Nell2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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94 records found for search term Nell2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155976165	CV2231602	single nucleotide variant	NM_001145108.2(NELL2):c.-23G>A	not specified [RCV004096645]	uncertain significance	12	44875892	44875892	Human		name
8654013	CV130588	single nucleotide variant	NM_001145110.1(NELL2):c.39-7798G>A	Lung cancer [RCV000111075]	uncertain significance	12	44883698	44883698	Human		name
8654011	CV130586	single nucleotide variant	NM_001145107.1(NELL2):c.1339+1955C>T	Lung cancer [RCV000111073]	uncertain significance	12	44709337	44709337	Human		name
8654010	CV130585	single nucleotide variant	NM_001145107.1(NELL2):c.1595-25737T>C	Lung cancer [RCV000111072]	uncertain significance	12	44636707	44636707	Human		name
8654012	CV130587	single nucleotide variant	NM_001145107.1(NELL2):c.1144+20237T>A	Lung cancer [RCV000111074]	uncertain significance	12	44754510	44754510	Human		name
405668871	CV3360256	single nucleotide variant	NM_001145108.2(NELL2):c.17T>C (p.Leu6Ser)	not specified [RCV004486063]	uncertain significance	12	44875853	44875853	Human		name
156222951	CV2344019	single nucleotide variant	NM_001145108.2(NELL2):c.67G>A (p.Gly23Ser)	not specified [RCV004195632]	uncertain significance	12	44875342	44875342	Human		name
407526328	CV3454913	single nucleotide variant	NM_001145108.2(NELL2):c.29T>G (p.Phe10Cys)	not specified [RCV004654773]	uncertain significance	12	44875841	44875841	Human		name
597639145	CV3565548	single nucleotide variant	NM_001145108.2(NELL2):c.89T>C (p.Ile30Thr)	not specified [RCV004831891]	uncertain significance	12	44875320	44875320	Human		name
156295511	CV2321510	single nucleotide variant	NM_001145108.2(NELL2):c.289C>T (p.His97Tyr)	not specified [RCV004177479]	uncertain significance	12	44816032	44816032	Human		name
401742298	CV2677554	single nucleotide variant	NM_001145108.2(NELL2):c.155A>G (p.His52Arg)	not specified [RCV004291658]	uncertain significance	12	44875254	44875254	Human		name
401729955	CV2683875	single nucleotide variant	NM_001145108.2(NELL2):c.146C>T (p.Pro49Leu)	not specified [RCV004284598]	uncertain significance	12	44875263	44875263	Human		name
401768216	CV2723225	single nucleotide variant	NM_001145108.2(NELL2):c.188C>T (p.Thr63Ile)	not specified [RCV004329461]	uncertain significance	12	44816133	44816133	Human		name
401887777	CV2770433	single nucleotide variant	NM_001145108.2(NELL2):c.212C>T (p.Thr71Ile)	not specified [RCV004358074]	uncertain significance	12	44816109	44816109	Human		name
405669201	CV3360323	single nucleotide variant	NM_001145108.2(NELL2):c.113T>C (p.Leu38Pro)	not specified [RCV004486130]	uncertain significance	12	44875296	44875296	Human		name
407526331	CV3454915	single nucleotide variant	NM_001145108.2(NELL2):c.228G>T (p.Gln76His)	not specified [RCV004654774]	uncertain significance	12	44816093	44816093	Human		name
597639123	CV3565544	single nucleotide variant	NM_001145108.2(NELL2):c.254A>G (p.His85Arg)	not specified [RCV004831887]	uncertain significance	12	44816067	44816067	Human		name
156068744	CV2237071	single nucleotide variant	NM_001145108.2(NELL2):c.613A>C (p.Met205Leu)	not specified [RCV004114832]	uncertain significance	12	44777308	44777308	Human		name
156256724	CV2264823	single nucleotide variant	NM_001145108.2(NELL2):c.674A>G (p.Asn225Ser)	not specified [RCV004134581]	uncertain significance	12	44777247	44777247	Human		name
156198628	CV2365144	single nucleotide variant	NM_001145108.2(NELL2):c.982A>G (p.Lys328Glu)	not specified [RCV004205166]	uncertain significance	12	44774759	44774759	Human		name
329359362	CV2436124	single nucleotide variant	NM_001145108.2(NELL2):c.841T>C (p.Tyr281His)	not specified [RCV004249367]	uncertain significance	12	44776072	44776072	Human		name
405669323	CV3360348	single nucleotide variant	NM_001145108.2(NELL2):c.364C>T (p.Arg122Trp)	not specified [RCV004486155]	uncertain significance	12	44779994	44779994	Human		name
405669375	CV3360359	single nucleotide variant	NM_001145108.2(NELL2):c.824C>G (p.Thr275Ser)	not specified [RCV004486166]	uncertain significance	12	44776089	44776089	Human		name
407526322	CV3454911	single nucleotide variant	NM_001145108.2(NELL2):c.593A>G (p.His198Arg)	not specified [RCV004654771]	uncertain significance	12	44779676	44779676	Human		name
407489630	CV3454914	single nucleotide variant	NM_001145108.2(NELL2):c.365G>A (p.Arg122Gln)	not specified [RCV004641504]	uncertain significance	12	44779993	44779993	Human		name
407489634	CV3454916	single nucleotide variant	NM_001145108.2(NELL2):c.613A>G (p.Met205Val)	not specified [RCV004641505]	uncertain significance	12	44777308	44777308	Human		name
407526333	CV3454917	single nucleotide variant	NM_001145108.2(NELL2):c.424C>T (p.Pro142Ser)	not specified [RCV004654775]	uncertain significance	12	44779934	44779934	Human		name
407526336	CV3454918	single nucleotide variant	NM_001145108.2(NELL2):c.644A>T (p.Gln215Leu)	not specified [RCV004654776]	uncertain significance	12	44777277	44777277	Human		name
597639129	CV3565545	single nucleotide variant	NM_001145108.2(NELL2):c.946A>C (p.Lys316Gln)	not specified [RCV004831888]	uncertain significance	12	44774795	44774795	Human		name
597639196	CV3565558	single nucleotide variant	NM_001145108.2(NELL2):c.818C>G (p.Thr273Ser)	not specified [RCV004831901]	uncertain significance	12	44776095	44776095	Human		name
598231999	CV3990773	single nucleotide variant	NM_001145108.2(NELL2):c.388C>T (p.Arg130Cys)	not specified [RCV005381461]	uncertain significance	12	44779970	44779970	Human		name
598232004	CV3990774	single nucleotide variant	NM_001145108.2(NELL2):c.562A>G (p.Thr188Ala)	not specified [RCV005381462]	uncertain significance	12	44779707	44779707	Human		name
598232016	CV3990777	single nucleotide variant	NM_001145108.2(NELL2):c.832G>A (p.Gly278Arg)	not specified [RCV005381464]	uncertain significance	12	44776081	44776081	Human		name
598232021	CV3990778	single nucleotide variant	NM_001145108.2(NELL2):c.520A>G (p.Arg174Gly)	not specified [RCV005381465]	uncertain significance	12	44779749	44779749	Human		name
156320826	CV2197414	single nucleotide variant	NM_001145108.2(NELL2):c.2159A>T (p.Gln720Leu)	not specified [RCV004081152]	uncertain significance	12	44522016	44522016	Human		name
155968205	CV2216986	single nucleotide variant	NM_001145108.2(NELL2):c.1324G>T (p.Asp442Tyr)	not specified [RCV004085351]	uncertain significance	12	44665604	44665604	Human		name
156312213	CV2256835	single nucleotide variant	NM_001145108.2(NELL2):c.1886G>A (p.Arg629Gln)	not specified [RCV004121051]	uncertain significance	12	44523403	44523403	Human		name
156171159	CV2267637	single nucleotide variant	NM_001145108.2(NELL2):c.2390G>A (p.Cys797Tyr)	not specified [RCV004134188]	uncertain significance	12	44520015	44520015	Human		name
156151796	CV2268977	single nucleotide variant	NM_001145108.2(NELL2):c.2021G>A (p.Arg674Gln)	not specified [RCV004128378]	uncertain significance	12	44522154	44522154	Human		name
156209332	CV2304474	single nucleotide variant	NM_001145108.2(NELL2):c.1991C>T (p.Ser664Leu)	not specified [RCV004164563]	uncertain significance	12	44523298	44523298	Human		name
156259955	CV2305020	single nucleotide variant	NM_001145108.2(NELL2):c.1783C>T (p.Pro595Ser)	not specified [RCV004168909]	uncertain significance	12	44532602	44532602	Human		name
156153070	CV2307684	single nucleotide variant	NM_001145108.2(NELL2):c.1896T>G (p.His632Gln)	not specified [RCV004168096]	uncertain significance	12	44523393	44523393	Human		name
156096123	CV2310156	single nucleotide variant	NM_001145108.2(NELL2):c.1072C>T (p.Leu358Phe)	not specified [RCV004163267]	uncertain significance	12	44714664	44714664	Human		name
156082688	CV2333619	single nucleotide variant	NM_001145108.2(NELL2):c.1619T>C (p.Val540Ala)	not specified [RCV004192464]	uncertain significance	12	44607213	44607213	Human		name
155978011	CV2339881	single nucleotide variant	NM_001145108.2(NELL2):c.1343G>A (p.Arg448His)	not specified [RCV004189987]	uncertain significance	12	44665585	44665585	Human		name
155922803	CV2340687	single nucleotide variant	NM_001145108.2(NELL2):c.1108G>A (p.Glu370Lys)	not specified [RCV004190359]	uncertain significance	12	44711373	44711373	Human		name
156273328	CV2344111	single nucleotide variant	NM_001145108.2(NELL2):c.2055T>A (p.Asp685Glu)	not specified [RCV004195710]	uncertain significance	12	44522120	44522120	Human		name
156178104	CV2374569	single nucleotide variant	NM_001145108.2(NELL2):c.1227G>T (p.Glu409Asp)	not specified [RCV004225198]	uncertain significance	12	44703817	44703817	Human		name
329372481	CV2424107	single nucleotide variant	NM_001145108.2(NELL2):c.2330T>C (p.Met777Thr)	not specified [RCV004248009]	uncertain significance	12	44520075	44520075	Human		name
329357354	CV2431353	single nucleotide variant	NM_001145108.2(NELL2):c.1324G>A (p.Asp442Asn)	not specified [RCV004252470]	uncertain significance	12	44665604	44665604	Human		name
329387240	CV2436326	single nucleotide variant	NM_001145108.2(NELL2):c.1469A>G (p.Gln490Arg)	not specified [RCV004251726]	uncertain significance	12	44610946	44610946	Human		name
401730377	CV2680287	single nucleotide variant	NM_001145108.2(NELL2):c.1273C>G (p.Arg425Gly)	not specified [RCV004288542]	uncertain significance	12	44703771	44703771	Human		name
401760144	CV2694938	single nucleotide variant	NM_001145108.2(NELL2):c.1601C>T (p.Ala534Val)	not specified [RCV004301325]	uncertain significance	12	44607231	44607231	Human		name
401743275	CV2715441	single nucleotide variant	NM_001145108.2(NELL2):c.2032G>A (p.Asp678Asn)	not specified [RCV004324757]	uncertain significance	12	44522143	44522143	Human		name
401760713	CV2715909	single nucleotide variant	NM_001145108.2(NELL2):c.1141G>C (p.Glu381Gln)	not specified [RCV004329015]	uncertain significance	12	44711340	44711340	Human		name
401896787	CV2788782	single nucleotide variant	NM_001145108.2(NELL2):c.2311A>G (p.Lys771Glu)	not specified [RCV004361244]	uncertain significance	12	44520094	44520094	Human		name
405668696	CV3360221	single nucleotide variant	NM_001145108.2(NELL2):c.1115C>T (p.Ser372Leu)	not specified [RCV004486028]	uncertain significance	12	44711366	44711366	Human		name
405668712	CV3360224	single nucleotide variant	NM_001145108.2(NELL2):c.1123C>A (p.Pro375Thr)	not specified [RCV004486031]	uncertain significance	12	44711358	44711358	Human		name
405668774	CV3360237	single nucleotide variant	NM_001145108.2(NELL2):c.1298A>T (p.Glu433Val)	not specified [RCV004486044]	uncertain significance	12	44703746	44703746	Human		name
405668834	CV3360249	single nucleotide variant	NM_001145108.2(NELL2):c.1412G>A (p.Gly471Glu)	not specified [RCV004486056]	uncertain significance	12	44665516	44665516	Human		name
405668903	CV3360262	single nucleotide variant	NM_001145108.2(NELL2):c.1706G>A (p.Arg569His)	not specified [RCV004486069]	uncertain significance	12	44532679	44532679	Human		name
405668913	CV3360264	single nucleotide variant	NM_001145108.2(NELL2):c.1754A>T (p.Asp585Val)	not specified [RCV004486071]	uncertain significance	12	44532631	44532631	Human		name
405668933	CV3360268	single nucleotide variant	NM_001145108.2(NELL2):c.1796C>T (p.Ser599Leu)	not specified [RCV004486075]	uncertain significance	12	44532589	44532589	Human		name
405669077	CV3360296	single nucleotide variant	NM_001145108.2(NELL2):c.2168G>A (p.Arg723His)	not specified [RCV004486103]	uncertain significance	12	44522007	44522007	Human		name
405669100	CV3360301	single nucleotide variant	NM_001145108.2(NELL2):c.2258C>T (p.Pro753Leu)	not specified [RCV004486108]	uncertain significance	12	44520147	44520147	Human		name
405669114	CV3360304	single nucleotide variant	NM_001145108.2(NELL2):c.2296C>T (p.Arg766Cys)	not specified [RCV004486111]	uncertain significance	12	44520109	44520109	Human		name
405669157	CV3360314	single nucleotide variant	NM_001145108.2(NELL2):c.2326G>A (p.Glu776Lys)	not specified [RCV004486121]	uncertain significance	12	44520079	44520079	Human		name
407526325	CV3454912	single nucleotide variant	NM_001145108.2(NELL2):c.1321A>G (p.Ile441Val)	not specified [RCV004654772]	uncertain significance	12	44665607	44665607	Human		name
597639662	CV3565543	single nucleotide variant	NM_001145108.2(NELL2):c.1825G>T (p.Gly609Trp)	not specified [RCV004831886]	uncertain significance	12	44523464	44523464	Human		name
597639140	CV3565547	single nucleotide variant	NM_001145108.2(NELL2):c.1925A>G (p.His642Arg)	not specified [RCV004831890]	uncertain significance	12	44523364	44523364	Human		name
597639150	CV3565549	single nucleotide variant	NM_001145108.2(NELL2):c.1844A>G (p.Asn615Ser)	not specified [RCV004831892]	uncertain significance	12	44523445	44523445	Human		name
597639154	CV3565550	single nucleotide variant	NM_001145108.2(NELL2):c.1144T>C (p.Ser382Pro)	not specified [RCV004831893]	uncertain significance	12	44711337	44711337	Human		name
597639160	CV3565551	single nucleotide variant	NM_001145108.2(NELL2):c.1564A>C (p.Lys522Gln)	not specified [RCV004831894]	uncertain significance	12	44610851	44610851	Human		name
597639165	CV3565552	single nucleotide variant	NM_001145108.2(NELL2):c.2444A>G (p.Glu815Gly)	not specified [RCV004831895]	uncertain significance	12	44508941	44508941	Human		name
597639169	CV3565553	single nucleotide variant	NM_001145108.2(NELL2):c.1342C>A (p.Arg448Ser)	not specified [RCV004831896]	uncertain significance	12	44665586	44665586	Human		name
597639174	CV3565554	single nucleotide variant	NM_001145108.2(NELL2):c.1417A>G (p.Ile473Val)	not specified [RCV004831897]	uncertain significance	12	44665511	44665511	Human		name
597639179	CV3565555	single nucleotide variant	NM_001145108.2(NELL2):c.2106T>A (p.His702Gln)	not specified [RCV004831898]	uncertain significance	12	44522069	44522069	Human		name
597639190	CV3565557	single nucleotide variant	NM_001145108.2(NELL2):c.1751G>A (p.Arg584Lys)	not specified [RCV004831900]	uncertain significance	12	44532634	44532634	Human		name
597639199	CV3565559	single nucleotide variant	NM_001145108.2(NELL2):c.1301A>G (p.Asp434Gly)	not specified [RCV004831902]	uncertain significance	12	44703743	44703743	Human		name
598254550	CV3990767	single nucleotide variant	NM_001145108.2(NELL2):c.2402A>G (p.Asn801Ser)	not specified [RCV005385515]	uncertain significance	12	44508983	44508983	Human		name
598231983	CV3990768	single nucleotide variant	NM_001145108.2(NELL2):c.1556C>T (p.Thr519Met)	not specified [RCV005381458]	uncertain significance	12	44610859	44610859	Human		name
598231988	CV3990769	single nucleotide variant	NM_001145108.2(NELL2):c.1342C>T (p.Arg448Cys)	not specified [RCV005381459]	uncertain significance	12	44665586	44665586	Human		name
598254558	CV3990770	single nucleotide variant	NM_001145108.2(NELL2):c.1953G>T (p.Gln651His)	not specified [RCV005385516]	uncertain significance	12	44523336	44523336	Human		name
598231994	CV3990771	single nucleotide variant	NM_001145108.2(NELL2):c.1368G>A (p.Met456Ile)	not specified [RCV005381460]	uncertain significance	12	44665560	44665560	Human		name
598254564	CV3990772	single nucleotide variant	NM_001145108.2(NELL2):c.1601C>G (p.Ala534Gly)	not specified [RCV005385517]	uncertain significance	12	44607231	44607231	Human		name
598254572	CV3990775	single nucleotide variant	NM_001145108.2(NELL2):c.2140A>T (p.Thr714Ser)	not specified [RCV005385518]	uncertain significance	12	44522035	44522035	Human		name
598232010	CV3990776	single nucleotide variant	NM_001145108.2(NELL2):c.2101C>G (p.Leu701Val)	not specified [RCV005381463]	uncertain significance	12	44522074	44522074	Human		name
598232027	CV3990779	single nucleotide variant	NM_001145108.2(NELL2):c.1612G>A (p.Ala538Thr)	not specified [RCV005381466]	uncertain significance	12	44607220	44607220	Human		name
598254579	CV3990780	single nucleotide variant	NM_001145108.2(NELL2):c.2260C>T (p.Arg754Cys)	not specified [RCV005385519]	uncertain significance	12	44520145	44520145	Human		name
598232033	CV3990781	single nucleotide variant	NM_001145108.2(NELL2):c.2008G>A (p.Val670Ile)	not specified [RCV005381467]	uncertain significance	12	44522167	44522167	Human		name
598254587	CV3990782	single nucleotide variant	NM_001145108.2(NELL2):c.2331G>C (p.Met777Ile)	not specified [RCV005385520]	uncertain significance	12	44520074	44520074	Human		name
8627270	CV82414	single nucleotide variant	NM_001145107.1(NELL2):c.2194C>T (p.Pro732Ser)	Malignant melanoma [RCV000062493]	not provided	12	44522131	44522131	Human		name
8627271	CV82415	single nucleotide variant	NM_001145107.1(NELL2):c.2081G>A (p.Gly694Glu)	Malignant melanoma [RCV000062494]	not provided	12	44523358	44523358	Human		name
8634675	CV89895	single nucleotide variant	NM_001145107.1(NELL2):c.2593G>A (p.Glu865Lys)	Malignant melanoma [RCV000069992]	not provided	12	44508942	44508942	Human		name

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