Zhx3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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190 records found for search term Zhx3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150466563	CV1255760	single nucleotide variant	NM_001384317.1(ZHX3):c.*102C>T	not provided [RCV001670394]	benign	20	41185089	41185089	Human		name
405253446	CV3174460	single nucleotide variant	NM_001384317.1(ZHX3):c.2861-8C>T	not provided [RCV003871089]	likely benign	20	41185209	41185209	Human		name
152070796	CV1628491	single nucleotide variant	NM_001384317.1(ZHX3):c.2860+16G>C	not provided [RCV002169263]	likely benign	20	41202041	41202041	Human		name
404996178	CV2992506	single nucleotide variant	NM_001384317.1(ZHX3):c.2861-11T>C	not provided [RCV003692728]	uncertain significance	20	41185212	41185212	Human		name
405243021	CV3164699	single nucleotide variant	NM_001384317.1(ZHX3):c.2861-17A>G	not provided [RCV003867780]	likely benign	20	41185218	41185218	Human		name
150448654	CV1275570	duplication	NM_001384317.1(ZHX3):c.2861-210dup	not provided [RCV001708025]	benign	20	41185409	41185410	Human		name
156242164	CV1981413	single nucleotide variant	NM_001384317.1(ZHX3):c.24C>G (p.Thr8=)	not provided [RCV002645611]	likely benign	20	41204893	41204893	Human		name
402496530	CV2875363	single nucleotide variant	NM_001384317.1(ZHX3):c.87C>T (p.Pro29=)	not provided [RCV003545476]	likely benign	20	41204830	41204830	Human		name
405094478	CV3045722	single nucleotide variant	NM_001384317.1(ZHX3):c.30A>G (p.Pro10=)	not provided [RCV003718059]	benign	20	41204887	41204887	Human		name
8628508	CV83652	single nucleotide variant	NM_015035.3(ZHX3):c.1338G>A (p.Thr446=)	Malignant melanoma [RCV000063733]	not provided	20	41203579	41203579	Human		name
8637308	CV92534	single nucleotide variant	NM_015035.3(ZHX3):c.1878C>T (p.Ala626=)	Malignant melanoma [RCV000072632]	not provided	20	41203039	41203039	Human		name
155992743	CV2112665	single nucleotide variant	NM_001384317.1(ZHX3):c.246C>T (p.Cys82=)	ZHX3-related disorder [RCV003926542]\|not provided [RCV002947407]	benign	20	41204671	41204671	Human		name , trait , alternate_id
404984188	CV3183616	single nucleotide variant	NM_001384317.1(ZHX3):c.219T>C (p.Asp73=)	not provided [RCV003880893]	likely benign	20	41204698	41204698	Human		name
152145641	CV1582697	single nucleotide variant	NM_001384317.1(ZHX3):c.756C>T (p.Ala252=)	ZHX3-related disorder [RCV003926310]\|not provided [RCV002201199]	benign	20	41204161	41204161	Human		name , trait , alternate_id
152127806	CV1596449	single nucleotide variant	NM_001384317.1(ZHX3):c.924G>A (p.Thr308=)	not provided [RCV002118682]	likely benign	20	41203993	41203993	Human		name
156016713	CV2019099	single nucleotide variant	NM_001384317.1(ZHX3):c.429C>T (p.Ala143=)	not provided [RCV002690803]	likely benign	20	41204488	41204488	Human		name
156029108	CV2039774	single nucleotide variant	NM_001384317.1(ZHX3):c.64G>C (p.Asp22His)	not provided [RCV002781035]	uncertain significance	20	41204853	41204853	Human		name
156044266	CV2127179	single nucleotide variant	NM_001384317.1(ZHX3):c.990C>T (p.Thr330=)	not provided [RCV002949738]	likely benign	20	41203927	41203927	Human		name
405225304	CV2881989	single nucleotide variant	NM_001384317.1(ZHX3):c.402G>T (p.Gly134=)	not provided [RCV003554553]	likely benign	20	41204515	41204515	Human		name
402516555	CV3003182	single nucleotide variant	NM_001384317.1(ZHX3):c.660T>A (p.Thr220=)	not provided [RCV003716112]	likely benign	20	41204257	41204257	Human		name
405040866	CV3063976	single nucleotide variant	NM_001384317.1(ZHX3):c.399C>T (p.Ser133=)	not provided [RCV003739910]	likely benign	20	41204518	41204518	Human		name
404990372	CV3131992	single nucleotide variant	NM_001384317.1(ZHX3):c.423C>T (p.Asn141=)	not provided [RCV003827121]	likely benign	20	41204494	41204494	Human		name
405235590	CV3168673	single nucleotide variant	NM_001384317.1(ZHX3):c.907C>T (p.Leu303=)	not provided [RCV003866147]	likely benign	20	41204010	41204010	Human		name
408367613	CV3511203	single nucleotide variant	NM_001384317.1(ZHX3):c.804A>C (p.Ile268=)	ZHX3-related disorder [RCV004759066]	likely benign	20	41204113	41204113	Human		name , trait , alternate_id
597728798	CV3625041	single nucleotide variant	NM_001384317.1(ZHX3):c.98T>C (p.Leu33Ser)	not specified [RCV004888565]	uncertain significance	20	41204819	41204819	Human		name
597888962	CV3766324	single nucleotide variant	NM_001384317.1(ZHX3):c.945T>C (p.Ser315=)	not provided [RCV005110441]	likely benign	20	41203972	41203972	Human		name
597853404	CV3805800	single nucleotide variant	NM_001384317.1(ZHX3):c.762C>T (p.Asn254=)	not provided [RCV005145730]	likely benign	20	41204155	41204155	Human		name
597951380	CV3843289	single nucleotide variant	NM_001384317.1(ZHX3):c.978C>T (p.Phe326=)	not provided [RCV005190339]	likely benign	20	41203939	41203939	Human		name
598260352	CV3934067	single nucleotide variant	NM_001384317.1(ZHX3):c.88G>A (p.Ala30Thr)	not specified [RCV005300406]	likely benign	20	41204829	41204829	Human		name
598159385	CV3934071	single nucleotide variant	NM_001384317.1(ZHX3):c.68C>A (p.Ala23Asp)	not specified [RCV005306559]	uncertain significance	20	41204849	41204849	Human		name
151718234	CV1458592	single nucleotide variant	NM_001384317.1(ZHX3):c.1167G>A (p.Thr389=)	not provided [RCV002003253]	likely benign\|uncertain significance	20	41203750	41203750	Human		name
151814748	CV1463186	single nucleotide variant	NM_001384317.1(ZHX3):c.233C>T (p.Ser78Phe)	not provided [RCV001900300]	uncertain significance	20	41204684	41204684	Human		name
152174694	CV1520388	single nucleotide variant	NM_001384317.1(ZHX3):c.154G>A (p.Ala52Thr)	not provided [RCV002184600]	likely benign	20	41204763	41204763	Human		name
152161354	CV1534732	single nucleotide variant	NM_001384317.1(ZHX3):c.2526T>C (p.Ile842=)	not provided [RCV002140976]	likely benign	20	41202391	41202391	Human		name
152114279	CV1574796	single nucleotide variant	NM_001384317.1(ZHX3):c.2070G>A (p.Glu690=)	not provided [RCV002116975]	benign	20	41202847	41202847	Human		name
152156995	CV1586078	single nucleotide variant	NM_001384317.1(ZHX3):c.2658A>G (p.Lys886=)	ZHX3-related disorder [RCV003958885]\|not provided [RCV002140281]	benign	20	41202259	41202259	Human		name , trait , alternate_id
152080873	CV1589321	single nucleotide variant	NM_001384317.1(ZHX3):c.2481C>T (p.Tyr827=)	not provided [RCV002112732]	likely benign	20	41202436	41202436	Human		name
152075668	CV1635448	single nucleotide variant	NM_001384317.1(ZHX3):c.1062C>G (p.Ala354=)	not provided [RCV002092187]	benign	20	41203855	41203855	Human		name
152093714	CV1648714	single nucleotide variant	NM_001384317.1(ZHX3):c.1599C>T (p.Leu533=)	not provided [RCV002078054]	likely benign	20	41203318	41203318	Human		name
152139791	CV1660698	single nucleotide variant	NM_001384317.1(ZHX3):c.1239C>T (p.His413=)	not provided [RCV002120201]	benign	20	41203678	41203678	Human		name
156308607	CV1895108	single nucleotide variant	NM_001384317.1(ZHX3):c.2523C>T (p.Val841=)	not provided [RCV003088307]	likely benign	20	41202394	41202394	Human		name
156354298	CV1920853	single nucleotide variant	NM_001384317.1(ZHX3):c.1857A>G (p.Arg619=)	not provided [RCV002632212]	likely benign	20	41203060	41203060	Human		name
156445175	CV1945173	single nucleotide variant	NM_001384317.1(ZHX3):c.1809A>G (p.Gln603=)	not provided [RCV003116113]	likely benign	20	41203108	41203108	Human		name
156272307	CV1970998	single nucleotide variant	NM_001384317.1(ZHX3):c.274T>A (p.Phe92Ile)	not provided [RCV002598131]	uncertain significance	20	41204643	41204643	Human		name
156279984	CV2005179	single nucleotide variant	NM_001384317.1(ZHX3):c.1101G>A (p.Glu367=)	not provided [RCV002646808]	likely benign	20	41203816	41203816	Human		name
156314637	CV2017904	single nucleotide variant	NM_001384317.1(ZHX3):c.1791C>T (p.His597=)	not provided [RCV002671832]	likely benign	20	41203126	41203126	Human		name
156153491	CV2098588	single nucleotide variant	NM_001384317.1(ZHX3):c.1215C>T (p.Leu405=)	not provided [RCV002890734]	likely benign	20	41203702	41203702	Human		name
156033896	CV2152764	single nucleotide variant	NM_001384317.1(ZHX3):c.170G>T (p.Ser57Ile)	not provided [RCV003018792]	uncertain significance	20	41204747	41204747	Human		name
402496463	CV2875354	single nucleotide variant	NM_001384317.1(ZHX3):c.1929C>T (p.Asp643=)	not provided [RCV003545470]	likely benign	20	41202988	41202988	Human		name
405216023	CV2876252	single nucleotide variant	NM_001384317.1(ZHX3):c.2451C>T (p.Tyr817=)	not provided [RCV003553206]	likely benign	20	41202466	41202466	Human		name
405132287	CV2905535	single nucleotide variant	NM_001384317.1(ZHX3):c.205C>T (p.Arg69Trp)	not provided [RCV003560141]	uncertain significance	20	41204712	41204712	Human		name
405175827	CV2951867	single nucleotide variant	NM_001384317.1(ZHX3):c.2835G>A (p.Ser945=)	not provided [RCV003675819]	likely benign	20	41202082	41202082	Human		name
405181899	CV2952595	single nucleotide variant	NM_001384317.1(ZHX3):c.2172C>A (p.Pro724=)	not provided [RCV003676357]	likely benign	20	41202745	41202745	Human		name
405224041	CV3035887	single nucleotide variant	NM_001384317.1(ZHX3):c.2628C>T (p.Ser876=)	not provided [RCV003710392]	likely benign	20	41202289	41202289	Human		name
405235760	CV3040818	single nucleotide variant	NM_001384317.1(ZHX3):c.1305G>T (p.Gly435=)	not provided [RCV003712218]	likely benign	20	41203612	41203612	Human		name
405254490	CV3055407	single nucleotide variant	NM_001384317.1(ZHX3):c.2454A>G (p.Ala818=)	not provided [RCV003723034]	likely benign	20	41202463	41202463	Human		name
405128292	CV3132976	single nucleotide variant	NM_001384317.1(ZHX3):c.1185C>T (p.Leu395=)	not provided [RCV003838139]	likely benign	20	41203732	41203732	Human		name
402499268	CV3170407	single nucleotide variant	NM_001384317.1(ZHX3):c.2109T>C (p.Ser703=)	not provided [RCV003877779]	likely benign	20	41202808	41202808	Human		name
405681834	CV3357124	single nucleotide variant	NM_001384317.1(ZHX3):c.291C>G (p.Asn97Lys)	not specified [RCV004488850]	uncertain significance	20	41204626	41204626	Human		name
407459721	CV3490337	single nucleotide variant	NM_001384317.1(ZHX3):c.221G>C (p.Gly74Ala)	not specified [RCV004687210]	uncertain significance	20	41204696	41204696	Human		name
407459726	CV3490338	single nucleotide variant	NM_001384317.1(ZHX3):c.224A>G (p.Tyr75Cys)	not specified [RCV004687211]	uncertain significance	20	41204693	41204693	Human		name
597728791	CV3625042	single nucleotide variant	NM_001384317.1(ZHX3):c.272A>C (p.Gln91Pro)	not specified [RCV004888566]	uncertain significance	20	41204645	41204645	Human		name
597728759	CV3625047	single nucleotide variant	NM_001384317.1(ZHX3):c.212C>T (p.Thr71Ile)	not specified [RCV004888570]	uncertain significance	20	41204705	41204705	Human		name
597963188	CV3753859	single nucleotide variant	NM_001384317.1(ZHX3):c.2403G>A (p.Thr801=)	not provided [RCV005082163]	likely benign	20	41202514	41202514	Human		name
597927396	CV3783455	single nucleotide variant	NM_001384317.1(ZHX3):c.1737G>A (p.Ser579=)	not provided [RCV005116142]	likely benign	20	41203180	41203180	Human		name
597871138	CV3835655	single nucleotide variant	NM_001384317.1(ZHX3):c.1278G>A (p.Leu426=)	not provided [RCV005176646]	likely benign	20	41203639	41203639	Human		name
597942248	CV3847212	single nucleotide variant	NM_001384317.1(ZHX3):c.1347C>T (p.Ser449=)	not provided [RCV005188132]	likely benign	20	41203570	41203570	Human		name
597938898	CV3852929	single nucleotide variant	NM_001384317.1(ZHX3):c.211A>C (p.Thr71Pro)	not provided [RCV005187330]	uncertain significance	20	41204706	41204706	Human		name
150504755	CV1224013	single nucleotide variant	NM_001384317.1(ZHX3):c.929A>G (p.Asn310Ser)	not provided [RCV001621662]	benign	20	41203988	41203988	Human	26	name
151874223	CV1369450	single nucleotide variant	NM_001384317.1(ZHX3):c.932C>T (p.Ala311Val)	not provided [RCV002036056]	uncertain significance	20	41203985	41203985	Human		name
151734103	CV1392962	single nucleotide variant	NM_001384317.1(ZHX3):c.787G>A (p.Val263Ile)	not provided [RCV001967409]	uncertain significance	20	41204130	41204130	Human		name
155953927	CV2043896	single nucleotide variant	NM_001384317.1(ZHX3):c.767C>T (p.Pro256Leu)	not provided [RCV002775921]\|not specified [RCV004686742]	uncertain significance	20	41204150	41204150	Human		name
156033224	CV2126850	single nucleotide variant	NM_001384317.1(ZHX3):c.757G>A (p.Ala253Thr)	not provided [RCV002949319]\|not specified [RCV004068278]	likely benign\|uncertain significance	20	41204160	41204160	Human		name
156377824	CV2207563	single nucleotide variant	NM_001384317.1(ZHX3):c.886C>T (p.Leu296Phe)	not specified [RCV004090354]	uncertain significance	20	41204031	41204031	Human		name
156133765	CV2235450	single nucleotide variant	NM_001384317.1(ZHX3):c.948C>G (p.Asn316Lys)	not specified [RCV004109498]	uncertain significance	20	41203969	41203969	Human		name
156098466	CV2250598	single nucleotide variant	NM_001384317.1(ZHX3):c.535A>G (p.Ile179Val)	not specified [RCV004129238]	uncertain significance	20	41204382	41204382	Human		name
156041410	CV2261377	single nucleotide variant	NM_001384317.1(ZHX3):c.710T>C (p.Val237Ala)	not specified [RCV004130017]	likely benign	20	41204207	41204207	Human		name
156287038	CV2288361	single nucleotide variant	NM_001384317.1(ZHX3):c.523G>A (p.Gly175Arg)	not specified [RCV004151919]	uncertain significance	20	41204394	41204394	Human		name
156282638	CV2288838	single nucleotide variant	NM_001384317.1(ZHX3):c.889C>G (p.Pro297Ala)	not specified [RCV004148043]	uncertain significance	20	41204028	41204028	Human		name
156262922	CV2329328	single nucleotide variant	NM_001384317.1(ZHX3):c.335G>A (p.Ser112Asn)	not specified [RCV004187347]	uncertain significance	20	41204582	41204582	Human		name
156250286	CV2359079	single nucleotide variant	NM_001384317.1(ZHX3):c.656C>T (p.Ser219Leu)	not provided [RCV003565606]\|not specified [RCV004214446]	uncertain significance	20	41204261	41204261	Human		name
156206367	CV2385316	single nucleotide variant	NM_001384317.1(ZHX3):c.494C>T (p.Ala165Val)	not provided [RCV003720744]\|not specified [RCV004230596]	uncertain significance	20	41204423	41204423	Human		name
329366192	CV2438215	single nucleotide variant	NM_001384317.1(ZHX3):c.838G>A (p.Val280Met)	not specified [RCV004256982]	uncertain significance	20	41204079	41204079	Human		name
329366836	CV2441924	single nucleotide variant	NM_001384317.1(ZHX3):c.370C>A (p.Leu124Ile)	not specified [RCV004262101]	uncertain significance	20	41204547	41204547	Human		name
401730769	CV2677338	single nucleotide variant	NM_001384317.1(ZHX3):c.347T>C (p.Phe116Ser)	not specified [RCV004295953]	uncertain significance	20	41204570	41204570	Human		name
401746113	CV2695504	single nucleotide variant	NM_001384317.1(ZHX3):c.884C>T (p.Ala295Val)	not provided [RCV003542478]\|not specified [RCV004305685]	uncertain significance	20	41204033	41204033	Human		name
401889727	CV2763347	single nucleotide variant	NM_001384317.1(ZHX3):c.400G>A (p.Gly134Arg)	not provided [RCV003720860]\|not specified [RCV004349243]	uncertain significance	20	41204517	41204517	Human		name
405028576	CV3076340	single nucleotide variant	NM_001384317.1(ZHX3):c.811T>C (p.Phe271Leu)	not provided [RCV003738970]	uncertain significance	20	41204106	41204106	Human		name
405681838	CV3357125	single nucleotide variant	NM_001384317.1(ZHX3):c.617T>C (p.Val206Ala)	not specified [RCV004488851]	uncertain significance	20	41204300	41204300	Human		name
405681843	CV3357126	single nucleotide variant	NM_001384317.1(ZHX3):c.674T>C (p.Val225Ala)	not specified [RCV004488852]	uncertain significance	20	41204243	41204243	Human		name
407459715	CV3490336	single nucleotide variant	NM_001384317.1(ZHX3):c.753T>G (p.His251Gln)	not specified [RCV004687209]	uncertain significance	20	41204164	41204164	Human		name
597728737	CV3625050	single nucleotide variant	NM_001384317.1(ZHX3):c.575G>A (p.Gly192Asp)	not specified [RCV004888573]	uncertain significance	20	41204342	41204342	Human		name
597728730	CV3625051	single nucleotide variant	NM_001384317.1(ZHX3):c.484C>G (p.Pro162Ala)	not specified [RCV004888574]	uncertain significance	20	41204433	41204433	Human		name
597929815	CV3742123	single nucleotide variant	NM_001384317.1(ZHX3):c.817T>A (p.Ser273Thr)	not provided [RCV005075755]	uncertain significance	20	41204100	41204100	Human		name
597858000	CV3769572	single nucleotide variant	NM_001384317.1(ZHX3):c.854A>G (p.His285Arg)	not provided [RCV005105614]	uncertain significance	20	41204063	41204063	Human		name
597953218	CV3795490	single nucleotide variant	NM_001384317.1(ZHX3):c.763G>A (p.Gly255Arg)	not provided [RCV005136500]	uncertain significance	20	41204154	41204154	Human		name
597858930	CV3822421	single nucleotide variant	NM_001384317.1(ZHX3):c.814C>T (p.Leu272Phe)	not provided [RCV005174719]	uncertain significance	20	41204103	41204103	Human		name
598260342	CV3934063	single nucleotide variant	NM_001384317.1(ZHX3):c.449T>C (p.Val150Ala)	not specified [RCV005300404]	uncertain significance	20	41204468	41204468	Human		name
598260347	CV3934065	single nucleotide variant	NM_001384317.1(ZHX3):c.707C>T (p.Ala236Val)	not specified [RCV005300405]	uncertain significance	20	41204210	41204210	Human		name
598159381	CV3934068	single nucleotide variant	NM_001384317.1(ZHX3):c.682G>A (p.Gly228Arg)	not specified [RCV005306558]	uncertain significance	20	41204235	41204235	Human		name
598159389	CV3934072	single nucleotide variant	NM_001384317.1(ZHX3):c.443A>C (p.His148Pro)	not specified [RCV005306560]	uncertain significance	20	41204474	41204474	Human		name
8689375	CV97463	single nucleotide variant	NM_001384317.1(ZHX3):c.496G>T (p.Gly166Cys)	not provided [RCV000122542]	uncertain significance	20	41204421	41204421	Human		name
151713893	CV1379593	single nucleotide variant	NM_001384317.1(ZHX3):c.1678C>A (p.Pro560Thr)	not provided [RCV001964838]	uncertain significance	20	41203239	41203239	Human		name
151818064	CV1397343	single nucleotide variant	NM_001384317.1(ZHX3):c.2164G>A (p.Val722Ile)	not provided [RCV001992496]	uncertain significance	20	41202753	41202753	Human		name
151775243	CV1424240	single nucleotide variant	NM_001384317.1(ZHX3):c.1778C>T (p.Thr593Ile)	not provided [RCV002025746]\|not specified [RCV004046091]	uncertain significance	20	41203139	41203139	Human		name
151723900	CV1436948	single nucleotide variant	NM_001384317.1(ZHX3):c.1229T>C (p.Leu410Pro)	not provided [RCV002004030]	uncertain significance	20	41203688	41203688	Human		name
151862582	CV1448891	single nucleotide variant	NM_001384317.1(ZHX3):c.2033A>G (p.Asn678Ser)	not provided [RCV001959410]	uncertain significance	20	41202884	41202884	Human		name
151754636	CV1453866	single nucleotide variant	NM_001384317.1(ZHX3):c.2755A>G (p.Thr919Ala)	not provided [RCV001913327]	uncertain significance	20	41202162	41202162	Human		name
151710291	CV1502189	single nucleotide variant	NM_001384317.1(ZHX3):c.2107T>C (p.Ser703Pro)	not provided [RCV001907856]	uncertain significance	20	41202810	41202810	Human		name
152076003	CV1528407	single nucleotide variant	NM_001384317.1(ZHX3):c.2011G>A (p.Glu671Lys)	ZHX3-related disorder [RCV003923571]\|not provided [RCV002112113]	likely benign	20	41202906	41202906	Human		name , trait , alternate_id
152031763	CV1546119	single nucleotide variant	NM_001384317.1(ZHX3):c.2209G>A (p.Ala737Thr)	not provided [RCV002124624]	benign	20	41202708	41202708	Human		name
152168326	CV1547965	single nucleotide variant	NM_001384317.1(ZHX3):c.2249A>T (p.Asp750Val)	ZHX3-related disorder [RCV003923803]\|not provided [RCV002161092]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	20	41202668	41202668	Human		name , trait , alternate_id
152073772	CV1638065	single nucleotide variant	NM_001384317.1(ZHX3):c.1186G>A (p.Val396Ile)	ZHX3-related disorder [RCV004758859]\|not provided [RCV002192142]	benign\|likely benign	20	41203731	41203731	Human		name , trait , alternate_id
152131730	CV1640129	single nucleotide variant	NM_001384317.1(ZHX3):c.1315A>G (p.Thr439Ala)	not provided [RCV002155630]	likely benign	20	41203602	41203602	Human		name
152121303	CV1662197	single nucleotide variant	NM_001384317.1(ZHX3):c.2262T>G (p.Asp754Glu)	not provided [RCV002117885]	benign	20	41202655	41202655	Human		name
156335344	CV1905961	single nucleotide variant	NM_001384317.1(ZHX3):c.2242G>A (p.Ala748Thr)	not provided [RCV003090034]	benign	20	41202675	41202675	Human		name
156355812	CV1917433	single nucleotide variant	NM_001384317.1(ZHX3):c.2495G>A (p.Arg832Gln)	not provided [RCV002632324]	uncertain significance	20	41202422	41202422	Human		name
156408887	CV1922094	single nucleotide variant	NM_001384317.1(ZHX3):c.1941T>A (p.Ser647Arg)	not provided [RCV002607384]	uncertain significance	20	41202976	41202976	Human		name
156310548	CV1928374	single nucleotide variant	NM_001384317.1(ZHX3):c.1421A>G (p.Asn474Ser)	not provided [RCV002630056]\|not specified [RCV004072123]	uncertain significance	20	41203496	41203496	Human		name
156215662	CV2084441	single nucleotide variant	NM_001384317.1(ZHX3):c.1441A>C (p.Thr481Pro)	not provided [RCV002853005]	uncertain significance	20	41203476	41203476	Human		name
156147546	CV2119152	single nucleotide variant	NM_001384317.1(ZHX3):c.2536A>T (p.Asn846Tyr)	not provided [RCV002954454]\|not specified [RCV004068193]	uncertain significance	20	41202381	41202381	Human		name
156344993	CV2120883	single nucleotide variant	NM_001384317.1(ZHX3):c.2082G>T (p.Glu694Asp)	not provided [RCV002939117]	uncertain significance	20	41202835	41202835	Human		name
156389552	CV2122323	single nucleotide variant	NM_001384317.1(ZHX3):c.1247G>T (p.Gly416Val)	not provided [RCV002943757]\|not specified [RCV004887707]	uncertain significance	20	41203670	41203670	Human		name
156074742	CV2141660	single nucleotide variant	NM_001384317.1(ZHX3):c.2150T>C (p.Leu717Ser)	not provided [RCV002979056]	uncertain significance	20	41202767	41202767	Human		name
156069739	CV2203826	single nucleotide variant	NM_001384317.1(ZHX3):c.1766C>T (p.Pro589Leu)	not specified [RCV004074461]	uncertain significance	20	41203151	41203151	Human		name
156130228	CV2209967	single nucleotide variant	NM_001384317.1(ZHX3):c.2090C>T (p.Ala697Val)	not specified [RCV004076409]	uncertain significance	20	41202827	41202827	Human		name
156279300	CV2227774	single nucleotide variant	NM_001384317.1(ZHX3):c.1115G>A (p.Arg372Gln)	not specified [RCV004094157]	uncertain significance	20	41203802	41203802	Human		name
156148608	CV2265288	single nucleotide variant	NM_001384317.1(ZHX3):c.2661G>A (p.Met887Ile)	not specified [RCV004128182]	uncertain significance	20	41202256	41202256	Human		name
156360704	CV2269088	single nucleotide variant	NM_001384317.1(ZHX3):c.2009A>C (p.Glu670Ala)	not specified [RCV004130265]	uncertain significance	20	41202908	41202908	Human		name
156239052	CV2269089	single nucleotide variant	NM_001384317.1(ZHX3):c.2010G>T (p.Glu670Asp)	not specified [RCV004130266]	uncertain significance	20	41202907	41202907	Human		name
156083605	CV2289608	single nucleotide variant	NM_001384317.1(ZHX3):c.2074G>A (p.Gly692Arg)	not specified [RCV004148532]	uncertain significance	20	41202843	41202843	Human		name
156183860	CV2292189	single nucleotide variant	NM_001384317.1(ZHX3):c.2537A>T (p.Asn846Ile)	not specified [RCV004148242]	uncertain significance	20	41202380	41202380	Human		name
155971257	CV2309278	single nucleotide variant	NM_001384317.1(ZHX3):c.2159G>A (p.Arg720His)	not specified [RCV004165440]	uncertain significance	20	41202758	41202758	Human		name
156070858	CV2325144	single nucleotide variant	NM_001384317.1(ZHX3):c.1658A>T (p.Lys553Met)	not specified [RCV004177569]	uncertain significance	20	41203259	41203259	Human		name
156063395	CV2331004	single nucleotide variant	NM_001384317.1(ZHX3):c.1343C>T (p.Thr448Ile)	not specified [RCV004188043]	uncertain significance	20	41203574	41203574	Human		name
156065482	CV2340837	single nucleotide variant	NM_001384317.1(ZHX3):c.1563G>C (p.Gln521His)	not specified [RCV004188194]	uncertain significance	20	41203354	41203354	Human		name
156188256	CV2346805	single nucleotide variant	NM_001384317.1(ZHX3):c.2852G>A (p.Arg951His)	not specified [RCV004199812]	uncertain significance	20	41202065	41202065	Human		name
156107386	CV2390121	single nucleotide variant	NM_001384317.1(ZHX3):c.2539C>T (p.Arg847Trp)	not specified [RCV004240510]	uncertain significance	20	41202378	41202378	Human		name
329374138	CV2443675	single nucleotide variant	NM_001384317.1(ZHX3):c.1348G>A (p.Val450Ile)	not specified [RCV004255979]	uncertain significance	20	41203569	41203569	Human		name
329394632	CV2461485	single nucleotide variant	NM_001384317.1(ZHX3):c.2108C>G (p.Ser703Cys)	not specified [RCV004269415]	uncertain significance	20	41202809	41202809	Human		name
401745110	CV2693182	single nucleotide variant	NM_001384317.1(ZHX3):c.1816C>T (p.His606Tyr)	not specified [RCV004293113]	uncertain significance	20	41203101	41203101	Human		name
401770245	CV2711013	single nucleotide variant	NM_001384317.1(ZHX3):c.1592C>T (p.Thr531Met)	not specified [RCV004310714]	uncertain significance	20	41203325	41203325	Human		name
401782565	CV2719880	single nucleotide variant	NM_001384317.1(ZHX3):c.1849A>G (p.Lys617Glu)	not specified [RCV004329288]	uncertain significance	20	41203068	41203068	Human		name
401889961	CV2763563	single nucleotide variant	NM_001384317.1(ZHX3):c.1130A>G (p.Asn377Ser)	not specified [RCV004343080]	uncertain significance	20	41203787	41203787	Human		name
401870272	CV2765778	single nucleotide variant	NM_001384317.1(ZHX3):c.1240G>A (p.Val414Ile)	not specified [RCV004335778]	uncertain significance	20	41203677	41203677	Human		name
405176863	CV2860981	single nucleotide variant	NM_001384317.1(ZHX3):c.1189G>A (p.Ala397Thr)	not provided [RCV003542835]	uncertain significance	20	41203728	41203728	Human		name
405056785	CV2932113	single nucleotide variant	NM_001384317.1(ZHX3):c.2290C>G (p.Pro764Ala)	not provided [RCV003580182]	uncertain significance	20	41202627	41202627	Human		name
405228792	CV2973692	single nucleotide variant	NM_001384317.1(ZHX3):c.2506C>G (p.Pro836Ala)	not provided [RCV003681837]	uncertain significance	20	41202411	41202411	Human		name
405052510	CV3022209	single nucleotide variant	NM_001384317.1(ZHX3):c.1399A>G (p.Thr467Ala)	not provided [RCV003697106]	uncertain significance	20	41203518	41203518	Human		name
405254005	CV3045100	single nucleotide variant	NM_001384317.1(ZHX3):c.2482G>A (p.Glu828Lys)	not provided [RCV003722745]	uncertain significance	20	41202435	41202435	Human		name
405245458	CV3054960	single nucleotide variant	NM_001384317.1(ZHX3):c.2770T>A (p.Ser924Thr)	not provided [RCV003720210]	uncertain significance	20	41202147	41202147	Human		name
405120935	CV3116553	single nucleotide variant	NM_001384317.1(ZHX3):c.2018A>G (p.Lys673Arg)	not provided [RCV003814855]	uncertain significance	20	41202899	41202899	Human		name
405162554	CV3153136	single nucleotide variant	NM_001384317.1(ZHX3):c.1424C>T (p.Ala475Val)	not provided [RCV003840871]	uncertain significance	20	41203493	41203493	Human		name
405235512	CV3155914	single nucleotide variant	NM_001384317.1(ZHX3):c.2558A>G (p.Tyr853Cys)	not provided [RCV003853647]	uncertain significance	20	41202359	41202359	Human		name
405803726	CV3357113	single nucleotide variant	NM_001384317.1(ZHX3):c.1136T>C (p.Val379Ala)	not specified [RCV004478924]	uncertain significance	20	41203781	41203781	Human		name
405803729	CV3357114	single nucleotide variant	NM_001384317.1(ZHX3):c.1632T>A (p.Asp544Glu)	not specified [RCV004478925]	uncertain significance	20	41203285	41203285	Human		name
405803733	CV3357116	single nucleotide variant	NM_001384317.1(ZHX3):c.2326C>T (p.Arg776Trp)	not specified [RCV004478927]	uncertain significance	20	41202591	41202591	Human		name
405803735	CV3357117	single nucleotide variant	NM_001384317.1(ZHX3):c.2372A>T (p.Asn791Ile)	not specified [RCV004478928]	uncertain significance	20	41202545	41202545	Human		name
405803737	CV3357118	single nucleotide variant	NM_001384317.1(ZHX3):c.2429G>A (p.Arg810His)	not specified [RCV004478929]	uncertain significance	20	41202488	41202488	Human		name
405803739	CV3357119	single nucleotide variant	NM_001384317.1(ZHX3):c.2473A>C (p.Lys825Gln)	not specified [RCV004478930]	uncertain significance	20	41202444	41202444	Human		name
405803741	CV3357120	single nucleotide variant	NM_001384317.1(ZHX3):c.2501A>G (p.Asn834Ser)	not specified [RCV004478931]	uncertain significance	20	41202416	41202416	Human		name
405803743	CV3357121	single nucleotide variant	NM_001384317.1(ZHX3):c.2689A>C (p.Thr897Pro)	not provided [RCV005065145]\|not specified [RCV004478932]	uncertain significance	20	41202228	41202228	Human		name
405803746	CV3357122	single nucleotide variant	NM_001384317.1(ZHX3):c.2834C>G (p.Ser945Trp)	not provided [RCV005065146]\|not specified [RCV004478933]	uncertain significance	20	41202083	41202083	Human		name
405803748	CV3357123	single nucleotide variant	NM_001384317.1(ZHX3):c.2837G>T (p.Ser946Ile)	not specified [RCV004478934]	uncertain significance	20	41202080	41202080	Human		name
407459697	CV3490333	single nucleotide variant	NM_001384317.1(ZHX3):c.2662G>C (p.Gly888Arg)	not specified [RCV004687206]	uncertain significance	20	41202255	41202255	Human		name
407459703	CV3490334	single nucleotide variant	NM_001384317.1(ZHX3):c.1300A>G (p.Asn434Asp)	not specified [RCV004687207]	uncertain significance	20	41203617	41203617	Human		name
407459709	CV3490335	single nucleotide variant	NM_001384317.1(ZHX3):c.2327G>A (p.Arg776Gln)	not specified [RCV004687208]	uncertain significance	20	41202590	41202590	Human		name
407459732	CV3490339	single nucleotide variant	NM_001384317.1(ZHX3):c.2803C>T (p.Pro935Ser)	not specified [RCV004687212]	uncertain significance	20	41202114	41202114	Human		name
407459739	CV3490340	single nucleotide variant	NM_001384317.1(ZHX3):c.1658A>G (p.Lys553Arg)	not specified [RCV004687213]	uncertain significance	20	41203259	41203259	Human		name
407459744	CV3490341	single nucleotide variant	NM_001384317.1(ZHX3):c.2158C>T (p.Arg720Cys)	not specified [RCV004687214]	uncertain significance	20	41202759	41202759	Human		name
407459751	CV3490342	single nucleotide variant	NM_001384317.1(ZHX3):c.1736C>T (p.Ser579Leu)	not specified [RCV004687215]	uncertain significance	20	41203181	41203181	Human		name
597728783	CV3625043	single nucleotide variant	NM_001384317.1(ZHX3):c.1301A>G (p.Asn434Ser)	not specified [RCV004888567]	uncertain significance	20	41203616	41203616	Human		name
597728775	CV3625044	single nucleotide variant	NM_001384317.1(ZHX3):c.1225G>A (p.Ala409Thr)	not specified [RCV004888568]	uncertain significance	20	41203692	41203692	Human		name
597728768	CV3625046	single nucleotide variant	NM_001384317.1(ZHX3):c.1857A>C (p.Arg619Ser)	not specified [RCV004888569]	uncertain significance	20	41203060	41203060	Human		name
597728752	CV3625048	single nucleotide variant	NM_001384317.1(ZHX3):c.2729C>A (p.Thr910Lys)	not specified [RCV004888571]	uncertain significance	20	41202188	41202188	Human		name
597728744	CV3625049	single nucleotide variant	NM_001384317.1(ZHX3):c.1103T>C (p.Ile368Thr)	not specified [RCV004888572]	uncertain significance	20	41203814	41203814	Human		name
597728723	CV3625052	single nucleotide variant	NM_001384317.1(ZHX3):c.1298C>T (p.Ala433Val)	not specified [RCV004888575]	uncertain significance	20	41203619	41203619	Human		name
597912611	CV3745730	single nucleotide variant	NM_001384317.1(ZHX3):c.2375A>G (p.Gln792Arg)	not provided [RCV005073731]	uncertain significance	20	41202542	41202542	Human		name
597953805	CV3757043	single nucleotide variant	NM_001384317.1(ZHX3):c.2809G>T (p.Ala937Ser)	not provided [RCV005079904]	uncertain significance	20	41202108	41202108	Human		name
597891205	CV3762967	single nucleotide variant	NM_001384317.1(ZHX3):c.2045A>G (p.Glu682Gly)	not provided [RCV005110740]	uncertain significance	20	41202872	41202872	Human		name
597877302	CV3766769	single nucleotide variant	NM_001384317.1(ZHX3):c.1655T>C (p.Leu552Ser)	not provided [RCV005108709]	uncertain significance	20	41203262	41203262	Human		name
597881359	CV3810373	single nucleotide variant	NM_001384317.1(ZHX3):c.1058C>T (p.Thr353Ile)	not provided [RCV005149834]	uncertain significance	20	41203859	41203859	Human		name
597843617	CV3827330	single nucleotide variant	NM_001384317.1(ZHX3):c.1867C>A (p.Gln623Lys)	not provided [RCV005172601]	uncertain significance	20	41203050	41203050	Human		name
597902761	CV3851492	single nucleotide variant	NM_001384317.1(ZHX3):c.1467A>T (p.Gln489His)	not provided [RCV005202269]	uncertain significance	20	41203450	41203450	Human		name
597862723	CV3860593	single nucleotide variant	NM_001384317.1(ZHX3):c.2540G>A (p.Arg847Gln)	not provided [RCV005196121]	uncertain significance	20	41202377	41202377	Human		name
598159378	CV3934066	single nucleotide variant	NM_001384317.1(ZHX3):c.2213A>G (p.Asn738Ser)	not specified [RCV005306557]	uncertain significance	20	41202704	41202704	Human		name
598260357	CV3934069	single nucleotide variant	NM_001384317.1(ZHX3):c.2452G>A (p.Ala818Thr)	not specified [RCV005300407]	uncertain significance	20	41202465	41202465	Human		name
598260360	CV3934070	single nucleotide variant	NM_001384317.1(ZHX3):c.1616G>A (p.Arg539Gln)	not specified [RCV005300408]	uncertain significance	20	41203301	41203301	Human		name
598159392	CV3934073	single nucleotide variant	NM_001384317.1(ZHX3):c.1874G>A (p.Arg625Lys)	not specified [RCV005306561]	uncertain significance	20	41203043	41203043	Human		name
597940330	CV3757220	deletion	NM_001384317.1(ZHX3):c.2519_2530del (p.Leu840_Ala843del)	not provided [RCV005077405]	uncertain significance	20	41202387	41202398	Human		name

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