Myh13 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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236 records found for search term Myh13

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401904142	CV2814948	single nucleotide variant	NM_003802.3(MYH13):c.348+7G>A	not provided [RCV003419654]	likely benign	17	10362353	10362353	Human		name
405269465	CV3201619	single nucleotide variant	NM_003802.3(MYH13):c.349-9T>C	MYH13-related disorder [RCV003899529]	likely benign	17	10362283	10362283	Human		name , trait , alternate_id
8585233	CV119816	single nucleotide variant	NM_003802.2(MYH13):c.1145-1030G>A	Lung cancer [RCV000100336]	uncertain significance	17	10347828	10347828	Human		name
8654353	CV130928	single nucleotide variant	NM_003802.2(MYH13):c.2691+1582G>T	Lung cancer [RCV000111415]	uncertain significance	17	10326284	10326284	Human		name
8635965	CV91188	single nucleotide variant	NM_003802.2(MYH13):c.48C>T (p.Tyr16=)	Malignant melanoma [RCV000071286]	not provided	17	10364483	10364483	Human		name
156346641	CV2382778	single nucleotide variant	NM_003802.3(MYH13):c.97G>A (p.Asp33Asn)	not specified [RCV004224123]	uncertain significance	17	10364434	10364434	Human		name
401774931	CV2713700	single nucleotide variant	NM_003802.3(MYH13):c.94T>C (p.Phe32Leu)	not specified [RCV004321058]	uncertain significance	17	10364437	10364437	Human		name
405294487	CV3211484	single nucleotide variant	NM_003802.3(MYH13):c.375C>T (p.Thr125=)	MYH13-related disorder [RCV003934384]	likely benign	17	10362248	10362248	Human		name , trait , alternate_id
405293211	CV3221276	single nucleotide variant	NM_003802.3(MYH13):c.606C>T (p.Thr202=)	MYH13-related disorder [RCV003966802]	likely benign	17	10359999	10359999	Human		name , trait , alternate_id
405755188	CV3316694	single nucleotide variant	NM_003802.3(MYH13):c.46T>G (p.Tyr16Asp)	not specified [RCV004454389]	uncertain significance	17	10364485	10364485	Human		name
407514885	CV3454364	single nucleotide variant	NM_003802.3(MYH13):c.77A>G (p.Glu26Gly)	not specified [RCV004649700]	uncertain significance	17	10364454	10364454	Human		name
597646397	CV3554997	single nucleotide variant	NM_003802.3(MYH13):c.52C>T (p.Arg18Trp)	not specified [RCV004826242]	uncertain significance	17	10364479	10364479	Human		name
598189272	CV3983333	single nucleotide variant	NM_003802.3(MYH13):c.534C>T (p.Thr178=)	not specified [RCV005373846]	likely benign	17	10360071	10360071	Human		name
156006425	CV2288797	single nucleotide variant	NM_003802.3(MYH13):c.230T>C (p.Val77Ala)	not specified [RCV004148008]	uncertain significance	17	10362478	10362478	Human		name
401778688	CV2735455	single nucleotide variant	NM_003802.3(MYH13):c.178G>A (p.Val60Ile)	not specified [RCV004331014]	uncertain significance	17	10364353	10364353	Human		name
401914035	CV2814947	single nucleotide variant	NM_003802.3(MYH13):c.1377C>T (p.Ile459=)	not provided [RCV003428141]	likely benign	17	10345503	10345503	Human		name
405739799	CV3316492	single nucleotide variant	NM_003802.3(MYH13):c.203G>A (p.Arg68Gln)	not specified [RCV004452203]	uncertain significance	17	10364328	10364328	Human		name
407514876	CV3454360	single nucleotide variant	NM_003802.3(MYH13):c.284C>T (p.Thr95Ile)	not specified [RCV004649697]	uncertain significance	17	10362424	10362424	Human		name
407504226	CV3454363	single nucleotide variant	NM_003802.3(MYH13):c.211A>G (p.Thr71Ala)	not specified [RCV004645737]	uncertain significance	17	10362497	10362497	Human		name
597646563	CV3555023	single nucleotide variant	NM_003802.3(MYH13):c.155T>C (p.Ile52Thr)	not specified [RCV004826266]	uncertain significance	17	10364376	10364376	Human		name
597646578	CV3555025	single nucleotide variant	NM_003802.3(MYH13):c.176A>G (p.Lys59Arg)	not specified [RCV004826268]	uncertain significance	17	10364355	10364355	Human		name
8627888	CV83032	single nucleotide variant	NM_003802.2(MYH13):c.1632G>A (p.Lys544=)	Malignant melanoma [RCV000063112]	not provided	17	10344062	10344062	Human		name
8627889	CV83033	single nucleotide variant	NM_003802.2(MYH13):c.242A>G (p.Asn81Ser)	Malignant melanoma [RCV000063113]	not provided	17	10362466	10362466	Human		name
155918999	CV2279332	single nucleotide variant	NM_003802.3(MYH13):c.973A>G (p.Ile325Val)	not specified [RCV004139848]	uncertain significance	17	10354712	10354712	Human		name
156060168	CV2305382	single nucleotide variant	NM_003802.3(MYH13):c.376G>A (p.Val126Ile)	not specified [RCV004171285]	uncertain significance	17	10362247	10362247	Human		name
156177952	CV2327302	single nucleotide variant	NM_003802.3(MYH13):c.749T>C (p.Ile250Thr)	not specified [RCV004174745]	uncertain significance	17	10355137	10355137	Human		name
156324950	CV2335130	single nucleotide variant	NM_003802.3(MYH13):c.398C>T (p.Pro133Leu)	not specified [RCV004184661]	uncertain significance	17	10362225	10362225	Human		name
155984588	CV2344437	single nucleotide variant	NM_003802.3(MYH13):c.442C>T (p.Arg148Cys)	not specified [RCV004195182]	uncertain significance	17	10362181	10362181	Human		name
155994217	CV2379517	single nucleotide variant	NM_003802.3(MYH13):c.931G>A (p.Asp311Asn)	not specified [RCV004217228]	uncertain significance	17	10354754	10354754	Human		name
155936444	CV2380455	single nucleotide variant	NM_003802.3(MYH13):c.838T>C (p.Ser280Pro)	not specified [RCV004218053]	uncertain significance	17	10354958	10354958	Human		name
329401613	CV2457215	single nucleotide variant	NM_003802.3(MYH13):c.350C>A (p.Thr117Asn)	not specified [RCV004265289]	uncertain significance	17	10362273	10362273	Human		name
401729796	CV2686950	single nucleotide variant	NM_003802.3(MYH13):c.424G>T (p.Ala142Ser)	not specified [RCV004304283]	uncertain significance	17	10362199	10362199	Human		name
401763790	CV2725299	single nucleotide variant	NM_003802.3(MYH13):c.878C>T (p.Ser293Leu)	not specified [RCV004319963]	uncertain significance	17	10354918	10354918	Human		name
401729708	CV2733255	single nucleotide variant	NM_003802.3(MYH13):c.571C>T (p.Arg191Cys)	not specified [RCV004332168]	uncertain significance	17	10360034	10360034	Human		name
401867050	CV2759081	single nucleotide variant	NM_003802.3(MYH13):c.680C>T (p.Pro227Leu)	not specified [RCV004342384]	uncertain significance	17	10357793	10357793	Human		name
401856167	CV2764425	single nucleotide variant	NM_003802.3(MYH13):c.608G>A (p.Gly203Glu)	not specified [RCV004338995]	uncertain significance	17	10359997	10359997	Human		name
401884414	CV2789676	single nucleotide variant	NM_003802.3(MYH13):c.827C>G (p.Thr276Arg)	not specified [RCV004360269]	uncertain significance	17	10354969	10354969	Human		name
401914030	CV2814944	single nucleotide variant	NM_003802.3(MYH13):c.4119C>T (p.Ala1373=)	not provided [RCV003428139]	likely benign	17	10313220	10313220	Human		name
405264080	CV3189869	single nucleotide variant	NM_003802.3(MYH13):c.595A>G (p.Ile199Val)	MYH13-related disorder [RCV003896917]	likely benign	17	10360010	10360010	Human		name , trait , alternate_id
405756134	CV3316831	single nucleotide variant	NM_003802.3(MYH13):c.898A>C (p.Ile300Leu)	not specified [RCV004454526]	uncertain significance	17	10354898	10354898	Human		name
407514897	CV3454372	single nucleotide variant	NM_003802.3(MYH13):c.602T>C (p.Val201Ala)	not specified [RCV004649704]	uncertain significance	17	10360003	10360003	Human		name
597646435	CV3555002	single nucleotide variant	NM_003802.3(MYH13):c.364T>C (p.Phe122Leu)	not specified [RCV004826247]	uncertain significance	17	10362259	10362259	Human		name
598189139	CV3983308	single nucleotide variant	NM_003802.3(MYH13):c.443G>A (p.Arg148His)	not specified [RCV005373829]	uncertain significance	17	10362180	10362180	Human		name
598189147	CV3983309	single nucleotide variant	NM_003802.3(MYH13):c.976G>A (p.Asp326Asn)	not specified [RCV005373830]	uncertain significance	17	10354709	10354709	Human		name
598189163	CV3983312	single nucleotide variant	NM_003802.3(MYH13):c.484G>A (p.Ala162Thr)	not specified [RCV005373832]	uncertain significance	17	10362139	10362139	Human		name
598189197	CV3983316	single nucleotide variant	NM_003802.3(MYH13):c.990A>T (p.Glu330Asp)	not specified [RCV005373836]	uncertain significance	17	10354695	10354695	Human		name
598273444	CV3983323	single nucleotide variant	NM_003802.3(MYH13):c.541T>C (p.Ser181Pro)	not specified [RCV005389686]	uncertain significance	17	10360064	10360064	Human		name
8635961	CV91184	single nucleotide variant	NM_003802.2(MYH13):c.5316G>A (p.Glu1772=)	Malignant melanoma [RCV000071282]	not provided	17	10306609	10306609	Human		name
8635962	CV91185	single nucleotide variant	NM_003802.2(MYH13):c.5310T>C (p.Ala1770=)	Malignant melanoma [RCV000071283]	not provided	17	10306615	10306615	Human		name
156132147	CV2206532	single nucleotide variant	NM_003802.3(MYH13):c.2375C>T (p.Thr792Met)	not specified [RCV004080884]	uncertain significance	17	10330447	10330447	Human		name
156208847	CV2250151	single nucleotide variant	NM_003802.3(MYH13):c.2033T>C (p.Ile678Thr)	not specified [RCV004116957]	uncertain significance	17	10340173	10340173	Human		name
156307152	CV2252814	single nucleotide variant	NM_003802.3(MYH13):c.1378G>A (p.Gly460Arg)	not specified [RCV004120437]	uncertain significance	17	10345502	10345502	Human		name
156302458	CV2258674	single nucleotide variant	NM_003802.3(MYH13):c.2039A>G (p.Asn680Ser)	not specified [RCV004117920]	uncertain significance	17	10340167	10340167	Human		name
156334082	CV2267025	single nucleotide variant	NM_003802.3(MYH13):c.1077G>A (p.Met359Ile)	not specified [RCV004131664]	uncertain significance	17	10350623	10350623	Human		name
156368528	CV2267026	single nucleotide variant	NM_003802.3(MYH13):c.1078C>A (p.His360Asn)	not specified [RCV004131665]	uncertain significance	17	10350622	10350622	Human		name
155998820	CV2287198	single nucleotide variant	NM_003802.3(MYH13):c.2784G>C (p.Glu928Asp)	not specified [RCV004146848]	uncertain significance	17	10324172	10324172	Human		name
156174720	CV2290371	single nucleotide variant	NM_003802.3(MYH13):c.2180G>A (p.Arg727Gln)	not specified [RCV004154797]	uncertain significance	17	10332217	10332217	Human		name
155971715	CV2309330	single nucleotide variant	NM_003802.3(MYH13):c.2534A>G (p.Lys845Arg)	not specified [RCV004165485]	uncertain significance	17	10328023	10328023	Human		name
156064585	CV2316166	single nucleotide variant	NM_003802.3(MYH13):c.2585G>A (p.Arg862Lys)	not specified [RCV004174210]	uncertain significance	17	10327972	10327972	Human		name
156065541	CV2323723	single nucleotide variant	NM_003802.3(MYH13):c.2249T>C (p.Leu750Pro)	not specified [RCV004174378]	uncertain significance	17	10332148	10332148	Human		name
156176893	CV2327138	single nucleotide variant	NM_003802.3(MYH13):c.1297G>A (p.Val433Ile)	not specified [RCV004178703]	uncertain significance	17	10345583	10345583	Human		name
156189507	CV2328825	single nucleotide variant	NM_003802.3(MYH13):c.1624T>C (p.Phe542Leu)	not specified [RCV004178043]	uncertain significance	17	10344070	10344070	Human		name
156034529	CV2338733	single nucleotide variant	NM_003802.3(MYH13):c.1951G>A (p.Val651Met)	not specified [RCV004182304]	uncertain significance	17	10340345	10340345	Human		name
156056583	CV2343483	single nucleotide variant	NM_003802.3(MYH13):c.1109A>G (p.Gln370Arg)	not specified [RCV004197552]	uncertain significance	17	10350591	10350591	Human		name
156182966	CV2353198	single nucleotide variant	NM_003802.3(MYH13):c.2537G>A (p.Ser846Asn)	not specified [RCV004203667]	uncertain significance	17	10328020	10328020	Human		name
156282529	CV2363133	single nucleotide variant	NM_003802.3(MYH13):c.2135G>T (p.Gly712Val)	not specified [RCV004211256]	uncertain significance	17	10333113	10333113	Human		name
156212505	CV2378423	single nucleotide variant	NM_003802.3(MYH13):c.2838T>A (p.Asn946Lys)	not specified [RCV004226438]	uncertain significance	17	10324118	10324118	Human		name
156392647	CV2386573	single nucleotide variant	NM_003802.3(MYH13):c.2260G>A (p.Asp754Asn)	not specified [RCV004230924]	uncertain significance	17	10332137	10332137	Human		name
155907382	CV2389870	single nucleotide variant	NM_003802.3(MYH13):c.2035C>T (p.Pro679Ser)	not specified [RCV004236085]	uncertain significance	17	10340171	10340171	Human		name
156193239	CV2397971	single nucleotide variant	NM_003802.3(MYH13):c.1013T>C (p.Ile338Thr)	not specified [RCV004241579]	uncertain significance	17	10350687	10350687	Human		name
329385286	CV2432076	single nucleotide variant	NM_003802.3(MYH13):c.1844C>T (p.Ser615Leu)	not specified [RCV004249227]	uncertain significance	17	10343850	10343850	Human		name
329365185	CV2440115	single nucleotide variant	NM_003802.3(MYH13):c.1921G>A (p.Gly641Arg)	not specified [RCV004260579]	uncertain significance	17	10340375	10340375	Human		name
329390738	CV2455421	single nucleotide variant	NM_003802.3(MYH13):c.1183G>A (p.Ala395Thr)	not specified [RCV004276695]	uncertain significance	17	10346760	10346760	Human		name
401741959	CV2676786	single nucleotide variant	NM_003802.3(MYH13):c.2560G>T (p.Ala854Ser)	not specified [RCV004290957]	uncertain significance	17	10327997	10327997	Human		name
401740804	CV2702641	single nucleotide variant	NM_003802.3(MYH13):c.2708T>G (p.Met903Arg)	not specified [RCV004318910]	uncertain significance	17	10324248	10324248	Human		name
401774247	CV2702672	single nucleotide variant	NM_003802.3(MYH13):c.2558T>A (p.Met853Lys)	not specified [RCV004318933]	uncertain significance	17	10327999	10327999	Human		name
401766224	CV2714315	single nucleotide variant	NM_003802.3(MYH13):c.1903G>A (p.Gly635Arg)	not specified [RCV004315996]	uncertain significance	17	10340393	10340393	Human		name
401778378	CV2714686	single nucleotide variant	NM_003802.3(MYH13):c.1159G>A (p.Gly387Arg)	not specified [RCV004320263]	uncertain significance	17	10346784	10346784	Human		name
401725316	CV2726112	single nucleotide variant	NM_003802.3(MYH13):c.1960G>T (p.Val654Leu)	not specified [RCV004324461]	uncertain significance	17	10340336	10340336	Human		name
405739821	CV3316495	single nucleotide variant	NM_003802.3(MYH13):c.2099A>G (p.Asn700Ser)	not specified [RCV004452206]	uncertain significance	17	10333149	10333149	Human		name
405739871	CV3316502	single nucleotide variant	NM_003802.3(MYH13):c.2173C>T (p.Arg725Trp)	not specified [RCV004452213]	uncertain significance	17	10333075	10333075	Human		name
405739988	CV3316519	single nucleotide variant	NM_003802.3(MYH13):c.2375C>G (p.Thr792Arg)	not specified [RCV004452230]	uncertain significance	17	10330447	10330447	Human		name
405740041	CV3316526	single nucleotide variant	NM_003802.3(MYH13):c.2414T>G (p.Phe805Cys)	not specified [RCV004452237]	uncertain significance	17	10330408	10330408	Human		name
405740063	CV3316529	single nucleotide variant	NM_003802.3(MYH13):c.2464A>G (p.Ile822Val)	not specified [RCV004452240]	uncertain significance	17	10328093	10328093	Human		name
405740070	CV3316530	single nucleotide variant	NM_003802.3(MYH13):c.2480A>G (p.Asn827Ser)	not specified [RCV004452241]	uncertain significance	17	10328077	10328077	Human		name
405740170	CV3316544	single nucleotide variant	NM_003802.3(MYH13):c.2538T>A (p.Ser846Arg)	not specified [RCV004452255]	uncertain significance	17	10328019	10328019	Human		name
405740208	CV3316550	single nucleotide variant	NM_003802.3(MYH13):c.2780C>T (p.Thr927Met)	not specified [RCV004452261]	uncertain significance	17	10324176	10324176	Human		name
405739307	CV3320310	single nucleotide variant	NM_003802.3(MYH13):c.1081T>C (p.Tyr361His)	not specified [RCV004452131]	uncertain significance	17	10350619	10350619	Human		name
405739321	CV3320312	single nucleotide variant	NM_003802.3(MYH13):c.1084G>A (p.Gly362Arg)	not specified [RCV004452133]	uncertain significance	17	10350616	10350616	Human		name
405739388	CV3320321	single nucleotide variant	NM_003802.3(MYH13):c.1214G>A (p.Arg405Lys)	not specified [RCV004452142]	uncertain significance	17	10346729	10346729	Human		name
405739418	CV3320325	single nucleotide variant	NM_003802.3(MYH13):c.1274C>T (p.Ser425Leu)	not specified [RCV004452146]	uncertain significance	17	10345606	10345606	Human		name
405739485	CV3320336	single nucleotide variant	NM_003802.3(MYH13):c.1556T>C (p.Leu519Pro)	not specified [RCV004452157]	uncertain significance	17	10345230	10345230	Human		name
405739674	CV3320364	single nucleotide variant	NM_003802.3(MYH13):c.1960G>A (p.Val654Met)	not specified [RCV004452185]	uncertain significance	17	10340336	10340336	Human		name
407514860	CV3454352	single nucleotide variant	NM_003802.3(MYH13):c.1489G>A (p.Val497Met)	not specified [RCV004649692]	uncertain significance	17	10345297	10345297	Human		name
407514863	CV3454353	single nucleotide variant	NM_003802.3(MYH13):c.1424T>C (p.Leu475Pro)	not specified [RCV004649693]	uncertain significance	17	10345362	10345362	Human		name
407514866	CV3454356	single nucleotide variant	NM_003802.3(MYH13):c.2269C>G (p.Arg757Gly)	not specified [RCV004649694]	uncertain significance	17	10332128	10332128	Human		name
407504238	CV3454368	single nucleotide variant	NM_003802.3(MYH13):c.1427A>G (p.Glu476Gly)	not specified [RCV004645741]	uncertain significance	17	10345359	10345359	Human		name
407514888	CV3454369	single nucleotide variant	NM_003802.3(MYH13):c.1604T>C (p.Ile535Thr)	not specified [RCV004649701]	uncertain significance	17	10344090	10344090	Human		name
597646384	CV3554994	single nucleotide variant	NM_003802.3(MYH13):c.2468G>A (p.Arg823His)	not specified [RCV004826240]	uncertain significance	17	10328089	10328089	Human		name
597646390	CV3554995	single nucleotide variant	NM_003802.3(MYH13):c.1438A>G (p.Ile480Val)	not specified [RCV004826241]	uncertain significance	17	10345348	10345348	Human		name
597646422	CV3555000	single nucleotide variant	NM_003802.3(MYH13):c.2145C>G (p.Ser715Arg)	not specified [RCV004826245]	uncertain significance	17	10333103	10333103	Human		name
597646460	CV3555007	single nucleotide variant	NM_003802.3(MYH13):c.2326C>T (p.Leu776Phe)	not specified [RCV004826251]	uncertain significance	17	10330496	10330496	Human		name
597646467	CV3555008	single nucleotide variant	NM_003802.3(MYH13):c.1156G>C (p.Ala386Pro)	not specified [RCV004826252]	uncertain significance	17	10346787	10346787	Human		name
597646481	CV3555010	single nucleotide variant	NM_003802.3(MYH13):c.1674T>A (p.His558Gln)	not specified [RCV004826254]	uncertain significance	17	10344020	10344020	Human		name
597646496	CV3555012	single nucleotide variant	NM_003802.3(MYH13):c.1378G>T (p.Gly460Trp)	not specified [RCV004826256]	uncertain significance	17	10345502	10345502	Human		name
597646504	CV3555013	single nucleotide variant	NM_003802.3(MYH13):c.2336A>C (p.Glu779Ala)	not specified [RCV004826257]	uncertain significance	17	10330486	10330486	Human		name
597646530	CV3555018	single nucleotide variant	NM_003802.3(MYH13):c.1717G>C (p.Gly573Arg)	not specified [RCV004826261]	uncertain significance	17	10343977	10343977	Human		name
597646543	CV3555020	single nucleotide variant	NM_003802.3(MYH13):c.2899A>G (p.Lys967Glu)	not specified [RCV004826263]	uncertain significance	17	10324057	10324057	Human		name
597646548	CV3555021	single nucleotide variant	NM_003802.3(MYH13):c.1422C>G (p.Ser474Arg)	not specified [RCV004826264]	uncertain significance	17	10345364	10345364	Human		name
598273429	CV3983310	single nucleotide variant	NM_003802.3(MYH13):c.2270G>A (p.Arg757Gln)	not specified [RCV005389681]	uncertain significance	17	10332127	10332127	Human		name
598273432	CV3983317	single nucleotide variant	NM_003802.3(MYH13):c.2162A>C (p.Asp721Ala)	not specified [RCV005389682]	uncertain significance	17	10333086	10333086	Human		name
598189205	CV3983318	single nucleotide variant	NM_003802.3(MYH13):c.2877T>A (p.Asp959Glu)	not specified [RCV005373837]	uncertain significance	17	10324079	10324079	Human		name
598273438	CV3983320	single nucleotide variant	NM_003802.3(MYH13):c.1048G>T (p.Gly350Trp)	not specified [RCV005389684]	uncertain significance	17	10350652	10350652	Human		name
598273441	CV3983322	single nucleotide variant	NM_003802.3(MYH13):c.1882G>A (p.Gly628Ser)	not specified [RCV005389685]	uncertain significance	17	10343812	10343812	Human		name
598189250	CV3983329	single nucleotide variant	NM_003802.3(MYH13):c.2708T>C (p.Met903Thr)	not specified [RCV005373843]	uncertain significance	17	10324248	10324248	Human		name
598273450	CV3983331	single nucleotide variant	NM_003802.3(MYH13):c.2876A>G (p.Asp959Gly)	not specified [RCV005389688]	uncertain significance	17	10324080	10324080	Human		name
8635963	CV91186	single nucleotide variant	NM_003802.2(MYH13):c.2129G>A (p.Arg710Lys)	Malignant melanoma [RCV000071284]	not provided	17	10333119	10333119	Human		name
8635964	CV91187	single nucleotide variant	NM_003802.2(MYH13):c.2024G>A (p.Arg675Gln)	Malignant melanoma [RCV000071285]	not provided	17	10340182	10340182	Human		name
38466242	CV919697	single nucleotide variant	NM_003802.3(MYH13):c.2117T>A (p.Ile706Asn)	See cases [RCV001198662]	uncertain significance	17	10333131	10333131	Human		name
156399070	CV2194964	single nucleotide variant	NM_003802.3(MYH13):c.5011C>T (p.Leu1671Phe)	not specified [RCV004075485]	uncertain significance	17	10309392	10309392	Human		name
156262604	CV2201105	single nucleotide variant	NM_003802.3(MYH13):c.5354G>A (p.Arg1785Gln)	not provided [RCV004695341]\|not specified [RCV004075226]	uncertain significance	17	10306571	10306571	Human		name
156376280	CV2210525	single nucleotide variant	NM_003802.3(MYH13):c.4156C>T (p.Arg1386Cys)	not specified [RCV004089653]	uncertain significance	17	10313183	10313183	Human		name
155979060	CV2215136	single nucleotide variant	NM_003802.3(MYH13):c.4589C>T (p.Ala1530Val)	not specified [RCV004086857]	likely benign	17	10311170	10311170	Human		name
156401816	CV2217797	single nucleotide variant	NM_003802.3(MYH13):c.4232C>T (p.Ala1411Val)	not specified [RCV004083973]	likely benign	17	10312707	10312707	Human		name
156331504	CV2218172	single nucleotide variant	NM_003802.3(MYH13):c.5577G>C (p.Glu1859Asp)	not specified [RCV004086593]	uncertain significance	17	10303286	10303286	Human		name
156380884	CV2218370	single nucleotide variant	NM_003802.3(MYH13):c.5017G>A (p.Glu1673Lys)	MYH13-related disorder [RCV003906579]\|not specified [RCV004088878]	likely benign\|uncertain significance	17	10309386	10309386	Human		name , trait , alternate_id
156037832	CV2218686	single nucleotide variant	NM_003802.3(MYH13):c.4960C>T (p.Leu1654Phe)	MYH13-related disorder [RCV003906580]\|not specified [RCV004090935]	likely benign\|uncertain significance	17	10309527	10309527	Human		name , trait , alternate_id
156022392	CV2223176	single nucleotide variant	NM_003802.3(MYH13):c.5384A>C (p.Lys1795Thr)	not specified [RCV004104019]	uncertain significance	17	10306541	10306541	Human		name
156154334	CV2242286	single nucleotide variant	NM_003802.3(MYH13):c.4250C>T (p.Ser1417Leu)	not specified [RCV004111306]	uncertain significance	17	10312689	10312689	Human		name
155915208	CV2243702	single nucleotide variant	NM_003802.3(MYH13):c.3129G>T (p.Glu1043Asp)	not specified [RCV004114405]	uncertain significance	17	10320479	10320479	Human		name
156175003	CV2254627	single nucleotide variant	NM_003802.3(MYH13):c.4802T>C (p.Leu1601Pro)	not specified [RCV004115115]	uncertain significance	17	10309685	10309685	Human		name
155967406	CV2261157	single nucleotide variant	NM_003802.3(MYH13):c.4007C>G (p.Ala1336Gly)	not specified [RCV004128051]	uncertain significance	17	10313332	10313332	Human		name
156113530	CV2261433	single nucleotide variant	NM_003802.3(MYH13):c.4043G>A (p.Arg1348Gln)	not specified [RCV004130057]	uncertain significance	17	10313296	10313296	Human		name
156167937	CV2279917	single nucleotide variant	NM_003802.3(MYH13):c.3836T>C (p.Met1279Thr)	not specified [RCV004146294]	uncertain significance	17	10315928	10315928	Human		name
156140952	CV2280873	single nucleotide variant	NM_003802.3(MYH13):c.3270A>T (p.Glu1090Asp)	not specified [RCV004145126]	uncertain significance	17	10320231	10320231	Human		name
156172770	CV2293395	single nucleotide variant	NM_003802.3(MYH13):c.3013G>C (p.Glu1005Gln)	not specified [RCV004150863]	uncertain significance	17	10321630	10321630	Human		name
156170876	CV2296892	single nucleotide variant	NM_003802.3(MYH13):c.4100A>G (p.Lys1367Arg)	not specified [RCV004148765]	uncertain significance	17	10313239	10313239	Human		name
156206653	CV2307764	single nucleotide variant	NM_003802.3(MYH13):c.5586C>A (p.His1862Gln)	not specified [RCV004168452]	uncertain significance	17	10303277	10303277	Human		name
156049136	CV2315826	single nucleotide variant	NM_003802.3(MYH13):c.4903C>A (p.His1635Asn)	not specified [RCV004171607]	uncertain significance	17	10309584	10309584	Human		name
156158726	CV2322678	single nucleotide variant	NM_003802.3(MYH13):c.4192G>T (p.Ala1398Ser)	not specified [RCV004182806]	uncertain significance	17	10312747	10312747	Human		name
156175353	CV2331085	single nucleotide variant	NM_003802.3(MYH13):c.3630G>C (p.Gln1210His)	not specified [RCV004181699]	uncertain significance	17	10318898	10318898	Human		name
156328163	CV2332210	single nucleotide variant	NM_003802.3(MYH13):c.3167A>G (p.Lys1056Arg)	not specified [RCV004189244]	uncertain significance	17	10320441	10320441	Human		name
155981329	CV2351306	single nucleotide variant	NM_003802.3(MYH13):c.3000G>C (p.Lys1000Asn)	not specified [RCV004193010]	uncertain significance	17	10321643	10321643	Human		name
155928291	CV2359990	single nucleotide variant	NM_003802.3(MYH13):c.3536G>A (p.Arg1179His)	not specified [RCV004212831]	uncertain significance	17	10318992	10318992	Human		name
156284712	CV2360686	single nucleotide variant	NM_003802.3(MYH13):c.5753A>T (p.Glu1918Val)	not specified [RCV004213480]	uncertain significance	17	10301618	10301618	Human		name
156402194	CV2368155	single nucleotide variant	NM_003802.3(MYH13):c.5124G>C (p.Gln1708His)	not specified [RCV004216500]	uncertain significance	17	10309279	10309279	Human		name
156251648	CV2368859	single nucleotide variant	NM_003802.3(MYH13):c.4313G>A (p.Arg1438His)	not specified [RCV004207818]	uncertain significance	17	10312626	10312626	Human		name
156270463	CV2379516	single nucleotide variant	NM_003802.3(MYH13):c.5423C>T (p.Ala1808Val)	not specified [RCV004217227]	uncertain significance	17	10306502	10306502	Human		name
156388478	CV2380454	single nucleotide variant	NM_003802.3(MYH13):c.3773A>T (p.Asp1258Val)	not specified [RCV004218052]	uncertain significance	17	10315991	10315991	Human		name
156059364	CV2383528	single nucleotide variant	NM_003802.3(MYH13):c.3293T>C (p.Ile1098Thr)	not specified [RCV004222534]	uncertain significance	17	10320208	10320208	Human		name
155904065	CV2385406	single nucleotide variant	NM_003802.3(MYH13):c.3568G>A (p.Glu1190Lys)	not specified [RCV004231053]	uncertain significance	17	10318960	10318960	Human		name
156227378	CV2388220	single nucleotide variant	NM_003802.3(MYH13):c.4360G>A (p.Asp1454Asn)	not specified [RCV004234678]	uncertain significance	17	10312579	10312579	Human		name
155960408	CV2390685	single nucleotide variant	NM_003802.3(MYH13):c.4866G>A (p.Met1622Ile)	not specified [RCV004239199]	uncertain significance	17	10309621	10309621	Human		name
156005150	CV2393961	single nucleotide variant	NM_003802.3(MYH13):c.3799G>A (p.Asp1267Asn)	not specified [RCV004603416]	uncertain significance	17	10315965	10315965	Human		name
156115312	CV2397270	single nucleotide variant	NM_003802.3(MYH13):c.4021C>T (p.Arg1341Cys)	not specified [RCV004238803]	uncertain significance	17	10313318	10313318	Human		name
329354104	CV2436963	single nucleotide variant	NM_003802.3(MYH13):c.5233G>A (p.Val1745Met)	not specified [RCV004260337]	uncertain significance	17	10307001	10307001	Human		name
329352232	CV2452129	single nucleotide variant	NM_003802.3(MYH13):c.5731G>A (p.Ala1911Thr)	not specified [RCV004278846]	uncertain significance	17	10301640	10301640	Human		name
401727875	CV2678540	single nucleotide variant	NM_003802.3(MYH13):c.5560A>G (p.Met1854Val)	not specified [RCV004292551]	uncertain significance	17	10303405	10303405	Human		name
401732802	CV2685338	single nucleotide variant	NM_003802.3(MYH13):c.4144G>A (p.Asp1382Asn)	not specified [RCV004292336]	uncertain significance	17	10313195	10313195	Human		name
401776318	CV2706969	single nucleotide variant	NM_003802.3(MYH13):c.4869G>C (p.Glu1623Asp)	not specified [RCV004321570]	uncertain significance	17	10309618	10309618	Human		name
401778528	CV2709221	single nucleotide variant	NM_003802.3(MYH13):c.5429A>G (p.Lys1810Arg)	not specified [RCV004316392]	uncertain significance	17	10306496	10306496	Human		name
401721646	CV2710084	single nucleotide variant	NM_003802.3(MYH13):c.3917C>T (p.Thr1306Ile)	not specified [RCV004315143]	uncertain significance	17	10315760	10315760	Human		name
401777695	CV2718305	single nucleotide variant	NM_003802.3(MYH13):c.4518C>A (p.Asn1506Lys)	not specified [RCV004318143]	uncertain significance	17	10311924	10311924	Human		name
401783702	CV2723860	single nucleotide variant	NM_003802.3(MYH13):c.3801C>G (p.Asp1267Glu)	not specified [RCV004326000]	uncertain significance	17	10315963	10315963	Human		name
401779481	CV2731843	single nucleotide variant	NM_003802.3(MYH13):c.3820A>T (p.Ile1274Phe)	not specified [RCV004333095]	uncertain significance	17	10315944	10315944	Human		name
401876626	CV2757184	single nucleotide variant	NM_003802.3(MYH13):c.5098G>A (p.Glu1700Lys)	not specified [RCV004338789]	uncertain significance	17	10309305	10309305	Human		name
401889612	CV2758331	single nucleotide variant	NM_003802.3(MYH13):c.5434G>A (p.Gly1812Arg)	not specified [RCV004341683]	uncertain significance	17	10306491	10306491	Human		name
401884174	CV2765081	single nucleotide variant	NM_003802.3(MYH13):c.3474T>A (p.Ser1158Arg)	not specified [RCV004337196]	uncertain significance	17	10319054	10319054	Human		name
401869135	CV2766901	single nucleotide variant	NM_003802.3(MYH13):c.3679G>A (p.Glu1227Lys)	not specified [RCV004343296]	uncertain significance	17	10318849	10318849	Human		name
401861314	CV2779621	single nucleotide variant	NM_003802.3(MYH13):c.4291G>T (p.Asp1431Tyr)	not specified [RCV004351326]	uncertain significance	17	10312648	10312648	Human		name
401914033	CV2814945	single nucleotide variant	NM_003802.3(MYH13):c.3897G>T (p.Glu1299Asp)	not provided [RCV003428140]	likely benign	17	10315780	10315780	Human		name
401944578	CV2839805	single nucleotide variant	NM_003802.3(MYH13):c.3647G>A (p.Arg1216Gln)	not specified [RCV003457225]	benign	17	10318881	10318881	Human		name
401944470	CV2839816	single nucleotide variant	NM_003802.3(MYH13):c.5003A>G (p.Asn1668Ser)	not specified [RCV003457236]	benign	17	10309400	10309400	Human		name
405284910	CV3190868	single nucleotide variant	NM_003802.3(MYH13):c.5326G>A (p.Glu1776Lys)	MYH13-related disorder [RCV003909434]	likely benign	17	10306599	10306599	Human		name , trait , alternate_id
405740313	CV3316566	single nucleotide variant	NM_003802.3(MYH13):c.3091C>T (p.Leu1031Phe)	not specified [RCV004452277]	uncertain significance	17	10321552	10321552	Human		name
405740373	CV3316574	single nucleotide variant	NM_003802.3(MYH13):c.3143T>C (p.Leu1048Pro)	not specified [RCV004452285]	uncertain significance	17	10320465	10320465	Human		name
405740408	CV3316579	single nucleotide variant	NM_003802.3(MYH13):c.3271C>T (p.Leu1091Phe)	not specified [RCV004452290]	uncertain significance	17	10320230	10320230	Human		name
405740570	CV3316601	single nucleotide variant	NM_003802.3(MYH13):c.3704T>A (p.Met1235Lys)	not specified [RCV004452312]	uncertain significance	17	10318824	10318824	Human		name
405740659	CV3316615	single nucleotide variant	NM_003802.3(MYH13):c.3814C>G (p.Gln1272Glu)	not specified [RCV004452326]	uncertain significance	17	10315950	10315950	Human		name
405740790	CV3316635	single nucleotide variant	NM_003802.3(MYH13):c.4001C>T (p.Ala1334Val)	not specified [RCV004452346]	uncertain significance	17	10313338	10313338	Human		name
405740856	CV3316645	single nucleotide variant	NM_003802.3(MYH13):c.4130C>T (p.Thr1377Ile)	not specified [RCV004452356]	uncertain significance	17	10313209	10313209	Human		name
405740904	CV3316652	single nucleotide variant	NM_003802.3(MYH13):c.4157G>A (p.Arg1386His)	not specified [RCV004452363]	uncertain significance	17	10313182	10313182	Human		name
405740955	CV3316659	single nucleotide variant	NM_003802.3(MYH13):c.4223C>T (p.Thr1408Met)	not specified [RCV004452370]	uncertain significance	17	10312716	10312716	Human		name
405741087	CV3316678	single nucleotide variant	NM_003802.3(MYH13):c.4363A>C (p.Lys1455Gln)	not specified [RCV004452389]	uncertain significance	17	10312576	10312576	Human		name
405741116	CV3316682	single nucleotide variant	NM_003802.3(MYH13):c.4511G>A (p.Arg1504Gln)	not specified [RCV004452393]	uncertain significance	17	10311931	10311931	Human		name
405755244	CV3316703	single nucleotide variant	NM_003802.3(MYH13):c.4843G>T (p.Ala1615Ser)	not specified [RCV004454398]	uncertain significance	17	10309644	10309644	Human		name
405755330	CV3316715	single nucleotide variant	NM_003802.3(MYH13):c.4946C>T (p.Thr1649Met)	not specified [RCV004454410]	uncertain significance	17	10309541	10309541	Human		name
405755511	CV3316741	single nucleotide variant	NM_003802.3(MYH13):c.5291C>T (p.Thr1764Met)	not specified [RCV004454436]	uncertain significance	17	10306943	10306943	Human		name
405755544	CV3316746	single nucleotide variant	NM_003802.3(MYH13):c.5353C>T (p.Arg1785Trp)	not specified [RCV004454441]	uncertain significance	17	10306572	10306572	Human		name
405755607	CV3316755	single nucleotide variant	NM_003802.3(MYH13):c.5378C>T (p.Thr1793Met)	not specified [RCV004454450]	uncertain significance	17	10306547	10306547	Human		name
405755708	CV3316769	single nucleotide variant	NM_003802.3(MYH13):c.5471G>A (p.Arg1824Gln)	not specified [RCV004454464]	uncertain significance	17	10303494	10303494	Human		name
405755728	CV3316772	single nucleotide variant	NM_003802.3(MYH13):c.5557G>C (p.Glu1853Gln)	not specified [RCV004454467]	uncertain significance	17	10303408	10303408	Human		name
405755832	CV3316786	single nucleotide variant	NM_003802.3(MYH13):c.5606A>T (p.Gln1869Leu)	not specified [RCV004454481]	uncertain significance	17	10303257	10303257	Human		name
407504212	CV3454350	single nucleotide variant	NM_003802.3(MYH13):c.4324G>A (p.Ala1442Thr)	not specified [RCV004645733]	uncertain significance	17	10312615	10312615	Human		name
407514858	CV3454351	single nucleotide variant	NM_003802.3(MYH13):c.4043G>C (p.Arg1348Pro)	not specified [RCV004649691]	uncertain significance	17	10313296	10313296	Human		name
407504215	CV3454354	single nucleotide variant	NM_003802.3(MYH13):c.3760C>T (p.Arg1254Trp)	not specified [RCV004645734]	uncertain significance	17	10316004	10316004	Human		name
407514869	CV3454357	single nucleotide variant	NM_003802.3(MYH13):c.4912C>G (p.Arg1638Gly)	not specified [RCV004649695]	uncertain significance	17	10309575	10309575	Human		name
407504223	CV3454358	single nucleotide variant	NM_003802.3(MYH13):c.5020C>A (p.Gln1674Lys)	not specified [RCV004645736]	uncertain significance	17	10309383	10309383	Human		name
407514873	CV3454359	single nucleotide variant	NM_003802.3(MYH13):c.3118G>A (p.Gly1040Ser)	not specified [RCV004649696]	uncertain significance	17	10320490	10320490	Human		name
407514879	CV3454361	single nucleotide variant	NM_003802.3(MYH13):c.3162G>C (p.Arg1054Ser)	not specified [RCV004649698]	uncertain significance	17	10320446	10320446	Human		name
407514883	CV3454362	single nucleotide variant	NM_003802.3(MYH13):c.3445G>A (p.Glu1149Lys)	not specified [RCV004649699]	uncertain significance	17	10319083	10319083	Human		name
407504229	CV3454365	single nucleotide variant	NM_003802.3(MYH13):c.4814T>A (p.Leu1605Gln)	not specified [RCV004645738]	uncertain significance	17	10309673	10309673	Human		name
407504235	CV3454367	single nucleotide variant	NM_003802.3(MYH13):c.3330G>C (p.Lys1110Asn)	not specified [RCV004645740]	uncertain significance	17	10320171	10320171	Human		name
407514890	CV3454370	single nucleotide variant	NM_003802.3(MYH13):c.3845C>A (p.Ala1282Glu)	not specified [RCV004649702]	uncertain significance	17	10315919	10315919	Human		name
407514893	CV3454371	single nucleotide variant	NM_003802.3(MYH13):c.5170A>G (p.Asn1724Asp)	not specified [RCV004649703]	uncertain significance	17	10307064	10307064	Human		name
597646405	CV3554998	single nucleotide variant	NM_003802.3(MYH13):c.5147G>A (p.Arg1716His)	not specified [RCV004826243]	uncertain significance	17	10309256	10309256	Human		name
597646413	CV3554999	single nucleotide variant	NM_003802.3(MYH13):c.4549A>G (p.Thr1517Ala)	not specified [RCV004826244]	uncertain significance	17	10311210	10311210	Human		name
597646428	CV3555001	single nucleotide variant	NM_003802.3(MYH13):c.3209T>C (p.Ile1070Thr)	not specified [RCV004826246]	uncertain significance	17	10320399	10320399	Human		name
597646441	CV3555003	single nucleotide variant	NM_003802.3(MYH13):c.5047G>A (p.Gly1683Ser)	not specified [RCV004826248]	uncertain significance	17	10309356	10309356	Human		name
597646447	CV3555004	single nucleotide variant	NM_003802.3(MYH13):c.5584C>T (p.His1862Tyr)	not specified [RCV004826249]	uncertain significance	17	10303279	10303279	Human		name
597646454	CV3555006	single nucleotide variant	NM_003802.3(MYH13):c.5246T>C (p.Ile1749Thr)	not specified [RCV004826250]	uncertain significance	17	10306988	10306988	Human		name
597646473	CV3555009	single nucleotide variant	NM_003802.3(MYH13):c.4199G>A (p.Arg1400Lys)	not specified [RCV004826253]	uncertain significance	17	10312740	10312740	Human		name
597646488	CV3555011	single nucleotide variant	NM_003802.3(MYH13):c.4690C>A (p.Arg1564Ser)	not specified [RCV004826255]	uncertain significance	17	10309797	10309797	Human		name
597646507	CV3555014	single nucleotide variant	NM_003802.3(MYH13):c.5582A>T (p.Asp1861Val)	not specified [RCV004826258]	uncertain significance	17	10303281	10303281	Human		name
597646514	CV3555016	single nucleotide variant	NM_003802.3(MYH13):c.3094G>A (p.Glu1032Lys)	not specified [RCV004826259]	uncertain significance	17	10321549	10321549	Human		name
597646522	CV3555017	single nucleotide variant	NM_003802.3(MYH13):c.4511G>T (p.Arg1504Leu)	not specified [RCV004826260]	uncertain significance	17	10311931	10311931	Human		name
597646535	CV3555019	single nucleotide variant	NM_003802.3(MYH13):c.5236G>A (p.Glu1746Lys)	not specified [RCV004826262]	uncertain significance	17	10306998	10306998	Human		name
597646556	CV3555022	single nucleotide variant	NM_003802.3(MYH13):c.4793C>G (p.Ala1598Gly)	not specified [RCV004826265]	uncertain significance	17	10309694	10309694	Human		name
597646570	CV3555024	single nucleotide variant	NM_003802.3(MYH13):c.4307T>C (p.Leu1436Pro)	not specified [RCV004826267]	uncertain significance	17	10312632	10312632	Human		name
597646584	CV3555026	single nucleotide variant	NM_003802.3(MYH13):c.5519C>G (p.Ala1840Gly)	not specified [RCV004826269]	uncertain significance	17	10303446	10303446	Human		name
597646592	CV3555027	single nucleotide variant	NM_003802.3(MYH13):c.5651G>A (p.Arg1884Lys)	not specified [RCV004826270]	uncertain significance	17	10303212	10303212	Human		name
598189125	CV3983304	single nucleotide variant	NM_003802.3(MYH13):c.3616G>A (p.Glu1206Lys)	not specified [RCV005373827]	uncertain significance	17	10318912	10318912	Human		name
598189132	CV3983305	single nucleotide variant	NM_003802.3(MYH13):c.5791G>A (p.Val1931Met)	not specified [RCV005373828]	uncertain significance	17	10301580	10301580	Human		name
598273426	CV3983307	single nucleotide variant	NM_003802.3(MYH13):c.4006G>A (p.Ala1336Thr)	not specified [RCV005389680]	uncertain significance	17	10313333	10313333	Human		name
598189155	CV3983311	single nucleotide variant	NM_003802.3(MYH13):c.3766G>A (p.Val1256Ile)	not specified [RCV005373831]	uncertain significance	17	10315998	10315998	Human		name
598189171	CV3983313	single nucleotide variant	NM_003802.3(MYH13):c.4147G>A (p.Ala1383Thr)	not specified [RCV005373833]	uncertain significance	17	10313192	10313192	Human		name
598189186	CV3983315	single nucleotide variant	NM_003802.3(MYH13):c.4409A>C (p.Glu1470Ala)	not specified [RCV005373835]	uncertain significance	17	10312033	10312033	Human		name
598273435	CV3983319	single nucleotide variant	NM_003802.3(MYH13):c.4466G>A (p.Arg1489Lys)	not specified [RCV005389683]	uncertain significance	17	10311976	10311976	Human		name
598189214	CV3983321	single nucleotide variant	NM_003802.3(MYH13):c.3052G>A (p.Glu1018Lys)	not specified [RCV005373838]	uncertain significance	17	10321591	10321591	Human		name
598189221	CV3983324	single nucleotide variant	NM_003802.3(MYH13):c.3463G>A (p.Glu1155Lys)	not specified [RCV005373839]	uncertain significance	17	10319065	10319065	Human		name
598189238	CV3983327	single nucleotide variant	NM_003802.3(MYH13):c.5684C>T (p.Thr1895Met)	not specified [RCV005373841]	uncertain significance	17	10301687	10301687	Human		name
598189244	CV3983328	single nucleotide variant	NM_003802.3(MYH13):c.3783T>G (p.Ser1261Arg)	not specified [RCV005373842]	uncertain significance	17	10315981	10315981	Human		name
598189256	CV3983330	single nucleotide variant	NM_003802.3(MYH13):c.3118G>T (p.Gly1040Cys)	not specified [RCV005373844]	uncertain significance	17	10320490	10320490	Human		name
598189265	CV3983332	single nucleotide variant	NM_003802.3(MYH13):c.5230G>A (p.Glu1744Lys)	not specified [RCV005373845]	uncertain significance	17	10307004	10307004	Human		name
401903833	CV2814946	microsatellite	NM_003802.3(MYH13):c.2417AGA[1] (p.Lys807del)	not provided [RCV003419653]	likely benign	17	10330400	10330402	Human		name
405283141	CV3191260	microsatellite	NM_003802.3(MYH13):c.3329AGA[1] (p.Lys1111del)	MYH13-related disorder [RCV003921665]	likely benign	17	10320167	10320169	Human		name , trait , alternate_id

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