Myo10 Variant Search Result - Rat Genome Database

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242 records found for search term Myo10

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8580598	CV115028	single nucleotide variant	NM_012334.2(MYO10):c.121-12303A>G	Lung cancer [RCV000095551]	uncertain significance	5	16830470	16830470	Human		name
156174090	CV2290233	single nucleotide variant	NM_012334.3(MYO10):c.23G>T (p.Gly8Val)	not specified [RCV004152883]	uncertain significance	5	16877706	16877706	Human		name
401942547	CV2839643	single nucleotide variant	NM_012334.3(MYO10):c.88G>A (p.Gly30Ser)	not provided [RCV003456591]	uncertain significance	5	16877641	16877641	Human		name
405762719	CV3321305	single nucleotide variant	NM_012334.3(MYO10):c.91A>G (p.Ile31Val)	not specified [RCV004455597]	likely benign	5	16877638	16877638	Human		name
156241500	CV2213943	single nucleotide variant	NM_012334.3(MYO10):c.190G>A (p.Gly64Ser)	not specified [RCV004083667]	uncertain significance	5	16818098	16818098	Human		name
155992255	CV2379293	single nucleotide variant	NM_012334.3(MYO10):c.113A>G (p.Tyr38Cys)	not specified [RCV004223762]	uncertain significance	5	16877616	16877616	Human		name
156059262	CV2383521	single nucleotide variant	NM_012334.3(MYO10):c.142A>C (p.Thr48Pro)	not specified [RCV004222528]	uncertain significance	5	16818146	16818146	Human		name
401732952	CV2691159	single nucleotide variant	NM_012334.3(MYO10):c.146T>A (p.Ile49Asn)	not specified [RCV004302939]	uncertain significance	5	16818142	16818142	Human		name
401925313	CV2827668	single nucleotide variant	NM_012334.3(MYO10):c.1620A>T (p.Ala540=)	not provided [RCV003436423]	likely benign	5	16762081	16762081	Human		name
405747572	CV3310983	single nucleotide variant	NM_012334.3(MYO10):c.103C>T (p.Arg35Trp)	not specified [RCV004453283]	uncertain significance	5	16877626	16877626	Human		name
597665062	CV3565020	single nucleotide variant	NM_012334.3(MYO10):c.238A>G (p.Met80Val)	not specified [RCV004828988]	uncertain significance	5	16818050	16818050	Human		name
597665093	CV3565024	single nucleotide variant	NM_012334.3(MYO10):c.259T>C (p.Tyr87His)	not specified [RCV004828992]	uncertain significance	5	16818029	16818029	Human		name
597665260	CV3565045	single nucleotide variant	NM_012334.3(MYO10):c.158A>G (p.Lys53Arg)	not specified [RCV004829013]	uncertain significance	5	16818130	16818130	Human		name
597665735	CV3565049	single nucleotide variant	NM_012334.3(MYO10):c.229G>A (p.Gly77Ser)	not specified [RCV004829017]	uncertain significance	5	16818059	16818059	Human		name
598225028	CV3894192	single nucleotide variant	NM_012334.3(MYO10):c.2826C>T (p.Leu942=)	not provided [RCV005257435]	likely benign	5	16701569	16701569	Human		name
598190459	CV3994136	single nucleotide variant	NM_012334.3(MYO10):c.175C>A (p.Pro59Thr)	not specified [RCV005374046]	uncertain significance	5	16818113	16818113	Human		name
617153093	CV4021066	single nucleotide variant	NM_012334.3(MYO10):c.2538C>T (p.Ala846=)	not provided [RCV005428819]	likely benign	5	16702561	16702561	Human		name
15145106	CV709803	single nucleotide variant	NM_012334.3(MYO10):c.2871C>T (p.Ile957=)	not provided [RCV000966939]	benign	5	16701524	16701524	Human		name
15153729	CV721370	single nucleotide variant	NM_012334.3(MYO10):c.179C>T (p.Thr60Met)	not provided [RCV000880069]	likely benign	5	16818109	16818109	Human		name
156149169	CV2197076	single nucleotide variant	NM_012334.3(MYO10):c.629C>T (p.Ala210Val)	not specified [RCV004071514]	uncertain significance	5	16781803	16781803	Human		name
156275342	CV2255661	single nucleotide variant	NM_012334.3(MYO10):c.632A>T (p.Lys211Met)	not specified [RCV004120064]	uncertain significance	5	16781800	16781800	Human		name
155914487	CV2268357	single nucleotide variant	NM_012334.3(MYO10):c.853A>C (p.Asn285His)	not specified [RCV004138636]	uncertain significance	5	16779622	16779622	Human		name
156338131	CV2271223	single nucleotide variant	NM_012334.3(MYO10):c.931A>G (p.Thr311Ala)	not specified [RCV004136371]	uncertain significance	5	16769203	16769203	Human		name
156306682	CV2315039	single nucleotide variant	NM_012334.3(MYO10):c.301G>A (p.Ala101Thr)	not specified [RCV004164949]	uncertain significance	5	16794812	16794812	Human		name
156186608	CV2332585	single nucleotide variant	NM_012334.3(MYO10):c.932C>T (p.Thr311Met)	not specified [RCV004196296]	uncertain significance	5	16769202	16769202	Human		name
155971954	CV2334278	single nucleotide variant	NM_012334.3(MYO10):c.370C>T (p.Arg124Cys)	not specified [RCV004188261]	likely benign	5	16794743	16794743	Human		name
156220172	CV2344997	single nucleotide variant	NM_012334.3(MYO10):c.976G>A (p.Val326Met)	not specified [RCV004193286]	uncertain significance	5	16769158	16769158	Human		name
155901950	CV2345898	single nucleotide variant	NM_012334.3(MYO10):c.637G>A (p.Val213Met)	not specified [RCV004198938]	uncertain significance	5	16781795	16781795	Human		name
156078843	CV2375215	single nucleotide variant	NM_012334.3(MYO10):c.425G>A (p.Arg142His)	not specified [RCV004230252]	uncertain significance	5	16794688	16794688	Human		name
329377012	CV2435777	single nucleotide variant	NM_012334.3(MYO10):c.580G>C (p.Glu194Gln)	not specified [RCV004253405]	uncertain significance	5	16783357	16783357	Human		name
401782451	CV2686866	single nucleotide variant	NM_012334.3(MYO10):c.707A>G (p.Gln236Arg)	not specified [RCV004302044]	uncertain significance	5	16781725	16781725	Human		name
401749996	CV2704883	single nucleotide variant	NM_012334.3(MYO10):c.352A>G (p.Met118Val)	not specified [RCV004307460]	uncertain significance	5	16794761	16794761	Human		name
401855471	CV2757399	single nucleotide variant	NM_012334.3(MYO10):c.563A>G (p.Glu188Gly)	not specified [RCV004340799]	uncertain significance	5	16783374	16783374	Human		name
405761820	CV3311159	single nucleotide variant	NM_012334.3(MYO10):c.344C>T (p.Pro115Leu)	not specified [RCV004455444]	uncertain significance	5	16794769	16794769	Human		name
405761990	CV3311187	single nucleotide variant	NM_012334.3(MYO10):c.391C>T (p.Pro131Ser)	not specified [RCV004455472]	uncertain significance	5	16794722	16794722	Human		name
405762106	CV3311206	single nucleotide variant	NM_012334.3(MYO10):c.445G>C (p.Asp149His)	not specified [RCV004455491]	uncertain significance	5	16794668	16794668	Human		name
405762292	CV3311239	single nucleotide variant	NM_012334.3(MYO10):c.542C>G (p.Ser181Cys)	not specified [RCV004455524]	uncertain significance	5	16783395	16783395	Human		name
596947104	CV3547168	single nucleotide variant	NM_012334.3(MYO10):c.367C>T (p.Arg123Trp)	not provided [RCV004810976]	benign	5	16794746	16794746	Human		name
597665009	CV3565014	single nucleotide variant	NM_012334.3(MYO10):c.371G>A (p.Arg124His)	not specified [RCV004828982]	uncertain significance	5	16794742	16794742	Human		name
597665100	CV3565025	single nucleotide variant	NM_012334.3(MYO10):c.941A>T (p.Asp314Val)	not specified [RCV004828993]	uncertain significance	5	16769193	16769193	Human		name
597665148	CV3565031	single nucleotide variant	NM_012334.3(MYO10):c.424C>T (p.Arg142Cys)	not specified [RCV004828999]	uncertain significance	5	16794689	16794689	Human		name
597665173	CV3565034	single nucleotide variant	NM_012334.3(MYO10):c.415G>A (p.Glu139Lys)	not specified [RCV004829002]	uncertain significance	5	16794698	16794698	Human		name
597665719	CV3565051	single nucleotide variant	NM_012334.3(MYO10):c.307G>A (p.Val103Met)	not specified [RCV004829019]	uncertain significance	5	16794806	16794806	Human		name
597665692	CV3565055	single nucleotide variant	NM_012334.3(MYO10):c.647A>G (p.Asn216Ser)	not specified [RCV004829023]	uncertain significance	5	16781785	16781785	Human		name
598190414	CV3994127	single nucleotide variant	NM_012334.3(MYO10):c.508A>G (p.Ile170Val)	not specified [RCV005374040]	uncertain significance	5	16783429	16783429	Human		name
15175813	CV699002	single nucleotide variant	NM_012334.3(MYO10):c.4143G>A (p.Arg1381=)	not provided [RCV000950676]	benign	5	16681917	16681917	Human		name
15099502	CV699003	single nucleotide variant	NM_012334.3(MYO10):c.4107G>A (p.Pro1369=)	not provided [RCV000958771]	benign	5	16681953	16681953	Human		name
15103977	CV699004	single nucleotide variant	NM_012334.3(MYO10):c.819A>C (p.Glu273Asp)	not provided [RCV000959590]	benign	5	16780531	16780531	Human		name
15182353	CV709799	single nucleotide variant	NM_012334.3(MYO10):c.5004C>T (p.Tyr1668=)	not provided [RCV000974611]	benign	5	16673850	16673850	Human		name
15145102	CV709800	single nucleotide variant	NM_012334.3(MYO10):c.4782G>A (p.Gln1594=)	not provided [RCV000966938]	benign	5	16675035	16675035	Human		name
15107243	CV709801	single nucleotide variant	NM_012334.3(MYO10):c.4629G>A (p.Pro1543=)	not provided [RCV000960251]	benign	5	16676068	16676068	Human		name
15174530	CV709802	single nucleotide variant	NM_012334.3(MYO10):c.4554G>A (p.Leu1518=)	not provided [RCV000972735]	benign	5	16676143	16676143	Human		name
15181402	CV721363	single nucleotide variant	NM_012334.3(MYO10):c.5370C>T (p.Cys1790=)	not provided [RCV000885760]	benign\|likely benign	5	16671482	16671482	Human		name
15159710	CV721364	single nucleotide variant	NM_012334.3(MYO10):c.4818G>A (p.Leu1606=)	not provided [RCV000881245]	benign	5	16674999	16674999	Human		name
15159712	CV721365	single nucleotide variant	NM_012334.3(MYO10):c.3990G>A (p.Val1330=)	not provided [RCV000881246]	benign	5	16685738	16685738	Human		name
15108242	CV721366	single nucleotide variant	NM_012334.3(MYO10):c.3207C>T (p.Gly1069=)	not provided [RCV000893630]	benign	5	16701188	16701188	Human		name
15201985	CV721369	single nucleotide variant	NM_012334.3(MYO10):c.976G>C (p.Val326Leu)	not provided [RCV000891350]	likely benign	5	16769158	16769158	Human		name
15135009	CV734990	single nucleotide variant	NM_012334.3(MYO10):c.4593G>A (p.Pro1531=)	not provided [RCV000898385]	benign	5	16676104	16676104	Human		name
15122000	CV734991	single nucleotide variant	NM_012334.3(MYO10):c.4482C>T (p.Asn1494=)	not provided [RCV000896165]	likely benign	5	16680007	16680007	Human		name
15135016	CV734992	single nucleotide variant	NM_012334.3(MYO10):c.3207C>A (p.Gly1069=)	not provided [RCV000898386]	likely benign	5	16701188	16701188	Human		name
15148264	CV749401	single nucleotide variant	NM_012334.3(MYO10):c.925G>A (p.Val309Ile)	not provided [RCV000923063]	likely benign	5	16779550	16779550	Human		name
156370708	CV2204302	single nucleotide variant	NM_012334.3(MYO10):c.2678T>C (p.Leu893Pro)	not specified [RCV004079129]	uncertain significance	5	16701717	16701717	Human		name
156002139	CV2257927	single nucleotide variant	NM_012334.3(MYO10):c.2459A>G (p.Glu820Gly)	not specified [RCV004129746]	uncertain significance	5	16702976	16702976	Human		name
155969125	CV2262078	single nucleotide variant	NM_012334.3(MYO10):c.1036G>T (p.Gly346Trp)	not specified [RCV004126549]	uncertain significance	5	16769098	16769098	Human		name
156039936	CV2279070	single nucleotide variant	NM_012334.3(MYO10):c.1822C>T (p.Arg608Trp)	not specified [RCV004145747]	uncertain significance	5	16758144	16758144	Human		name
156085813	CV2289867	single nucleotide variant	NM_012334.3(MYO10):c.2477A>G (p.Glu826Gly)	not specified [RCV004150527]	uncertain significance	5	16702958	16702958	Human		name
156014809	CV2301583	single nucleotide variant	NM_012334.3(MYO10):c.1451T>C (p.Ile484Thr)	not specified [RCV004162490]	uncertain significance	5	16763524	16763524	Human		name
156273945	CV2319894	single nucleotide variant	NM_012334.3(MYO10):c.2650A>G (p.Asn884Asp)	not specified [RCV004167774]	uncertain significance	5	16701745	16701745	Human		name
156134797	CV2347121	single nucleotide variant	NM_012334.3(MYO10):c.1112A>C (p.Asp371Ala)	not specified [RCV004204601]	uncertain significance	5	16766147	16766147	Human		name
155918939	CV2360108	single nucleotide variant	NM_012334.3(MYO10):c.2847G>C (p.Glu949Asp)	not specified [RCV004215383]	uncertain significance	5	16701548	16701548	Human		name
156336926	CV2360844	single nucleotide variant	NM_012334.3(MYO10):c.1758T>A (p.Asp586Glu)	not specified [RCV004213615]	uncertain significance	5	16758208	16758208	Human		name
156387155	CV2372657	single nucleotide variant	NM_012334.3(MYO10):c.2772C>G (p.Asp924Glu)	not specified [RCV004221857]	uncertain significance	5	16701623	16701623	Human		name
156084862	CV2382035	single nucleotide variant	NM_012334.3(MYO10):c.1169A>G (p.Asn390Ser)	not specified [RCV004228004]	likely benign	5	16766090	16766090	Human		name
155908778	CV2387439	single nucleotide variant	NM_012334.3(MYO10):c.2795A>G (p.Glu932Gly)	not specified [RCV004240304]	uncertain significance	5	16701600	16701600	Human		name
329359865	CV2462346	single nucleotide variant	NM_012334.3(MYO10):c.2875C>T (p.Arg959Trp)	not specified [RCV004266329]	uncertain significance	5	16701520	16701520	Human		name
329398543	CV2471168	single nucleotide variant	NM_012334.3(MYO10):c.2371G>A (p.Ala791Thr)	not specified [RCV004278416]	uncertain significance	5	16703064	16703064	Human		name
401735973	CV2672790	single nucleotide variant	NM_012334.3(MYO10):c.1439T>C (p.Val480Ala)	not specified [RCV004281571]	uncertain significance	5	16763536	16763536	Human		name
401747065	CV2678998	single nucleotide variant	NM_012334.3(MYO10):c.1817A>G (p.His606Arg)	not specified [RCV004295009]	uncertain significance	5	16758149	16758149	Human		name
401721762	CV2680668	single nucleotide variant	NM_012334.3(MYO10):c.2129A>G (p.Tyr710Cys)	not specified [RCV004291285]	uncertain significance	5	16710948	16710948	Human		name
401754996	CV2682352	single nucleotide variant	NM_012334.3(MYO10):c.1780C>T (p.Arg594Cys)	not specified [RCV004290386]	uncertain significance	5	16758186	16758186	Human		name
401782569	CV2686929	single nucleotide variant	NM_012334.3(MYO10):c.2764C>T (p.Arg922Trp)	not specified [RCV004302099]	uncertain significance	5	16701631	16701631	Human		name
401747403	CV2691583	single nucleotide variant	NM_012334.3(MYO10):c.2449G>A (p.Glu817Lys)	not specified [RCV004305411]	uncertain significance	5	16702986	16702986	Human		name
401724774	CV2693414	single nucleotide variant	NM_012334.3(MYO10):c.1408G>C (p.Glu470Gln)	not specified [RCV004295366]	uncertain significance	5	16763674	16763674	Human		name
401757985	CV2731605	single nucleotide variant	NM_012334.3(MYO10):c.2674C>T (p.Arg892Cys)	not specified [RCV004330950]	uncertain significance	5	16701721	16701721	Human		name
401877847	CV2757637	single nucleotide variant	NM_012334.3(MYO10):c.2729C>T (p.Ser910Leu)	not specified [RCV004334755]	uncertain significance	5	16701666	16701666	Human		name
401884279	CV2762837	single nucleotide variant	NM_012334.3(MYO10):c.1586C>T (p.Ala529Val)	not specified [RCV004340384]	uncertain significance	5	16762546	16762546	Human		name
401894637	CV2785063	single nucleotide variant	NM_012334.3(MYO10):c.1873A>G (p.Thr625Ala)	not specified [RCV004355079]	uncertain significance	5	16754884	16754884	Human		name
405747667	CV3310997	single nucleotide variant	NM_012334.3(MYO10):c.1267G>C (p.Gly423Arg)	not specified [RCV004453297]	uncertain significance	5	16764309	16764309	Human		name
405747765	CV3311012	single nucleotide variant	NM_012334.3(MYO10):c.1625A>G (p.Asn542Ser)	not specified [RCV004453312]	uncertain significance	5	16762076	16762076	Human		name
405747793	CV3311017	single nucleotide variant	NM_012334.3(MYO10):c.1664A>G (p.Tyr555Cys)	not specified [RCV004453317]	uncertain significance	5	16761539	16761539	Human		name
405747806	CV3311019	single nucleotide variant	NM_012334.3(MYO10):c.1721A>G (p.Asn574Ser)	not specified [RCV004453319]	uncertain significance	5	16761482	16761482	Human		name
405747931	CV3311036	single nucleotide variant	NM_012334.3(MYO10):c.1979C>T (p.Ser660Leu)	not specified [RCV004453337]	uncertain significance	5	16711196	16711196	Human		name
405747967	CV3311041	single nucleotide variant	NM_012334.3(MYO10):c.2102G>A (p.Gly701Glu)	not specified [RCV004453342]	uncertain significance	5	16710975	16710975	Human		name
405747985	CV3311044	single nucleotide variant	NM_012334.3(MYO10):c.2111C>T (p.Thr704Met)	not specified [RCV004453345]	uncertain significance	5	16710966	16710966	Human		name
405748008	CV3311048	single nucleotide variant	NM_012334.3(MYO10):c.2195A>G (p.Gln732Arg)	not specified [RCV004453349]	uncertain significance	5	16704660	16704660	Human		name
405748058	CV3311056	single nucleotide variant	NM_012334.3(MYO10):c.2407A>C (p.Ile803Leu)	not specified [RCV004453357]	uncertain significance	5	16703028	16703028	Human		name
405748079	CV3311060	single nucleotide variant	NM_012334.3(MYO10):c.2425A>G (p.Arg809Gly)	not specified [RCV004453361]	uncertain significance	5	16703010	16703010	Human		name
405748243	CV3311082	single nucleotide variant	NM_012334.3(MYO10):c.2726T>G (p.Leu909Arg)	not specified [RCV004453383]	uncertain significance	5	16701669	16701669	Human		name
405748262	CV3311085	single nucleotide variant	NM_012334.3(MYO10):c.2737G>A (p.Glu913Lys)	not specified [RCV004453386]	uncertain significance	5	16701658	16701658	Human		name
405748298	CV3311091	single nucleotide variant	NM_012334.3(MYO10):c.2773C>A (p.Gln925Lys)	not specified [RCV004453392]	uncertain significance	5	16701622	16701622	Human		name
407515326	CV3450679	single nucleotide variant	NM_012334.3(MYO10):c.1163C>T (p.Pro388Leu)	not specified [RCV004649854]	uncertain significance	5	16766096	16766096	Human		name
407515332	CV3450681	single nucleotide variant	NM_012334.3(MYO10):c.2617G>A (p.Glu873Lys)	not specified [RCV004649856]	uncertain significance	5	16701778	16701778	Human		name
407504525	CV3450682	single nucleotide variant	NM_012334.3(MYO10):c.2837A>G (p.Asn946Ser)	not specified [RCV004645852]	uncertain significance	5	16701558	16701558	Human		name
597665045	CV3565018	single nucleotide variant	NM_012334.3(MYO10):c.1271A>G (p.Asn424Ser)	not specified [RCV004828986]	uncertain significance	5	16764305	16764305	Human		name
597665072	CV3565021	single nucleotide variant	NM_012334.3(MYO10):c.2534A>G (p.Glu845Gly)	not specified [RCV004828989]	uncertain significance	5	16702565	16702565	Human		name
597665123	CV3565028	single nucleotide variant	NM_012334.3(MYO10):c.2921G>A (p.Ser974Asn)	not specified [RCV004828996]	uncertain significance	5	16701474	16701474	Human		name
597665138	CV3565030	single nucleotide variant	NM_012334.3(MYO10):c.1921A>C (p.Met641Leu)	not specified [RCV004828998]	uncertain significance	5	16754836	16754836	Human		name
597665188	CV3565036	single nucleotide variant	NM_012334.3(MYO10):c.2593T>A (p.Leu865Met)	not specified [RCV004829004]	uncertain significance	5	16701802	16701802	Human		name
597665197	CV3565037	single nucleotide variant	NM_012334.3(MYO10):c.1352T>C (p.Ile451Thr)	not specified [RCV004829005]	uncertain significance	5	16763730	16763730	Human		name
597665213	CV3565039	single nucleotide variant	NM_012334.3(MYO10):c.2401G>A (p.Gly801Ser)	not specified [RCV004829007]	uncertain significance	5	16703034	16703034	Human		name
597665245	CV3565043	single nucleotide variant	NM_012334.3(MYO10):c.2569A>G (p.Arg857Gly)	not specified [RCV004829011]	uncertain significance	5	16701826	16701826	Human		name
597665251	CV3565044	single nucleotide variant	NM_012334.3(MYO10):c.1673G>A (p.Arg558Gln)	not specified [RCV004829012]	uncertain significance	5	16761530	16761530	Human		name
597665728	CV3565050	single nucleotide variant	NM_012334.3(MYO10):c.1850A>G (p.Asp617Gly)	not specified [RCV004829018]	uncertain significance	5	16754907	16754907	Human		name
597665713	CV3565052	single nucleotide variant	NM_012334.3(MYO10):c.1160C>A (p.Thr387Lys)	not specified [RCV004829020]	uncertain significance	5	16766099	16766099	Human		name
598190407	CV3994126	single nucleotide variant	NM_012334.3(MYO10):c.1349A>G (p.Asn450Ser)	not specified [RCV005374039]	uncertain significance	5	16763733	16763733	Human		name
598190430	CV3994129	single nucleotide variant	NM_012334.3(MYO10):c.2810C>T (p.Ala937Val)	not specified [RCV005374042]	uncertain significance	5	16701585	16701585	Human		name
598273706	CV3994140	single nucleotide variant	NM_012334.3(MYO10):c.2282A>G (p.Gln761Arg)	not specified [RCV005389785]	uncertain significance	5	16703153	16703153	Human		name
598273713	CV3994144	single nucleotide variant	NM_012334.3(MYO10):c.1312T>C (p.Phe438Leu)	not specified [RCV005389788]	uncertain significance	5	16764264	16764264	Human		name
598273715	CV3994145	single nucleotide variant	NM_012334.3(MYO10):c.2942A>G (p.Asn981Ser)	not specified [RCV005389789]	likely benign	5	16701453	16701453	Human		name
598190506	CV3994150	single nucleotide variant	NM_012334.3(MYO10):c.2815C>G (p.Gln939Glu)	not specified [RCV005374053]	uncertain significance	5	16701580	16701580	Human		name
598190521	CV3994152	single nucleotide variant	NM_012334.3(MYO10):c.1211C>T (p.Ala404Val)	not specified [RCV005374055]	uncertain significance	5	16764365	16764365	Human		name
598190530	CV3994153	single nucleotide variant	NM_012334.3(MYO10):c.1010G>A (p.Gly337Glu)	not specified [RCV005374056]	uncertain significance	5	16769124	16769124	Human		name
15149899	CV721367	single nucleotide variant	NM_012334.3(MYO10):c.2708T>C (p.Met903Thr)	not provided [RCV000879263]	benign	5	16701687	16701687	Human		name
15192174	CV721368	single nucleotide variant	NM_012334.3(MYO10):c.1889A>G (p.Asn630Ser)	not provided [RCV000888589]	benign	5	16754868	16754868	Human		name
156079966	CV2198426	single nucleotide variant	NM_012334.3(MYO10):c.3007G>A (p.Ala1003Thr)	not specified [RCV004081957]	uncertain significance	5	16701388	16701388	Human		name
156261035	CV2204866	single nucleotide variant	NM_012334.3(MYO10):c.3668G>C (p.Gly1223Ala)	not specified [RCV004075111]	uncertain significance	5	16694503	16694503	Human		name
156043489	CV2215854	single nucleotide variant	NM_012334.3(MYO10):c.4426C>T (p.Arg1476Trp)	not specified [RCV004096953]	uncertain significance	5	16680063	16680063	Human		name
156283757	CV2231035	single nucleotide variant	NM_012334.3(MYO10):c.3686T>C (p.Leu1229Pro)	not specified [RCV004094270]	uncertain significance	5	16694485	16694485	Human		name
156238529	CV2235804	single nucleotide variant	NM_012334.3(MYO10):c.3426G>T (p.Gln1142His)	not specified [RCV004111926]	uncertain significance	5	16700969	16700969	Human		name
156197081	CV2241595	single nucleotide variant	NM_012334.3(MYO10):c.5698C>T (p.Arg1900Trp)	not specified [RCV004104481]	uncertain significance	5	16670711	16670711	Human		name
155912717	CV2245625	single nucleotide variant	NM_012334.3(MYO10):c.3612C>G (p.Phe1204Leu)	not specified [RCV004111516]	uncertain significance	5	16694559	16694559	Human		name
155995263	CV2250327	single nucleotide variant	NM_012334.3(MYO10):c.4448A>G (p.Asn1483Ser)	not specified [RCV004127222]	uncertain significance	5	16680041	16680041	Human		name
155993375	CV2252250	single nucleotide variant	NM_012334.3(MYO10):c.5362C>G (p.Leu1788Val)	not specified [RCV004116118]	uncertain significance	5	16671490	16671490	Human		name
156025808	CV2274018	single nucleotide variant	NM_012334.3(MYO10):c.5281G>A (p.Val1761Ile)	not specified [RCV004134405]	uncertain significance	5	16672717	16672717	Human		name
155901043	CV2275310	single nucleotide variant	NM_012334.3(MYO10):c.5549C>T (p.Pro1850Leu)	not specified [RCV004137082]	uncertain significance	5	16670860	16670860	Human		name
155923731	CV2280370	single nucleotide variant	NM_012334.3(MYO10):c.3895A>G (p.Ser1299Gly)	not specified [RCV004140556]	uncertain significance	5	16689825	16689825	Human		name
156237196	CV2285783	single nucleotide variant	NM_012334.3(MYO10):c.4234C>A (p.Leu1412Met)	not specified [RCV004143737]	uncertain significance	5	16681459	16681459	Human		name
155999421	CV2287270	single nucleotide variant	NM_012334.3(MYO10):c.5551C>T (p.Leu1851Phe)	not specified [RCV004146909]	uncertain significance	5	16670858	16670858	Human		name
156087959	CV2290633	single nucleotide variant	NM_012334.3(MYO10):c.5146A>G (p.Ile1716Val)	not specified [RCV004149169]	uncertain significance	5	16673708	16673708	Human		name
156082878	CV2292972	single nucleotide variant	NM_012334.3(MYO10):c.3853G>A (p.Asp1285Asn)	not specified [RCV004148457]	uncertain significance	5	16689867	16689867	Human		name
156003442	CV2295662	single nucleotide variant	NM_012334.3(MYO10):c.3190C>T (p.His1064Tyr)	not specified [RCV004149818]	uncertain significance	5	16701205	16701205	Human		name
156267242	CV2296588	single nucleotide variant	NM_012334.3(MYO10):c.3857G>C (p.Arg1286Thr)	not specified [RCV004154653]	uncertain significance	5	16689863	16689863	Human		name
156289880	CV2299410	single nucleotide variant	NM_012334.3(MYO10):c.3181G>A (p.Gly1061Arg)	not specified [RCV004154496]	uncertain significance	5	16701214	16701214	Human		name
156240875	CV2310074	single nucleotide variant	NM_012334.3(MYO10):c.3000C>A (p.Asp1000Glu)	not specified [RCV004163205]	uncertain significance	5	16701395	16701395	Human		name
156169806	CV2315481	single nucleotide variant	NM_012334.3(MYO10):c.4592C>T (p.Pro1531Leu)	not specified [RCV004167428]	uncertain significance	5	16676105	16676105	Human		name
156183207	CV2353215	single nucleotide variant	NM_012334.3(MYO10):c.5564A>T (p.Tyr1855Phe)	not specified [RCV004203683]	uncertain significance	5	16670845	16670845	Human		name
155908829	CV2354757	single nucleotide variant	NM_012334.3(MYO10):c.5014A>G (p.Thr1672Ala)	not specified [RCV004204748]	uncertain significance	5	16673840	16673840	Human		name
156402340	CV2363835	single nucleotide variant	NM_012334.3(MYO10):c.6146G>A (p.Arg2049His)	not specified [RCV004218815]	uncertain significance	5	16666723	16666723	Human		name
155996465	CV2373075	single nucleotide variant	NM_012334.3(MYO10):c.3358G>A (p.Asp1120Asn)	not specified [RCV004217772]	uncertain significance	5	16701037	16701037	Human		name
155992926	CV2381642	single nucleotide variant	NM_012334.3(MYO10):c.4103C>T (p.Thr1368Met)	not specified [RCV004232113]	uncertain significance	5	16681957	16681957	Human		name
156247055	CV2396862	single nucleotide variant	NM_012334.3(MYO10):c.5528C>T (p.Thr1843Ile)	not specified [RCV004603415]	uncertain significance	5	16670881	16670881	Human		name
329375952	CV2441231	single nucleotide variant	NM_012334.3(MYO10):c.5465C>T (p.Ala1822Val)	not specified [RCV004263620]	uncertain significance	5	16670944	16670944	Human		name
329389036	CV2448654	single nucleotide variant	NM_012334.3(MYO10):c.6092A>G (p.Lys2031Arg)	not specified [RCV004259323]	uncertain significance	5	16666777	16666777	Human		name
329354907	CV2449167	single nucleotide variant	NM_012334.3(MYO10):c.4970G>A (p.Arg1657Gln)	not specified [RCV004264225]	uncertain significance	5	16673884	16673884	Human		name
329358448	CV2450320	single nucleotide variant	NM_012334.3(MYO10):c.5387A>G (p.Asn1796Ser)	not specified [RCV004271408]	uncertain significance	5	16671465	16671465	Human		name
329391101	CV2452033	single nucleotide variant	NM_012334.3(MYO10):c.5824A>C (p.Lys1942Gln)	not specified [RCV004278764]	uncertain significance	5	16670585	16670585	Human		name
329397386	CV2460218	single nucleotide variant	NM_012334.3(MYO10):c.4460G>T (p.Arg1487Leu)	not specified [RCV004273310]	uncertain significance	5	16680029	16680029	Human		name
329401428	CV2460833	single nucleotide variant	NM_012334.3(MYO10):c.4097C>T (p.Ala1366Val)	not specified [RCV004271145]	uncertain significance	5	16681963	16681963	Human		name
329397857	CV2464081	single nucleotide variant	NM_012334.3(MYO10):c.3431C>T (p.Ser1144Leu)	not specified [RCV004273779]	uncertain significance	5	16700964	16700964	Human		name
329389256	CV2467221	single nucleotide variant	NM_012334.3(MYO10):c.3845T>A (p.Ile1282Asn)	not specified [RCV004285034]	uncertain significance	5	16689875	16689875	Human		name
401751446	CV2672456	single nucleotide variant	NM_012334.3(MYO10):c.5467C>G (p.Pro1823Ala)	not specified [RCV004285710]	uncertain significance	5	16670942	16670942	Human		name
401726827	CV2674561	single nucleotide variant	NM_012334.3(MYO10):c.3794C>T (p.Thr1265Met)	not specified [RCV004291438]	uncertain significance	5	16694377	16694377	Human		name
401725186	CV2697305	single nucleotide variant	NM_012334.3(MYO10):c.3404G>A (p.Arg1135Gln)	not specified [RCV004304063]	uncertain significance	5	16700991	16700991	Human		name
401783091	CV2703778	single nucleotide variant	NM_012334.3(MYO10):c.3088T>G (p.Ser1030Ala)	not specified [RCV004306652]	uncertain significance	5	16701307	16701307	Human		name
401776712	CV2711290	single nucleotide variant	NM_012334.3(MYO10):c.3319G>A (p.Val1107Met)	not specified [RCV004313069]	uncertain significance	5	16701076	16701076	Human		name
401743255	CV2715436	single nucleotide variant	NM_012334.3(MYO10):c.3271T>C (p.Tyr1091His)	not specified [RCV004324753]	uncertain significance	5	16701124	16701124	Human		name
401781579	CV2722173	single nucleotide variant	NM_012334.3(MYO10):c.4511C>G (p.Thr1504Ser)	not specified [RCV004328743]	uncertain significance	5	16679978	16679978	Human		name
401728426	CV2731719	single nucleotide variant	NM_012334.3(MYO10):c.3710G>A (p.Arg1237His)	not specified [RCV004331820]	uncertain significance	5	16694461	16694461	Human		name
401865782	CV2755635	single nucleotide variant	NM_012334.3(MYO10):c.5321C>T (p.Thr1774Ile)	not specified [RCV004342021]	uncertain significance	5	16671531	16671531	Human		name
401874290	CV2759155	single nucleotide variant	NM_012334.3(MYO10):c.3938A>G (p.Asp1313Gly)	not specified [RCV004342451]	uncertain significance	5	16685790	16685790	Human		name
401878825	CV2777917	single nucleotide variant	NM_012334.3(MYO10):c.5753C>T (p.Ser1918Phe)	not specified [RCV004347885]	uncertain significance	5	16670656	16670656	Human		name
401894886	CV2782019	single nucleotide variant	NM_012334.3(MYO10):c.5479C>T (p.Leu1827Phe)	not specified [RCV004359029]	uncertain significance	5	16670930	16670930	Human		name
405761558	CV3311115	single nucleotide variant	NM_012334.3(MYO10):c.3149C>T (p.Thr1050Met)	not specified [RCV004455400]	uncertain significance	5	16701246	16701246	Human		name
405761579	CV3311118	single nucleotide variant	NM_012334.3(MYO10):c.3185G>A (p.Ser1062Asn)	not specified [RCV004455403]	uncertain significance	5	16701210	16701210	Human		name
405761629	CV3311126	single nucleotide variant	NM_012334.3(MYO10):c.3194A>G (p.Asn1065Ser)	not specified [RCV004455411]	uncertain significance	5	16701201	16701201	Human		name
405761650	CV3311130	single nucleotide variant	NM_012334.3(MYO10):c.3205G>A (p.Gly1069Ser)	not specified [RCV004455415]	uncertain significance	5	16701190	16701190	Human		name
405761720	CV3311142	single nucleotide variant	NM_012334.3(MYO10):c.3340G>T (p.Gly1114Cys)	not specified [RCV004455427]	uncertain significance	5	16701055	16701055	Human		name
405761769	CV3311150	single nucleotide variant	NM_012334.3(MYO10):c.3392C>T (p.Ser1131Leu)	not specified [RCV004455435]	uncertain significance	5	16701003	16701003	Human		name
405761844	CV3311163	single nucleotide variant	NM_012334.3(MYO10):c.3541T>C (p.Phe1181Leu)	not specified [RCV004455448]	uncertain significance	5	16699465	16699465	Human		name
405761859	CV3311166	single nucleotide variant	NM_012334.3(MYO10):c.3563T>C (p.Leu1188Pro)	not specified [RCV004455451]	uncertain significance	5	16694608	16694608	Human		name
405762028	CV3311193	single nucleotide variant	NM_012334.3(MYO10):c.4019C>G (p.Ser1340Cys)	not specified [RCV004455478]	uncertain significance	5	16683907	16683907	Human		name
405762144	CV3311213	single nucleotide variant	NM_012334.3(MYO10):c.4651G>T (p.Asp1551Tyr)	not specified [RCV004455498]	uncertain significance	5	16676046	16676046	Human		name
405762155	CV3311215	single nucleotide variant	NM_012334.3(MYO10):c.4808G>A (p.Arg1603Gln)	not specified [RCV004455500]	uncertain significance	5	16675009	16675009	Human		name
405762185	CV3311220	single nucleotide variant	NM_012334.3(MYO10):c.4980T>G (p.Phe1660Leu)	not specified [RCV004455505]	uncertain significance	5	16673874	16673874	Human		name
405762218	CV3311226	single nucleotide variant	NM_012334.3(MYO10):c.5158A>G (p.Thr1720Ala)	not specified [RCV004455511]	uncertain significance	5	16673696	16673696	Human		name
405762259	CV3311233	single nucleotide variant	NM_012334.3(MYO10):c.5354A>T (p.Tyr1785Phe)	not specified [RCV004455518]	uncertain significance	5	16671498	16671498	Human		name
405762299	CV3311240	single nucleotide variant	NM_012334.3(MYO10):c.5453G>T (p.Gly1818Val)	not specified [RCV004455525]	uncertain significance	5	16670956	16670956	Human		name
405762411	CV3321254	single nucleotide variant	NM_012334.3(MYO10):c.5582A>G (p.Lys1861Arg)	not specified [RCV004455546]	uncertain significance	5	16670827	16670827	Human		name
405762438	CV3321258	single nucleotide variant	NM_012334.3(MYO10):c.5627G>A (p.Arg1876Gln)	not specified [RCV004455550]	uncertain significance	5	16670782	16670782	Human		name
405762467	CV3321263	single nucleotide variant	NM_012334.3(MYO10):c.5645C>A (p.Thr1882Lys)	not specified [RCV004455555]	uncertain significance	5	16670764	16670764	Human		name
405762486	CV3321266	single nucleotide variant	NM_012334.3(MYO10):c.5672G>A (p.Arg1891Gln)	not specified [RCV004455558]	uncertain significance	5	16670737	16670737	Human		name
405762509	CV3321270	single nucleotide variant	NM_012334.3(MYO10):c.5753C>A (p.Ser1918Tyr)	not specified [RCV004455562]	uncertain significance	5	16670656	16670656	Human		name
405762534	CV3321274	single nucleotide variant	NM_012334.3(MYO10):c.5762G>A (p.Arg1921Gln)	not specified [RCV004455566]	uncertain significance	5	16670647	16670647	Human		name
405762554	CV3321277	single nucleotide variant	NM_012334.3(MYO10):c.5802G>T (p.Met1934Ile)	not specified [RCV004455569]	uncertain significance	5	16670607	16670607	Human		name
405762571	CV3321280	single nucleotide variant	NM_012334.3(MYO10):c.5932G>A (p.Asp1978Asn)	not specified [RCV004455572]	uncertain significance	5	16668420	16668420	Human		name
405762591	CV3321283	single nucleotide variant	NM_012334.3(MYO10):c.6026C>T (p.Thr2009Met)	not specified [RCV004455575]	uncertain significance	5	16668326	16668326	Human		name
405762611	CV3321287	single nucleotide variant	NM_012334.3(MYO10):c.6043G>A (p.Asp2015Asn)	not specified [RCV004455579]	uncertain significance	5	16668309	16668309	Human		name
405762678	CV3321298	single nucleotide variant	NM_012334.3(MYO10):c.6160C>A (p.Gln2054Lys)	not specified [RCV004455590]	uncertain significance	5	16666709	16666709	Human		name
407504521	CV3450675	single nucleotide variant	NM_012334.3(MYO10):c.4079G>A (p.Arg1360Gln)	not specified [RCV004645851]	uncertain significance	5	16681981	16681981	Human		name
407515320	CV3450677	single nucleotide variant	NM_012334.3(MYO10):c.5235T>G (p.Phe1745Leu)	not specified [RCV004649852]	uncertain significance	5	16672763	16672763	Human		name
407515323	CV3450678	single nucleotide variant	NM_012334.3(MYO10):c.5818A>C (p.Met1940Leu)	not specified [RCV004649853]	uncertain significance	5	16670591	16670591	Human		name
407515329	CV3450680	single nucleotide variant	NM_012334.3(MYO10):c.4563T>A (p.Asp1521Glu)	not specified [RCV004649855]	uncertain significance	5	16676134	16676134	Human		name
407515335	CV3450683	single nucleotide variant	NM_012334.3(MYO10):c.5587C>T (p.Arg1863Cys)	not specified [RCV004649857]	uncertain significance	5	16670822	16670822	Human		name
407515338	CV3450684	single nucleotide variant	NM_012334.3(MYO10):c.3818C>A (p.Thr1273Asn)	not specified [RCV004649858]	uncertain significance	5	16689902	16689902	Human		name
407504528	CV3450685	single nucleotide variant	NM_012334.3(MYO10):c.3229C>A (p.Gln1077Lys)	not specified [RCV004645853]	uncertain significance	5	16701166	16701166	Human		name
597665018	CV3565015	single nucleotide variant	NM_012334.3(MYO10):c.5554G>A (p.Glu1852Lys)	not specified [RCV004828983]	uncertain significance	5	16670855	16670855	Human		name
597665028	CV3565016	single nucleotide variant	NM_012334.3(MYO10):c.6058C>G (p.Leu2020Val)	not specified [RCV004828984]	uncertain significance	5	16668294	16668294	Human		name
597665037	CV3565017	single nucleotide variant	NM_012334.3(MYO10):c.5710G>A (p.Glu1904Lys)	not specified [RCV004828985]	uncertain significance	5	16670699	16670699	Human		name
597665054	CV3565019	single nucleotide variant	NM_012334.3(MYO10):c.4460G>A (p.Arg1487Gln)	not specified [RCV004828987]	uncertain significance	5	16680029	16680029	Human		name
597665087	CV3565023	single nucleotide variant	NM_012334.3(MYO10):c.3781G>A (p.Val1261Ile)	not specified [RCV004828991]	uncertain significance	5	16694390	16694390	Human		name
597665107	CV3565026	single nucleotide variant	NM_012334.3(MYO10):c.5864C>T (p.Ser1955Leu)	not specified [RCV004828994]	uncertain significance	5	16670545	16670545	Human		name
597665115	CV3565027	single nucleotide variant	NM_012334.3(MYO10):c.3668G>T (p.Gly1223Val)	not specified [RCV004828995]	uncertain significance	5	16694503	16694503	Human		name
597665129	CV3565029	single nucleotide variant	NM_012334.3(MYO10):c.3274G>A (p.Asp1092Asn)	not specified [RCV004828997]	uncertain significance	5	16701121	16701121	Human		name
597665165	CV3565033	single nucleotide variant	NM_012334.3(MYO10):c.5245G>A (p.Gly1749Ser)	not specified [RCV004829001]	uncertain significance	5	16672753	16672753	Human		name
597665181	CV3565035	single nucleotide variant	NM_012334.3(MYO10):c.3779C>T (p.Thr1260Ile)	not specified [RCV004829003]	uncertain significance	5	16694392	16694392	Human		name
597665204	CV3565038	single nucleotide variant	NM_012334.3(MYO10):c.5559G>C (p.Glu1853Asp)	not specified [RCV004829006]	uncertain significance	5	16670850	16670850	Human		name
597665221	CV3565040	single nucleotide variant	NM_012334.3(MYO10):c.2998G>A (p.Asp1000Asn)	not specified [RCV004829008]	uncertain significance	5	16701397	16701397	Human		name
597665230	CV3565041	single nucleotide variant	NM_012334.3(MYO10):c.5626C>T (p.Arg1876Trp)	not specified [RCV004829009]	uncertain significance	5	16670783	16670783	Human		name
597665759	CV3565046	single nucleotide variant	NM_012334.3(MYO10):c.3278A>T (p.Gln1093Leu)	not specified [RCV004829014]	uncertain significance	5	16701117	16701117	Human		name
597665750	CV3565047	single nucleotide variant	NM_012334.3(MYO10):c.3584G>A (p.Arg1195His)	not specified [RCV004829015]	uncertain significance	5	16694587	16694587	Human		name
597665741	CV3565048	single nucleotide variant	NM_012334.3(MYO10):c.3501C>G (p.Asp1167Glu)	not specified [RCV004829016]	uncertain significance	5	16699505	16699505	Human		name
597665699	CV3565054	single nucleotide variant	NM_012334.3(MYO10):c.3668G>A (p.Gly1223Glu)	not specified [RCV004829022]	uncertain significance	5	16694503	16694503	Human		name
598273694	CV3994125	single nucleotide variant	NM_012334.3(MYO10):c.3364C>T (p.Arg1122Cys)	not specified [RCV005389779]	uncertain significance	5	16701031	16701031	Human		name
598190423	CV3994128	single nucleotide variant	NM_012334.3(MYO10):c.3497G>A (p.Arg1166His)	not specified [RCV005374041]	uncertain significance	5	16699509	16699509	Human		name
598273696	CV3994131	single nucleotide variant	NM_012334.3(MYO10):c.3839A>G (p.Asp1280Gly)	not specified [RCV005389780]	uncertain significance	5	16689881	16689881	Human		name
598190445	CV3994132	single nucleotide variant	NM_012334.3(MYO10):c.3838G>A (p.Asp1280Asn)	not specified [RCV005374044]	uncertain significance	5	16689882	16689882	Human		name
598190452	CV3994133	single nucleotide variant	NM_012334.3(MYO10):c.4157C>T (p.Thr1386Ile)	not specified [RCV005374045]	uncertain significance	5	16681903	16681903	Human		name
598273698	CV3994134	single nucleotide variant	NM_012334.3(MYO10):c.4472C>T (p.Ala1491Val)	not specified [RCV005389781]	uncertain significance	5	16680017	16680017	Human		name
598273700	CV3994135	single nucleotide variant	NM_012334.3(MYO10):c.6170C>G (p.Ser2057Cys)	not specified [RCV005389782]	uncertain significance	5	16666699	16666699	Human		name
598190466	CV3994138	single nucleotide variant	NM_012334.3(MYO10):c.3343A>G (p.Ser1115Gly)	not specified [RCV005374047]	uncertain significance	5	16701052	16701052	Human		name
598273704	CV3994139	single nucleotide variant	NM_012334.3(MYO10):c.3329C>T (p.Ser1110Phe)	not specified [RCV005389784]	uncertain significance	5	16701066	16701066	Human		name
598273708	CV3994141	single nucleotide variant	NM_012334.3(MYO10):c.2999A>C (p.Asp1000Ala)	not specified [RCV005389786]	uncertain significance	5	16701396	16701396	Human		name
598190472	CV3994142	single nucleotide variant	NM_012334.3(MYO10):c.4690A>T (p.Thr1564Ser)	not specified [RCV005374048]	uncertain significance	5	16675127	16675127	Human		name
598273711	CV3994143	single nucleotide variant	NM_012334.3(MYO10):c.5081T>G (p.Leu1694Arg)	not specified [RCV005389787]	uncertain significance	5	16673773	16673773	Human		name
598190479	CV3994146	single nucleotide variant	NM_012334.3(MYO10):c.5457C>A (p.His1819Gln)	not specified [RCV005374049]	uncertain significance	5	16670952	16670952	Human		name
598190484	CV3994147	single nucleotide variant	NM_012334.3(MYO10):c.3750A>C (p.Glu1250Asp)	not specified [RCV005374050]	uncertain significance	5	16694421	16694421	Human		name
598190499	CV3994149	single nucleotide variant	NM_012334.3(MYO10):c.5464G>T (p.Ala1822Ser)	not specified [RCV005374052]	uncertain significance	5	16670945	16670945	Human		name
598190513	CV3994151	single nucleotide variant	NM_012334.3(MYO10):c.4583A>G (p.Lys1528Arg)	not specified [RCV005374054]	uncertain significance	5	16676114	16676114	Human		name
598190537	CV3994154	single nucleotide variant	NM_012334.3(MYO10):c.3959A>C (p.His1320Pro)	not specified [RCV005374057]	uncertain significance	5	16685769	16685769	Human		name
15172897	CV699001	single nucleotide variant	NM_012334.3(MYO10):c.4559C>T (p.Ser1520Leu)	not provided [RCV000950129]	benign	5	16676138	16676138	Human		name
15167939	CV709798	single nucleotide variant	NM_012334.3(MYO10):c.6071G>C (p.Ser2024Thr)	not provided [RCV000971506]	benign	5	16668281	16668281	Human		name
405705228	CV3225085	deletion	NM_012334.3(MYO10):c.841_844del (p.Ser281fs)	not provided [RCV003990041]	likely pathogenic	5	16779631	16779634	Human		name

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