Wdr90 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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287 records found for search term Wdr90

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401904830	CV2810716	single nucleotide variant	NM_145294.5(WDR90):c.560-7C>T	not provided [RCV003395124]	likely benign	16	650988	650988	Human		name
15152268	CV780048	single nucleotide variant	NM_145294.5(WDR90):c.3674-5C>G	not provided [RCV000968317]	benign	16	661592	661592	Human		name
156297672	CV2328973	single nucleotide variant	NM_145294.5(WDR90):c.4G>C (p.Ala2Pro)	not specified [RCV004180267]	uncertain significance	16	649420	649420	Human		name
401867379	CV2766672	single nucleotide variant	NM_145294.5(WDR90):c.22C>T (p.Pro8Ser)	not specified [RCV004347281]	uncertain significance	16	649774	649774	Human		name
156077579	CV2281672	single nucleotide variant	NM_145294.5(WDR90):c.158A>G (p.Asn53Ser)	not specified [RCV004153959]	uncertain significance	16	650046	650046	Human		name
156254454	CV2359214	single nucleotide variant	NM_145294.5(WDR90):c.206G>A (p.Gly69Glu)	not specified [RCV004212509]	uncertain significance	16	650094	650094	Human		name
401760341	CV2695009	single nucleotide variant	NM_145294.5(WDR90):c.272C>T (p.Ser91Phe)	not specified [RCV004301383]	uncertain significance	16	650160	650160	Human		name
401759066	CV2712388	single nucleotide variant	NM_145294.5(WDR90):c.233C>T (p.Pro78Leu)	not specified [RCV004313865]	uncertain significance	16	650121	650121	Human		name
401882243	CV2781593	single nucleotide variant	NM_145294.5(WDR90):c.185C>T (p.Thr62Ile)	not specified [RCV004354804]	uncertain significance	16	650073	650073	Human		name
401904831	CV2810718	single nucleotide variant	NM_145294.5(WDR90):c.1089C>T (p.Gly363=)	not provided [RCV003395126]	likely benign	16	652502	652502	Human		name
401930277	CV2810719	single nucleotide variant	NM_145294.5(WDR90):c.1594C>A (p.Arg532=)	not provided [RCV003390592]	likely benign	16	655344	655344	Human		name
405807672	CV3356540	single nucleotide variant	NM_145294.5(WDR90):c.172C>T (p.Pro58Ser)	not specified [RCV004480800]	uncertain significance	16	650060	650060	Human		name
405807682	CV3356545	single nucleotide variant	NM_145294.5(WDR90):c.202A>G (p.Thr68Ala)	not specified [RCV004480805]	uncertain significance	16	650090	650090	Human		name
405807694	CV3356551	single nucleotide variant	NM_145294.5(WDR90):c.278A>G (p.Lys93Arg)	not specified [RCV004480811]	uncertain significance	16	650166	650166	Human		name
596947971	CV3547562	single nucleotide variant	NM_145294.5(WDR90):c.1605C>T (p.Gly535=)	not provided [RCV004811866]	likely benign	16	655355	655355	Human		name
597792100	CV3630126	single nucleotide variant	NM_145294.5(WDR90):c.191C>T (p.Ser64Phe)	not specified [RCV004876880]	uncertain significance	16	650079	650079	Human		name
598267064	CV3933535	single nucleotide variant	NM_145294.5(WDR90):c.257T>A (p.Ile86Asn)	not specified [RCV005302091]	uncertain significance	16	650145	650145	Human		name
156114406	CV2208902	single nucleotide variant	NM_145294.5(WDR90):c.844G>A (p.Gly282Ser)	not specified [RCV004085269]	likely benign	16	651830	651830	Human		name
156290609	CV2226203	single nucleotide variant	NM_145294.5(WDR90):c.313C>G (p.Leu105Val)	not specified [RCV004105601]	uncertain significance	16	650287	650287	Human		name
156070575	CV2251349	single nucleotide variant	NM_145294.5(WDR90):c.899G>A (p.Arg300His)	not specified [RCV004115554]	likely benign	16	651885	651885	Human		name
156034771	CV2252893	single nucleotide variant	NM_145294.5(WDR90):c.370G>A (p.Ala124Thr)	not specified [RCV004120724]	uncertain significance	16	650344	650344	Human		name
155987604	CV2259484	single nucleotide variant	NM_145294.5(WDR90):c.667C>T (p.Arg223Trp)	not provided [RCV004695447]\|not specified [RCV004122686]	uncertain significance	16	651102	651102	Human		name
156038075	CV2259889	single nucleotide variant	NM_145294.5(WDR90):c.818T>C (p.Val273Ala)	not specified [RCV004118925]	uncertain significance	16	651725	651725	Human		name
155999178	CV2261062	single nucleotide variant	NM_145294.5(WDR90):c.313C>T (p.Leu105Phe)	not specified [RCV004127712]	uncertain significance	16	650287	650287	Human		name
155954246	CV2274303	single nucleotide variant	NM_145294.5(WDR90):c.653G>A (p.Arg218His)	not specified [RCV004136698]	likely benign	16	651088	651088	Human		name
156244210	CV2283332	single nucleotide variant	NM_145294.5(WDR90):c.830G>A (p.Ser277Asn)	not specified [RCV004145990]	uncertain significance	16	651737	651737	Human		name
156070494	CV2325092	single nucleotide variant	NM_145294.5(WDR90):c.958C>G (p.Leu320Val)	not specified [RCV004175625]	likely benign	16	651944	651944	Human		name
155926412	CV2345183	single nucleotide variant	NM_145294.5(WDR90):c.707T>C (p.Ile236Thr)	not specified [RCV004195922]	uncertain significance	16	651237	651237	Human		name
156068778	CV2355706	single nucleotide variant	NM_145294.5(WDR90):c.853G>A (p.Ala285Thr)	not specified [RCV004199068]	uncertain significance	16	651839	651839	Human		name
156339366	CV2367510	single nucleotide variant	NM_145294.5(WDR90):c.773C>T (p.Pro258Leu)	not specified [RCV004211446]	uncertain significance	16	651680	651680	Human		name
156391890	CV2382711	single nucleotide variant	NM_145294.5(WDR90):c.848G>A (p.Arg283Gln)	not specified [RCV004233020]	likely benign	16	651834	651834	Human		name
329359223	CV2435351	single nucleotide variant	NM_145294.5(WDR90):c.928G>A (p.Gly310Ser)	not specified [RCV004253010]	likely benign	16	651914	651914	Human		name
401777713	CV2704289	single nucleotide variant	NM_145294.5(WDR90):c.415G>T (p.Ala139Ser)	not specified [RCV004311277]	uncertain significance	16	650565	650565	Human		name
401904620	CV2810717	single nucleotide variant	NM_145294.5(WDR90):c.687G>T (p.Leu229Phe)	not provided [RCV003395125]	likely benign	16	651217	651217	Human		name
401904832	CV2810720	single nucleotide variant	NM_145294.5(WDR90):c.3060C>T (p.Gly1020=)	not provided [RCV003395127]	likely benign	16	659252	659252	Human		name
401904833	CV2810721	single nucleotide variant	NM_145294.5(WDR90):c.3831C>G (p.Leu1277=)	not provided [RCV003395128]	likely benign	16	661754	661754	Human		name
401930279	CV2810722	single nucleotide variant	NM_145294.5(WDR90):c.3990C>T (p.Ala1330=)	not provided [RCV003390593]	likely benign	16	662016	662016	Human		name
401904834	CV2810723	single nucleotide variant	NM_145294.5(WDR90):c.5154C>T (p.Asn1718=)	not provided [RCV003395129]	likely benign	16	667496	667496	Human		name
405807969	CV3356569	single nucleotide variant	NM_145294.5(WDR90):c.481G>A (p.Gly161Ser)	not specified [RCV004480829]	likely benign	16	650631	650631	Human		name
407524383	CV3489978	single nucleotide variant	NM_145294.5(WDR90):c.967T>C (p.Ser323Pro)	not specified [RCV004678404]	uncertain significance	16	651953	651953	Human		name
597792027	CV3630086	single nucleotide variant	NM_145294.5(WDR90):c.512G>C (p.Ser171Thr)	not specified [RCV004876855]	uncertain significance	16	650662	650662	Human		name
597792036	CV3630089	single nucleotide variant	NM_145294.5(WDR90):c.991G>A (p.Gly331Ser)	not specified [RCV004876858]	uncertain significance	16	651977	651977	Human		name
597739610	CV3630101	single nucleotide variant	NM_145294.5(WDR90):c.988G>A (p.Ala330Thr)	not specified [RCV004890363]	uncertain significance	16	651974	651974	Human		name
597792074	CV3630113	single nucleotide variant	NM_145294.5(WDR90):c.791C>G (p.Pro264Arg)	not specified [RCV004876871]	uncertain significance	16	651698	651698	Human		name
597739634	CV3630114	single nucleotide variant	NM_145294.5(WDR90):c.868C>G (p.Pro290Ala)	not specified [RCV004890368]	uncertain significance	16	651854	651854	Human		name
598232907	CV3933512	single nucleotide variant	NM_145294.5(WDR90):c.641G>A (p.Ser214Asn)	not specified [RCV005295484]	uncertain significance	16	651076	651076	Human		name
598267047	CV3933527	single nucleotide variant	NM_145294.5(WDR90):c.662A>C (p.His221Pro)	not specified [RCV005302087]	uncertain significance	16	651097	651097	Human		name
598232963	CV3933534	single nucleotide variant	NM_145294.5(WDR90):c.664G>T (p.Val222Phe)	not specified [RCV005295493]	uncertain significance	16	651099	651099	Human		name
15163081	CV726729	single nucleotide variant	NM_145294.5(WDR90):c.4017G>A (p.Ala1339=)	not provided [RCV000881891]	benign	16	662043	662043	Human		name
155962920	CV2197675	single nucleotide variant	NM_145294.5(WDR90):c.2164C>T (p.Arg722Cys)	not specified [RCV004074884]	uncertain significance	16	656499	656499	Human		name
156323527	CV2201730	single nucleotide variant	NM_145294.5(WDR90):c.2195T>C (p.Leu732Pro)	not specified [RCV004082175]	uncertain significance	16	656530	656530	Human		name
156181374	CV2201809	single nucleotide variant	NM_145294.5(WDR90):c.2036C>T (p.Ser679Leu)	not specified [RCV004082243]	uncertain significance	16	656371	656371	Human		name
156326914	CV2217167	single nucleotide variant	NM_145294.5(WDR90):c.1684C>T (p.Arg562Trp)	not specified [RCV004087626]	uncertain significance	16	655434	655434	Human		name
155923395	CV2217624	single nucleotide variant	NM_145294.5(WDR90):c.2974G>A (p.Ala992Thr)	not specified [RCV004090145]	uncertain significance	16	658974	658974	Human		name
156112543	CV2218096	single nucleotide variant	NM_145294.5(WDR90):c.1825C>A (p.Pro609Thr)	not specified [RCV004086528]	uncertain significance	16	655679	655679	Human		name
156071150	CV2229122	single nucleotide variant	NM_145294.5(WDR90):c.2894A>G (p.Gln965Arg)	not specified [RCV004099169]	uncertain significance	16	658652	658652	Human		name
156028594	CV2238244	single nucleotide variant	NM_145294.5(WDR90):c.2122A>G (p.Met708Val)	not specified [RCV004113332]	uncertain significance	16	656457	656457	Human		name
156233523	CV2245266	single nucleotide variant	NM_145294.5(WDR90):c.2173C>T (p.Arg725Cys)	not specified [RCV004107032]	uncertain significance	16	656508	656508	Human		name
156316125	CV2250867	single nucleotide variant	NM_145294.5(WDR90):c.2445C>A (p.Asp815Glu)	not specified [RCV004123461]	uncertain significance	16	657193	657193	Human		name
156317455	CV2251049	single nucleotide variant	NM_145294.5(WDR90):c.1648G>A (p.Ala550Thr)	not specified [RCV004123605]	uncertain significance	16	655398	655398	Human		name
156017426	CV2262860	single nucleotide variant	NM_145294.5(WDR90):c.2965G>A (p.Ala989Thr)	not provided [RCV004695473]\|not specified [RCV004125008]	uncertain significance	16	658965	658965	Human		name
155907055	CV2279652	single nucleotide variant	NM_145294.5(WDR90):c.2255C>T (p.Pro752Leu)	not specified [RCV004142148]	uncertain significance	16	656784	656784	Human		name
155932847	CV2299970	single nucleotide variant	NM_145294.5(WDR90):c.2234C>G (p.Pro745Arg)	not specified [RCV004151186]	uncertain significance	16	656763	656763	Human		name
156047334	CV2304334	single nucleotide variant	NM_145294.5(WDR90):c.1606G>T (p.Gly536Trp)	not specified [RCV004164451]	uncertain significance	16	655356	655356	Human		name
155971247	CV2309277	single nucleotide variant	NM_145294.5(WDR90):c.2834T>C (p.Ile945Thr)	not specified [RCV004165439]	likely benign	16	658592	658592	Human		name
156305690	CV2314705	single nucleotide variant	NM_145294.5(WDR90):c.1770G>A (p.Met590Ile)	not specified [RCV004170850]	uncertain significance	16	655624	655624	Human		name
156325261	CV2335213	single nucleotide variant	NM_145294.5(WDR90):c.1565C>T (p.Ser522Leu)	not specified [RCV004186786]	uncertain significance	16	655315	655315	Human		name
156279900	CV2338348	single nucleotide variant	NM_145294.5(WDR90):c.2390G>A (p.Arg797His)	not specified [RCV004186399]	uncertain significance	16	657138	657138	Human		name
156060218	CV2343762	single nucleotide variant	NM_145294.5(WDR90):c.1822C>A (p.His608Asn)	not specified [RCV004190783]	uncertain significance	16	655676	655676	Human		name
155923826	CV2347570	single nucleotide variant	NM_145294.5(WDR90):c.2072T>G (p.Val691Gly)	not specified [RCV004200508]	uncertain significance	16	656407	656407	Human		name
156279272	CV2348318	single nucleotide variant	NM_145294.5(WDR90):c.2717C>T (p.Ser906Phe)	not specified [RCV004193517]	uncertain significance	16	658295	658295	Human		name
156283475	CV2348942	single nucleotide variant	NM_145294.5(WDR90):c.2345G>A (p.Cys782Tyr)	not specified [RCV004203376]	uncertain significance	16	657093	657093	Human		name
156283761	CV2348966	single nucleotide variant	NM_145294.5(WDR90):c.1327G>A (p.Gly443Arg)	not specified [RCV004203399]	uncertain significance	16	653618	653618	Human		name
156117626	CV2349487	single nucleotide variant	NM_145294.5(WDR90):c.2089C>T (p.Arg697Cys)	not specified [RCV004201455]	uncertain significance	16	656424	656424	Human		name
156117643	CV2349488	single nucleotide variant	NM_145294.5(WDR90):c.2804C>T (p.Thr935Met)	not specified [RCV004201456]	likely benign	16	658562	658562	Human		name
156182677	CV2353172	single nucleotide variant	NM_145294.5(WDR90):c.1549G>A (p.Glu517Lys)	not specified [RCV004203644]	uncertain significance	16	655140	655140	Human		name
155988335	CV2355067	single nucleotide variant	NM_145294.5(WDR90):c.2296G>A (p.Val766Met)	not specified [RCV004198461]	uncertain significance	16	656825	656825	Human		name
156343137	CV2364069	single nucleotide variant	NM_145294.5(WDR90):c.2405C>T (p.Ser802Phe)	not specified [RCV004221453]	uncertain significance	16	657153	657153	Human		name
155907963	CV2387173	single nucleotide variant	NM_145294.5(WDR90):c.1789C>G (p.Arg597Gly)	not specified [RCV004238278]	uncertain significance	16	655643	655643	Human		name
155998281	CV2393407	single nucleotide variant	NM_145294.5(WDR90):c.1627G>A (p.Val543Met)	not specified [RCV004228905]	uncertain significance	16	655377	655377	Human		name
329392332	CV2441453	single nucleotide variant	NM_145294.5(WDR90):c.2230G>A (p.Ala744Thr)	not specified [RCV004257248]	uncertain significance	16	656759	656759	Human		name
329399977	CV2444474	single nucleotide variant	NM_145294.5(WDR90):c.2582T>C (p.Met861Thr)	not specified [RCV004263205]	uncertain significance	16	657870	657870	Human		name
329391475	CV2448608	single nucleotide variant	NM_145294.5(WDR90):c.1531C>T (p.Arg511Trp)	not specified [RCV004259281]	uncertain significance	16	655122	655122	Human		name
329352312	CV2452345	single nucleotide variant	NM_145294.5(WDR90):c.1136C>T (p.Pro379Leu)	not specified [RCV004272673]	uncertain significance	16	653354	653354	Human		name
329395626	CV2454407	single nucleotide variant	NM_145294.5(WDR90):c.2240C>G (p.Ala747Gly)	not specified [RCV004267918]	uncertain significance	16	656769	656769	Human		name
401746992	CV2678980	single nucleotide variant	NM_145294.5(WDR90):c.2755A>G (p.Ile919Val)	not specified [RCV004294993]	likely benign	16	658333	658333	Human		name
401733554	CV2682567	single nucleotide variant	NM_145294.5(WDR90):c.2290G>A (p.Gly764Arg)	not specified [RCV004290577]	uncertain significance	16	656819	656819	Human		name
401721501	CV2683529	single nucleotide variant	NM_145294.5(WDR90):c.1436C>T (p.Thr479Met)	not specified [RCV004282463]	uncertain significance	16	653802	653802	Human		name
401781856	CV2689963	single nucleotide variant	NM_145294.5(WDR90):c.2500G>A (p.Ala834Thr)	not specified [RCV004297847]	uncertain significance	16	657788	657788	Human		name
401734290	CV2690540	single nucleotide variant	NM_145294.5(WDR90):c.2747C>T (p.Ser916Leu)	not specified [RCV004304649]	uncertain significance	16	658325	658325	Human		name
401722833	CV2703514	single nucleotide variant	NM_145294.5(WDR90):c.2165G>A (p.Arg722His)	not specified [RCV004317693]	likely benign	16	656500	656500	Human		name
401773331	CV2716529	single nucleotide variant	NM_145294.5(WDR90):c.2761C>T (p.Arg921Trp)	not specified [RCV004327610]	uncertain significance	16	658339	658339	Human		name
401769960	CV2718969	single nucleotide variant	NM_145294.5(WDR90):c.1777C>G (p.Arg593Gly)	not specified [RCV004322560]	uncertain significance	16	655631	655631	Human		name
401743827	CV2726174	single nucleotide variant	NM_145294.5(WDR90):c.1489G>A (p.Val497Ile)	not specified [RCV004326651]	likely benign	16	655080	655080	Human		name
401781072	CV2726416	single nucleotide variant	NM_145294.5(WDR90):c.1363G>T (p.Val455Phe)	not specified [RCV004328626]	uncertain significance	16	653654	653654	Human		name
401755882	CV2731167	single nucleotide variant	NM_145294.5(WDR90):c.2465G>A (p.Arg822Gln)	not specified [RCV004332667]	uncertain significance	16	657213	657213	Human		name
401855497	CV2757366	single nucleotide variant	NM_145294.5(WDR90):c.2438G>A (p.Cys813Tyr)	not specified [RCV004340768]	uncertain significance	16	657186	657186	Human		name
401854339	CV2766660	single nucleotide variant	NM_145294.5(WDR90):c.1805G>A (p.Arg602Gln)	not specified [RCV004347269]	likely benign	16	655659	655659	Human		name
401863551	CV2770696	single nucleotide variant	NM_145294.5(WDR90):c.1951G>A (p.Val651Met)	not specified [RCV004349744]	uncertain significance	16	655874	655874	Human		name
401897684	CV2772779	single nucleotide variant	NM_145294.5(WDR90):c.2620A>G (p.Ile874Val)	not specified [RCV004357577]	likely benign	16	658198	658198	Human		name
401866414	CV2782835	single nucleotide variant	NM_145294.5(WDR90):c.2423T>C (p.Leu808Pro)	not specified [RCV004361647]	uncertain significance	16	657171	657171	Human		name
405807667	CV3356537	single nucleotide variant	NM_145294.5(WDR90):c.1393G>A (p.Gly465Arg)	not specified [RCV004480797]	uncertain significance	16	653759	653759	Human		name
405807669	CV3356538	single nucleotide variant	NM_145294.5(WDR90):c.1502C>T (p.Ala501Val)	not specified [RCV004480798]	likely benign	16	655093	655093	Human		name
405807670	CV3356539	single nucleotide variant	NM_145294.5(WDR90):c.1580G>C (p.Ser527Thr)	not specified [RCV004480799]	uncertain significance	16	655330	655330	Human		name
405807674	CV3356541	single nucleotide variant	NM_145294.5(WDR90):c.1754T>C (p.Ile585Thr)	not specified [RCV004480801]	uncertain significance	16	655608	655608	Human		name
405807676	CV3356542	single nucleotide variant	NM_145294.5(WDR90):c.1768A>G (p.Met590Val)	not specified [RCV004480802]	uncertain significance	16	655622	655622	Human		name
405807678	CV3356543	single nucleotide variant	NM_145294.5(WDR90):c.1789C>T (p.Arg597Cys)	not specified [RCV004480803]	uncertain significance	16	655643	655643	Human		name
405807680	CV3356544	single nucleotide variant	NM_145294.5(WDR90):c.2014C>T (p.Arg672Cys)	not specified [RCV004480804]	uncertain significance	16	656349	656349	Human		name
405807684	CV3356546	single nucleotide variant	NM_145294.5(WDR90):c.2068C>T (p.Arg690Trp)	not specified [RCV004480806]	uncertain significance	16	656403	656403	Human		name
405807686	CV3356547	single nucleotide variant	NM_145294.5(WDR90):c.2239G>A (p.Ala747Thr)	not specified [RCV004480807]	likely benign	16	656768	656768	Human		name
405807690	CV3356549	single nucleotide variant	NM_145294.5(WDR90):c.2385C>G (p.Asp795Glu)	not specified [RCV004480809]	uncertain significance	16	657133	657133	Human		name
405807692	CV3356550	single nucleotide variant	NM_145294.5(WDR90):c.2663T>C (p.Met888Thr)	not specified [RCV004480810]	uncertain significance	16	658241	658241	Human		name
405807697	CV3356552	single nucleotide variant	NM_145294.5(WDR90):c.2912C>T (p.Ser971Leu)	not specified [RCV004480812]	uncertain significance	16	658912	658912	Human		name
405807699	CV3356553	single nucleotide variant	NM_145294.5(WDR90):c.2966C>T (p.Ala989Val)	not specified [RCV004480813]	likely benign	16	658966	658966	Human		name
407524361	CV3489966	single nucleotide variant	NM_145294.5(WDR90):c.2465G>C (p.Arg822Pro)	not specified [RCV004678396]	uncertain significance	16	657213	657213	Human		name
407524364	CV3489967	single nucleotide variant	NM_145294.5(WDR90):c.1981G>A (p.Val661Ile)	not specified [RCV004678397]	likely benign	16	656316	656316	Human		name
407524366	CV3489968	single nucleotide variant	NM_145294.5(WDR90):c.1777C>T (p.Arg593Trp)	not specified [RCV004678398]	uncertain significance	16	655631	655631	Human		name
407524369	CV3489970	single nucleotide variant	NM_145294.5(WDR90):c.2537G>A (p.Arg846His)	not specified [RCV004678399]	uncertain significance	16	657825	657825	Human		name
407524374	CV3489972	single nucleotide variant	NM_145294.5(WDR90):c.1546G>A (p.Asp516Asn)	not specified [RCV004678401]	uncertain significance	16	655137	655137	Human		name
407465370	CV3489973	single nucleotide variant	NM_145294.5(WDR90):c.1766G>A (p.Arg589His)	not specified [RCV004688751]	uncertain significance	16	655620	655620	Human		name
407524379	CV3489976	single nucleotide variant	NM_145294.5(WDR90):c.1720T>A (p.Phe574Ile)	not specified [RCV004678403]	uncertain significance	16	655574	655574	Human		name
407465378	CV3489977	single nucleotide variant	NM_145294.5(WDR90):c.1309C>T (p.Leu437Phe)	not specified [RCV004688753]	uncertain significance	16	653600	653600	Human		name
407465382	CV3489979	single nucleotide variant	NM_145294.5(WDR90):c.2902A>G (p.Ile968Val)	not specified [RCV004688754]	uncertain significance	16	658902	658902	Human		name
597792013	CV3630079	single nucleotide variant	NM_145294.5(WDR90):c.2714C>T (p.Ser905Leu)	not specified [RCV004876850]	uncertain significance	16	658292	658292	Human		name
597792016	CV3630081	single nucleotide variant	NM_145294.5(WDR90):c.1534G>C (p.Val512Leu)	not specified [RCV004876851]	uncertain significance	16	655125	655125	Human		name
597739584	CV3630082	single nucleotide variant	NM_145294.5(WDR90):c.2119G>A (p.Ala707Thr)	not specified [RCV004890357]	uncertain significance	16	656454	656454	Human		name
597792018	CV3630083	single nucleotide variant	NM_145294.5(WDR90):c.2246C>T (p.Thr749Ile)	not specified [RCV004876852]	uncertain significance	16	656775	656775	Human		name
597792025	CV3630085	single nucleotide variant	NM_145294.5(WDR90):c.2327T>C (p.Val776Ala)	not specified [RCV004876854]	uncertain significance	16	656856	656856	Human		name
597792029	CV3630087	single nucleotide variant	NM_145294.5(WDR90):c.2170G>A (p.Val724Ile)	not specified [RCV004876856]	uncertain significance	16	656505	656505	Human		name
597739589	CV3630090	single nucleotide variant	NM_145294.5(WDR90):c.1208G>A (p.Arg403His)	not specified [RCV004890358]	uncertain significance	16	653426	653426	Human		name
597792040	CV3630093	single nucleotide variant	NM_145294.5(WDR90):c.1786C>T (p.Arg596Cys)	not specified [RCV004876859]	uncertain significance	16	655640	655640	Human		name
597792046	CV3630096	single nucleotide variant	NM_145294.5(WDR90):c.1090G>A (p.Val364Ile)	not specified [RCV004876861]	uncertain significance	16	652503	652503	Human		name
597739601	CV3630098	single nucleotide variant	NM_145294.5(WDR90):c.1474G>A (p.Gly492Ser)	not specified [RCV004890361]	uncertain significance	16	655065	655065	Human		name
597792050	CV3630100	single nucleotide variant	NM_145294.5(WDR90):c.1562C>T (p.Ala521Val)	not specified [RCV004876863]	uncertain significance	16	655312	655312	Human		name
597792056	CV3630104	single nucleotide variant	NM_145294.5(WDR90):c.1528T>A (p.Phe510Ile)	not specified [RCV004876865]	uncertain significance	16	655119	655119	Human		name
597792062	CV3630107	single nucleotide variant	NM_145294.5(WDR90):c.2794C>A (p.Pro932Thr)	not specified [RCV004876867]	uncertain significance	16	658552	658552	Human		name
597739625	CV3630108	single nucleotide variant	NM_145294.5(WDR90):c.2543T>G (p.Leu848Arg)	not specified [RCV004890366]	uncertain significance	16	657831	657831	Human		name
597739629	CV3630109	single nucleotide variant	NM_145294.5(WDR90):c.2164C>G (p.Arg722Gly)	not specified [RCV004890367]	uncertain significance	16	656499	656499	Human		name
597792072	CV3630112	single nucleotide variant	NM_145294.5(WDR90):c.2821C>T (p.Arg941Cys)	not specified [RCV004876870]	uncertain significance	16	658579	658579	Human		name
597792080	CV3630116	single nucleotide variant	NM_145294.5(WDR90):c.1990G>A (p.Val664Ile)	not specified [RCV004876873]	uncertain significance	16	656325	656325	Human		name
597739638	CV3630118	single nucleotide variant	NM_145294.5(WDR90):c.1150G>T (p.Val384Phe)	not specified [RCV004890369]	uncertain significance	16	653368	653368	Human		name
597792089	CV3630121	single nucleotide variant	NM_145294.5(WDR90):c.2381C>T (p.Pro794Leu)	not specified [RCV004876876]	uncertain significance	16	657129	657129	Human		name
597792091	CV3630123	single nucleotide variant	NM_145294.5(WDR90):c.2918C>G (p.Pro973Arg)	not specified [RCV004876877]	uncertain significance	16	658918	658918	Human		name
597792098	CV3630125	single nucleotide variant	NM_145294.5(WDR90):c.2489C>T (p.Pro830Leu)	not specified [RCV004876879]	uncertain significance	16	657777	657777	Human		name
597792108	CV3630129	single nucleotide variant	NM_145294.5(WDR90):c.2837C>T (p.Ala946Val)	not specified [RCV004876883]	uncertain significance	16	658595	658595	Human		name
597792124	CV3630135	single nucleotide variant	NM_145294.5(WDR90):c.1942T>A (p.Phe648Ile)	not specified [RCV004876888]	uncertain significance	16	655865	655865	Human		name
598232858	CV3933495	single nucleotide variant	NM_145294.5(WDR90):c.1285G>A (p.Ala429Thr)	not specified [RCV005295476]	uncertain significance	16	653576	653576	Human		name
598232865	CV3933496	single nucleotide variant	NM_145294.5(WDR90):c.1537A>G (p.Thr513Ala)	not specified [RCV005295477]	likely benign	16	655128	655128	Human		name
598232878	CV3933500	single nucleotide variant	NM_145294.5(WDR90):c.1036C>T (p.Arg346Cys)	not specified [RCV005295479]	uncertain significance	16	652022	652022	Human		name
598266978	CV3933501	single nucleotide variant	NM_145294.5(WDR90):c.1196C>T (p.Thr399Met)	not specified [RCV005302071]	uncertain significance	16	653414	653414	Human		name
598232888	CV3933503	single nucleotide variant	NM_145294.5(WDR90):c.2762G>A (p.Arg921Gln)	not specified [RCV005295481]	uncertain significance	16	658340	658340	Human		name
598266984	CV3933505	single nucleotide variant	NM_145294.5(WDR90):c.1141G>A (p.Gly381Arg)	not specified [RCV005302072]	uncertain significance	16	653359	653359	Human		name
598266996	CV3933509	single nucleotide variant	NM_145294.5(WDR90):c.2567G>A (p.Cys856Tyr)	not specified [RCV005302075]	likely benign	16	657855	657855	Human		name
598267009	CV3933513	single nucleotide variant	NM_145294.5(WDR90):c.2822G>A (p.Arg941His)	not specified [RCV005302078]	uncertain significance	16	658580	658580	Human		name
598267017	CV3933515	single nucleotide variant	NM_145294.5(WDR90):c.2227G>A (p.Asp743Asn)	not specified [RCV005302080]	uncertain significance	16	656756	656756	Human		name
598267030	CV3933518	single nucleotide variant	NM_145294.5(WDR90):c.1424A>G (p.His475Arg)	not specified [RCV005302083]	likely benign	16	653790	653790	Human		name
598267035	CV3933519	single nucleotide variant	NM_145294.5(WDR90):c.2333T>C (p.Val778Ala)	not specified [RCV005302084]	uncertain significance	16	656862	656862	Human		name
598267039	CV3933523	single nucleotide variant	NM_145294.5(WDR90):c.1165C>T (p.His389Tyr)	not specified [RCV005302085]	uncertain significance	16	653383	653383	Human		name
598232933	CV3933524	single nucleotide variant	NM_145294.5(WDR90):c.1879G>A (p.Val627Ile)	not specified [RCV005295488]	likely benign	16	655802	655802	Human		name
598232938	CV3933525	single nucleotide variant	NM_145294.5(WDR90):c.2826C>A (p.Phe942Leu)	not specified [RCV005295489]	uncertain significance	16	658584	658584	Human		name
598267043	CV3933526	single nucleotide variant	NM_145294.5(WDR90):c.2015G>C (p.Arg672Pro)	not specified [RCV005302086]	uncertain significance	16	656350	656350	Human		name
598267056	CV3933529	single nucleotide variant	NM_145294.5(WDR90):c.2363C>T (p.Thr788Ile)	not specified [RCV005302089]	uncertain significance	16	657111	657111	Human		name
598232945	CV3933530	single nucleotide variant	NM_145294.5(WDR90):c.2192C>T (p.Thr731Ile)	not specified [RCV005295490]	uncertain significance	16	656527	656527	Human		name
598232957	CV3933532	single nucleotide variant	NM_145294.5(WDR90):c.1519G>A (p.Val507Ile)	not specified [RCV005295492]	likely benign	16	655110	655110	Human		name
598267060	CV3933533	single nucleotide variant	NM_145294.5(WDR90):c.1717C>T (p.Leu573Phe)	not specified [RCV005302090]	uncertain significance	16	655467	655467	Human		name
598267069	CV3933536	single nucleotide variant	NM_145294.5(WDR90):c.2885C>T (p.Pro962Leu)	not specified [RCV005302092]	uncertain significance	16	658643	658643	Human		name
15161344	CV703767	single nucleotide variant	NM_145294.5(WDR90):c.1111G>A (p.Gly371Ser)	not provided [RCV000947656]	benign	16	652524	652524	Human		name
156377981	CV2207604	single nucleotide variant	NM_145294.5(WDR90):c.4490G>A (p.Arg1497Gln)	not specified [RCV004090386]	likely benign	16	666005	666005	Human		name
156251271	CV2212307	single nucleotide variant	NM_145294.5(WDR90):c.4580C>T (p.Ala1527Val)	not specified [RCV004091258]	uncertain significance	16	666095	666095	Human		name
156281909	CV2220666	single nucleotide variant	NM_145294.5(WDR90):c.5074G>T (p.Ala1692Ser)	not specified [RCV004097843]	uncertain significance	16	666974	666974	Human		name
156332349	CV2220667	single nucleotide variant	NM_145294.5(WDR90):c.5185G>C (p.Ala1729Pro)	not specified [RCV004097844]	uncertain significance	16	667527	667527	Human		name
156239865	CV2221287	single nucleotide variant	NM_145294.5(WDR90):c.5020C>T (p.Pro1674Ser)	not specified [RCV004094717]	uncertain significance	16	666920	666920	Human		name
155968934	CV2244386	single nucleotide variant	NM_145294.5(WDR90):c.3079G>T (p.Ala1027Ser)	not specified [RCV004100361]	uncertain significance	16	659271	659271	Human		name
156275221	CV2255642	single nucleotide variant	NM_145294.5(WDR90):c.3998G>A (p.Cys1333Tyr)	not specified [RCV004120049]	uncertain significance	16	662024	662024	Human		name
156112091	CV2261848	single nucleotide variant	NM_145294.5(WDR90):c.5042C>T (p.Ser1681Phe)	not specified [RCV004126115]	uncertain significance	16	666942	666942	Human		name
156249038	CV2264051	single nucleotide variant	NM_145294.5(WDR90):c.4321G>T (p.Val1441Leu)	not specified [RCV004138065]	uncertain significance	16	665688	665688	Human		name
155904810	CV2276161	single nucleotide variant	NM_145294.5(WDR90):c.5137T>C (p.Phe1713Leu)	not specified [RCV004141822]	uncertain significance	16	667479	667479	Human		name
156030481	CV2278723	single nucleotide variant	NM_145294.5(WDR90):c.4666A>G (p.Thr1556Ala)	not specified [RCV004134915]	uncertain significance	16	666276	666276	Human		name
156077595	CV2281673	single nucleotide variant	NM_145294.5(WDR90):c.4541G>A (p.Arg1514His)	not specified [RCV004153960]	uncertain significance	16	666056	666056	Human		name
155926802	CV2284989	single nucleotide variant	NM_145294.5(WDR90):c.3361C>T (p.Arg1121Trp)	not specified [RCV004143423]	uncertain significance	16	660684	660684	Human		name
156003181	CV2293436	single nucleotide variant	NM_145294.5(WDR90):c.3005C>T (p.Thr1002Ile)	not specified [RCV004152684]	uncertain significance	16	659005	659005	Human		name
155932854	CV2299971	single nucleotide variant	NM_145294.5(WDR90):c.3577G>A (p.Val1193Met)	not specified [RCV004151187]	uncertain significance	16	661405	661405	Human		name
156279912	CV2338349	single nucleotide variant	NM_145294.5(WDR90):c.4336G>A (p.Gly1446Arg)	not specified [RCV004186400]	uncertain significance	16	665703	665703	Human		name
155977722	CV2338825	single nucleotide variant	NM_145294.5(WDR90):c.4522C>T (p.Arg1508Cys)	not specified [RCV004182381]	uncertain significance	16	666037	666037	Human		name
156045886	CV2340212	single nucleotide variant	NM_145294.5(WDR90):c.3551C>G (p.Ala1184Gly)	not specified [RCV004192445]	uncertain significance	16	661379	661379	Human		name
156244943	CV2347202	single nucleotide variant	NM_145294.5(WDR90):c.3041C>G (p.Ala1014Gly)	not specified [RCV004204673]	uncertain significance	16	659115	659115	Human		name
156064179	CV2352927	single nucleotide variant	NM_145294.5(WDR90):c.3299C>T (p.Pro1100Leu)	not specified [RCV004200972]	likely benign	16	660622	660622	Human		name
156109079	CV2355452	single nucleotide variant	NM_145294.5(WDR90):c.5143G>A (p.Gly1715Ser)	not specified [RCV004205303]	uncertain significance	16	667485	667485	Human		name
155906999	CV2357423	single nucleotide variant	NM_145294.5(WDR90):c.5177C>T (p.Thr1726Ile)	not specified [RCV004200301]	uncertain significance	16	667519	667519	Human		name
156304310	CV2359592	single nucleotide variant	NM_145294.5(WDR90):c.4079C>T (p.Thr1360Met)	not specified [RCV004214892]	uncertain significance	16	662265	662265	Human		name
156344594	CV2364306	single nucleotide variant	NM_145294.5(WDR90):c.3038C>A (p.Pro1013Gln)	not specified [RCV004223529]	uncertain significance	16	659112	659112	Human		name
156210983	CV2370303	single nucleotide variant	NM_145294.5(WDR90):c.4660C>T (p.Pro1554Ser)	not specified [RCV004213218]	likely benign	16	666270	666270	Human		name
155993723	CV2377278	single nucleotide variant	NM_145294.5(WDR90):c.3565C>T (p.Arg1189Cys)	not specified [RCV004225467]	uncertain significance	16	661393	661393	Human		name
156141643	CV2383710	single nucleotide variant	NM_145294.5(WDR90):c.5102G>C (p.Arg1701Thr)	not specified [RCV004231598]	uncertain significance	16	667444	667444	Human		name
156091261	CV2389438	single nucleotide variant	NM_145294.5(WDR90):c.4817C>T (p.Ser1606Phe)	not specified [RCV004238164]	uncertain significance	16	666531	666531	Human		name
156221959	CV2394550	single nucleotide variant	NM_145294.5(WDR90):c.4570C>T (p.His1524Tyr)	not specified [RCV004240903]	uncertain significance	16	666085	666085	Human		name
329382819	CV2424565	single nucleotide variant	NM_145294.5(WDR90):c.4937C>T (p.Ala1646Val)	not specified [RCV004254066]	uncertain significance	16	666725	666725	Human		name
329367308	CV2438803	single nucleotide variant	NM_145294.5(WDR90):c.4645G>A (p.Val1549Met)	not specified [RCV004264343]	uncertain significance	16	666255	666255	Human		name
329359188	CV2450912	single nucleotide variant	NM_145294.5(WDR90):c.4049C>T (p.Ser1350Leu)	not specified [RCV004267811]	uncertain significance	16	662235	662235	Human		name
329402850	CV2451455	single nucleotide variant	NM_145294.5(WDR90):c.3972T>G (p.Cys1324Trp)	not specified [RCV004272126]	uncertain significance	16	661998	661998	Human		name
401780584	CV2674091	single nucleotide variant	NM_145294.5(WDR90):c.4780G>A (p.Ala1594Thr)	not specified [RCV004295497]	uncertain significance	16	666494	666494	Human		name
401727487	CV2681055	single nucleotide variant	NM_145294.5(WDR90):c.3068C>T (p.Pro1023Leu)	not specified [RCV004296116]	uncertain significance	16	659260	659260	Human		name
401752205	CV2682739	single nucleotide variant	NM_145294.5(WDR90):c.3256G>A (p.Ala1086Thr)	not specified [RCV004281715]	uncertain significance	16	660129	660129	Human		name
401770931	CV2686095	single nucleotide variant	NM_145294.5(WDR90):c.5029T>G (p.Phe1677Val)	not specified [RCV004297104]	uncertain significance	16	666929	666929	Human		name
401769353	CV2689652	single nucleotide variant	NM_145294.5(WDR90):c.3932C>G (p.Pro1311Arg)	not specified [RCV004297579]	uncertain significance	16	661958	661958	Human		name
401731251	CV2693692	single nucleotide variant	NM_145294.5(WDR90):c.3364G>T (p.Ala1122Ser)	not specified [RCV004298022]	uncertain significance	16	660687	660687	Human		name
401772508	CV2712769	single nucleotide variant	NM_145294.5(WDR90):c.4247C>T (p.Thr1416Met)	not specified [RCV004310110]	uncertain significance	16	662780	662780	Human		name
401750798	CV2715766	single nucleotide variant	NM_145294.5(WDR90):c.3032C>T (p.Ala1011Val)	not specified [RCV004328903]	uncertain significance	16	659106	659106	Human		name
401723822	CV2725045	single nucleotide variant	NM_145294.5(WDR90):c.3739C>T (p.Arg1247Cys)	not specified [RCV004319799]	uncertain significance	16	661662	661662	Human		name
401865936	CV2762462	single nucleotide variant	NM_145294.5(WDR90):c.5059G>A (p.Gly1687Arg)	not specified [RCV004337999]	uncertain significance	16	666959	666959	Human		name
401884189	CV2762775	single nucleotide variant	NM_145294.5(WDR90):c.5209C>G (p.Arg1737Gly)	not specified [RCV004340329]	uncertain significance	16	667551	667551	Human		name
401890035	CV2763601	single nucleotide variant	NM_145294.5(WDR90):c.4193G>A (p.Ser1398Asn)	not specified [RCV004343110]	uncertain significance	16	662726	662726	Human		name
401857882	CV2766062	single nucleotide variant	NM_145294.5(WDR90):c.3206C>T (p.Ser1069Leu)	not specified [RCV004340520]	uncertain significance	16	660079	660079	Human		name
401885727	CV2775058	single nucleotide variant	NM_145294.5(WDR90):c.3227A>C (p.Tyr1076Ser)	not specified [RCV004346434]	uncertain significance	16	660100	660100	Human		name
401898772	CV2782679	single nucleotide variant	NM_145294.5(WDR90):c.3898G>A (p.Ala1300Thr)	not specified [RCV004359692]	uncertain significance	16	661924	661924	Human		name
401881451	CV2783839	single nucleotide variant	NM_145294.5(WDR90):c.4262G>C (p.Ser1421Thr)	not specified [RCV004360742]	uncertain significance	16	662795	662795	Human		name
405807701	CV3356554	single nucleotide variant	NM_145294.5(WDR90):c.3175G>A (p.Gly1059Ser)	not specified [RCV004480814]	uncertain significance	16	659367	659367	Human		name
405807703	CV3356555	single nucleotide variant	NM_145294.5(WDR90):c.3217C>G (p.Arg1073Gly)	not specified [RCV004480815]	uncertain significance	16	660090	660090	Human		name
405807705	CV3356556	single nucleotide variant	NM_145294.5(WDR90):c.3307G>A (p.Ala1103Thr)	not specified [RCV004480816]	uncertain significance	16	660630	660630	Human		name
405807707	CV3356557	single nucleotide variant	NM_145294.5(WDR90):c.3362G>A (p.Arg1121Gln)	not specified [RCV004480817]	uncertain significance	16	660685	660685	Human		name
405807709	CV3356558	single nucleotide variant	NM_145294.5(WDR90):c.3746C>T (p.Pro1249Leu)	not specified [RCV004480818]	likely benign	16	661669	661669	Human		name
405807711	CV3356559	single nucleotide variant	NM_145294.5(WDR90):c.3784G>T (p.Ala1262Ser)	not specified [RCV004480819]	uncertain significance	16	661707	661707	Human		name
405807713	CV3356560	single nucleotide variant	NM_145294.5(WDR90):c.3806G>A (p.Gly1269Asp)	not specified [RCV004480820]	uncertain significance	16	661729	661729	Human		name
405807715	CV3356561	single nucleotide variant	NM_145294.5(WDR90):c.3991G>A (p.Gly1331Ser)	not specified [RCV004480821]	uncertain significance	16	662017	662017	Human		name
405807717	CV3356562	single nucleotide variant	NM_145294.5(WDR90):c.4024G>A (p.Gly1342Ser)	not specified [RCV004480822]	likely benign	16	662050	662050	Human		name
405807719	CV3356563	single nucleotide variant	NM_145294.5(WDR90):c.4085G>A (p.Arg1362Gln)	not specified [RCV004480823]	uncertain significance	16	662271	662271	Human		name
405807721	CV3356564	single nucleotide variant	NM_145294.5(WDR90):c.4130A>G (p.Lys1377Arg)	not specified [RCV004480824]	uncertain significance	16	662316	662316	Human		name
405807723	CV3356565	single nucleotide variant	NM_145294.5(WDR90):c.4346A>G (p.His1449Arg)	not specified [RCV004480825]	uncertain significance	16	665713	665713	Human		name
405807975	CV3356566	single nucleotide variant	NM_145294.5(WDR90):c.4423G>T (p.Val1475Leu)	not specified [RCV004480826]	uncertain significance	16	665790	665790	Human		name
405807973	CV3356567	single nucleotide variant	NM_145294.5(WDR90):c.4445G>T (p.Cys1482Phe)	not specified [RCV004480827]	uncertain significance	16	665960	665960	Human		name
405807970	CV3356568	single nucleotide variant	NM_145294.5(WDR90):c.4450G>T (p.Ala1484Ser)	not specified [RCV004480828]	uncertain significance	16	665965	665965	Human		name
405807967	CV3356570	single nucleotide variant	NM_145294.5(WDR90):c.5026C>A (p.Pro1676Thr)	not specified [RCV004480830]	uncertain significance	16	666926	666926	Human		name
405807965	CV3356571	single nucleotide variant	NM_145294.5(WDR90):c.5239G>A (p.Gly1747Ser)	not specified [RCV004480831]	uncertain significance	16	667581	667581	Human		name
407524358	CV3489965	single nucleotide variant	NM_145294.5(WDR90):c.3752C>T (p.Pro1251Leu)	not specified [RCV004678395]	uncertain significance	16	661675	661675	Human		name
407465364	CV3489969	single nucleotide variant	NM_145294.5(WDR90):c.3868C>G (p.Arg1290Gly)	not specified [RCV004688750]	uncertain significance	16	661894	661894	Human		name
407465374	CV3489974	single nucleotide variant	NM_145294.5(WDR90):c.3415C>T (p.Arg1139Cys)	not specified [RCV004688752]	likely benign	16	661074	661074	Human		name
407524376	CV3489975	single nucleotide variant	NM_145294.5(WDR90):c.3122A>G (p.Lys1041Arg)	not specified [RCV004678402]	uncertain significance	16	659314	659314	Human		name
407524386	CV3489980	single nucleotide variant	NM_145294.5(WDR90):c.5086G>T (p.Ala1696Ser)	not specified [RCV004678405]	uncertain significance	16	666986	666986	Human		name
407524388	CV3489981	single nucleotide variant	NM_145294.5(WDR90):c.4241C>T (p.Ala1414Val)	not specified [RCV004678406]	uncertain significance	16	662774	662774	Human		name
407465387	CV3489984	single nucleotide variant	NM_145294.5(WDR90):c.3986G>A (p.Arg1329His)	not specified [RCV004688755]	uncertain significance	16	662012	662012	Human		name
407459634	CV3496851	single nucleotide variant	NM_145294.5(WDR90):c.4489C>T (p.Arg1497Trp)	Autism [RCV004698666]	uncertain significance	16	666004	666004	Human	2	name
596947146	CV3547210	single nucleotide variant	NM_145294.5(WDR90):c.4084C>T (p.Arg1362Trp)	not provided [RCV004811018]	likely benign	16	662270	662270	Human		name
597739579	CV3630080	single nucleotide variant	NM_145294.5(WDR90):c.3403T>C (p.Tyr1135His)	not specified [RCV004890356]	uncertain significance	16	661062	661062	Human		name
597792021	CV3630084	single nucleotide variant	NM_145294.5(WDR90):c.4549A>G (p.Met1517Val)	not specified [RCV004876853]	uncertain significance	16	666064	666064	Human		name
597792034	CV3630088	single nucleotide variant	NM_145294.5(WDR90):c.3638C>T (p.Ala1213Val)	not specified [RCV004876857]	uncertain significance	16	661466	661466	Human		name
597739591	CV3630091	single nucleotide variant	NM_145294.5(WDR90):c.3290G>A (p.Gly1097Asp)	not specified [RCV004890359]	uncertain significance	16	660613	660613	Human		name
597739596	CV3630092	single nucleotide variant	NM_145294.5(WDR90):c.3325C>T (p.Arg1109Cys)	not specified [RCV004890360]	uncertain significance	16	660648	660648	Human		name
597792043	CV3630094	single nucleotide variant	NM_145294.5(WDR90):c.4766C>G (p.Thr1589Arg)	not specified [RCV004876860]	uncertain significance	16	666480	666480	Human		name
597792048	CV3630097	single nucleotide variant	NM_145294.5(WDR90):c.3028G>A (p.Gly1010Arg)	not specified [RCV004876862]	uncertain significance	16	659102	659102	Human		name
597739606	CV3630099	single nucleotide variant	NM_145294.5(WDR90):c.4213G>A (p.Val1405Met)	not specified [RCV004890362]	likely benign	16	662746	662746	Human		name
597739615	CV3630102	single nucleotide variant	NM_145294.5(WDR90):c.3107G>A (p.Arg1036Gln)	not specified [RCV004890364]	likely benign	16	659299	659299	Human		name
597792053	CV3630103	single nucleotide variant	NM_145294.5(WDR90):c.5149G>A (p.Asp1717Asn)	not specified [RCV004876864]	likely benign	16	667491	667491	Human		name
597792059	CV3630105	single nucleotide variant	NM_145294.5(WDR90):c.4957C>T (p.Pro1653Ser)	not specified [RCV004876866]	uncertain significance	16	666745	666745	Human		name
597739620	CV3630106	single nucleotide variant	NM_145294.5(WDR90):c.3932C>T (p.Pro1311Leu)	not specified [RCV004890365]	uncertain significance	16	661958	661958	Human		name
597792066	CV3630110	single nucleotide variant	NM_145294.5(WDR90):c.4894C>T (p.His1632Tyr)	not specified [RCV004876868]	uncertain significance	16	666682	666682	Human		name
597792068	CV3630111	single nucleotide variant	NM_145294.5(WDR90):c.5188A>T (p.Arg1730Trp)	not specified [RCV004876869]	uncertain significance	16	667530	667530	Human		name
597792076	CV3630115	single nucleotide variant	NM_145294.5(WDR90):c.3689G>A (p.Arg1230His)	not specified [RCV004876872]	uncertain significance	16	661612	661612	Human		name
597792083	CV3630117	single nucleotide variant	NM_145294.5(WDR90):c.4763G>A (p.Gly1588Asp)	not specified [RCV004876874]	uncertain significance	16	666477	666477	Human		name
597792086	CV3630119	single nucleotide variant	NM_145294.5(WDR90):c.4109C>T (p.Ala1370Val)	not specified [RCV004876875]	uncertain significance	16	662295	662295	Human		name
597739642	CV3630120	single nucleotide variant	NM_145294.5(WDR90):c.4393G>T (p.Ala1465Ser)	not specified [RCV004890370]	uncertain significance	16	665760	665760	Human		name
597739647	CV3630122	single nucleotide variant	NM_145294.5(WDR90):c.5210G>C (p.Arg1737Pro)	not specified [RCV004890371]	uncertain significance	16	667552	667552	Human		name
597792094	CV3630124	single nucleotide variant	NM_145294.5(WDR90):c.3344G>T (p.Gly1115Val)	not specified [RCV004876878]	uncertain significance	16	660667	660667	Human		name
597792103	CV3630127	single nucleotide variant	NM_145294.5(WDR90):c.3713C>T (p.Ala1238Val)	not specified [RCV004876881]	uncertain significance	16	661636	661636	Human		name
597792105	CV3630128	single nucleotide variant	NM_145294.5(WDR90):c.4847T>C (p.Val1616Ala)	not specified [RCV004876882]	uncertain significance	16	666561	666561	Human		name
597739652	CV3630130	single nucleotide variant	NM_145294.5(WDR90):c.3745C>T (p.Pro1249Ser)	not specified [RCV004890372]	uncertain significance	16	661668	661668	Human		name
597792111	CV3630131	single nucleotide variant	NM_145294.5(WDR90):c.5086G>A (p.Ala1696Thr)	not specified [RCV004876884]	uncertain significance	16	666986	666986	Human		name
597792114	CV3630132	single nucleotide variant	NM_145294.5(WDR90):c.5138T>C (p.Phe1713Ser)	not specified [RCV004876885]	uncertain significance	16	667480	667480	Human		name
597792117	CV3630133	single nucleotide variant	NM_145294.5(WDR90):c.5239G>C (p.Gly1747Arg)	not specified [RCV004876886]	uncertain significance	16	667581	667581	Human		name
597792121	CV3630134	single nucleotide variant	NM_145294.5(WDR90):c.3017A>C (p.Gln1006Pro)	not specified [RCV004876887]	uncertain significance	16	659091	659091	Human		name
597739657	CV3630136	single nucleotide variant	NM_145294.5(WDR90):c.3416G>A (p.Arg1139His)	not specified [RCV004890373]	uncertain significance	16	661075	661075	Human		name
598232845	CV3933492	single nucleotide variant	NM_145294.5(WDR90):c.3914C>T (p.Ser1305Leu)	not specified [RCV005295474]	uncertain significance	16	661940	661940	Human		name
598266967	CV3933493	single nucleotide variant	NM_145294.5(WDR90):c.4828C>T (p.Arg1610Trp)	not specified [RCV005302068]	uncertain significance	16	666542	666542	Human		name
598232852	CV3933494	single nucleotide variant	NM_145294.5(WDR90):c.4603A>G (p.Thr1535Ala)	not specified [RCV005295475]	likely benign	16	666118	666118	Human		name
598266971	CV3933497	single nucleotide variant	NM_145294.5(WDR90):c.3842G>A (p.Arg1281His)	not specified [RCV005302069]	likely benign	16	661765	661765	Human		name
598266975	CV3933499	single nucleotide variant	NM_145294.5(WDR90):c.3618C>A (p.Ser1206Arg)	not specified [RCV005302070]	uncertain significance	16	661446	661446	Human		name
598232883	CV3933502	single nucleotide variant	NM_145294.5(WDR90):c.3466G>T (p.Gly1156Cys)	not specified [RCV005295480]	uncertain significance	16	661125	661125	Human		name
598232894	CV3933504	single nucleotide variant	NM_145294.5(WDR90):c.5146C>T (p.His1716Tyr)	not specified [RCV005295482]	uncertain significance	16	667488	667488	Human		name
598266988	CV3933506	single nucleotide variant	NM_145294.5(WDR90):c.4270G>A (p.Glu1424Lys)	not specified [RCV005302073]	uncertain significance	16	662803	662803	Human		name
598232900	CV3933508	single nucleotide variant	NM_145294.5(WDR90):c.4219A>G (p.Met1407Val)	not specified [RCV005295483]	uncertain significance	16	662752	662752	Human		name
598267000	CV3933510	single nucleotide variant	NM_145294.5(WDR90):c.3986G>C (p.Arg1329Pro)	not specified [RCV005302076]	uncertain significance	16	662012	662012	Human		name
598267005	CV3933511	single nucleotide variant	NM_145294.5(WDR90):c.4570C>G (p.His1524Asp)	not specified [RCV005302077]	uncertain significance	16	666085	666085	Human		name
598267013	CV3933514	single nucleotide variant	NM_145294.5(WDR90):c.3013G>A (p.Asp1005Asn)	not specified [RCV005302079]	likely benign	16	659087	659087	Human		name
598267021	CV3933516	single nucleotide variant	NM_145294.5(WDR90):c.3472T>G (p.Ser1158Ala)	not specified [RCV005302081]	uncertain significance	16	661131	661131	Human		name
598232913	CV3933520	single nucleotide variant	NM_145294.5(WDR90):c.4106G>A (p.Gly1369Glu)	not specified [RCV005295485]	uncertain significance	16	662292	662292	Human		name
598232921	CV3933521	single nucleotide variant	NM_145294.5(WDR90):c.3727G>A (p.Val1243Met)	not specified [RCV005295486]	uncertain significance	16	661650	661650	Human		name
598232927	CV3933522	single nucleotide variant	NM_145294.5(WDR90):c.4474C>T (p.Arg1492Cys)	not specified [RCV005295487]	uncertain significance	16	665989	665989	Human		name
598232951	CV3933531	single nucleotide variant	NM_145294.5(WDR90):c.4111G>C (p.Val1371Leu)	not specified [RCV005295491]	uncertain significance	16	662297	662297	Human		name

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