Myh15 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

233 records found for search term Myh15

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155920257	CV2343318	single nucleotide variant	NM_014981.3(MYH15):c.-38C>T	not specified [RCV004194935]	uncertain significance	3	108510568	108510568	Human		name
15165705	CV777360	deletion	NM_014981.3(MYH15):c.89-10del	not provided [RCV000948655]	benign	3	108505839	108505839	Human		name
15168813	CV730170	single nucleotide variant	NM_014981.3(MYH15):c.5632-4A>T	not provided [RCV000883143]	likely benign	3	108383733	108383733	Human		name
15131169	CV743894	single nucleotide variant	NM_014981.3(MYH15):c.5431-7G>T	not provided [RCV000897727]	benign	3	108389081	108389081	Human		name
15183894	CV744007	single nucleotide variant	NM_014981.3(MYH15):c.3702+6T>C	not provided [RCV000908157]	benign	3	108428486	108428486	Human		name
15142894	CV759163	single nucleotide variant	NM_014981.3(MYH15):c.2021-5T>C	not provided [RCV000922098]	benign	3	108456888	108456888	Human		name
15156722	CV777329	single nucleotide variant	NM_014981.3(MYH15):c.5632-4A>G	not provided [RCV000946753]	benign	3	108383733	108383733	Human		name
15196158	CV777359	single nucleotide variant	NM_014981.3(MYH15):c.3221+5G>T	not provided [RCV000956118]	benign	3	108437549	108437549	Human		name
15183968	CV778941	duplication	NM_014981.3(MYH15):c.5632-5dup	not provided [RCV000975000]	benign	3	108383733	108383734	Human		name
15183977	CV779004	single nucleotide variant	NM_014981.3(MYH15):c.4496-1G>T	not provided [RCV000975002]	benign	3	108408405	108408405	Human		name
15144713	CV779009	single nucleotide variant	NM_014981.3(MYH15):c.4145+7A>G	not provided [RCV000966878]	benign	3	108414225	108414225	Human		name
15196162	CV777331	deletion	NM_014981.3(MYH15):c.89-11_89-10del	not provided [RCV000956119]	benign	3	108505839	108505840	Human		name
15162579	CV778934	duplication	NM_014981.3(MYH15):c.5632-6_5632-5dup	not provided [RCV000970298]	benign	3	108383733	108383734	Human		name
401926512	CV2827614	single nucleotide variant	NM_014981.3(MYH15):c.294C>T (p.Ser98=)	not provided [RCV003437939]	likely benign	3	108501757	108501757	Human		name
155905958	CV2303215	single nucleotide variant	NM_014981.3(MYH15):c.80C>T (p.Ala27Val)	not specified [RCV004156974]	uncertain significance	3	108510451	108510451	Human		name
401739210	CV2708371	single nucleotide variant	NM_014981.3(MYH15):c.32C>G (p.Ala11Gly)	not provided [RCV004696452]\|not specified [RCV004313488]	uncertain significance	3	108510499	108510499	Human		name
401869014	CV2767411	single nucleotide variant	NM_014981.3(MYH15):c.28G>A (p.Ala10Thr)	not specified [RCV004349567]	uncertain significance	3	108510503	108510503	Human		name
401922351	CV2827613	single nucleotide variant	NM_014981.3(MYH15):c.552G>A (p.Val184=)	not provided [RCV003433691]	benign	3	108498118	108498118	Human		name
598128405	CV3887609	single nucleotide variant	NM_014981.3(MYH15):c.363G>A (p.Val121=)	not provided [RCV005243782]	likely benign	3	108500251	108500251	Human		name
15144718	CV708454	single nucleotide variant	NM_014981.3(MYH15):c.993G>A (p.Leu331=)	not provided [RCV000966879]	benign	3	108485212	108485212	Human		name
15188261	CV733669	single nucleotide variant	NM_014981.3(MYH15):c.606C>T (p.Ser202=)	not provided [RCV000909319]	likely benign	3	108498064	108498064	Human		name
15164142	CV777314	insertion	NM_014981.3(MYH15):c.5632-9_5632-8insTG	not provided [RCV000948266]	benign	3	108383737	108383738	Human		name
156093371	CV2216975	single nucleotide variant	NM_014981.3(MYH15):c.256G>A (p.Glu86Lys)	not specified [RCV004085341]	uncertain significance	3	108501795	108501795	Human		name
329394320	CV2450174	single nucleotide variant	NM_014981.3(MYH15):c.266C>T (p.Ala89Val)	not specified [RCV004270993]	uncertain significance	3	108501785	108501785	Human		name
401926511	CV2827611	single nucleotide variant	NM_014981.3(MYH15):c.2853A>C (p.Thr951=)	not provided [RCV003437938]	likely benign	3	108441063	108441063	Human		name
401922350	CV2827612	single nucleotide variant	NM_014981.3(MYH15):c.2740C>T (p.Leu914=)	not provided [RCV003433690]	likely benign	3	108441176	108441176	Human		name
15166821	CV708452	single nucleotide variant	NM_014981.3(MYH15):c.2583G>A (p.Gln861=)	not provided [RCV000971267]	benign	3	108444712	108444712	Human		name
15112836	CV720061	single nucleotide variant	NM_014981.3(MYH15):c.2736G>A (p.Lys912=)	not provided [RCV000894545]	benign	3	108441180	108441180	Human		name
15144451	CV733668	single nucleotide variant	NM_014981.3(MYH15):c.1713T>C (p.Leu571=)	not provided [RCV000900006]	likely benign	3	108464656	108464656	Human		name
15164309	CV747867	single nucleotide variant	NM_014981.3(MYH15):c.1656G>A (p.Ser552=)	not provided [RCV000926351]	likely benign	3	108464713	108464713	Human		name
156200405	CV2237701	single nucleotide variant	NM_014981.3(MYH15):c.487A>G (p.Met163Val)	not specified [RCV004100493]	uncertain significance	3	108500127	108500127	Human		name
156106991	CV2257323	single nucleotide variant	NM_014981.3(MYH15):c.795G>C (p.Arg265Ser)	not specified [RCV004125424]	uncertain significance	3	108492576	108492576	Human		name
156113499	CV2263823	single nucleotide variant	NM_014981.3(MYH15):c.760G>C (p.Val254Leu)	not specified [RCV004136100]	uncertain significance	3	108493129	108493129	Human		name
156358190	CV2318441	single nucleotide variant	NM_014981.3(MYH15):c.313C>T (p.Arg105Trp)	not specified [RCV004179594]	uncertain significance	3	108501738	108501738	Human		name
329382235	CV2424378	single nucleotide variant	NM_014981.3(MYH15):c.622G>T (p.Ala208Ser)	not specified [RCV004252279]	uncertain significance	3	108495869	108495869	Human		name
329395668	CV2462921	single nucleotide variant	NM_014981.3(MYH15):c.701C>T (p.Ser234Phe)	not specified [RCV004272762]	uncertain significance	3	108495790	108495790	Human		name
401729258	CV2690118	single nucleotide variant	NM_014981.3(MYH15):c.667T>C (p.Phe223Leu)	not specified [RCV004300348]	uncertain significance	3	108495824	108495824	Human		name
401771542	CV2711745	single nucleotide variant	NM_014981.3(MYH15):c.425G>A (p.Gly142Glu)	not specified [RCV004309402]	uncertain significance	3	108500189	108500189	Human		name
401760908	CV2726579	single nucleotide variant	NM_014981.3(MYH15):c.682A>G (p.Thr228Ala)	not specified [RCV004329073]	uncertain significance	3	108495809	108495809	Human		name
401866790	CV2748725	single nucleotide variant	NM_014981.3(MYH15):c.616C>T (p.Gln206Ter)	not provided [RCV003331552]	not provided	3	108498054	108498054	Human		name
405701050	CV3310032	single nucleotide variant	NM_014981.3(MYH15):c.415G>T (p.Ala139Ser)	not specified [RCV004447110]	uncertain significance	3	108500199	108500199	Human		name
405701262	CV3310045	single nucleotide variant	NM_014981.3(MYH15):c.432G>C (p.Arg144Ser)	not specified [RCV004447123]	uncertain significance	3	108500182	108500182	Human		name
405701667	CV3310104	single nucleotide variant	NM_014981.3(MYH15):c.531A>C (p.Glu177Asp)	not specified [RCV004447182]	uncertain significance	3	108498139	108498139	Human		name
405701692	CV3310107	single nucleotide variant	NM_014981.3(MYH15):c.623C>T (p.Ala208Val)	not specified [RCV004447185]	uncertain significance	3	108495868	108495868	Human		name
405701753	CV3310115	single nucleotide variant	NM_014981.3(MYH15):c.908A>G (p.His303Arg)	not specified [RCV004447193]	uncertain significance	3	108486490	108486490	Human		name
597646605	CV3555051	single nucleotide variant	NM_014981.3(MYH15):c.707G>A (p.Arg236His)	not specified [RCV004826272]	uncertain significance	3	108495784	108495784	Human		name
597663242	CV3555070	single nucleotide variant	NM_014981.3(MYH15):c.755C>T (p.Ser252Leu)	not specified [RCV004828769]	uncertain significance	3	108493134	108493134	Human		name
597663273	CV3555074	single nucleotide variant	NM_014981.3(MYH15):c.892A>G (p.Asn298Asp)	not specified [RCV004828773]	uncertain significance	3	108486506	108486506	Human		name
597663292	CV3555077	single nucleotide variant	NM_014981.3(MYH15):c.955G>A (p.Glu319Lys)	not specified [RCV004828776]	uncertain significance	3	108486443	108486443	Human		name
15183972	CV708450	single nucleotide variant	NM_014981.3(MYH15):c.4515A>G (p.Thr1505=)	not provided [RCV000975001]	benign	3	108408385	108408385	Human		name
15185755	CV720059	single nucleotide variant	NM_014981.3(MYH15):c.3531T>C (p.Phe1177=)	not provided [RCV000886784]	benign\|likely benign	3	108428663	108428663	Human		name
15195626	CV720060	single nucleotide variant	NM_014981.3(MYH15):c.3366C>T (p.Ala1122=)	not provided [RCV000889554]	benign	3	108428828	108428828	Human		name
15143246	CV733667	single nucleotide variant	NM_014981.3(MYH15):c.4035C>T (p.Val1345=)	not provided [RCV000899806]	benign	3	108414342	108414342	Human		name
8630519	CV85674	single nucleotide variant	NM_014981.1(MYH15):c.3474G>A (p.Leu1158=)	Malignant melanoma [RCV000065757]	not provided	3	108428780	108428780	Human		name
156313601	CV2196523	single nucleotide variant	NM_014981.3(MYH15):c.1507A>G (p.Ile503Val)	not specified [RCV004073813]	uncertain significance	3	108470089	108470089	Human		name
156366613	CV2203363	single nucleotide variant	NM_014981.3(MYH15):c.2738A>C (p.Glu913Ala)	not specified [RCV004072592]	likely benign	3	108441178	108441178	Human		name
156399197	CV2204972	single nucleotide variant	NM_014981.3(MYH15):c.2630A>T (p.Asn877Ile)	not specified [RCV004077594]	uncertain significance	3	108444665	108444665	Human		name
156387703	CV2221586	single nucleotide variant	NM_014981.3(MYH15):c.1694T>C (p.Phe565Ser)	not specified [RCV004096845]	uncertain significance	3	108464675	108464675	Human		name
156293763	CV2233576	single nucleotide variant	NM_014981.3(MYH15):c.1268T>C (p.Met423Thr)	not specified [RCV004100051]	uncertain significance	3	108470813	108470813	Human		name
156294812	CV2233676	single nucleotide variant	NM_014981.3(MYH15):c.1584A>C (p.Glu528Asp)	not specified [RCV004100127]	uncertain significance	3	108464785	108464785	Human		name
156140608	CV2260337	single nucleotide variant	NM_014981.3(MYH15):c.2855T>C (p.Met952Thr)	not specified [RCV004129422]	uncertain significance	3	108441061	108441061	Human		name
156144788	CV2265005	single nucleotide variant	NM_014981.3(MYH15):c.2839G>A (p.Asp947Asn)	not specified [RCV004126170]	uncertain significance	3	108441077	108441077	Human		name
156031184	CV2278788	single nucleotide variant	NM_014981.3(MYH15):c.2628A>T (p.Lys876Asn)	not specified [RCV004134966]	uncertain significance	3	108444667	108444667	Human		name
155999711	CV2296229	single nucleotide variant	NM_014981.3(MYH15):c.2447T>A (p.Val816Glu)	not specified [RCV004154141]	uncertain significance	3	108444848	108444848	Human		name
156082233	CV2301148	single nucleotide variant	NM_014981.3(MYH15):c.1258T>A (p.Ser420Thr)	not specified [RCV004160060]	uncertain significance	3	108470823	108470823	Human		name
155907844	CV2302302	single nucleotide variant	NM_014981.3(MYH15):c.1501G>A (p.Val501Met)	not specified [RCV004161065]	uncertain significance	3	108470095	108470095	Human		name
155970789	CV2335618	single nucleotide variant	NM_014981.3(MYH15):c.2016A>G (p.Ile672Met)	not specified [RCV004193822]	likely benign	3	108459366	108459366	Human		name
156133776	CV2361916	single nucleotide variant	NM_014981.3(MYH15):c.1280T>C (p.Met427Thr)	not specified [RCV004207688]	uncertain significance	3	108470801	108470801	Human		name
156343333	CV2364097	single nucleotide variant	NM_014981.3(MYH15):c.1867A>G (p.Ile623Val)	not specified [RCV004221478]	uncertain significance	3	108460365	108460365	Human		name
156153142	CV2367215	single nucleotide variant	NM_014981.3(MYH15):c.1641C>A (p.Asn547Lys)	not specified [RCV004215641]	uncertain significance	3	108464728	108464728	Human		name
155937738	CV2373802	single nucleotide variant	NM_014981.3(MYH15):c.1684A>G (p.Lys562Glu)	not specified [RCV004224742]	uncertain significance	3	108464685	108464685	Human		name
156188116	CV2375287	single nucleotide variant	NM_014981.3(MYH15):c.1346T>C (p.Ile449Thr)	not specified [RCV004232697]	likely benign	3	108470735	108470735	Human		name
156035271	CV2376748	single nucleotide variant	NM_014981.3(MYH15):c.1138A>G (p.Met380Val)	not specified [RCV004227029]	uncertain significance	3	108476492	108476492	Human		name
156348140	CV2383048	single nucleotide variant	NM_014981.3(MYH15):c.1833C>G (p.Ser611Arg)	not specified [RCV004217628]	likely benign	3	108463142	108463142	Human		name
156181315	CV2384064	single nucleotide variant	NM_014981.3(MYH15):c.1375A>G (p.Ile459Val)	not specified [RCV004225427]	uncertain significance	3	108470706	108470706	Human		name
329377578	CV2449807	single nucleotide variant	NM_014981.3(MYH15):c.1118C>T (p.Ala373Val)	not specified [RCV004268911]	uncertain significance	3	108476512	108476512	Human		name
329361891	CV2468417	single nucleotide variant	NM_014981.3(MYH15):c.2582A>G (p.Gln861Arg)	not specified [RCV004277727]	uncertain significance	3	108444713	108444713	Human		name
401760829	CV2695175	single nucleotide variant	NM_014981.3(MYH15):c.1094T>A (p.Leu365Gln)	not specified [RCV004303321]	uncertain significance	3	108485111	108485111	Human		name
401784291	CV2721237	single nucleotide variant	NM_014981.3(MYH15):c.2608G>A (p.Val870Ile)	not specified [RCV004330177]	uncertain significance	3	108444687	108444687	Human		name
401746601	CV2731876	single nucleotide variant	NM_014981.3(MYH15):c.1006G>T (p.Asp336Tyr)	not specified [RCV004333121]	uncertain significance	3	108485199	108485199	Human		name
401866478	CV2762657	single nucleotide variant	NM_014981.3(MYH15):c.2350G>A (p.Ala784Thr)	not specified [RCV004340219]	uncertain significance	3	108454055	108454055	Human		name
401882482	CV2767963	single nucleotide variant	NM_014981.3(MYH15):c.1592T>C (p.Met531Thr)	not specified [RCV004348212]	uncertain significance	3	108464777	108464777	Human		name
401887565	CV2773509	single nucleotide variant	NM_014981.3(MYH15):c.2719C>A (p.Leu907Met)	not specified [RCV004354134]	uncertain significance	3	108441197	108441197	Human		name
401898701	CV2782607	single nucleotide variant	NM_014981.3(MYH15):c.2275G>A (p.Ala759Thr)	not specified [RCV004359632]	uncertain significance	3	108454130	108454130	Human		name
405700059	CV3313737	single nucleotide variant	NM_014981.3(MYH15):c.1573A>G (p.Ile525Val)	not specified [RCV004446923]	uncertain significance	3	108464796	108464796	Human		name
405700101	CV3313743	single nucleotide variant	NM_014981.3(MYH15):c.1631T>A (p.Leu544His)	not specified [RCV004446929]	uncertain significance	3	108464738	108464738	Human		name
405700157	CV3313751	single nucleotide variant	NM_014981.3(MYH15):c.1678C>A (p.Pro560Thr)	not specified [RCV004446937]	uncertain significance	3	108464691	108464691	Human		name
405700234	CV3313762	single nucleotide variant	NM_014981.3(MYH15):c.1818C>A (p.Asn606Lys)	not specified [RCV004446948]	uncertain significance	3	108463157	108463157	Human		name
405700268	CV3313767	single nucleotide variant	NM_014981.3(MYH15):c.1877G>C (p.Gly626Ala)	not specified [RCV004446953]	uncertain significance	3	108460355	108460355	Human		name
405700323	CV3313776	single nucleotide variant	NM_014981.3(MYH15):c.2509G>A (p.Val837Ile)	not specified [RCV004446962]	uncertain significance	3	108444786	108444786	Human		name
405700357	CV3313782	single nucleotide variant	NM_014981.3(MYH15):c.2668C>A (p.Leu890Met)	not specified [RCV004446968]	uncertain significance	3	108441248	108441248	Human		name
405700406	CV3313789	single nucleotide variant	NM_014981.3(MYH15):c.2789C>T (p.Ala930Val)	not specified [RCV004446975]	uncertain significance	3	108441127	108441127	Human		name
405700427	CV3313793	single nucleotide variant	NM_014981.3(MYH15):c.2798G>A (p.Arg933Gln)	not specified [RCV004446979]	uncertain significance	3	108441118	108441118	Human		name
405700435	CV3313794	single nucleotide variant	NM_014981.3(MYH15):c.2831A>C (p.Lys944Thr)	not specified [RCV004446980]	uncertain significance	3	108441085	108441085	Human		name
405700480	CV3313802	single nucleotide variant	NM_014981.3(MYH15):c.2885C>T (p.Thr962Ile)	not specified [RCV004446988]	uncertain significance	3	108441031	108441031	Human		name
407514912	CV3454383	single nucleotide variant	NM_014981.3(MYH15):c.1281G>A (p.Met427Ile)	not specified [RCV004649710]	uncertain significance	3	108470800	108470800	Human		name
407504254	CV3454384	single nucleotide variant	NM_014981.3(MYH15):c.1198A>G (p.Asn400Asp)	not specified [RCV004645747]	uncertain significance	3	108476432	108476432	Human		name
407514918	CV3454391	single nucleotide variant	NM_014981.3(MYH15):c.2962G>T (p.Ala988Ser)	not specified [RCV004649712]	uncertain significance	3	108439850	108439850	Human		name
407514924	CV3454393	single nucleotide variant	NM_014981.3(MYH15):c.1392C>A (p.Ser464Arg)	not specified [RCV004649714]	uncertain significance	3	108470204	108470204	Human		name
407504276	CV3454397	single nucleotide variant	NM_014981.3(MYH15):c.1798G>T (p.Val600Leu)	not specified [RCV004645754]	uncertain significance	3	108463177	108463177	Human		name
407504284	CV3454399	single nucleotide variant	NM_014981.3(MYH15):c.1611C>A (p.Asp537Glu)	not specified [RCV004645756]	uncertain significance	3	108464758	108464758	Human		name
407504292	CV3454401	single nucleotide variant	NM_014981.3(MYH15):c.2814A>T (p.Glu938Asp)	not specified [RCV004645758]	uncertain significance	3	108441102	108441102	Human		name
407504294	CV3454402	single nucleotide variant	NM_014981.3(MYH15):c.1832G>A (p.Ser611Asn)	not specified [RCV004645759]	likely benign	3	108463143	108463143	Human		name
597663128	CV3555054	single nucleotide variant	NM_014981.3(MYH15):c.1839T>G (p.Phe613Leu)	not specified [RCV004828754]	uncertain significance	3	108463136	108463136	Human		name
597663137	CV3555055	single nucleotide variant	NM_014981.3(MYH15):c.2369G>A (p.Arg790Gln)	not specified [RCV004828755]	uncertain significance	3	108454036	108454036	Human		name
597663145	CV3555056	single nucleotide variant	NM_014981.3(MYH15):c.2404G>A (p.Ala802Thr)	not specified [RCV004828756]	uncertain significance	3	108444891	108444891	Human		name
597663185	CV3555061	single nucleotide variant	NM_014981.3(MYH15):c.2762A>G (p.Glu921Gly)	not specified [RCV004828761]	uncertain significance	3	108441154	108441154	Human		name
597663193	CV3555063	single nucleotide variant	NM_014981.3(MYH15):c.1399C>A (p.Gln467Lys)	not specified [RCV004828762]	uncertain significance	3	108470197	108470197	Human		name
597663228	CV3555068	single nucleotide variant	NM_014981.3(MYH15):c.2051A>C (p.Gln684Pro)	not specified [RCV004828767]	uncertain significance	3	108456853	108456853	Human		name
597663248	CV3555071	single nucleotide variant	NM_014981.3(MYH15):c.1904C>T (p.Ser635Leu)	not specified [RCV004828770]	uncertain significance	3	108460328	108460328	Human		name
597663257	CV3555072	single nucleotide variant	NM_014981.3(MYH15):c.2896A>G (p.Lys966Glu)	not specified [RCV004828771]	uncertain significance	3	108441020	108441020	Human		name
597663286	CV3555076	single nucleotide variant	NM_014981.3(MYH15):c.1047G>A (p.Met349Ile)	not specified [RCV004828775]	uncertain significance	3	108485158	108485158	Human		name
598189333	CV3993858	single nucleotide variant	NM_014981.3(MYH15):c.1193T>C (p.Val398Ala)	not specified [RCV005373857]	uncertain significance	3	108476437	108476437	Human		name
598189340	CV3993860	single nucleotide variant	NM_014981.3(MYH15):c.1391G>A (p.Ser464Asn)	not specified [RCV005373858]	uncertain significance	3	108470205	108470205	Human		name
598273469	CV3993863	single nucleotide variant	NM_014981.3(MYH15):c.1643A>C (p.His548Pro)	not specified [RCV005389695]	uncertain significance	3	108464726	108464726	Human		name
598189361	CV3993864	single nucleotide variant	NM_014981.3(MYH15):c.2897A>G (p.Lys966Arg)	not specified [RCV005373861]	uncertain significance	3	108441019	108441019	Human		name
598189368	CV3993865	single nucleotide variant	NM_014981.3(MYH15):c.1115A>T (p.Asn372Ile)	not specified [RCV005373862]	uncertain significance	3	108476515	108476515	Human		name
598189402	CV3993870	single nucleotide variant	NM_014981.3(MYH15):c.2864A>G (p.Lys955Arg)	not specified [RCV005373867]	uncertain significance	3	108441052	108441052	Human		name
598189409	CV3993873	single nucleotide variant	NM_014981.3(MYH15):c.2254A>G (p.Ile752Val)	not specified [RCV005373868]	uncertain significance	3	108455744	108455744	Human		name
616938793	CV4015881	single nucleotide variant	NM_014981.3(MYH15):c.1301G>A (p.Arg434Gln)	Thalidomide response [RCV005414433]	drug response	3	108470780	108470780	Human		name
15123704	CV708453	single nucleotide variant	NM_014981.3(MYH15):c.2233C>G (p.His745Asp)	not provided [RCV000963291]	likely benign	3	108455765	108455765	Human		name
15194961	CV747868	single nucleotide variant	NM_014981.3(MYH15):c.1655C>T (p.Ser552Leu)	not provided [RCV000911276]	benign	3	108464714	108464714	Human		name
8630520	CV85675	single nucleotide variant	NM_014981.1(MYH15):c.1261G>A (p.Glu421Lys)	Malignant melanoma [RCV000065758]	not provided	3	108476429	108476429	Human		name
156068109	CV2193690	single nucleotide variant	NM_014981.3(MYH15):c.4007G>A (p.Arg1336Gln)	not specified [RCV004074285]	uncertain significance	3	108414370	108414370	Human		name
156133856	CV2195982	single nucleotide variant	NM_014981.3(MYH15):c.3482C>T (p.Thr1161Ile)	not specified [RCV004072233]	uncertain significance	3	108428712	108428712	Human		name
156260851	CV2204844	single nucleotide variant	NM_014981.3(MYH15):c.5227G>A (p.Ala1743Thr)	not specified [RCV004075094]	uncertain significance	3	108394063	108394063	Human		name
155972789	CV2214378	single nucleotide variant	NM_014981.3(MYH15):c.5197G>A (p.Ala1733Thr)	not specified [RCV004088150]	uncertain significance	3	108394093	108394093	Human		name
155969695	CV2244632	single nucleotide variant	NM_014981.3(MYH15):c.5510G>A (p.Arg1837Gln)	not specified [RCV004102348]	uncertain significance	3	108388995	108388995	Human		name
156235552	CV2245443	single nucleotide variant	NM_014981.3(MYH15):c.4474A>G (p.Arg1492Gly)	not specified [RCV004109223]	uncertain significance	3	108410604	108410604	Human		name
156036648	CV2249992	single nucleotide variant	NM_014981.3(MYH15):c.5758G>C (p.Gly1920Arg)	not specified [RCV004122958]	uncertain significance	3	108383603	108383603	Human		name
156306292	CV2252711	single nucleotide variant	NM_014981.3(MYH15):c.3745C>T (p.His1249Tyr)	not specified [RCV004118567]	uncertain significance	3	108421172	108421172	Human		name
156245857	CV2267549	single nucleotide variant	NM_014981.3(MYH15):c.5206G>A (p.Val1736Met)	not specified [RCV004135968]	uncertain significance	3	108394084	108394084	Human		name
156164685	CV2270286	single nucleotide variant	NM_014981.3(MYH15):c.3362G>A (p.Arg1121Gln)	not specified [RCV004135500]	uncertain significance	3	108428832	108428832	Human		name
156142313	CV2288691	single nucleotide variant	NM_014981.3(MYH15):c.4071T>A (p.Asn1357Lys)	not specified [RCV004153983]	uncertain significance	3	108414306	108414306	Human		name
156011627	CV2291164	single nucleotide variant	NM_014981.3(MYH15):c.3298G>T (p.Val1100Phe)	not specified [RCV004153468]	uncertain significance	3	108430846	108430846	Human		name
156285005	CV2291950	single nucleotide variant	NM_014981.3(MYH15):c.5339A>G (p.Gln1780Arg)	not specified [RCV004158462]	uncertain significance	3	108391851	108391851	Human		name
156271818	CV2297051	single nucleotide variant	NM_014981.3(MYH15):c.4603A>G (p.Thr1535Ala)	not specified [RCV004150969]	likely benign	3	108408297	108408297	Human		name
156080268	CV2300990	single nucleotide variant	NM_014981.3(MYH15):c.3912T>G (p.Ile1304Met)	not specified [RCV004158158]	uncertain significance	3	108416848	108416848	Human		name
155911297	CV2303791	single nucleotide variant	NM_014981.3(MYH15):c.4255G>C (p.Asp1419His)	not specified [RCV004163632]	uncertain significance	3	108410823	108410823	Human		name
156296249	CV2318126	single nucleotide variant	NM_014981.3(MYH15):c.5611A>C (p.Lys1871Gln)	not specified [RCV004177539]	uncertain significance	3	108384707	108384707	Human		name
156356030	CV2320712	single nucleotide variant	NM_014981.3(MYH15):c.5058G>C (p.Gln1686His)	not specified [RCV004179067]	uncertain significance	3	108398712	108398712	Human		name
156062018	CV2320957	single nucleotide variant	NM_014981.3(MYH15):c.3173T>C (p.Met1058Thr)	not specified [RCV004172760]	uncertain significance	3	108437602	108437602	Human		name
156352226	CV2323928	single nucleotide variant	NM_014981.3(MYH15):c.3385G>A (p.Ala1129Thr)	not specified [RCV004176454]	uncertain significance	3	108428809	108428809	Human		name
156073226	CV2325421	single nucleotide variant	NM_014981.3(MYH15):c.3083G>C (p.Gly1028Ala)	not specified [RCV004177781]	uncertain significance	3	108437692	108437692	Human		name
156178324	CV2327386	single nucleotide variant	NM_014981.3(MYH15):c.4876C>T (p.Arg1626Trp)	not specified [RCV004174812]	uncertain significance	3	108399128	108399128	Human		name
156359987	CV2328358	single nucleotide variant	NM_014981.3(MYH15):c.4411A>G (p.Thr1471Ala)	not specified [RCV004175473]	uncertain significance	3	108410667	108410667	Human		name
156395467	CV2329208	single nucleotide variant	NM_014981.3(MYH15):c.5566A>T (p.Met1856Leu)	not specified [RCV004173956]	uncertain significance	3	108384752	108384752	Human		name
156047858	CV2336400	single nucleotide variant	NM_014981.3(MYH15):c.4882G>T (p.Val1628Leu)	not specified [RCV004194619]	uncertain significance	3	108399122	108399122	Human		name
156281906	CV2348815	single nucleotide variant	NM_014981.3(MYH15):c.4901C>G (p.Ser1634Cys)	not specified [RCV004203260]	uncertain significance	3	108399103	108399103	Human		name
156103983	CV2352418	single nucleotide variant	NM_014981.3(MYH15):c.3739C>T (p.Arg1247Cys)	not specified [RCV004200883]	uncertain significance	3	108421178	108421178	Human		name
156282061	CV2363096	single nucleotide variant	NM_014981.3(MYH15):c.4633C>T (p.Arg1545Cys)	not specified [RCV004211222]	uncertain significance	3	108405441	108405441	Human		name
156342732	CV2368610	single nucleotide variant	NM_014981.3(MYH15):c.3745C>G (p.His1249Asp)	not specified [RCV004221389]	uncertain significance	3	108421172	108421172	Human		name
156174093	CV2377147	single nucleotide variant	NM_014981.3(MYH15):c.3107C>T (p.Ala1036Val)	not specified [RCV004231824]	uncertain significance	3	108437668	108437668	Human		name
155994777	CV2377647	single nucleotide variant	NM_014981.3(MYH15):c.4634G>A (p.Arg1545His)	not specified [RCV004227826]	uncertain significance	3	108405440	108405440	Human		name
156063155	CV2380456	single nucleotide variant	NM_014981.3(MYH15):c.3281C>T (p.Ala1094Val)	not specified [RCV004218054]	uncertain significance	3	108430863	108430863	Human		name
156264152	CV2384572	single nucleotide variant	NM_014981.3(MYH15):c.3127G>C (p.Glu1043Gln)	not specified [RCV004232362]	uncertain significance	3	108437648	108437648	Human		name
156227887	CV2388347	single nucleotide variant	NM_014981.3(MYH15):c.5630C>T (p.Ala1877Val)	not specified [RCV004234798]	likely benign	3	108384688	108384688	Human		name
156185811	CV2397505	single nucleotide variant	NM_014981.3(MYH15):c.3503G>A (p.Arg1168Gln)	not specified [RCV004236975]	likely benign	3	108428691	108428691	Human		name
156005531	CV2401100	single nucleotide variant	NM_014981.3(MYH15):c.4178C>T (p.Ala1393Val)	not specified [RCV004245671]	uncertain significance	3	108410900	108410900	Human		name
329356049	CV2430554	single nucleotide variant	NM_014981.3(MYH15):c.3904C>T (p.Arg1302Trp)	not specified [RCV004252136]	likely benign	3	108416856	108416856	Human		name
329374264	CV2434755	single nucleotide variant	NM_014981.3(MYH15):c.4051C>T (p.Arg1351Trp)	not specified [RCV004248458]	uncertain significance	3	108414326	108414326	Human		name
329365237	CV2440175	single nucleotide variant	NM_014981.3(MYH15):c.5179G>T (p.Ala1727Ser)	not specified [RCV004260627]	uncertain significance	3	108394111	108394111	Human		name
329371740	CV2442881	single nucleotide variant	NM_014981.3(MYH15):c.5072G>A (p.Arg1691His)	not specified [RCV004253488]	uncertain significance	3	108398698	108398698	Human		name
329368741	CV2450399	single nucleotide variant	NM_014981.3(MYH15):c.4195G>A (p.Ala1399Thr)	not specified [RCV004265332]	uncertain significance	3	108410883	108410883	Human		name
329393547	CV2467090	single nucleotide variant	NM_014981.3(MYH15):c.5412C>G (p.Ile1804Met)	not specified [RCV004282823]	uncertain significance	3	108391778	108391778	Human		name
401743335	CV2674636	single nucleotide variant	NM_014981.3(MYH15):c.4436C>T (p.Thr1479Ile)	not specified [RCV004293934]	uncertain significance	3	108410642	108410642	Human		name
401766518	CV2676197	single nucleotide variant	NM_014981.3(MYH15):c.5173G>C (p.Asp1725His)	not specified [RCV004286245]	uncertain significance	3	108394117	108394117	Human		name
401777963	CV2704489	single nucleotide variant	NM_014981.3(MYH15):c.4688A>G (p.Glu1563Gly)	not specified [RCV004313231]	uncertain significance	3	108405386	108405386	Human		name
401754756	CV2717518	single nucleotide variant	NM_014981.3(MYH15):c.4201G>A (p.Ala1401Thr)	not specified [RCV004330264]	uncertain significance	3	108410877	108410877	Human		name
401725321	CV2726114	single nucleotide variant	NM_014981.3(MYH15):c.4070A>G (p.Asn1357Ser)	not specified [RCV004324463]	uncertain significance	3	108414307	108414307	Human		name
401771062	CV2726350	single nucleotide variant	NM_014981.3(MYH15):c.4983G>T (p.Glu1661Asp)	not specified [RCV004326787]	uncertain significance	3	108398787	108398787	Human		name
401773803	CV2727638	single nucleotide variant	NM_014981.3(MYH15):c.4837G>A (p.Asp1613Asn)	not specified [RCV004329819]	uncertain significance	3	108399167	108399167	Human		name
401764374	CV2727924	single nucleotide variant	NM_014981.3(MYH15):c.3284A>G (p.Gln1095Arg)	not specified [RCV004324105]	uncertain significance	3	108430860	108430860	Human		name
401884577	CV2755897	single nucleotide variant	NM_014981.3(MYH15):c.5707G>C (p.Glu1903Gln)	not specified [RCV004335989]	uncertain significance	3	108383654	108383654	Human		name
401864314	CV2760802	single nucleotide variant	NM_014981.3(MYH15):c.4192G>A (p.Val1398Met)	not specified [RCV004336444]	uncertain significance	3	108410886	108410886	Human		name
401866522	CV2762670	single nucleotide variant	NM_014981.3(MYH15):c.4824G>T (p.Lys1608Asn)	not specified [RCV004340232]	uncertain significance	3	108399180	108399180	Human		name
401860268	CV2765508	single nucleotide variant	NM_014981.3(MYH15):c.3686A>G (p.Gln1229Arg)	not specified [RCV004341818]	uncertain significance	3	108428508	108428508	Human		name
401870063	CV2765612	single nucleotide variant	NM_014981.3(MYH15):c.5006G>A (p.Arg1669His)	not specified [RCV004335625]	likely benign	3	108398764	108398764	Human		name
401895897	CV2775802	single nucleotide variant	NM_014981.3(MYH15):c.5604A>C (p.Gln1868His)	not specified [RCV004344845]	likely benign	3	108384714	108384714	Human		name
401895978	CV2776236	single nucleotide variant	NM_014981.3(MYH15):c.5474G>C (p.Ser1825Thr)	not specified [RCV004353605]	uncertain significance	3	108389031	108389031	Human		name
401922349	CV2827610	single nucleotide variant	NM_014981.3(MYH15):c.4273G>T (p.Gly1425Trp)	not provided [RCV003433689]	uncertain significance	3	108410805	108410805	Human		name
405700742	CV3309956	single nucleotide variant	NM_014981.3(MYH15):c.3424C>A (p.Leu1142Met)	not specified [RCV004447034]	uncertain significance	3	108428770	108428770	Human		name
405701159	CV3309980	single nucleotide variant	NM_014981.3(MYH15):c.3989G>A (p.Arg1330His)	not specified [RCV004447058]	likely benign	3	108414388	108414388	Human		name
405700808	CV3309991	single nucleotide variant	NM_014981.3(MYH15):c.4052G>A (p.Arg1351Gln)	not specified [RCV004447069]	uncertain significance	3	108414325	108414325	Human		name
405700837	CV3309997	single nucleotide variant	NM_014981.3(MYH15):c.4252G>C (p.Gly1418Arg)	not specified [RCV004447075]	uncertain significance	3	108410826	108410826	Human		name
405700903	CV3310008	single nucleotide variant	NM_014981.3(MYH15):c.4357G>A (p.Glu1453Lys)	not specified [RCV004447086]	uncertain significance	3	108410721	108410721	Human		name
405701316	CV3310055	single nucleotide variant	NM_014981.3(MYH15):c.4960C>A (p.Gln1654Lys)	not specified [RCV004447133]	uncertain significance	3	108398810	108398810	Human		name
405701508	CV3310085	single nucleotide variant	NM_014981.3(MYH15):c.5255T>C (p.Ile1752Thr)	not specified [RCV004447163]	likely benign	3	108394035	108394035	Human		name
405701599	CV3310097	single nucleotide variant	NM_014981.3(MYH15):c.5623G>A (p.Glu1875Lys)	not specified [RCV004447175]	uncertain significance	3	108384695	108384695	Human		name
405700527	CV3313810	single nucleotide variant	NM_014981.3(MYH15):c.3129A>C (p.Glu1043Asp)	not specified [RCV004446996]	uncertain significance	3	108437646	108437646	Human		name
405700548	CV3313814	single nucleotide variant	NM_014981.3(MYH15):c.3163C>T (p.Arg1055Trp)	not specified [RCV004447000]	uncertain significance	3	108437612	108437612	Human		name
405700620	CV3313826	single nucleotide variant	NM_014981.3(MYH15):c.3245T>C (p.Met1082Thr)	not specified [RCV004447012]	uncertain significance	3	108430899	108430899	Human		name
405700641	CV3313830	single nucleotide variant	NM_014981.3(MYH15):c.3275T>G (p.Leu1092Arg)	not specified [RCV004447016]	uncertain significance	3	108430869	108430869	Human		name
407504257	CV3454385	single nucleotide variant	NM_014981.3(MYH15):c.3356C>T (p.Thr1119Ile)	not specified [RCV004645748]	uncertain significance	3	108428838	108428838	Human		name
407504260	CV3454386	single nucleotide variant	NM_014981.3(MYH15):c.5014C>T (p.Leu1672Phe)	not specified [RCV004645749]	uncertain significance	3	108398756	108398756	Human		name
407504264	CV3454387	single nucleotide variant	NM_014981.3(MYH15):c.4844A>G (p.Asn1615Ser)	not specified [RCV004645750]	likely benign	3	108399160	108399160	Human		name
407504266	CV3454388	single nucleotide variant	NM_014981.3(MYH15):c.3118T>A (p.Cys1040Ser)	not specified [RCV004645751]	uncertain significance	3	108437657	108437657	Human		name
407514915	CV3454390	single nucleotide variant	NM_014981.3(MYH15):c.3296C>T (p.Thr1099Met)	not specified [RCV004649711]	likely benign	3	108430848	108430848	Human		name
407514921	CV3454392	single nucleotide variant	NM_014981.3(MYH15):c.3869T>G (p.Ile1290Arg)	not specified [RCV004649713]	uncertain significance	3	108416891	108416891	Human		name
407504273	CV3454394	single nucleotide variant	NM_014981.3(MYH15):c.4477G>A (p.Glu1493Lys)	not specified [RCV004645753]	uncertain significance	3	108410601	108410601	Human		name
407514927	CV3454395	single nucleotide variant	NM_014981.3(MYH15):c.3329T>C (p.Leu1110Ser)	not specified [RCV004649715]	uncertain significance	3	108428865	108428865	Human		name
407514930	CV3454396	single nucleotide variant	NM_014981.3(MYH15):c.5071C>T (p.Arg1691Cys)	not specified [RCV004649716]	uncertain significance	3	108398699	108398699	Human		name
407504288	CV3454400	single nucleotide variant	NM_014981.3(MYH15):c.3740G>A (p.Arg1247His)	not specified [RCV004645757]	uncertain significance	3	108421177	108421177	Human		name
597663119	CV3555053	single nucleotide variant	NM_014981.3(MYH15):c.4775G>A (p.Ser1592Asn)	not specified [RCV004828753]	uncertain significance	3	108399229	108399229	Human		name
597663153	CV3555057	single nucleotide variant	NM_014981.3(MYH15):c.5254A>G (p.Ile1752Val)	not specified [RCV004828757]	uncertain significance	3	108394036	108394036	Human		name
597663160	CV3555058	single nucleotide variant	NM_014981.3(MYH15):c.4258G>A (p.Ala1420Thr)	not specified [RCV004828758]	likely benign	3	108410820	108410820	Human		name
597663168	CV3555059	single nucleotide variant	NM_014981.3(MYH15):c.3631A>G (p.Lys1211Glu)	not specified [RCV004828759]	uncertain significance	3	108428563	108428563	Human		name
597663176	CV3555060	single nucleotide variant	NM_014981.3(MYH15):c.4585A>G (p.Lys1529Glu)	not specified [RCV004828760]	uncertain significance	3	108408315	108408315	Human		name
597663203	CV3555064	single nucleotide variant	NM_014981.3(MYH15):c.4985A>G (p.Gln1662Arg)	not specified [RCV004828763]	uncertain significance	3	108398785	108398785	Human		name
597663211	CV3555065	single nucleotide variant	NM_014981.3(MYH15):c.4265C>T (p.Ser1422Phe)	not specified [RCV004828764]	uncertain significance	3	108410813	108410813	Human		name
597663218	CV3555066	single nucleotide variant	NM_014981.3(MYH15):c.3718C>T (p.Leu1240Phe)	not specified [RCV004828765]	uncertain significance	3	108421199	108421199	Human		name
597663223	CV3555067	single nucleotide variant	NM_014981.3(MYH15):c.3176A>G (p.Glu1059Gly)	not specified [RCV004828766]	uncertain significance	3	108437599	108437599	Human		name
597663236	CV3555069	single nucleotide variant	NM_014981.3(MYH15):c.3679G>C (p.Val1227Leu)	not specified [RCV004828768]	uncertain significance	3	108428515	108428515	Human		name
597663279	CV3555075	single nucleotide variant	NM_014981.3(MYH15):c.3692C>G (p.Thr1231Arg)	not specified [RCV004828774]	uncertain significance	3	108428502	108428502	Human		name
598203438	CV3896480	microsatellite	NM_014981.3(MYH15):c.4736+2592_4736+2593del	Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome [RCV005356716]	likely pathogenic	3	108402745	108402746	Human		name
598189326	CV3993857	single nucleotide variant	NM_014981.3(MYH15):c.5324G>C (p.Arg1775Thr)	not specified [RCV005373856]	uncertain significance	3	108391866	108391866	Human		name
598273466	CV3993859	single nucleotide variant	NM_014981.3(MYH15):c.4547C>T (p.Thr1516Ile)	not specified [RCV005389694]	uncertain significance	3	108408353	108408353	Human		name
598189348	CV3993861	single nucleotide variant	NM_014981.3(MYH15):c.4901C>A (p.Ser1634Tyr)	not specified [RCV005373859]	uncertain significance	3	108399103	108399103	Human		name
598189376	CV3993866	single nucleotide variant	NM_014981.3(MYH15):c.3677G>A (p.Arg1226His)	not specified [RCV005373863]	likely benign	3	108428517	108428517	Human		name
598189383	CV3993867	single nucleotide variant	NM_014981.3(MYH15):c.3887A>G (p.Glu1296Gly)	not specified [RCV005373864]	uncertain significance	3	108416873	108416873	Human		name
598189390	CV3993868	single nucleotide variant	NM_014981.3(MYH15):c.4684G>A (p.Ala1562Thr)	not specified [RCV005373865]	uncertain significance	3	108405390	108405390	Human		name
598189397	CV3993869	single nucleotide variant	NM_014981.3(MYH15):c.3994T>C (p.Cys1332Arg)	not specified [RCV005373866]	uncertain significance	3	108414383	108414383	Human		name
598273477	CV3993872	single nucleotide variant	NM_014981.3(MYH15):c.4198A>G (p.Asn1400Asp)	not specified [RCV005389697]	uncertain significance	3	108410880	108410880	Human		name
598189416	CV3993874	single nucleotide variant	NM_014981.3(MYH15):c.4080G>A (p.Met1360Ile)	not specified [RCV005373869]	uncertain significance	3	108414297	108414297	Human		name
598273480	CV3993875	single nucleotide variant	NM_014981.3(MYH15):c.3771G>C (p.Lys1257Asn)	not specified [RCV005389698]	uncertain significance	3	108421146	108421146	Human		name
15190884	CV697740	single nucleotide variant	NM_014981.3(MYH15):c.5183G>A (p.Arg1728Gln)	not provided [RCV000954610]	benign	3	108394107	108394107	Human		name
15192741	CV697741	single nucleotide variant	NM_014981.3(MYH15):c.3361C>T (p.Arg1121Ter)	not provided [RCV000955162]	likely benign	3	108428833	108428833	Human		name
15165320	CV708449	single nucleotide variant	NM_014981.3(MYH15):c.5005C>T (p.Arg1669Cys)	not provided [RCV000970923]	benign\|likely benign	3	108398765	108398765	Human		name
15126946	CV708451	single nucleotide variant	NM_014981.3(MYH15):c.4339G>A (p.Asp1447Asn)	not provided [RCV000963823]	benign	3	108410739	108410739	Human		name
15159567	CV720057	single nucleotide variant	NM_014981.3(MYH15):c.5767G>T (p.Val1923Phe)	not provided [RCV000881219]	benign	3	108381559	108381559	Human		name
15195622	CV720058	single nucleotide variant	NM_014981.3(MYH15):c.5503C>T (p.Leu1835Phe)	not provided [RCV000889553]	benign	3	108389002	108389002	Human		name
21068615	CV795302	single nucleotide variant	NM_014981.3(MYH15):c.4599G>C (p.Gln1533His)	not provided [RCV000998120]\|not specified [RCV004649398]	uncertain significance	3	108408301	108408301	Human		name
8630518	CV85673	single nucleotide variant	NM_014981.1(MYH15):c.4210G>A (p.Glu1404Lys)	Malignant melanoma [RCV000065756]	not provided	3	108410928	108410928	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message