Klhl29 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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101 records found for search term Klhl29

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8577070	CV111440	single nucleotide variant	NM_052920.1(KLHL29):c.940+9901T>G	Lung cancer [RCV000091963]	uncertain significance	2	23652751	23652751	Human		name
8577065	CV111435	single nucleotide variant	NM_052920.1(KLHL29):c.-154+31657G>T	Lung cancer [RCV000091958]	uncertain significance	2	23417437	23417437	Human		name
156165720	CV2348619	single nucleotide variant	NM_052920.2(KLHL29):c.8G>A (p.Arg3Gln)	not specified [RCV004195844]	uncertain significance	2	23562204	23562204	Human		name
329392846	CV2439221	single nucleotide variant	NM_052920.2(KLHL29):c.25G>A (p.Glu9Lys)	not specified [RCV004266492]	uncertain significance	2	23562221	23562221	Human		name
597640348	CV3692424	single nucleotide variant	NM_052920.2(KLHL29):c.20G>A (p.Arg7His)	not specified [RCV004941507]	uncertain significance	2	23562216	23562216	Human		name
156288029	CV2288451	single nucleotide variant	NM_052920.2(KLHL29):c.83G>A (p.Gly28Glu)	not specified [RCV004151996]	uncertain significance	2	23562279	23562279	Human		name
155913914	CV2341885	single nucleotide variant	NM_052920.2(KLHL29):c.67G>A (p.Val23Ile)	not specified [RCV004184833]	uncertain significance	2	23562263	23562263	Human		name
156067975	CV2356777	single nucleotide variant	NM_052920.2(KLHL29):c.92G>A (p.Ser31Asn)	not specified [RCV004202120]	uncertain significance	2	23562288	23562288	Human		name
155932006	CV2362698	single nucleotide variant	NM_052920.2(KLHL29):c.38G>A (p.Arg13Gln)	not specified [RCV004215341]	uncertain significance	2	23562234	23562234	Human		name
156005649	CV2357686	single nucleotide variant	NM_052920.2(KLHL29):c.235G>A (p.Glu79Lys)	not specified [RCV004202943]	uncertain significance	2	23562431	23562431	Human		name
329357538	CV2453645	single nucleotide variant	NM_052920.2(KLHL29):c.281C>A (p.Thr94Asn)	not specified [RCV004269304]	uncertain significance	2	23562477	23562477	Human		name
401723396	CV2724881	single nucleotide variant	NM_052920.2(KLHL29):c.157C>T (p.Leu53Phe)	not specified [RCV004319660]	uncertain significance	2	23562353	23562353	Human		name
401864810	CV2757204	single nucleotide variant	NM_052920.2(KLHL29):c.1080G>A (p.Arg360=)	not specified [RCV004338808]	likely benign	2	23691674	23691674	Human		name
401857468	CV2760182	single nucleotide variant	NM_052920.2(KLHL29):c.145G>A (p.Val49Ile)	not specified [RCV004347360]	uncertain significance	2	23562341	23562341	Human		name
401937476	CV2815570	single nucleotide variant	NM_052920.2(KLHL29):c.2121C>T (p.Thr707=)	not provided [RCV003415511]	likely benign	2	23703201	23703201	Human		name
405813468	CV3276177	single nucleotide variant	NM_052920.2(KLHL29):c.113G>C (p.Gly38Ala)	not specified [RCV004409413]	uncertain significance	2	23562309	23562309	Human		name
405813470	CV3276178	single nucleotide variant	NM_052920.2(KLHL29):c.118G>A (p.Gly40Ser)	not specified [RCV004409414]	uncertain significance	2	23562314	23562314	Human		name
405813472	CV3276179	single nucleotide variant	NM_052920.2(KLHL29):c.125G>T (p.Gly42Val)	not specified [RCV004409415]	uncertain significance	2	23562321	23562321	Human		name
405813480	CV3276183	single nucleotide variant	NM_052920.2(KLHL29):c.185G>A (p.Arg62Gln)	not specified [RCV004409419]	uncertain significance	2	23562381	23562381	Human		name
405813485	CV3276185	single nucleotide variant	NM_052920.2(KLHL29):c.226G>A (p.Gly76Ser)	not specified [RCV004409421]	uncertain significance	2	23562422	23562422	Human		name
407524960	CV3448575	single nucleotide variant	NM_052920.2(KLHL29):c.217T>A (p.Cys73Ser)	not specified [RCV004631564]	uncertain significance	2	23562413	23562413	Human		name
407498812	CV3448580	single nucleotide variant	NM_052920.2(KLHL29):c.259A>C (p.Ser87Arg)	not specified [RCV004644140]	uncertain significance	2	23562455	23562455	Human		name
597640310	CV3692416	single nucleotide variant	NM_052920.2(KLHL29):c.203C>T (p.Thr68Ile)	not specified [RCV004941501]	uncertain significance	2	23562399	23562399	Human		name
598161610	CV3987366	single nucleotide variant	NM_052920.2(KLHL29):c.172G>A (p.Val58Met)	not specified [RCV005368469]	uncertain significance	2	23562368	23562368	Human		name
155940754	CV2294132	single nucleotide variant	NM_052920.2(KLHL29):c.898G>A (p.Gly300Ser)	not specified [RCV004149502]	uncertain significance	2	23642808	23642808	Human		name
156291472	CV2306082	single nucleotide variant	NM_052920.2(KLHL29):c.521C>A (p.Pro174Gln)	not specified [RCV004162847]	uncertain significance	2	23642431	23642431	Human		name
156149579	CV2318552	single nucleotide variant	NM_052920.2(KLHL29):c.340C>T (p.Arg114Trp)	not specified [RCV004173460]	uncertain significance	2	23639193	23639193	Human		name
156190715	CV2325517	single nucleotide variant	NM_052920.2(KLHL29):c.974C>T (p.Ala325Val)	not specified [RCV004179957]	uncertain significance	2	23684432	23684432	Human		name
156184442	CV2335593	single nucleotide variant	NM_052920.2(KLHL29):c.862G>A (p.Asp288Asn)	not specified [RCV004193799]	uncertain significance	2	23642772	23642772	Human		name
155979518	CV2339133	single nucleotide variant	NM_052920.2(KLHL29):c.778C>A (p.Pro260Thr)	not specified [RCV004187173]	uncertain significance	2	23642688	23642688	Human		name
156155109	CV2359695	single nucleotide variant	NM_052920.2(KLHL29):c.496G>A (p.Val166Met)	not specified [RCV004210518]	uncertain significance	2	23642406	23642406	Human		name
156249305	CV2394077	single nucleotide variant	NM_052920.2(KLHL29):c.845A>G (p.Asn282Ser)	not specified [RCV004236291]	uncertain significance	2	23642755	23642755	Human		name
156003922	CV2396827	single nucleotide variant	NM_052920.2(KLHL29):c.593C>T (p.Pro198Leu)	not specified [RCV004233960]	uncertain significance	2	23642503	23642503	Human		name
329391600	CV2448747	single nucleotide variant	NM_052920.2(KLHL29):c.408G>A (p.Met136Ile)	not specified [RCV004259400]	uncertain significance	2	23639261	23639261	Human		name
329402215	CV2454057	single nucleotide variant	NM_052920.2(KLHL29):c.896T>C (p.Ile299Thr)	not specified [RCV004271704]	uncertain significance	2	23642806	23642806	Human		name
401721704	CV2680638	single nucleotide variant	NM_052920.2(KLHL29):c.626C>T (p.Pro209Leu)	not specified [RCV004291257]	uncertain significance	2	23642536	23642536	Human		name
401758919	CV2694344	single nucleotide variant	NM_052920.2(KLHL29):c.859A>C (p.Thr287Pro)	not specified [RCV004304535]	uncertain significance	2	23642769	23642769	Human		name
401782960	CV2716062	single nucleotide variant	NM_052920.2(KLHL29):c.505C>A (p.Pro169Thr)	not specified [RCV004323309]	uncertain significance	2	23642415	23642415	Human		name
401862668	CV2762320	single nucleotide variant	NM_052920.2(KLHL29):c.353C>T (p.Thr118Met)	not specified [RCV004335436]	uncertain significance	2	23639206	23639206	Human		name
401880548	CV2763084	single nucleotide variant	NM_052920.2(KLHL29):c.763G>A (p.Gly255Ser)	not specified [RCV004336134]	uncertain significance	2	23642673	23642673	Human		name
401878892	CV2773763	single nucleotide variant	NM_052920.2(KLHL29):c.652G>A (p.Val218Met)	not specified [RCV004356432]	uncertain significance	2	23642562	23642562	Human		name
405813491	CV3276188	single nucleotide variant	NM_052920.2(KLHL29):c.390G>C (p.Glu130Asp)	not specified [RCV004409424]	uncertain significance	2	23639243	23639243	Human		name
405813493	CV3276189	single nucleotide variant	NM_052920.2(KLHL29):c.901G>A (p.Val301Met)	not specified [RCV004409425]	uncertain significance	2	23642811	23642811	Human		name
405813495	CV3276190	single nucleotide variant	NM_052920.2(KLHL29):c.973G>A (p.Ala325Thr)	not specified [RCV004409426]	uncertain significance	2	23684431	23684431	Human		name
407498789	CV3448571	single nucleotide variant	NM_052920.2(KLHL29):c.751G>A (p.Ala251Thr)	not specified [RCV004644133]	uncertain significance	2	23642661	23642661	Human		name
407498798	CV3448574	single nucleotide variant	NM_052920.2(KLHL29):c.980C>A (p.Ala327Glu)	not specified [RCV004644136]	uncertain significance	2	23684438	23684438	Human		name
407498808	CV3448578	single nucleotide variant	NM_052920.2(KLHL29):c.536A>G (p.Gln179Arg)	not specified [RCV004644139]	uncertain significance	2	23642446	23642446	Human		name
407498816	CV3448581	single nucleotide variant	NM_052920.2(KLHL29):c.423T>G (p.Asn141Lys)	not specified [RCV004644141]	uncertain significance	2	23639276	23639276	Human		name
597640277	CV3692411	single nucleotide variant	NM_052920.2(KLHL29):c.457G>T (p.Ala153Ser)	not specified [RCV004941496]	uncertain significance	2	23642367	23642367	Human		name
597640290	CV3692413	single nucleotide variant	NM_052920.2(KLHL29):c.751G>T (p.Ala251Ser)	not specified [RCV004941498]	uncertain significance	2	23642661	23642661	Human		name
597640303	CV3692415	single nucleotide variant	NM_052920.2(KLHL29):c.484C>T (p.His162Tyr)	not specified [RCV004941500]	uncertain significance	2	23642394	23642394	Human		name
598182825	CV3987358	single nucleotide variant	NM_052920.2(KLHL29):c.803C>T (p.Ala268Val)	not specified [RCV005352797]	uncertain significance	2	23642713	23642713	Human		name
598182836	CV3987361	single nucleotide variant	NM_052920.2(KLHL29):c.532G>A (p.Val178Ile)	not specified [RCV005352799]	uncertain significance	2	23642442	23642442	Human		name
598182842	CV3987362	single nucleotide variant	NM_052920.2(KLHL29):c.703G>A (p.Val235Met)	not specified [RCV005352800]	uncertain significance	2	23642613	23642613	Human		name
598161615	CV3987368	single nucleotide variant	NM_052920.2(KLHL29):c.519C>A (p.Ser173Arg)	not specified [RCV005368470]	uncertain significance	2	23642429	23642429	Human		name
598182879	CV3987371	single nucleotide variant	NM_052920.2(KLHL29):c.685A>C (p.Ser229Arg)	not specified [RCV005352806]	uncertain significance	2	23642595	23642595	Human		name
598221211	CV3987373	single nucleotide variant	NM_052920.2(KLHL29):c.827G>C (p.Ser276Thr)	not specified [RCV005360775]	uncertain significance	2	23642737	23642737	Human		name
598182887	CV3987374	single nucleotide variant	NM_052920.2(KLHL29):c.526G>A (p.Val176Met)	not specified [RCV005352807]	uncertain significance	2	23642436	23642436	Human		name
156144074	CV2208700	single nucleotide variant	NM_052920.2(KLHL29):c.1204G>A (p.Ala402Thr)	not specified [RCV004084894]	uncertain significance	2	23691798	23691798	Human		name
156329702	CV2213888	single nucleotide variant	NM_052920.2(KLHL29):c.1692C>A (p.His564Gln)	not specified [RCV004083621]	uncertain significance	2	23695772	23695772	Human		name
156364691	CV2271973	single nucleotide variant	NM_052920.2(KLHL29):c.1195A>G (p.Ile399Val)	not specified [RCV004124787]	uncertain significance	2	23691789	23691789	Human		name
156237804	CV2285834	single nucleotide variant	NM_052920.2(KLHL29):c.2324C>G (p.Thr775Arg)	not specified [RCV004143779]	uncertain significance	2	23703743	23703743	Human		name
156292965	CV2296886	single nucleotide variant	NM_052920.2(KLHL29):c.2236G>A (p.Gly746Ser)	not specified [RCV004148760]	uncertain significance	2	23703316	23703316	Human		name
156285358	CV2334835	single nucleotide variant	NM_052920.2(KLHL29):c.1096G>A (p.Gly366Ser)	not specified [RCV004181945]	likely benign	2	23691690	23691690	Human		name
156391291	CV2385235	single nucleotide variant	NM_052920.2(KLHL29):c.2140G>A (p.Ala714Thr)	not specified [RCV004228480]	uncertain significance	2	23703220	23703220	Human		name
155969967	CV2400825	single nucleotide variant	NM_052920.2(KLHL29):c.2144C>G (p.Pro715Arg)	not specified [RCV004242482]	uncertain significance	2	23703224	23703224	Human		name
329377755	CV2436024	single nucleotide variant	NM_052920.2(KLHL29):c.2540C>T (p.Thr847Ile)	not specified [RCV004255244]	uncertain significance	2	23706576	23706576	Human		name
401730054	CV2700399	single nucleotide variant	NM_052920.2(KLHL29):c.1383G>T (p.Gln461His)	not specified [RCV004311047]	uncertain significance	2	23693369	23693369	Human		name
401779279	CV2709660	single nucleotide variant	NM_052920.2(KLHL29):c.2024G>A (p.Arg675Gln)	not specified [RCV004318872]	uncertain significance	2	23696432	23696432	Human		name
401736849	CV2717806	single nucleotide variant	NM_052920.2(KLHL29):c.2507C>T (p.Ala836Val)	not specified [RCV004321789]	uncertain significance	2	23706543	23706543	Human		name
401900060	CV2780293	single nucleotide variant	NM_052920.2(KLHL29):c.1249C>T (p.His417Tyr)	not specified [RCV004355919]	uncertain significance	2	23691843	23691843	Human		name
401877421	CV2790164	single nucleotide variant	NM_052920.2(KLHL29):c.2093A>G (p.Asp698Gly)	not specified [RCV004364093]	uncertain significance	2	23696501	23696501	Human		name
405813463	CV3276175	single nucleotide variant	NM_052920.2(KLHL29):c.1084G>A (p.Val362Met)	not specified [RCV004409411]	uncertain significance	2	23691678	23691678	Human		name
405813465	CV3276176	single nucleotide variant	NM_052920.2(KLHL29):c.1126G>A (p.Val376Ile)	not specified [RCV004409412]	uncertain significance	2	23691720	23691720	Human		name
405813474	CV3276180	single nucleotide variant	NM_052920.2(KLHL29):c.1283A>G (p.Glu428Gly)	not specified [RCV004409416]	uncertain significance	2	23693269	23693269	Human		name
405813476	CV3276181	single nucleotide variant	NM_052920.2(KLHL29):c.1450G>A (p.Val484Ile)	not specified [RCV004409417]	likely benign	2	23693436	23693436	Human		name
405813478	CV3276182	single nucleotide variant	NM_052920.2(KLHL29):c.1547C>T (p.Ala516Val)	not specified [RCV004409418]	uncertain significance	2	23695627	23695627	Human		name
405813482	CV3276184	single nucleotide variant	NM_052920.2(KLHL29):c.2161C>T (p.His721Tyr)	not specified [RCV004409420]	uncertain significance	2	23703241	23703241	Human		name
405813487	CV3276186	single nucleotide variant	NM_052920.2(KLHL29):c.2372C>T (p.Thr791Ile)	not specified [RCV004409422]	uncertain significance	2	23703791	23703791	Human		name
407498792	CV3448572	single nucleotide variant	NM_052920.2(KLHL29):c.1000G>A (p.Val334Ile)	not specified [RCV004644134]	uncertain significance	2	23684458	23684458	Human		name
407498795	CV3448573	single nucleotide variant	NM_052920.2(KLHL29):c.1013G>A (p.Arg338Lys)	not specified [RCV004644135]	uncertain significance	2	23684471	23684471	Human		name
407498801	CV3448576	single nucleotide variant	NM_052920.2(KLHL29):c.1406A>G (p.Gln469Arg)	not specified [RCV004644137]	uncertain significance	2	23693392	23693392	Human		name
407498805	CV3448577	single nucleotide variant	NM_052920.2(KLHL29):c.1105G>A (p.Gly369Ser)	not specified [RCV004644138]	uncertain significance	2	23691699	23691699	Human		name
407524962	CV3448579	single nucleotide variant	NM_052920.2(KLHL29):c.2198A>G (p.Tyr733Cys)	not specified [RCV004631565]	uncertain significance	2	23703278	23703278	Human		name
597640283	CV3692412	single nucleotide variant	NM_052920.2(KLHL29):c.2239G>A (p.Val747Ile)	not specified [RCV004941497]	uncertain significance	2	23703319	23703319	Human		name
597640297	CV3692414	single nucleotide variant	NM_052920.2(KLHL29):c.1946C>T (p.Thr649Met)	not specified [RCV004941499]	uncertain significance	2	23696354	23696354	Human		name
597640318	CV3692417	single nucleotide variant	NM_052920.2(KLHL29):c.2096A>G (p.His699Arg)	not specified [RCV004941502]	uncertain significance	2	23696504	23696504	Human		name
597640331	CV3692419	single nucleotide variant	NM_052920.2(KLHL29):c.1258T>G (p.Cys420Gly)	not specified [RCV004941504]	uncertain significance	2	23691852	23691852	Human		name
597640337	CV3692420	single nucleotide variant	NM_052920.2(KLHL29):c.1109G>A (p.Arg370Gln)	not specified [RCV004941505]	uncertain significance	2	23691703	23691703	Human		name
597768746	CV3692421	single nucleotide variant	NM_052920.2(KLHL29):c.2609A>G (p.Lys870Arg)	not specified [RCV004927555]	uncertain significance	2	23706645	23706645	Human		name
597640343	CV3692422	single nucleotide variant	NM_052920.2(KLHL29):c.2116A>G (p.Ile706Val)	not specified [RCV004941506]	uncertain significance	2	23703196	23703196	Human		name
597768750	CV3692423	single nucleotide variant	NM_052920.2(KLHL29):c.1286A>G (p.Lys429Arg)	not specified [RCV004927556]	uncertain significance	2	23693272	23693272	Human		name
598182831	CV3987359	single nucleotide variant	NM_052920.2(KLHL29):c.1876C>T (p.Arg626Cys)	not specified [RCV005352798]	uncertain significance	2	23696085	23696085	Human		name
598221197	CV3987360	single nucleotide variant	NM_052920.2(KLHL29):c.1210G>A (p.Ala404Thr)	not specified [RCV005360773]	uncertain significance	2	23691804	23691804	Human		name
598182848	CV3987363	single nucleotide variant	NM_052920.2(KLHL29):c.2599G>A (p.Val867Met)	not specified [RCV005352801]	uncertain significance	2	23706635	23706635	Human		name
598182854	CV3987364	single nucleotide variant	NM_052920.2(KLHL29):c.2568G>T (p.Met856Ile)	not specified [RCV005352802]	uncertain significance	2	23706604	23706604	Human		name
598221202	CV3987365	single nucleotide variant	NM_052920.2(KLHL29):c.1405C>G (p.Gln469Glu)	not specified [RCV005360774]	uncertain significance	2	23693391	23693391	Human		name
598182866	CV3987369	single nucleotide variant	NM_052920.2(KLHL29):c.2554C>T (p.Leu852Phe)	not specified [RCV005352804]	uncertain significance	2	23706590	23706590	Human		name
598182873	CV3987370	single nucleotide variant	NM_052920.2(KLHL29):c.2569C>G (p.Pro857Ala)	not specified [RCV005352805]	uncertain significance	2	23706605	23706605	Human		name
598161620	CV3987372	single nucleotide variant	NM_052920.2(KLHL29):c.2383G>A (p.Asp795Asn)	not specified [RCV005368471]	uncertain significance	2	23703802	23703802	Human		name
598161625	CV3987375	single nucleotide variant	NM_052920.2(KLHL29):c.2081C>T (p.Ala694Val)	not specified [RCV005368472]	uncertain significance	2	23696489	23696489	Human		name

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