	uncertain significance	17	75574633	75574633	Human		name
405809450	CV3287565	single nucleotide variant	NM_001031803.2(LLGL2):c.3032G>C (p.Gly1011Ala)	not specified [RCV004407527]	uncertain significance	17	75574645	75574645	Human		name
405809452	CV3287566	single nucleotide variant	NM_001031803.2(LLGL2):c.3038G>A (p.Ser1013Asn)	not specified [RCV004407528]	uncertain significance	17	75574651	75574651	Human		name
407470714	CV3449158	single nucleotide variant	NM_001031803.2(LLGL2):c.3017A>G (p.His1006Arg)	not specified [RCV004637175]	uncertain significance	17	75574630	75574630	Human		name
598237828	CV3980978	single nucleotide variant	NM_001031803.2(LLGL2):c.3031G>C (p.Gly1011Arg)	not specified [RCV005364147]	uncertain significance	17	75574644	75574644	Human		name
15187394	CV727426	single nucleotide variant	NM_001031803.2(LLGL2):c.3010C>T (p.Arg1004Cys)	not provided [RCV000887242]	benign	17	75574623	75574623	Human		name

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