Mical1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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More than 1000 records found for search term Mical1 (Displaying 1000)
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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156326735	CV1982155	single nucleotide variant	NM_022765.4(MICAL1):c.-4C>T	not provided [RCV002649598]	likely benign	6	109454200	109454200	Human		name
597908783	CV3781573	single nucleotide variant	NM_022765.4(MICAL1):c.-1C>G	not provided [RCV005128261]	likely benign	6	109454197	109454197	Human		name
151776667	CV1381669	single nucleotide variant	NM_022765.4(MICAL1):c.-30C>G	not provided [RCV001950676]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	6	109454226	109454226	Human		name
152033437	CV1610361	single nucleotide variant	NM_022765.4(MICAL1):c.-37A>G	not provided [RCV002124933]	benign	6	109454233	109454233	Human		name
156054632	CV1928653	single nucleotide variant	NM_022765.4(MICAL1):c.-18C>A	not provided [RCV002620725]	uncertain significance	6	109454214	109454214	Human		name
156444316	CV1938172	single nucleotide variant	NM_022765.4(MICAL1):c.-33C>T	not provided [RCV003115240]	likely benign	6	109454229	109454229	Human		name
156371893	CV2031199	single nucleotide variant	NM_022765.4(MICAL1):c.-25C>A	not provided [RCV002721583]	uncertain significance	6	109454221	109454221	Human		name
156238681	CV2115740	single nucleotide variant	NM_022765.4(MICAL1):c.-14C>T	not provided [RCV002919215]	likely benign	6	109454210	109454210	Human		name
405072031	CV2876626	single nucleotide variant	NM_022765.4(MICAL1):c.-27A>G	not provided [RCV003548589]	uncertain significance	6	109454223	109454223	Human		name
402475575	CV2915957	single nucleotide variant	NM_022765.4(MICAL1):c.-19C>T	not provided [RCV003571246]	likely benign	6	109454215	109454215	Human		name
405239670	CV2997108	single nucleotide variant	NM_022765.4(MICAL1):c.-39T>G	not provided [RCV003718852]	uncertain significance	6	109454235	109454235	Human		name
405034786	CV3072478	single nucleotide variant	NM_022765.4(MICAL1):c.-15C>T	not provided [RCV003739425]	uncertain significance	6	109454211	109454211	Human		name
597864422	CV3742185	single nucleotide variant	NM_022765.4(MICAL1):c.-32T>C	not provided [RCV005067801]	uncertain significance	6	109454228	109454228	Human		name
597841771	CV3752779	single nucleotide variant	NM_022765.4(MICAL1):c.-11A>G	not provided [RCV005086508]	uncertain significance	6	109454207	109454207	Human		name
597874055	CV3805559	single nucleotide variant	NM_022765.4(MICAL1):c.-41A>G	not provided [RCV005148837]	uncertain significance	6	109454237	109454237	Human		name
151750431	CV1415659	single nucleotide variant	NM_022765.4(MICAL1):c.466+5G>A	not provided [RCV001927469]	uncertain significance	6	109453633	109453633	Human		name
151725973	CV1517355	single nucleotide variant	NM_022765.4(MICAL1):c.-43-1G>A	Epilepsy, familial temporal lobe, 1 [RCV002051606]	pathogenic	6	109454240	109454240	Human	1	name
152080987	CV1663729	single nucleotide variant	NM_022765.4(MICAL1):c.571+1G>T	not provided [RCV002149307]	likely benign	6	109453262	109453262	Human		name
156442499	CV1938778	single nucleotide variant	NM_022765.4(MICAL1):c.833-3C>T	not provided [RCV003112844]	uncertain significance	6	109451703	109451703	Human		name
156440492	CV1943543	single nucleotide variant	NM_022765.4(MICAL1):c.934-6A>G	not provided [RCV003110527]	benign	6	109450563	109450563	Human		name
156377058	CV1956769	single nucleotide variant	NM_022765.4(MICAL1):c.934-4A>T	not provided [RCV002582889]	likely benign	6	109450561	109450561	Human		name
156016694	CV2010365	single nucleotide variant	NM_022765.4(MICAL1):c.-43-7T>A	not provided [RCV002735177]	likely benign	6	109454246	109454246	Human		name
156011032	CV2011468	single nucleotide variant	NM_022765.4(MICAL1):c.466+4A>G	not provided [RCV002690514]	uncertain significance	6	109453634	109453634	Human		name
156231330	CV2085289	single nucleotide variant	NM_022765.4(MICAL1):c.571+5G>C	not provided [RCV002876248]	uncertain significance	6	109453258	109453258	Human		name
156196069	CV2175523	single nucleotide variant	NM_022765.4(MICAL1):c.832+3C>T	not provided [RCV003057997]	uncertain significance	6	109452243	109452243	Human		name
405136668	CV2963147	single nucleotide variant	NM_022765.4(MICAL1):c.572-6C>T	not provided [RCV003668847]	likely benign	6	109452621	109452621	Human		name
405221710	CV2966061	single nucleotide variant	NM_022765.4(MICAL1):c.258+8C>T	not provided [RCV003680699]	likely benign	6	109453931	109453931	Human		name
405183223	CV3057760	single nucleotide variant	NM_022765.4(MICAL1):c.466+9C>G	not provided [RCV003729000]	uncertain significance	6	109453629	109453629	Human		name
597867307	CV3739139	deletion	NM_022765.4(MICAL1):c.572-8del	not provided [RCV005068206]	likely benign	6	109452623	109452623	Human		name
597968462	CV3761091	single nucleotide variant	NM_022765.4(MICAL1):c.676+3G>A	not provided [RCV005083478]	uncertain significance	6	109452508	109452508	Human		name
597968549	CV3795049	single nucleotide variant	NM_022765.4(MICAL1):c.259-9T>A	not provided [RCV005141017]	uncertain significance	6	109453854	109453854	Human		name
597870166	CV3803580	single nucleotide variant	NM_022765.4(MICAL1):c.571+1G>C	not provided [RCV005148178]	uncertain significance	6	109453262	109453262	Human		name
597952725	CV3815781	single nucleotide variant	NM_022765.4(MICAL1):c.259-3C>T	not provided [RCV005161534]	uncertain significance	6	109453848	109453848	Human		name
597976301	CV3829326	single nucleotide variant	NM_022765.4(MICAL1):c.934-4A>G	not provided [RCV005169775]	likely benign	6	109450561	109450561	Human		name
597975144	CV3832243	single nucleotide variant	NM_022765.4(MICAL1):c.833-8A>G	not provided [RCV005168979]	likely benign	6	109451708	109451708	Human		name
151857374	CV1348066	single nucleotide variant	NM_022765.4(MICAL1):c.2228-1G>A	not provided [RCV001979692]	uncertain significance	6	109446773	109446773	Human		name
151728621	CV1410029	single nucleotide variant	NM_022765.4(MICAL1):c.1986+6T>G	not provided [RCV001910638]	uncertain significance	6	109447675	109447675	Human		name
151774033	CV1413356	single nucleotide variant	NM_022765.4(MICAL1):c.1665-3C>T	not provided [RCV001971458]	uncertain significance	6	109448396	109448396	Human		name
151828193	CV1438065	single nucleotide variant	NM_022765.4(MICAL1):c.1192-1G>A	not provided [RCV001920229]	uncertain significance	6	109450086	109450086	Human		name
152056475	CV1523045	single nucleotide variant	NM_022765.4(MICAL1):c.2981+6G>C	not provided [RCV002167500]	likely benign	6	109444890	109444890	Human		name
152075127	CV1544815	single nucleotide variant	NM_022765.4(MICAL1):c.467-20T>C	not provided [RCV002169810]	benign	6	109453387	109453387	Human		name
152171927	CV1575666	single nucleotide variant	NM_022765.4(MICAL1):c.934-13G>A	not provided [RCV002183670]	likely benign	6	109450570	109450570	Human		name
152088112	CV1626089	single nucleotide variant	NM_022765.4(MICAL1):c.677-15T>C	not provided [RCV002131704]	likely benign	6	109452416	109452416	Human		name
156394972	CV1877038	single nucleotide variant	NM_022765.4(MICAL1):c.1856-4G>A	not provided [RCV003068491]	likely benign	6	109447967	109447967	Human		name
156047262	CV1887558	single nucleotide variant	NM_022765.4(MICAL1):c.1308-9C>T	not provided [RCV003078744]	likely benign	6	109449792	109449792	Human		name
156214963	CV1903256	single nucleotide variant	NM_022765.4(MICAL1):c.1664+1G>C	not provided [RCV003084758]	uncertain significance	6	109448731	109448731	Human		name
156005267	CV1906401	single nucleotide variant	NM_022765.4(MICAL1):c.2881+1G>C	not provided [RCV003098997]	uncertain significance	6	109445196	109445196	Human		name
156436903	CV1936721	single nucleotide variant	NM_022765.4(MICAL1):c.1191+2T>C	not provided [RCV003106427]	uncertain significance	6	109450298	109450298	Human		name
156444494	CV1948292	single nucleotide variant	NM_022765.4(MICAL1):c.2787+9C>T	not provided [RCV003115418]	likely benign	6	109445407	109445407	Human		name
156446193	CV1951284	single nucleotide variant	NM_022765.4(MICAL1):c.1986+8C>T	not provided [RCV003117160]	likely benign	6	109447673	109447673	Human		name
156377210	CV1956813	single nucleotide variant	NM_022765.4(MICAL1):c.3055+6T>C	not provided [RCV002582901]	uncertain significance	6	109444719	109444719	Human		name
156375996	CV1960330	single nucleotide variant	NM_022765.4(MICAL1):c.259-13T>C	not provided [RCV002582803]	likely benign	6	109453858	109453858	Human		name
156410093	CV1962106	single nucleotide variant	NM_022765.4(MICAL1):c.1855+5C>T	not provided [RCV002587044]	uncertain significance	6	109448198	109448198	Human		name
156135886	CV1962914	single nucleotide variant	NM_022765.4(MICAL1):c.2071-2A>G	not provided [RCV002572394]	uncertain significance	6	109447231	109447231	Human		name
156250979	CV1963700	single nucleotide variant	NM_022765.4(MICAL1):c.258+11G>A	not provided [RCV002576538]	likely benign	6	109453928	109453928	Human		name
156413313	CV1969025	single nucleotide variant	NM_022765.4(MICAL1):c.571+13A>G	not provided [RCV002608801]	likely benign	6	109453250	109453250	Human		name
156330180	CV1969899	single nucleotide variant	NM_022765.4(MICAL1):c.833-19C>G	not provided [RCV002600751]	likely benign	6	109451719	109451719	Human		name
156411365	CV1977158	single nucleotide variant	NM_022765.4(MICAL1):c.2982-8C>G	not provided [RCV002608233]	likely benign	6	109444806	109444806	Human		name
156179863	CV1978776	single nucleotide variant	NM_022765.4(MICAL1):c.2071-5C>T	not provided [RCV002595030]	likely benign	6	109447234	109447234	Human		name
156078922	CV1982530	single nucleotide variant	NM_022765.4(MICAL1):c.1308-5C>T	not provided [RCV002638834]	likely benign	6	109449788	109449788	Human		name
156388430	CV1989882	single nucleotide variant	NM_022765.4(MICAL1):c.1191+7G>T	not provided [RCV002604459]	likely benign	6	109450293	109450293	Human		name
156391140	CV1990141	single nucleotide variant	NM_022765.4(MICAL1):c.677-17C>T	not provided [RCV002604678]	benign	6	109452418	109452418	Human		name
156328649	CV1992439	single nucleotide variant	NM_022765.4(MICAL1):c.466+12G>A	not provided [RCV002649695]	likely benign	6	109453626	109453626	Human		name
156240433	CV1992531	single nucleotide variant	NM_022765.4(MICAL1):c.1516+9G>A	not provided [RCV002627113]	likely benign	6	109449391	109449391	Human		name
156150155	CV1999283	single nucleotide variant	NM_022765.4(MICAL1):c.2674-7C>T	not provided [RCV002663866]	likely benign	6	109445536	109445536	Human		name
156181736	CV2001400	single nucleotide variant	NM_022765.4(MICAL1):c.572-11C>G	not provided [RCV002643043]	likely benign	6	109452626	109452626	Human		name
156364715	CV2003479	single nucleotide variant	NM_022765.4(MICAL1):c.1516+1G>C	not provided [RCV002676478]	uncertain significance	6	109449399	109449399	Human		name
156016464	CV2010342	single nucleotide variant	NM_022765.4(MICAL1):c.1308-3C>A	not provided [RCV002735167]	uncertain significance	6	109449786	109449786	Human		name
156118217	CV2017287	single nucleotide variant	NM_022765.4(MICAL1):c.2228-5T>G	not provided [RCV002740097]	likely benign	6	109446777	109446777	Human		name
156211827	CV2028448	single nucleotide variant	NM_022765.4(MICAL1):c.832+13C>T	not provided [RCV002711792]	likely benign	6	109452233	109452233	Human		name
156019401	CV2029176	single nucleotide variant	NM_022765.4(MICAL1):c.2071-6A>G	not provided [RCV002735303]	likely benign	6	109447235	109447235	Human		name
156262901	CV2030222	single nucleotide variant	NM_022765.4(MICAL1):c.2673+1G>A	not provided [RCV002746370]	uncertain significance	6	109445770	109445770	Human		name
155942616	CV2032376	single nucleotide variant	NM_022765.4(MICAL1):c.3056-9T>G	not provided [RCV002730216]	likely benign	6	109444348	109444348	Human		name
156253217	CV2041150	single nucleotide variant	NM_022765.4(MICAL1):c.467-15T>C	not provided [RCV002806082]	likely benign	6	109453382	109453382	Human		name
156109417	CV2042376	single nucleotide variant	NM_022765.4(MICAL1):c.1517-5C>A	not provided [RCV002785337]	likely benign	6	109448884	109448884	Human		name
156068892	CV2050862	single nucleotide variant	NM_022765.4(MICAL1):c.1944+5A>G	not provided [RCV002797339]	uncertain significance	6	109447870	109447870	Human		name
156254798	CV2060606	single nucleotide variant	NM_022765.4(MICAL1):c.2304+1G>A	not provided [RCV002791816]	uncertain significance	6	109446695	109446695	Human		name
155973884	CV2062643	single nucleotide variant	NM_022765.4(MICAL1):c.1434+2T>G	not provided [RCV002842202]	uncertain significance	6	109449655	109449655	Human		name
156235754	CV2094047	single nucleotide variant	NM_022765.4(MICAL1):c.1307+7C>T	not provided [RCV002894729]	likely benign	6	109449963	109449963	Human		name
156008397	CV2126709	single nucleotide variant	NM_022765.4(MICAL1):c.259-14C>T	not provided [RCV002975511]	likely benign	6	109453859	109453859	Human		name
156144446	CV2134359	single nucleotide variant	NM_022765.4(MICAL1):c.1987-9C>T	not provided [RCV002982432]	likely benign	6	109447449	109447449	Human		name
155945147	CV2139386	single nucleotide variant	NM_022765.4(MICAL1):c.1308-7C>T	not provided [RCV002994298]	likely benign	6	109449790	109449790	Human		name
156313548	CV2160626	deletion	NM_022765.4(MICAL1):c.258+12del	not provided [RCV003046170]	likely benign	6	109453927	109453927	Human		name
156311417	CV2164128	single nucleotide variant	NM_022765.4(MICAL1):c.3055+9A>C	not provided [RCV003046051]	likely benign	6	109444716	109444716	Human		name
156090161	CV2166949	single nucleotide variant	NM_022765.4(MICAL1):c.1308-8C>T	not provided [RCV003038186]	likely benign	6	109449791	109449791	Human		name
156023879	CV2184797	single nucleotide variant	NM_022765.4(MICAL1):c.933+13C>G	not provided [RCV003035866]	likely benign	6	109451587	109451587	Human		name
156201008	CV2192148	single nucleotide variant	NM_022765.4(MICAL1):c.259-10G>A	not provided [RCV003058160]	likely benign	6	109453855	109453855	Human		name
405214457	CV2875898	single nucleotide variant	NM_022765.4(MICAL1):c.2304+3A>G	not provided [RCV003553035]	uncertain significance	6	109446693	109446693	Human		name
405207253	CV2913654	single nucleotide variant	NM_022765.4(MICAL1):c.2881+8A>T	not provided [RCV003566617]	likely benign	6	109445189	109445189	Human		name
402476511	CV2917058	duplication	NM_022765.4(MICAL1):c.933+15dup	not provided [RCV003571515]	likely benign	6	109451584	109451585	Human		name
405189831	CV2924598	single nucleotide variant	NM_022765.4(MICAL1):c.2070+2T>C	not provided [RCV003564804]	uncertain significance	6	109447355	109447355	Human		name
405123222	CV2942393	single nucleotide variant	NM_022765.4(MICAL1):c.1307+3A>T	not provided [RCV003671618]	uncertain significance	6	109449967	109449967	Human		name
405094709	CV2947350	single nucleotide variant	NM_022765.4(MICAL1):c.2787+9C>G	not provided [RCV003665547]	likely benign	6	109445407	109445407	Human		name
405152770	CV2949242	single nucleotide variant	NM_022765.4(MICAL1):c.2673+7G>A	not provided [RCV003674127]	likely benign	6	109445764	109445764	Human		name
405188450	CV2964207	single nucleotide variant	NM_022765.4(MICAL1):c.467-12T>C	not provided [RCV003676890]	likely benign	6	109453379	109453379	Human		name
405221833	CV2966254	single nucleotide variant	NM_022765.4(MICAL1):c.2788-5C>G	not provided [RCV003680784]	likely benign	6	109445295	109445295	Human		name
405226739	CV2967200	single nucleotide variant	NM_022765.4(MICAL1):c.677-11G>A	not provided [RCV003681552]	likely benign	6	109452412	109452412	Human		name
405220114	CV2969609	single nucleotide variant	NM_022765.4(MICAL1):c.572-13C>A	not provided [RCV003680552]	likely benign	6	109452628	109452628	Human		name
405243316	CV2971531	single nucleotide variant	NM_022765.4(MICAL1):c.2582-1G>A	not provided [RCV003684560]	uncertain significance	6	109445863	109445863	Human		name
402495054	CV2978588	single nucleotide variant	NM_022765.4(MICAL1):c.259-16C>T	not provided [RCV003714169]	likely benign	6	109453861	109453861	Human		name
405212167	CV2984028	single nucleotide variant	NM_022765.4(MICAL1):c.1192-1G>T	not provided [RCV003708853]	uncertain significance	6	109450086	109450086	Human		name
405075918	CV3007910	single nucleotide variant	NM_022765.4(MICAL1):c.571+16C>A	not provided [RCV003716756]	likely benign	6	109453247	109453247	Human		name
402500936	CV3013740	single nucleotide variant	NM_022765.4(MICAL1):c.2882-5C>G	not provided [RCV003688410]	likely benign	6	109445000	109445000	Human		name
405165570	CV3018794	single nucleotide variant	NM_022765.4(MICAL1):c.1517-7T>C	not provided [RCV003704282]	likely benign	6	109448886	109448886	Human		name
405204867	CV3033591	single nucleotide variant	NM_022765.4(MICAL1):c.2305-3C>T	not provided [RCV003707872]\|not specified [RCV003988141]	uncertain significance	6	109446415	109446415	Human		name
402508692	CV3034182	single nucleotide variant	NM_022765.4(MICAL1):c.1191+3G>A	not provided [RCV003715466]	uncertain significance	6	109450297	109450297	Human		name
405224330	CV3035781	single nucleotide variant	NM_022765.4(MICAL1):c.2070+7G>A	not provided [RCV003710322]	likely benign	6	109447350	109447350	Human		name
405237779	CV3077756	single nucleotide variant	NM_022765.4(MICAL1):c.1945-6T>C	not provided [RCV003736231]	uncertain significance	6	109447728	109447728	Human		name
405132833	CV3115251	single nucleotide variant	NM_022765.4(MICAL1):c.2674-1G>A	not provided [RCV003816096]	uncertain significance	6	109445530	109445530	Human		name
405204238	CV3116919	single nucleotide variant	NM_022765.4(MICAL1):c.832+19G>A	not provided [RCV003822403]	likely benign	6	109452227	109452227	Human		name
405204787	CV3116991	single nucleotide variant	NM_022765.4(MICAL1):c.572-16A>T	not provided [RCV003822475]	likely benign	6	109452631	109452631	Human		name
405006617	CV3117533	single nucleotide variant	NM_022765.4(MICAL1):c.832+15T>A	not provided [RCV003828588]	likely benign	6	109452231	109452231	Human		name
405094148	CV3118879	single nucleotide variant	NM_022765.4(MICAL1):c.2982-2A>G	not provided [RCV003811330]	uncertain significance	6	109444800	109444800	Human		name
405168110	CV3125740	single nucleotide variant	NM_022765.4(MICAL1):c.677-12C>T	not provided [RCV003818823]	likely benign	6	109452413	109452413	Human		name
405142446	CV3125988	single nucleotide variant	NM_022765.4(MICAL1):c.2070+8C>T	not provided [RCV003816904]	likely benign	6	109447349	109447349	Human		name
404979479	CV3127825	single nucleotide variant	NM_022765.4(MICAL1):c.258+10C>T	not provided [RCV003825857]	likely benign	6	109453929	109453929	Human		name
405025062	CV3133030	single nucleotide variant	NM_022765.4(MICAL1):c.2981+1G>T	not provided [RCV003830177]	uncertain significance	6	109444895	109444895	Human		name
405218558	CV3135725	single nucleotide variant	NM_022765.4(MICAL1):c.2787+5A>G	not provided [RCV003824350]	uncertain significance	6	109445411	109445411	Human		name
405015702	CV3139028	single nucleotide variant	NM_022765.4(MICAL1):c.1944+4G>A	not provided [RCV003829365]	uncertain significance	6	109447871	109447871	Human		name
405212963	CV3142738	single nucleotide variant	NM_022765.4(MICAL1):c.259-10G>T	not provided [RCV003846095]	likely benign	6	109453855	109453855	Human		name
405227968	CV3142899	single nucleotide variant	NM_022765.4(MICAL1):c.2981+1G>A	not provided [RCV003848242]	uncertain significance	6	109444895	109444895	Human		name
405209269	CV3145762	single nucleotide variant	NM_022765.4(MICAL1):c.466+12G>T	not provided [RCV003845492]	uncertain significance	6	109453626	109453626	Human		name
405177315	CV3148599	single nucleotide variant	NM_022765.4(MICAL1):c.2673+8G>A	not provided [RCV003858376]	likely benign	6	109445763	109445763	Human		name
405173019	CV3151763	single nucleotide variant	NM_022765.4(MICAL1):c.2581+1G>A	not provided [RCV003857914]	uncertain significance	6	109446135	109446135	Human		name
405219706	CV3154304	single nucleotide variant	NM_022765.4(MICAL1):c.2788-5C>T	not provided [RCV003846996]	likely benign	6	109445295	109445295	Human		name
405245532	CV3161858	single nucleotide variant	NM_022765.4(MICAL1):c.1435-7G>A	not provided [RCV003868571]	likely benign	6	109449488	109449488	Human		name
405255531	CV3172512	single nucleotide variant	NM_022765.4(MICAL1):c.572-16A>G	not provided [RCV003872450]	likely benign	6	109452631	109452631	Human		name
404991306	CV3176222	single nucleotide variant	NM_022765.4(MICAL1):c.2071-4G>A	not provided [RCV003881547]	likely benign	6	109447233	109447233	Human		name
597922467	CV3738508	single nucleotide variant	NM_022765.4(MICAL1):c.3056-8C>T	not provided [RCV005074915]	likely benign	6	109444347	109444347	Human		name
597946274	CV3755554	single nucleotide variant	NM_022765.4(MICAL1):c.1435-7G>T	not provided [RCV005078564]	likely benign	6	109449488	109449488	Human		name
597950947	CV3756356	single nucleotide variant	NM_022765.4(MICAL1):c.933+17G>A	not provided [RCV005079413]	likely benign	6	109451583	109451583	Human		name
597942481	CV3779925	single nucleotide variant	NM_022765.4(MICAL1):c.3055+2T>G	not provided [RCV005118934]	uncertain significance	6	109444723	109444723	Human		name
597951650	CV3798386	single nucleotide variant	NM_022765.4(MICAL1):c.1944+8G>A	not provided [RCV005136166]	likely benign	6	109447867	109447867	Human		name
597874081	CV3805564	single nucleotide variant	NM_022765.4(MICAL1):c.2674-8T>C	not provided [RCV005148842]	likely benign	6	109445537	109445537	Human		name
597953430	CV3808849	single nucleotide variant	NM_022765.4(MICAL1):c.934-12T>C	not provided [RCV005161767]	likely benign	6	109450569	109450569	Human		name
597962543	CV3809200	single nucleotide variant	NM_022765.4(MICAL1):c.2982-3C>T	not provided [RCV005164102]	uncertain significance	6	109444801	109444801	Human		name
597916882	CV3811036	single nucleotide variant	NM_022765.4(MICAL1):c.2882-5C>T	not provided [RCV005155071]	likely benign	6	109445000	109445000	Human		name
597878836	CV3826159	single nucleotide variant	NM_022765.4(MICAL1):c.1192-4G>A	not provided [RCV005177855]	likely benign	6	109450089	109450089	Human		name
597836459	CV3828436	single nucleotide variant	NM_022765.4(MICAL1):c.677-15T>G	not provided [RCV005171328]	likely benign	6	109452416	109452416	Human		name
597837194	CV3828736	single nucleotide variant	NM_022765.4(MICAL1):c.934-17C>T	not provided [RCV005171429]	likely benign	6	109450574	109450574	Human		name
597972028	CV3829440	single nucleotide variant	NM_022765.4(MICAL1):c.1517-1G>A	not provided [RCV005167227]	uncertain significance	6	109448880	109448880	Human		name
597972288	CV3829557	single nucleotide variant	NM_022765.4(MICAL1):c.832+17C>G	not provided [RCV005167344]	likely benign	6	109452229	109452229	Human		name
597909569	CV3830039	single nucleotide variant	NM_022765.4(MICAL1):c.2581+6C>G	not provided [RCV005182608]	uncertain significance	6	109446130	109446130	Human		name
597975148	CV3832245	single nucleotide variant	NM_022765.4(MICAL1):c.2581+5C>G	not provided [RCV005168981]	uncertain significance	6	109446131	109446131	Human		name
597975424	CV3832390	single nucleotide variant	NM_022765.4(MICAL1):c.832+10C>A	not provided [RCV005169127]	likely benign	6	109452236	109452236	Human		name
597866587	CV3834480	single nucleotide variant	NM_022765.4(MICAL1):c.832+13C>G	not provided [RCV005175847]	likely benign	6	109452233	109452233	Human		name
597949804	CV3846777	single nucleotide variant	NM_022765.4(MICAL1):c.2673+4A>T	not provided [RCV005189948]	uncertain significance	6	109445767	109445767	Human		name
15176969	CV730380	single nucleotide variant	NM_022765.4(MICAL1):c.2982-8C>T	not provided [RCV000884712]	benign\|likely benign	6	109444806	109444806	Human		name
151872380	CV1351583	single nucleotide variant	NM_022765.4(MICAL1):c.1855+18C>T	not provided [RCV001998519]	uncertain significance	6	109448185	109448185	Human		name
151716406	CV1470627	duplication	NM_022765.4(MICAL1):c.1987-10dup	not provided [RCV001909035]	likely benign\|uncertain significance	6	109447449	109447450	Human		name
152103195	CV1524027	single nucleotide variant	NM_022765.4(MICAL1):c.1517-11T>C	not provided [RCV002133526]	likely benign	6	109448890	109448890	Human		name
152062371	CV1533050	single nucleotide variant	NM_022765.4(MICAL1):c.2787+10G>A	not provided [RCV002090408]	likely benign	6	109445406	109445406	Human		name
152071065	CV1552013	single nucleotide variant	NM_022765.4(MICAL1):c.1435-13G>A	not provided [RCV002148083]	benign	6	109449494	109449494	Human		name
152056657	CV1567150	single nucleotide variant	NM_022765.4(MICAL1):c.2787+12G>A	not provided [RCV002146317]	likely benign	6	109445404	109445404	Human		name
152029266	CV1568207	single nucleotide variant	NM_022765.4(MICAL1):c.2304+13G>A	not provided [RCV002105527]	benign	6	109446683	109446683	Human		name
152084389	CV1577036	single nucleotide variant	NM_022765.4(MICAL1):c.2788-11G>A	not provided [RCV002193437]	benign	6	109445301	109445301	Human		name
152084629	CV1577085	duplication	NM_022765.4(MICAL1):c.1855+15dup	not provided [RCV002193470]	likely benign	6	109448187	109448188	Human		name
152128841	CV1596619	deletion	NM_022765.4(MICAL1):c.1986+13del	not provided [RCV002118809]	likely benign	6	109447668	109447668	Human		name
152041394	CV1603189	single nucleotide variant	NM_022765.4(MICAL1):c.2982-16T>C	not provided [RCV002071062]	likely benign	6	109444814	109444814	Human		name
152064314	CV1612256	single nucleotide variant	NM_022765.4(MICAL1):c.2981+13G>A	not provided [RCV002128756]	likely benign	6	109444883	109444883	Human		name
152109154	CV1623575	single nucleotide variant	NM_022765.4(MICAL1):c.1434+17A>G	not provided [RCV002215236]	likely benign	6	109449640	109449640	Human		name
152104134	CV1624611	single nucleotide variant	NM_022765.4(MICAL1):c.1308-13C>G	not provided [RCV002173486]	benign	6	109449796	109449796	Human		name
152122004	CV1631729	single nucleotide variant	NM_022765.4(MICAL1):c.2673+20G>A	not provided [RCV002117966]	benign	6	109445751	109445751	Human		name
152077173	CV1632843	single nucleotide variant	NM_022765.4(MICAL1):c.1192-18A>G	not provided [RCV002170076]	benign	6	109450103	109450103	Human		name
156103875	CV1907300	single nucleotide variant	NM_022765.4(MICAL1):c.2305-10G>A	not provided [RCV003080707]	benign	6	109446422	109446422	Human		name
156334062	CV1954310	single nucleotide variant	NM_022765.4(MICAL1):c.2304+15C>T	not provided [RCV002580157]	likely benign	6	109446681	109446681	Human		name
156302520	CV1955653	single nucleotide variant	NM_022765.4(MICAL1):c.1855+19G>A	not provided [RCV002578290]	likely benign	6	109448184	109448184	Human		name
156415422	CV1958430	single nucleotide variant	NM_022765.4(MICAL1):c.2582-20G>A	not provided [RCV002589160]	benign	6	109445882	109445882	Human		name
156148999	CV1964158	single nucleotide variant	NM_022765.4(MICAL1):c.1307+15G>A	not provided [RCV002572838]	likely benign	6	109449955	109449955	Human		name
156252059	CV1967249	single nucleotide variant	NM_022765.4(MICAL1):c.1517-16C>T	not provided [RCV002597502]	likely benign	6	109448895	109448895	Human		name
156312185	CV1969753	single nucleotide variant	NM_022765.4(MICAL1):c.1987-14A>C	not provided [RCV002578756]	likely benign	6	109447454	109447454	Human		name
155979546	CV1972342	single nucleotide variant	NM_022765.4(MICAL1):c.1516+10C>G	not provided [RCV002617536]	likely benign	6	109449390	109449390	Human		name
156310201	CV1973200	single nucleotide variant	NM_022765.4(MICAL1):c.1986+19G>A	not provided [RCV002578647]	uncertain significance	6	109447662	109447662	Human		name
156054595	CV1974510	single nucleotide variant	NM_022765.4(MICAL1):c.2227+19C>T	not provided [RCV002590770]	likely benign	6	109447054	109447054	Human		name
156411396	CV1976271	single nucleotide variant	NM_022765.4(MICAL1):c.2227+11C>T	not provided [RCV002587477]	benign	6	109447062	109447062	Human		name
155971095	CV1978333	single nucleotide variant	NM_022765.4(MICAL1):c.1192-20C>T	not provided [RCV002617184]	likely benign	6	109450105	109450105	Human		name
156392081	CV1986366	single nucleotide variant	NM_022765.4(MICAL1):c.1664+18C>A	not provided [RCV002604763]	likely benign	6	109448714	109448714	Human		name
156207479	CV1986788	duplication	NM_022765.4(MICAL1):c.2071-10dup	not provided [RCV002625956]	benign	6	109447238	109447239	Human		name
156109595	CV1988651	single nucleotide variant	NM_022765.4(MICAL1):c.2882-11C>A	not provided [RCV002622523]	likely benign	6	109445006	109445006	Human		name
156102600	CV1992017	single nucleotide variant	NM_022765.4(MICAL1):c.2071-10G>A	not provided [RCV002622271]	likely benign	6	109447239	109447239	Human		name
156112580	CV1993692	single nucleotide variant	NM_022765.4(MICAL1):c.1945-11A>G	not provided [RCV002662547]	likely benign	6	109447733	109447733	Human		name
156041384	CV1999039	single nucleotide variant	NM_022765.4(MICAL1):c.3056-17T>C	not provided [RCV002659051]	likely benign	6	109444356	109444356	Human		name
156375253	CV2003998	single nucleotide variant	NM_022765.4(MICAL1):c.2304+17T>C	not provided [RCV002653242]	uncertain significance	6	109446679	109446679	Human		name
156270142	CV2004077	single nucleotide variant	NM_022765.4(MICAL1):c.1435-14C>T	not provided [RCV002646504]	likely benign	6	109449495	109449495	Human		name
156355210	CV2005128	single nucleotide variant	NM_022765.4(MICAL1):c.2787+14G>A	not provided [RCV002675871]	likely benign	6	109445402	109445402	Human		name
156010569	CV2011437	single nucleotide variant	NM_022765.4(MICAL1):c.2582-12T>A	not provided [RCV002690489]	uncertain significance	6	109445874	109445874	Human		name
156116238	CV2016954	single nucleotide variant	NM_022765.4(MICAL1):c.2228-19C>T	not provided [RCV002740024]	likely benign	6	109446791	109446791	Human		name
156356299	CV2020008	single nucleotide variant	NM_022765.4(MICAL1):c.1945-20G>T	not provided [RCV002720557]	likely benign	6	109447742	109447742	Human		name
155990835	CV2026952	single nucleotide variant	NM_022765.4(MICAL1):c.2882-18C>T	not provided [RCV002755742]	likely benign	6	109445013	109445013	Human		name
156212506	CV2028478	single nucleotide variant	NM_022765.4(MICAL1):c.2674-16C>A	not provided [RCV002711818]	likely benign	6	109445545	109445545	Human		name
156033315	CV2037085	single nucleotide variant	NM_022765.4(MICAL1):c.1664+17C>T	not provided [RCV002781201]	likely benign	6	109448715	109448715	Human		name
156134451	CV2044260	single nucleotide variant	NM_022765.4(MICAL1):c.1856-10C>G	not provided [RCV002786294]	uncertain significance	6	109447973	109447973	Human		name
156028919	CV2052126	single nucleotide variant	NM_022765.4(MICAL1):c.2582-13T>C	not provided [RCV002820976]	likely benign	6	109445875	109445875	Human		name
156001483	CV2074645	inversion	NM_022765.4(MICAL1):c.-38_-37inv	not provided [RCV002843426]	uncertain significance	6	109454233	109454234	Human		name
155950206	CV2084329	single nucleotide variant	NM_022765.4(MICAL1):c.2581+16A>G	not provided [RCV002880457]	likely benign	6	109446120	109446120	Human		name
156091172	CV2093063	single nucleotide variant	NM_022765.4(MICAL1):c.2228-16T>A	not provided [RCV002926686]	likely benign	6	109446788	109446788	Human		name
156321196	CV2101016	deletion	NM_022765.4(MICAL1):c.1191+10del	not provided [RCV002899302]	likely benign	6	109450290	109450290	Human		name
156003133	CV2103456	single nucleotide variant	NM_022765.4(MICAL1):c.3056-13C>A	not provided [RCV002908730]	likely benign	6	109444352	109444352	Human		name
156017714	CV2121502	single nucleotide variant	NM_022765.4(MICAL1):c.1944+19G>T	not provided [RCV002948619]	uncertain significance	6	109447856	109447856	Human		name
156128943	CV2125048	single nucleotide variant	NM_022765.4(MICAL1):c.2787+14G>T	not provided [RCV002953803]	likely benign	6	109445402	109445402	Human		name
156067460	CV2147788	single nucleotide variant	NM_022765.4(MICAL1):c.1986+18C>A	not provided [RCV003037462]	likely benign	6	109447663	109447663	Human		name
156081926	CV2158632	single nucleotide variant	NM_022765.4(MICAL1):c.1987-14A>T	not provided [RCV003037912]	likely benign	6	109447454	109447454	Human		name
155955074	CV2166457	single nucleotide variant	NM_022765.4(MICAL1):c.1855+11G>A	not provided [RCV003015056]	likely benign	6	109448192	109448192	Human		name
155997777	CV2168830	single nucleotide variant	NM_022765.4(MICAL1):c.3056-10C>T	not provided [RCV003017132]	likely benign	6	109444349	109444349	Human		name
156050241	CV2169073	single nucleotide variant	NM_022765.4(MICAL1):c.1856-18C>A	not provided [RCV003019370]	likely benign	6	109447981	109447981	Human		name
155958505	CV2172899	single nucleotide variant	NM_022765.4(MICAL1):c.2673+13G>A	not provided [RCV003032820]	likely benign	6	109445758	109445758	Human		name
156234860	CV2180664	single nucleotide variant	NM_022765.4(MICAL1):c.1855+15A>G	not provided [RCV003043227]	likely benign	6	109448188	109448188	Human		name
156327815	CV2184533	single nucleotide variant	NM_022765.4(MICAL1):c.3055+15G>A	not provided [RCV003047034]	likely benign	6	109444710	109444710	Human		name
156399512	CV2185914	single nucleotide variant	NM_022765.4(MICAL1):c.1192-16T>C	not provided [RCV003052182]	likely benign	6	109450101	109450101	Human		name
156201239	CV2192186	single nucleotide variant	NM_022765.4(MICAL1):c.1435-11G>A	not provided [RCV003058167]	uncertain significance	6	109449492	109449492	Human		name
405221805	CV2880917	single nucleotide variant	NM_022765.4(MICAL1):c.1986+12C>T	not provided [RCV003554042]	uncertain significance	6	109447669	109447669	Human		name
405156294	CV2890802	single nucleotide variant	NM_022765.4(MICAL1):c.1308-10A>T	not provided [RCV003562075]	likely benign	6	109449793	109449793	Human		name
405091463	CV2937384	single nucleotide variant	NM_022765.4(MICAL1):c.2305-13G>A	not provided [RCV003665266]	likely benign	6	109446425	109446425	Human		name
405112655	CV2939016	single nucleotide variant	NM_022765.4(MICAL1):c.1192-10G>A	not provided [RCV003666510]	likely benign	6	109450095	109450095	Human		name
405088426	CV2943421	single nucleotide variant	NM_022765.4(MICAL1):c.2071-12G>C	not provided [RCV003665116]	likely benign	6	109447241	109447241	Human		name
405213129	CV2971236	single nucleotide variant	NM_022765.4(MICAL1):c.1855+13A>G	not provided [RCV003679670]	likely benign	6	109448190	109448190	Human		name
402507626	CV2979052	single nucleotide variant	NM_022765.4(MICAL1):c.1191+15A>T	not provided [RCV003689218]	likely benign	6	109450285	109450285	Human		name
405248133	CV2984647	single nucleotide variant	NM_022765.4(MICAL1):c.2070+13C>T	not provided [RCV003721020]	likely benign	6	109447344	109447344	Human		name
405001405	CV3005597	single nucleotide variant	NM_022765.4(MICAL1):c.2982-15C>A	not provided [RCV003693214]	likely benign	6	109444813	109444813	Human		name
405134313	CV3018446	single nucleotide variant	NM_022765.4(MICAL1):c.1944+19G>C	not provided [RCV003701969]	likely benign	6	109447856	109447856	Human		name
405102378	CV3119152	single nucleotide variant	NM_022765.4(MICAL1):c.1434+12G>A	not provided [RCV003811603]	likely benign	6	109449645	109449645	Human		name
404981065	CV3120978	single nucleotide variant	NM_022765.4(MICAL1):c.2070+18T>A	not provided [RCV003825970]	likely benign	6	109447339	109447339	Human		name
405151943	CV3123430	single nucleotide variant	NM_022765.4(MICAL1):c.2227+18A>C	not provided [RCV003817663]	likely benign	6	109447055	109447055	Human		name
405117775	CV3130997	single nucleotide variant	NM_022765.4(MICAL1):c.1944+17G>A	not provided [RCV003837053]	uncertain significance	6	109447858	109447858	Human		name
405141136	CV3131217	single nucleotide variant	NM_022765.4(MICAL1):c.2304+16G>A	not provided [RCV003839257]	uncertain significance	6	109446680	109446680	Human		name
405072135	CV3140286	single nucleotide variant	NM_022765.4(MICAL1):c.1944+13G>A	not provided [RCV003833441]	likely benign	6	109447862	109447862	Human		name
405207725	CV3145598	single nucleotide variant	NM_022765.4(MICAL1):c.2304+20A>G	not provided [RCV003845328]	likely benign\|uncertain significance	6	109446676	109446676	Human		name
405050237	CV3150901	single nucleotide variant	NM_022765.4(MICAL1):c.1192-19T>C	not provided [RCV003849505]	likely benign	6	109450104	109450104	Human		name
405052487	CV3151258	single nucleotide variant	NM_022765.4(MICAL1):c.1434+11C>T	not provided [RCV003849667]	likely benign	6	109449646	109449646	Human		name
405238240	CV3167049	single nucleotide variant	NM_022765.4(MICAL1):c.2674-19T>C	not provided [RCV003854304]	likely benign	6	109445548	109445548	Human		name
405234449	CV3168426	single nucleotide variant	NM_022765.4(MICAL1):c.2071-18T>C	not provided [RCV003865900]	likely benign	6	109447247	109447247	Human		name
405226531	CV3169436	single nucleotide variant	NM_022765.4(MICAL1):c.1986+17G>A	not provided [RCV003864460]	likely benign	6	109447664	109447664	Human		name
405255391	CV3172372	single nucleotide variant	NM_022765.4(MICAL1):c.2228-11A>G	not provided [RCV003872310]	likely benign	6	109446783	109446783	Human		name
597916566	CV3737426	single nucleotide variant	NM_022765.4(MICAL1):c.2673+15G>A	not provided [RCV005074215]	likely benign	6	109445756	109445756	Human		name
597916573	CV3737427	single nucleotide variant	NM_022765.4(MICAL1):c.2673+16T>C	not provided [RCV005074216]	likely benign	6	109445755	109445755	Human		name
597921837	CV3738430	single nucleotide variant	NM_022765.4(MICAL1):c.1856-13G>A	not provided [RCV005074837]	likely benign	6	109447976	109447976	Human		name
597866452	CV3742460	single nucleotide variant	NM_022765.4(MICAL1):c.1516+10C>A	not provided [RCV005068076]	likely benign	6	109449390	109449390	Human		name
597939233	CV3775301	single nucleotide variant	NM_022765.4(MICAL1):c.1987-16G>A	not provided [RCV005118127]	likely benign	6	109447456	109447456	Human		name
597926893	CV3783378	single nucleotide variant	NM_022765.4(MICAL1):c.2582-18C>A	not provided [RCV005116065]	likely benign	6	109445880	109445880	Human		name
597973202	CV3820346	single nucleotide variant	NM_022765.4(MICAL1):c.2981+17G>A	not provided [RCV005167863]	likely benign	6	109444879	109444879	Human		name
597968680	CV3821008	duplication	NM_022765.4(MICAL1):c.1192-11dup	not provided [RCV005165849]	likely benign	6	109450095	109450096	Human		name
597837223	CV3828742	single nucleotide variant	NM_022765.4(MICAL1):c.2882-11C>T	not provided [RCV005171435]	likely benign	6	109445006	109445006	Human		name
597832400	CV3831231	single nucleotide variant	NM_022765.4(MICAL1):c.2673+18C>T	not provided [RCV005170433]	likely benign	6	109445753	109445753	Human		name
597975279	CV3832314	single nucleotide variant	NM_022765.4(MICAL1):c.1307+10G>T	not provided [RCV005169051]	likely benign	6	109449960	109449960	Human		name
597970659	CV3832572	single nucleotide variant	NM_022765.4(MICAL1):c.2981+14G>T	not provided [RCV005166651]	likely benign	6	109444882	109444882	Human		name
597893945	CV3833505	single nucleotide variant	NM_022765.4(MICAL1):c.1986+15G>A	not provided [RCV005180197]	likely benign	6	109447666	109447666	Human		name
156067721	CV1927958	microsatellite	NM_022765.4(MICAL1):c.2582-12TCT[2]	not provided [RCV002638499]	likely benign	6	109445866	109445868	Human		name
156175598	CV2000344	deletion	NM_022765.4(MICAL1):c.571+4_571+7del	not provided [RCV002642861]	uncertain significance	6	109453256	109453259	Human		name
597945270	CV3844193	duplication	NM_022765.4(MICAL1):c.1435-15_1447dup	not provided [RCV005188802]	uncertain significance	6	109449468	109449469	Human		name
151840617	CV1342121	insertion	NM_022765.4(MICAL1):c.-43-5_-43-4insGC	not provided [RCV001956705]	uncertain significance	6	109454243	109454244	Human		name
156317486	CV1971253	single nucleotide variant	NM_022765.4(MICAL1):c.51C>T (p.Phe17=)	not provided [RCV002630144]	likely benign	6	109454146	109454146	Human		name
156352186	CV1978536	single nucleotide variant	NM_022765.4(MICAL1):c.5C>T (p.Ala2Val)	not provided [RCV002601905]	uncertain significance	6	109454192	109454192	Human		name
156041534	CV1999044	duplication	NM_022765.4(MICAL1):c.466+11_466+12dup	not provided [RCV002659056]	likely benign\|uncertain significance	6	109453625	109453626	Human		name
156279021	CV2011508	microsatellite	NM_022765.4(MICAL1):c.1664+2_1664+3del	not provided [RCV002715236]	uncertain significance	6	109448729	109448730	Human		name
156230246	CV2019685	single nucleotide variant	NM_022765.4(MICAL1):c.36C>T (p.Ala12=)	not provided [RCV002701332]	uncertain significance	6	109454161	109454161	Human		name
155966703	CV2304787	single nucleotide variant	NM_022765.4(MICAL1):c.8C>T (p.Ser3Leu)	not specified [RCV004166929]	uncertain significance	6	109454189	109454189	Human		name
405177957	CV2912990	deletion	NM_022765.4(MICAL1):c.676+13_676+15del	not provided [RCV003563704]	likely benign	6	109452496	109452498	Human		name
405064159	CV2939862	single nucleotide variant	NM_022765.4(MICAL1):c.54G>A (p.Leu18=)	not provided [RCV003659001]	likely benign	6	109454143	109454143	Human		name
405187515	CV2964211	deletion	NM_022765.4(MICAL1):c.15del (p.Ser6fs)	not provided [RCV003676893]	likely benign	6	109454182	109454182	Human		name
405225026	CV3041981	single nucleotide variant	NM_022765.4(MICAL1):c.79C>T (p.Leu27=)	not provided [RCV003710491]	likely benign	6	109454118	109454118	Human		name
405129998	CV3054593	single nucleotide variant	NM_022765.4(MICAL1):c.84C>T (p.Ser28=)	not provided [RCV003724741]	likely benign	6	109454113	109454113	Human		name
405230266	CV3153850	microsatellite	NM_022765.4(MICAL1):c.572-18_572-17del	not provided [RCV003848717]	likely benign	6	109452632	109452633	Human		name
405247664	CV3159072	single nucleotide variant	NM_022765.4(MICAL1):c.30G>A (p.Ala10=)	not provided [RCV003869217]	likely benign	6	109454167	109454167	Human		name
597952243	CV3795089	single nucleotide variant	NM_022765.4(MICAL1):c.4G>A (p.Ala2Thr)	not provided [RCV005136301]	uncertain significance	6	109454193	109454193	Human		name
151873100	CV1351920	deletion	NM_022765.4(MICAL1):c.85del (p.Ser29fs)	not provided [RCV001998604]	uncertain significance	6	109454112	109454112	Human		name
152078707	CV1579737	single nucleotide variant	NM_022765.4(MICAL1):c.288G>T (p.Gly96=)	not provided [RCV002076081]	benign	6	109453816	109453816	Human		name
152117960	CV1601119	single nucleotide variant	NM_022765.4(MICAL1):c.297C>T (p.Val99=)	not provided [RCV002097754]	likely benign	6	109453807	109453807	Human		name
152081406	CV1645072	single nucleotide variant	NM_022765.4(MICAL1):c.123C>T (p.Pro41=)	not provided [RCV002149359]	benign	6	109454074	109454074	Human		name
152055867	CV1662752	single nucleotide variant	NM_022765.4(MICAL1):c.240G>A (p.Arg80=)	not provided [RCV002146216]	likely benign	6	109453957	109453957	Human		name
156376121	CV1960358	single nucleotide variant	NM_022765.4(MICAL1):c.129G>A (p.Gly43=)	not provided [RCV002582814]	likely benign	6	109454068	109454068	Human		name
156394009	CV1983521	single nucleotide variant	NM_022765.4(MICAL1):c.267G>C (p.Val89=)	not provided [RCV002604950]	likely benign	6	109453837	109453837	Human		name
156350584	CV2005699	single nucleotide variant	NM_022765.4(MICAL1):c.183G>A (p.Lys61=)	not provided [RCV002650852]	likely benign	6	109454014	109454014	Human		name
156301744	CV2013499	single nucleotide variant	NM_022765.4(MICAL1):c.132G>A (p.Gly44=)	not provided [RCV002716093]	likely benign	6	109454065	109454065	Human		name
155981042	CV2025170	single nucleotide variant	NM_022765.4(MICAL1):c.177C>T (p.Ser59=)	not provided [RCV002755327]	likely benign	6	109454020	109454020	Human		name
155954259	CV2143846	single nucleotide variant	NM_022765.4(MICAL1):c.285C>T (p.Cys95=)	not provided [RCV002994805]	likely benign	6	109453819	109453819	Human		name
156037739	CV2150324	microsatellite	NM_022765.4(MICAL1):c.2882-11_2882-8del	not provided [RCV003018937]	likely benign	6	109445003	109445006	Human		name
156230116	CV2156688	single nucleotide variant	NM_022765.4(MICAL1):c.267G>A (p.Val89=)	not provided [RCV003025610]	likely benign	6	109453837	109453837	Human		name
405119313	CV2891478	single nucleotide variant	NM_022765.4(MICAL1):c.138C>G (p.Pro46=)	not provided [RCV003558889]	likely benign	6	109454059	109454059	Human		name
405216705	CV2972145	single nucleotide variant	NM_022765.4(MICAL1):c.225C>A (p.Val75=)	not provided [RCV003680118]	likely benign	6	109453972	109453972	Human		name
405228353	CV2973672	single nucleotide variant	NM_022765.4(MICAL1):c.129G>C (p.Gly43=)	not provided [RCV003681824]	likely benign	6	109454068	109454068	Human		name
402487763	CV2995444	single nucleotide variant	NM_022765.4(MICAL1):c.267G>T (p.Val89=)	not provided [RCV003687234]	likely benign	6	109453837	109453837	Human		name
405204458	CV3033503	single nucleotide variant	NM_022765.4(MICAL1):c.180C>T (p.Ala60=)	not provided [RCV003707823]	likely benign	6	109454017	109454017	Human		name
405205085	CV3117032	single nucleotide variant	NM_022765.4(MICAL1):c.171C>T (p.Tyr57=)	not provided [RCV003822516]	likely benign	6	109454026	109454026	Human		name
405145801	CV3141748	single nucleotide variant	NM_022765.4(MICAL1):c.11C>T (p.Pro4Leu)	not provided [RCV003839670]	uncertain significance	6	109454186	109454186	Human		name
405233894	CV3157981	single nucleotide variant	NM_022765.4(MICAL1):c.108C>T (p.Ala36=)	not provided [RCV003865737]	likely benign	6	109454089	109454089	Human		name
405246464	CV3162243	single nucleotide variant	NM_022765.4(MICAL1):c.279A>G (p.Gly93=)	not provided [RCV003868762]	likely benign	6	109453825	109453825	Human		name
151797757	CV1449461	single nucleotide variant	NM_022765.4(MICAL1):c.71A>G (p.Gln24Arg)	not provided [RCV002011283]\|not specified [RCV004046205]	uncertain significance	6	109454126	109454126	Human		name
151717235	CV1472940	single nucleotide variant	NM_022765.4(MICAL1):c.29C>T (p.Ala10Val)	not provided [RCV002039514]\|not specified [RCV004038860]	uncertain significance	6	109454168	109454168	Human		name
152158909	CV1521774	single nucleotide variant	NM_022765.4(MICAL1):c.870C>T (p.Asp290=)	not provided [RCV002180572]	likely benign	6	109451663	109451663	Human		name
152102036	CV1540295	single nucleotide variant	NM_022765.4(MICAL1):c.417T>C (p.Gly139=)	not provided [RCV002095658]	likely benign	6	109453687	109453687	Human		name
152035430	CV1552947	single nucleotide variant	NM_022765.4(MICAL1):c.564T>C (p.Pro188=)	not provided [RCV002187410]	likely benign	6	109453270	109453270	Human		name
152125763	CV1565652	single nucleotide variant	NM_022765.4(MICAL1):c.609T>C (p.Pro203=)	not provided [RCV002136292]	likely benign	6	109452578	109452578	Human		name
152067991	CV1567009	single nucleotide variant	NM_022765.4(MICAL1):c.930C>T (p.Arg310=)	not provided [RCV002091189]	likely benign	6	109451603	109451603	Human		name
152170523	CV1578158	single nucleotide variant	NM_022765.4(MICAL1):c.804C>T (p.Ser268=)	not provided [RCV002183181]	likely benign	6	109452274	109452274	Human		name
152101440	CV1578890	deletion	NM_022765.4(MICAL1):c.1855+13_1855+17del	not provided [RCV002079047]	benign	6	109448186	109448190	Human		name
152105447	CV1609489	single nucleotide variant	NM_022765.4(MICAL1):c.34G>A (p.Ala12Thr)	not provided [RCV002115877]	benign	6	109454163	109454163	Human		name
156312012	CV1896302	single nucleotide variant	NM_022765.4(MICAL1):c.453C>T (p.Thr151=)	not provided [RCV003088505]	likely benign	6	109453651	109453651	Human		name
156296584	CV1904798	single nucleotide variant	NM_022765.4(MICAL1):c.867C>T (p.Asp289=)	not provided [RCV002598975]	likely benign	6	109451666	109451666	Human		name
156306679	CV1912606	single nucleotide variant	NM_022765.4(MICAL1):c.316C>T (p.Leu106=)	not provided [RCV002599434]	likely benign	6	109453788	109453788	Human		name
156102666	CV1916996	single nucleotide variant	NM_022765.4(MICAL1):c.432C>T (p.Tyr144=)	not provided [RCV002592334]	likely benign	6	109453672	109453672	Human		name
156449561	CV1941818	single nucleotide variant	NM_022765.4(MICAL1):c.540T>C (p.Thr180=)	not provided [RCV003121685]	likely benign	6	109453294	109453294	Human		name
156437609	CV1947618	single nucleotide variant	NM_022765.4(MICAL1):c.399C>T (p.His133=)	not provided [RCV003107149]	likely benign	6	109453705	109453705	Human		name
156172303	CV1956342	single nucleotide variant	NM_022765.4(MICAL1):c.447C>T (p.Thr149=)	not provided [RCV002573848]	likely benign	6	109453657	109453657	Human		name
156133601	CV1962818	single nucleotide variant	NM_022765.4(MICAL1):c.393C>T (p.Thr131=)	not provided [RCV002572318]	likely benign	6	109453711	109453711	Human		name
156221344	CV1965383	single nucleotide variant	NM_022765.4(MICAL1):c.414C>T (p.Leu138=)	not provided [RCV002596472]	likely benign	6	109453690	109453690	Human		name
156416527	CV1976663	single nucleotide variant	NM_022765.4(MICAL1):c.636C>T (p.Asp212=)	not provided [RCV002589740]	likely benign	6	109452551	109452551	Human		name
156092567	CV1984167	single nucleotide variant	NM_022765.4(MICAL1):c.792C>T (p.Ile264=)	not provided [RCV002621912]	likely benign	6	109452286	109452286	Human		name
156393488	CV1988066	single nucleotide variant	NM_022765.4(MICAL1):c.300T>C (p.Ala100=)	not provided [RCV002635218]	likely benign	6	109453804	109453804	Human		name
156007374	CV1989430	single nucleotide variant	NM_022765.4(MICAL1):c.76G>A (p.Val26Met)	not provided [RCV002636046]	uncertain significance	6	109454121	109454121	Human		name
156086943	CV1989470	single nucleotide variant	NM_022765.4(MICAL1):c.73G>A (p.Asp25Asn)	not provided [RCV002639086]	uncertain significance	6	109454124	109454124	Human		name
156183926	CV2020595	single nucleotide variant	NM_022765.4(MICAL1):c.39C>G (p.His13Gln)	not provided [RCV002710868]\|not specified [RCV004827900]	uncertain significance	6	109454158	109454158	Human		name
156022191	CV2025478	single nucleotide variant	NM_022765.4(MICAL1):c.83G>T (p.Ser28Ile)	not provided [RCV002735428]	uncertain significance	6	109454114	109454114	Human		name
156200024	CV2034679	single nucleotide variant	NM_022765.4(MICAL1):c.981C>T (p.Pro327=)	not provided [RCV002766200]	likely benign	6	109450510	109450510	Human		name
156017282	CV2035370	single nucleotide variant	NM_022765.4(MICAL1):c.774C>T (p.Ile258=)	not provided [RCV002780473]	likely benign	6	109452304	109452304	Human		name
155911439	CV2037684	single nucleotide variant	NM_022765.4(MICAL1):c.768G>A (p.Pro256=)	not provided [RCV002771614]	likely benign	6	109452310	109452310	Human		name
156292043	CV2047278	single nucleotide variant	NM_022765.4(MICAL1):c.312G>A (p.Ala104=)	not provided [RCV002770813]	benign	6	109453792	109453792	Human		name
156378796	CV2050722	single nucleotide variant	NM_022765.4(MICAL1):c.952C>A (p.Arg318=)	not provided [RCV002814922]	likely benign	6	109450539	109450539	Human		name
156019230	CV2081305	single nucleotide variant	NM_022765.4(MICAL1):c.306G>A (p.Glu102=)	not provided [RCV002866520]	likely benign	6	109453798	109453798	Human		name
155954339	CV2086861	single nucleotide variant	NM_022765.4(MICAL1):c.484C>T (p.Leu162=)	not provided [RCV002862518]	likely benign	6	109453350	109453350	Human		name
156134015	CV2113190	single nucleotide variant	NM_022765.4(MICAL1):c.864G>A (p.Lys288=)	not provided [RCV002928310]	benign	6	109451669	109451669	Human		name
156324746	CV2134433	single nucleotide variant	NM_022765.4(MICAL1):c.444C>T (p.Cys148=)	not provided [RCV002963448]	likely benign	6	109453660	109453660	Human		name
156177825	CV2144887	single nucleotide variant	NM_022765.4(MICAL1):c.792C>A (p.Ile264=)	not provided [RCV003005610]	likely benign	6	109452286	109452286	Human		name
155911798	CV2153299	single nucleotide variant	NM_022765.4(MICAL1):c.909G>T (p.Leu303=)	not provided [RCV003012311]	likely benign	6	109451624	109451624	Human		name
156130012	CV2158717	single nucleotide variant	NM_022765.4(MICAL1):c.76G>C (p.Val26Leu)	not provided [RCV003022140]	uncertain significance	6	109454121	109454121	Human		name
156377586	CV2189189	single nucleotide variant	NM_022765.4(MICAL1):c.336G>A (p.Leu112=)	not provided [RCV003050238]	likely benign	6	109453768	109453768	Human		name
156370314	CV2263517	single nucleotide variant	NM_022765.4(MICAL1):c.33T>G (p.His11Gln)	not specified [RCV004133749]	uncertain significance	6	109454164	109454164	Human		name
405182599	CV2909530	single nucleotide variant	NM_022765.4(MICAL1):c.807C>T (p.Phe269=)	not provided [RCV003564055]	likely benign	6	109452271	109452271	Human		name
405014221	CV2930349	single nucleotide variant	NM_022765.4(MICAL1):c.61C>T (p.Gln21Ter)	not provided [RCV003576998]	likely benign	6	109454136	109454136	Human		name
402484605	CV2931445	single nucleotide variant	NM_022765.4(MICAL1):c.441C>T (p.Phe147=)	not provided [RCV003572409]	likely benign	6	109453663	109453663	Human		name
405229003	CV2973849	single nucleotide variant	NM_022765.4(MICAL1):c.558C>A (p.Pro186=)	not provided [RCV003681931]	likely benign	6	109453276	109453276	Human		name
404977959	CV3015274	single nucleotide variant	NM_022765.4(MICAL1):c.435G>A (p.Gly145=)	not provided [RCV003690626]	likely benign	6	109453669	109453669	Human		name
405145920	CV3052261	single nucleotide variant	NM_022765.4(MICAL1):c.672T>C (p.Pro224=)	not provided [RCV003725978]	likely benign	6	109452515	109452515	Human		name
405135097	CV3115580	single nucleotide variant	NM_022765.4(MICAL1):c.333G>A (p.Val111=)	not provided [RCV003816237]	likely benign	6	109453771	109453771	Human		name
405186389	CV3124367	single nucleotide variant	NM_022765.4(MICAL1):c.57G>T (p.Gln19His)	not provided [RCV003820566]	uncertain significance	6	109454140	109454140	Human		name
405214782	CV3124493	duplication	NM_022765.4(MICAL1):c.132dup (p.Leu45fs)	not provided [RCV003823855]	likely benign	6	109454064	109454065	Human		name
405142172	CV3131311	single nucleotide variant	NM_022765.4(MICAL1):c.300T>A (p.Ala100=)	not provided [RCV003839351]	likely benign	6	109453804	109453804	Human		name
405110335	CV3133130	single nucleotide variant	NM_022765.4(MICAL1):c.618G>A (p.Leu206=)	not provided [RCV003836116]	likely benign	6	109452569	109452569	Human		name
405229879	CV3153583	single nucleotide variant	NM_022765.4(MICAL1):c.495G>A (p.Leu165=)	not provided [RCV003848648]	likely benign	6	109453339	109453339	Human		name
405222041	CV3154813	single nucleotide variant	NM_022765.4(MICAL1):c.882T>C (p.Phe294=)	not provided [RCV003847308]	likely benign	6	109451651	109451651	Human		name
405190187	CV3156975	single nucleotide variant	NM_022765.4(MICAL1):c.855G>A (p.Val285=)	not provided [RCV003859663]	likely benign	6	109451678	109451678	Human		name
402467766	CV3174171	single nucleotide variant	NM_022765.4(MICAL1):c.678C>A (p.Gly226=)	not provided [RCV003873454]	likely benign	6	109452400	109452400	Human		name
405250399	CV3180728	single nucleotide variant	NM_022765.4(MICAL1):c.723A>G (p.Thr241=)	not provided [RCV003870005]	likely benign	6	109452355	109452355	Human		name
597853366	CV3737737	single nucleotide variant	NM_022765.4(MICAL1):c.381C>T (p.Leu127=)	not provided [RCV005066510]	likely benign	6	109453723	109453723	Human		name
597906066	CV3738717	single nucleotide variant	NM_022765.4(MICAL1):c.369C>T (p.Asn123=)	not provided [RCV005072951]	likely benign	6	109453735	109453735	Human		name
597830555	CV3743092	single nucleotide variant	NM_022765.4(MICAL1):c.597A>G (p.Gln199=)	not provided [RCV005062100]	likely benign	6	109452590	109452590	Human		name
597897210	CV3782263	single nucleotide variant	NM_022765.4(MICAL1):c.501A>G (p.Val167=)	not provided [RCV005126488]	likely benign	6	109453333	109453333	Human		name
597943231	CV3786403	single nucleotide variant	NM_022765.4(MICAL1):c.492G>A (p.Leu164=)	not provided [RCV005134094]	likely benign	6	109453342	109453342	Human		name
597946290	CV3807479	single nucleotide variant	NM_022765.4(MICAL1):c.876C>T (p.His292=)	not provided [RCV005160114]	likely benign	6	109451657	109451657	Human		name
597974035	CV3821049	single nucleotide variant	NM_022765.4(MICAL1):c.975G>A (p.Val325=)	not provided [RCV005168370]	likely benign	6	109450516	109450516	Human		name
597975832	CV3832790	single nucleotide variant	NM_022765.4(MICAL1):c.621C>T (p.Ala207=)	not provided [RCV005169349]	likely benign	6	109452566	109452566	Human		name
15117185	CV710111	single nucleotide variant	NM_022765.4(MICAL1):c.648G>A (p.Ser216=)	not provided [RCV000962160]	benign	6	109452539	109452539	Human		name
15166649	CV721640	single nucleotide variant	NM_022765.4(MICAL1):c.747C>T (p.Thr249=)	not provided [RCV000882676]	benign	6	109452331	109452331	Human		name
15161113	CV735329	single nucleotide variant	NM_022765.4(MICAL1):c.56A>T (p.Gln19Leu)	not provided [RCV000903282]	likely benign	6	109454141	109454141	Human		name
151765887	CV1418784	single nucleotide variant	NM_022765.4(MICAL1):c.169T>C (p.Tyr57His)	not provided [RCV001929044]\|not specified [RCV004044207]	uncertain significance	6	109454028	109454028	Human		name
151886112	CV1435448	insertion	NM_022765.4(MICAL1):c.-43-2_-43-1insCCTCT	not provided [RCV001962693]	uncertain significance	6	109454240	109454241	Human		name
151833308	CV1478935	single nucleotide variant	NM_022765.4(MICAL1):c.2475G>A (p.Pro825=)	not provided [RCV002050938]	likely benign\|uncertain significance	6	109446242	109446242	Human		name
152053709	CV1523763	single nucleotide variant	NM_022765.4(MICAL1):c.1425C>T (p.Thr475=)	not provided [RCV002127528]	benign	6	109449666	109449666	Human		name
152136618	CV1528501	single nucleotide variant	NM_022765.4(MICAL1):c.1539G>A (p.Glu513=)	not provided [RCV002100203]	likely benign	6	109448857	109448857	Human		name
152116759	CV1541031	single nucleotide variant	NM_022765.4(MICAL1):c.2058C>G (p.Ser686=)	not provided [RCV002197495]	likely benign	6	109447369	109447369	Human		name
152063130	CV1542243	single nucleotide variant	NM_022765.4(MICAL1):c.245G>A (p.Cys82Tyr)	not provided [RCV002208943]	likely benign	6	109453952	109453952	Human		name
152098060	CV1542363	single nucleotide variant	NM_022765.4(MICAL1):c.1782G>C (p.Gly594=)	not provided [RCV002195181]	benign	6	109448276	109448276	Human		name
152080150	CV1546466	single nucleotide variant	NM_022765.4(MICAL1):c.2208C>T (p.Tyr736=)	not provided [RCV002130722]	benign	6	109447092	109447092	Human		name
152166031	CV1557218	single nucleotide variant	NM_022765.4(MICAL1):c.1095C>T (p.Asp365=)	not provided [RCV002181854]	likely benign	6	109450396	109450396	Human		name
152093587	CV1561630	single nucleotide variant	NM_022765.4(MICAL1):c.2508C>T (p.Ser836=)	not provided [RCV002194614]	likely benign	6	109446209	109446209	Human		name
152088249	CV1562894	single nucleotide variant	NM_022765.4(MICAL1):c.2898A>G (p.Gln966=)	not provided [RCV002113713]	likely benign	6	109444979	109444979	Human		name
152124856	CV1565439	single nucleotide variant	NM_022765.4(MICAL1):c.1188G>A (p.Val396=)	not provided [RCV002136185]	likely benign	6	109450303	109450303	Human		name
152093265	CV1570467	single nucleotide variant	NM_022765.4(MICAL1):c.251G>T (p.Ser84Ile)	not provided [RCV002213021]	benign	6	109453946	109453946	Human		name
152111054	CV1581906	single nucleotide variant	NM_022765.4(MICAL1):c.1029T>C (p.His343=)	not provided [RCV002096853]	likely benign	6	109450462	109450462	Human		name
152111179	CV1582258	single nucleotide variant	NM_022765.4(MICAL1):c.2514C>T (p.Ser838=)	not provided [RCV002080270]	likely benign	6	109446203	109446203	Human		name
152097006	CV1587013	single nucleotide variant	NM_022765.4(MICAL1):c.1086T>C (p.Ser362=)	not provided [RCV002078485]	likely benign	6	109450405	109450405	Human		name
152114999	CV1623142	single nucleotide variant	NM_022765.4(MICAL1):c.2574C>T (p.Ser858=)	not provided [RCV002174814]	likely benign	6	109446143	109446143	Human		name
152038854	CV1643820	single nucleotide variant	NM_022765.4(MICAL1):c.2376C>T (p.Ala792=)	not provided [RCV002125780]	likely benign	6	109446341	109446341	Human		name
152066081	CV1646957	single nucleotide variant	NM_022765.4(MICAL1):c.1599G>A (p.Leu533=)	Epilepsy, familial temporal lobe, 1 [RCV002500265]\|not provided [RCV002128995]	benign\|likely benign	6	109448797	109448797	Human	1	name
152146039	CV1658459	single nucleotide variant	NM_022765.4(MICAL1):c.2139C>T (p.Asn713=)	not provided [RCV002220060]	likely benign	6	109447161	109447161	Human		name
156393486	CV1876155	single nucleotide variant	NM_022765.4(MICAL1):c.2433G>A (p.Pro811=)	not provided [RCV003068300]	likely benign	6	109446284	109446284	Human		name
156225250	CV1896321	single nucleotide variant	NM_022765.4(MICAL1):c.1839C>T (p.Ser613=)	not provided [RCV003085149]	likely benign	6	109448219	109448219	Human		name
156028255	CV1906917	single nucleotide variant	NM_022765.4(MICAL1):c.1374T>C (p.Tyr458=)	not provided [RCV003100528]	likely benign	6	109449717	109449717	Human		name
156084306	CV1909141	single nucleotide variant	NM_022765.4(MICAL1):c.1605C>T (p.Ser535=)	not provided [RCV002591682]	likely benign	6	109448791	109448791	Human		name
156015279	CV1912742	single nucleotide variant	NM_022765.4(MICAL1):c.1521G>A (p.Ser507=)	not provided [RCV002619113]	likely benign	6	109448875	109448875	Human		name
156016169	CV1912822	single nucleotide variant	NM_022765.4(MICAL1):c.2967C>T (p.Ala989=)	not provided [RCV002619156]	likely benign	6	109444910	109444910	Human		name
156418218	CV1914581	single nucleotide variant	NM_022765.4(MICAL1):c.292C>T (p.Arg98Trp)	not provided [RCV002611397]	uncertain significance	6	109453812	109453812	Human		name
156418263	CV1914641	single nucleotide variant	NM_022765.4(MICAL1):c.1278C>T (p.Gly426=)	not provided [RCV002611442]	likely benign	6	109449999	109449999	Human		name
155935090	CV1916344	single nucleotide variant	NM_022765.4(MICAL1):c.2433G>T (p.Pro811=)	not provided [RCV002615245]	likely benign	6	109446284	109446284	Human		name
155937344	CV1917146	single nucleotide variant	NM_022765.4(MICAL1):c.2086C>T (p.Leu696=)	not provided [RCV002615400]	likely benign	6	109447214	109447214	Human		name
156376809	CV1917749	single nucleotide variant	NM_022765.4(MICAL1):c.1597T>C (p.Leu533=)	not provided [RCV002603650]	likely benign	6	109448799	109448799	Human		name
156437182	CV1937011	single nucleotide variant	NM_022765.4(MICAL1):c.248C>G (p.Thr83Ser)	not provided [RCV003106713]	uncertain significance	6	109453949	109453949	Human		name
156435660	CV1940864	single nucleotide variant	NM_022765.4(MICAL1):c.268G>A (p.Val90Met)	not provided [RCV003104967]	uncertain significance	6	109453836	109453836	Human		name
156444924	CV1948973	single nucleotide variant	NM_022765.4(MICAL1):c.2064C>T (p.His688=)	not provided [RCV003115858]	likely benign	6	109447363	109447363	Human		name
156105852	CV1953640	single nucleotide variant	NM_022765.4(MICAL1):c.2304G>A (p.Pro768=)	not provided [RCV002571016]	uncertain significance	6	109446696	109446696	Human		name
156329290	CV1957424	single nucleotide variant	NM_022765.4(MICAL1):c.1635C>T (p.Ala545=)	not provided [RCV002579904]	likely benign	6	109448761	109448761	Human		name
156408273	CV1957787	single nucleotide variant	NM_022765.4(MICAL1):c.2082G>A (p.Gly694=)	not provided [RCV002586472]	likely benign	6	109447218	109447218	Human		name
156343769	CV1958041	single nucleotide variant	NM_022765.4(MICAL1):c.2025C>T (p.Asp675=)	not provided [RCV002580652]	likely benign	6	109447402	109447402	Human		name
156167752	CV1959979	single nucleotide variant	NM_022765.4(MICAL1):c.2253G>T (p.Leu751=)	not provided [RCV002573720]	likely benign	6	109446747	109446747	Human		name
156384724	CV1961134	single nucleotide variant	NM_022765.4(MICAL1):c.127G>C (p.Gly43Arg)	not provided [RCV002583404]\|not specified [RCV004064455]	uncertain significance	6	109454070	109454070	Human		name
156288035	CV1964732	single nucleotide variant	NM_022765.4(MICAL1):c.239G>A (p.Arg80Gln)	not provided [RCV002577717]	uncertain significance	6	109453958	109453958	Human		name
156414996	CV1964867	single nucleotide variant	NM_022765.4(MICAL1):c.1608C>T (p.Ser536=)	not provided [RCV002588920]	likely benign	6	109448788	109448788	Human		name
156333204	CV1966661	single nucleotide variant	NM_022765.4(MICAL1):c.1896A>G (p.Val632=)	not provided [RCV002600905]	likely benign	6	109447923	109447923	Human		name
156253067	CV1967293	single nucleotide variant	NM_022765.4(MICAL1):c.1101G>T (p.Thr367=)	not provided [RCV002597534]	likely benign	6	109450390	109450390	Human		name
156145096	CV1973788	single nucleotide variant	NM_022765.4(MICAL1):c.1038C>T (p.Leu346=)	not provided [RCV002593961]	likely benign	6	109450453	109450453	Human		name
156383352	CV1975360	single nucleotide variant	NM_022765.4(MICAL1):c.281C>T (p.Pro94Leu)	not provided [RCV002604123]\|not specified [RCV004641987]	uncertain significance	6	109453823	109453823	Human		name
156078228	CV1975570	single nucleotide variant	NM_022765.4(MICAL1):c.2283C>T (p.Ser761=)	not provided [RCV002621458]	likely benign	6	109446717	109446717	Human		name
156416710	CV1976781	single nucleotide variant	NM_022765.4(MICAL1):c.226T>A (p.Tyr76Asn)	not provided [RCV002589832]	likely benign	6	109453971	109453971	Human		name
156132960	CV1977126	duplication	NM_022765.4(MICAL1):c.454dup (p.Leu152fs)	not provided [RCV002593562]	uncertain significance	6	109453649	109453650	Human		name
156162086	CV1977845	single nucleotide variant	NM_022765.4(MICAL1):c.1167A>G (p.Gly389=)	not provided [RCV002594501]	likely benign	6	109450324	109450324	Human		name
156007227	CV1981222	single nucleotide variant	NM_022765.4(MICAL1):c.2835A>G (p.Leu945=)	not provided [RCV002618725]	likely benign	6	109445243	109445243	Human		name
156400674	CV1982280	single nucleotide variant	NM_022765.4(MICAL1):c.2454C>T (p.Ser818=)	not provided [RCV002635938]	likely benign	6	109446263	109446263	Human		name
155906857	CV1983260	single nucleotide variant	NM_022765.4(MICAL1):c.2280C>G (p.Gly760=)	not provided [RCV002613724]	likely benign	6	109446720	109446720	Human		name
156393149	CV1983360	single nucleotide variant	NM_022765.4(MICAL1):c.1518G>A (p.Gly506=)	not provided [RCV002604862]	likely benign	6	109448878	109448878	Human		name
156112437	CV1988857	single nucleotide variant	NM_022765.4(MICAL1):c.212C>T (p.Ala71Val)	not provided [RCV002622632]	uncertain significance	6	109453985	109453985	Human		name
156009248	CV1991525	single nucleotide variant	NM_022765.4(MICAL1):c.2973C>T (p.Leu991=)	not provided [RCV002618818]	likely benign	6	109444904	109444904	Human		name
156237942	CV1992424	single nucleotide variant	NM_022765.4(MICAL1):c.1752G>A (p.Pro584=)	not provided [RCV002627034]	likely benign	6	109448306	109448306	Human		name
156196294	CV1994935	single nucleotide variant	NM_022765.4(MICAL1):c.2847C>T (p.Gly949=)	not provided [RCV002643477]	likely benign	6	109445231	109445231	Human		name
156216426	CV1995431	single nucleotide variant	NM_022765.4(MICAL1):c.256A>G (p.Lys86Glu)	not provided [RCV002667050]	uncertain significance	6	109453941	109453941	Human		name
156110150	CV2002263	single nucleotide variant	NM_022765.4(MICAL1):c.2151C>T (p.Phe717=)	not provided [RCV002639906]	likely benign	6	109447149	109447149	Human		name
156228841	CV2002295	single nucleotide variant	NM_022765.4(MICAL1):c.124G>A (p.Gly42Ser)	not provided [RCV002667499]	uncertain significance	6	109454073	109454073	Human		name
156143625	CV2002874	single nucleotide variant	NM_022765.4(MICAL1):c.120A>T (p.Glu40Asp)	not provided [RCV002663658]	uncertain significance	6	109454077	109454077	Human		name
156269290	CV2004022	single nucleotide variant	NM_022765.4(MICAL1):c.2601G>A (p.Lys867=)	not provided [RCV002646478]	likely benign	6	109445843	109445843	Human		name
156406050	CV2004580	single nucleotide variant	NM_022765.4(MICAL1):c.1209C>A (p.Gly403=)	not provided [RCV002658459]	likely benign	6	109450068	109450068	Human		name
156360294	CV2006984	single nucleotide variant	NM_022765.4(MICAL1):c.209G>A (p.Arg70Gln)	not provided [RCV002676202]\|not specified [RCV004827899]	uncertain significance	6	109453988	109453988	Human		name
156060264	CV2008225	single nucleotide variant	NM_022765.4(MICAL1):c.1173G>A (p.Val391=)	not provided [RCV002705360]	uncertain significance	6	109450318	109450318	Human		name
156352587	CV2015424	single nucleotide variant	NM_022765.4(MICAL1):c.2073C>T (p.Ala691=)	not provided [RCV002720293]	likely benign	6	109447227	109447227	Human		name
156394053	CV2019455	single nucleotide variant	NM_022765.4(MICAL1):c.1788C>T (p.Asp596=)	not provided [RCV002725353]	likely benign	6	109448270	109448270	Human		name
155967957	CV2034424	single nucleotide variant	NM_022765.4(MICAL1):c.1617T>C (p.Asp539=)	not provided [RCV002731485]	likely benign	6	109448779	109448779	Human		name
155910054	CV2041117	single nucleotide variant	NM_022765.4(MICAL1):c.1587C>T (p.His529=)	not provided [RCV002771514]	likely benign	6	109448809	109448809	Human		name
156253704	CV2041171	single nucleotide variant	NM_022765.4(MICAL1):c.1485C>T (p.Asn495=)	not provided [RCV002806096]	likely benign	6	109449431	109449431	Human		name
156139462	CV2044403	single nucleotide variant	NM_022765.4(MICAL1):c.1068T>C (p.His356=)	not provided [RCV002800897]	likely benign	6	109450423	109450423	Human		name
156156391	CV2049320	single nucleotide variant	NM_022765.4(MICAL1):c.2496G>A (p.Lys832=)	not provided [RCV002801469]	likely benign	6	109446221	109446221	Human		name
156248615	CV2049581	single nucleotide variant	NM_022765.4(MICAL1):c.207G>T (p.Lys69Asn)	not provided [RCV002791613]	uncertain significance	6	109453990	109453990	Human		name
156210459	CV2074207	single nucleotide variant	NM_022765.4(MICAL1):c.2760G>A (p.Glu920=)	not provided [RCV002829277]	likely benign	6	109445443	109445443	Human		name
156018410	CV2079954	single nucleotide variant	NM_022765.4(MICAL1):c.2022T>G (p.Pro674=)	not provided [RCV002866479]	likely benign	6	109447405	109447405	Human		name
155968660	CV2082931	single nucleotide variant	NM_022765.4(MICAL1):c.1717C>T (p.Leu573=)	not provided [RCV002881379]	likely benign	6	109448341	109448341	Human		name
156056022	CV2089859	single nucleotide variant	NM_022765.4(MICAL1):c.235G>C (p.Gly79Arg)	not provided [RCV002867941]	uncertain significance	6	109453962	109453962	Human		name
156271554	CV2093760	single nucleotide variant	NM_022765.4(MICAL1):c.1645C>A (p.Arg549=)	not provided [RCV002877622]	likely benign	6	109448751	109448751	Human		name
156091989	CV2102716	single nucleotide variant	NM_022765.4(MICAL1):c.1288C>T (p.Leu430=)	not provided [RCV002913073]	likely benign	6	109449989	109449989	Human		name
156019233	CV2110867	single nucleotide variant	NM_022765.4(MICAL1):c.1101G>A (p.Thr367=)	not provided [RCV002909530]	likely benign	6	109450390	109450390	Human		name
156144327	CV2113353	single nucleotide variant	NM_022765.4(MICAL1):c.1629G>A (p.Leu543=)	not provided [RCV002915023]	likely benign	6	109448767	109448767	Human		name
156351921	CV2118656	single nucleotide variant	NM_022765.4(MICAL1):c.2286T>C (p.Asp762=)	not provided [RCV002966362]	likely benign	6	109446714	109446714	Human		name
155993543	CV2125982	single nucleotide variant	NM_022765.4(MICAL1):c.286G>A (p.Gly96Arg)	not provided [RCV002974843]	likely benign	6	109453818	109453818	Human		name
156385414	CV2128398	single nucleotide variant	NM_022765.4(MICAL1):c.209G>C (p.Arg70Pro)	not provided [RCV002943449]\|not specified [RCV004068016]	uncertain significance	6	109453988	109453988	Human		name
156138021	CV2129183	single nucleotide variant	NM_022765.4(MICAL1):c.1897T>C (p.Leu633=)	not provided [RCV002954122]	likely benign	6	109447922	109447922	Human		name
155961917	CV2131927	single nucleotide variant	NM_022765.4(MICAL1):c.1995C>T (p.Ala665=)	not provided [RCV002995198]	likely benign	6	109447432	109447432	Human		name
156033760	CV2132772	single nucleotide variant	NM_022765.4(MICAL1):c.1149C>T (p.Gly383=)	not provided [RCV002999250]	likely benign	6	109450342	109450342	Human		name
156030076	CV2135422	duplication	NM_001286613.2(MICAL1):c.11dup (p.Ser5fs)	not provided [RCV002999104]	uncertain significance	6	109465666	109465667	Human		name
156024049	CV2137647	single nucleotide variant	NM_022765.4(MICAL1):c.293G>A (p.Arg98Gln)	not provided [RCV002976296]\|not specified [RCV004065053]	uncertain significance	6	109453811	109453811	Human		name
155976889	CV2146607	single nucleotide variant	NM_022765.4(MICAL1):c.1869G>A (p.Gln623=)	not provided [RCV003016193]	likely benign	6	109447950	109447950	Human		name
155916951	CV2152307	single nucleotide variant	NM_022765.4(MICAL1):c.1041G>A (p.Gly347=)	not provided [RCV002991706]	likely benign	6	109450450	109450450	Human		name
156295507	CV2153076	single nucleotide variant	NM_022765.4(MICAL1):c.1245T>C (p.Asp415=)	not provided [RCV003010145]	likely benign	6	109450032	109450032	Human		name
156315112	CV2165039	single nucleotide variant	NM_022765.4(MICAL1):c.1302T>C (p.Ala434=)	not provided [RCV003046254]	likely benign	6	109449975	109449975	Human		name
156220645	CV2168281	single nucleotide variant	NM_022765.4(MICAL1):c.1116A>G (p.Ala372=)	not provided [RCV003042706]	likely benign	6	109450375	109450375	Human		name
156190118	CV2175142	single nucleotide variant	NM_022765.4(MICAL1):c.2313C>A (p.Pro771=)	not provided [RCV003057805]	likely benign	6	109446404	109446404	Human		name
156237205	CV2176865	single nucleotide variant	NM_022765.4(MICAL1):c.2109C>T (p.His703=)	not provided [RCV003043311]	likely benign	6	109447191	109447191	Human		name
156147902	CV2188489	single nucleotide variant	NM_022765.4(MICAL1):c.2016G>A (p.Val672=)	not provided [RCV003056426]	likely benign	6	109447411	109447411	Human		name
156372891	CV2204644	single nucleotide variant	NM_022765.4(MICAL1):c.174G>T (p.Trp58Cys)	not specified [RCV004081749]	uncertain significance	6	109454023	109454023	Human		name
155907133	CV2302156	single nucleotide variant	NM_022765.4(MICAL1):c.242C>T (p.Ala81Val)	not specified [RCV004159167]	uncertain significance	6	109453955	109453955	Human		name
401920839	CV2820615	single nucleotide variant	NM_022765.4(MICAL1):c.1578G>A (p.Pro526=)	not provided [RCV003431988]	likely benign	6	109448818	109448818	Human		name
402481439	CV2864222	single nucleotide variant	NM_022765.4(MICAL1):c.1572G>A (p.Gly524=)	not provided [RCV003544073]	likely benign	6	109448824	109448824	Human		name
402524038	CV2868233	single nucleotide variant	NM_022765.4(MICAL1):c.2529C>T (p.His843=)	not provided [RCV003547954]	likely benign	6	109446188	109446188	Human		name
405208802	CV2870504	single nucleotide variant	NM_022765.4(MICAL1):c.1521G>T (p.Ser507=)	not provided [RCV003552231]	uncertain significance	6	109448875	109448875	Human		name
405221783	CV2880903	single nucleotide variant	NM_022765.4(MICAL1):c.1629G>C (p.Leu543=)	not provided [RCV003554039]	likely benign	6	109448767	109448767	Human		name
405237184	CV2881070	single nucleotide variant	NM_022765.4(MICAL1):c.128G>C (p.Gly43Ala)	not provided [RCV003556627]	uncertain significance	6	109454069	109454069	Human		name
405222944	CV2891207	single nucleotide variant	NM_022765.4(MICAL1):c.251G>A (p.Ser84Asn)	not provided [RCV003554201]	uncertain significance	6	109453946	109453946	Human		name
405171438	CV2911982	single nucleotide variant	NM_022765.4(MICAL1):c.1470T>C (p.Pro490=)	not provided [RCV003563086]	likely benign	6	109449446	109449446	Human		name
402474846	CV2915970	duplication	NM_022765.4(MICAL1):c.322dup (p.Ala108fs)	not provided [RCV003571250]	uncertain significance	6	109453781	109453782	Human		name
405126536	CV2939536	single nucleotide variant	NM_022765.4(MICAL1):c.2358A>G (p.Thr786=)	not provided [RCV003672009]	uncertain significance	6	109446359	109446359	Human		name
405123672	CV2942593	single nucleotide variant	NM_022765.4(MICAL1):c.2040A>G (p.Val680=)	not provided [RCV003671742]	likely benign	6	109447387	109447387	Human		name
405128341	CV2954890	single nucleotide variant	NM_022765.4(MICAL1):c.1158G>A (p.Leu386=)	not provided [RCV003668147]	likely benign	6	109450333	109450333	Human		name
405132033	CV2959169	single nucleotide variant	NM_022765.4(MICAL1):c.2397C>T (p.Ser799=)	not provided [RCV003668465]	likely benign	6	109446320	109446320	Human		name
405164747	CV2960605	single nucleotide variant	NM_022765.4(MICAL1):c.239G>C (p.Arg80Pro)	not provided [RCV003674893]	uncertain significance	6	109453958	109453958	Human		name
405214737	CV2971469	single nucleotide variant	NM_022765.4(MICAL1):c.1002C>A (p.Thr334=)	not provided [RCV003679818]	likely benign	6	109450489	109450489	Human		name
404982336	CV2979229	single nucleotide variant	NM_022765.4(MICAL1):c.181A>G (p.Lys61Glu)	not provided [RCV003691427]	uncertain significance	6	109454016	109454016	Human		name
402492408	CV2981244	single nucleotide variant	NM_022765.4(MICAL1):c.1212T>G (p.Thr404=)	not provided [RCV003713904]	likely benign	6	109450065	109450065	Human		name
404984350	CV2986835	single nucleotide variant	NM_022765.4(MICAL1):c.2298G>A (p.Glu766=)	not provided [RCV003691647]	likely benign	6	109446702	109446702	Human		name
405230393	CV2987437	single nucleotide variant	NM_022765.4(MICAL1):c.2718C>T (p.Tyr906=)	not provided [RCV003711420]	likely benign	6	109445485	109445485	Human		name
402520508	CV3000354	single nucleotide variant	NM_022765.4(MICAL1):c.177C>G (p.Ser59Arg)	not provided [RCV003716392]	uncertain significance	6	109454020	109454020	Human		name
402494579	CV3004935	single nucleotide variant	NM_022765.4(MICAL1):c.2803C>T (p.Leu935=)	not provided [RCV003687877]	likely benign	6	109445275	109445275	Human		name
405032083	CV3012737	single nucleotide variant	NM_022765.4(MICAL1):c.185C>A (p.Ser62Ter)	not provided [RCV003695546]	uncertain significance	6	109454012	109454012	Human		name
405053823	CV3022385	single nucleotide variant	NM_022765.4(MICAL1):c.2451C>T (p.Ser817=)	not provided [RCV003697196]	likely benign	6	109446266	109446266	Human		name
405184776	CV3040289	single nucleotide variant	NM_022765.4(MICAL1):c.2121G>A (p.Leu707=)	not provided [RCV003705910]	uncertain significance	6	109447179	109447179	Human		name
405093801	CV3045615	single nucleotide variant	NM_022765.4(MICAL1):c.2364G>A (p.Ser788=)	not provided [RCV003718011]	uncertain significance	6	109446353	109446353	Human		name
405131729	CV3050978	single nucleotide variant	NM_022765.4(MICAL1):c.1218G>T (p.Val406=)	not provided [RCV003724772]	likely benign	6	109450059	109450059	Human		name
405144969	CV3052256	single nucleotide variant	NM_022765.4(MICAL1):c.1992G>A (p.Glu664=)	not provided [RCV003725973]	likely benign	6	109447435	109447435	Human		name
405204397	CV3058027	single nucleotide variant	NM_022765.4(MICAL1):c.2841C>T (p.Ala947=)	not provided [RCV003731147]	benign	6	109445237	109445237	Human		name
405228204	CV3065740	single nucleotide variant	NM_022765.4(MICAL1):c.2811G>A (p.Glu937=)	not provided [RCV003734427]	likely benign	6	109445267	109445267	Human		name
405209405	CV3117314	single nucleotide variant	NM_022765.4(MICAL1):c.1281T>C (p.Ala427=)	not provided [RCV003823101]	likely benign	6	109449996	109449996	Human		name
404984837	CV3121768	single nucleotide variant	NM_022765.4(MICAL1):c.2751G>A (p.Ala917=)	not provided [RCV003826567]	likely benign	6	109445452	109445452	Human		name
405179340	CV3123529	single nucleotide variant	NM_022765.4(MICAL1):c.127G>T (p.Gly43Trp)	not provided [RCV003819738]	uncertain significance	6	109454070	109454070	Human		name
404977720	CV3127257	single nucleotide variant	NM_022765.4(MICAL1):c.2310C>T (p.Leu770=)	not provided [RCV003825481]	likely benign	6	109446407	109446407	Human		name
405118559	CV3131083	single nucleotide variant	NM_022765.4(MICAL1):c.2421C>T (p.Arg807=)	not provided [RCV003837139]	likely benign	6	109446296	109446296	Human		name
405121204	CV3131490	single nucleotide variant	NM_022765.4(MICAL1):c.1671C>T (p.Pro557=)	not provided [RCV003837354]	likely benign	6	109448387	109448387	Human		name
405128108	CV3132957	single nucleotide variant	NM_022765.4(MICAL1):c.1017C>T (p.Asp339=)	not provided [RCV003838120]	likely benign	6	109450474	109450474	Human		name
405049867	CV3137990	single nucleotide variant	NM_022765.4(MICAL1):c.106G>A (p.Ala36Thr)	not provided [RCV003832028]	uncertain significance	6	109454091	109454091	Human		name
405213415	CV3142797	single nucleotide variant	NM_022765.4(MICAL1):c.1680G>A (p.Leu560=)	not provided [RCV003846155]	likely benign	6	109448378	109448378	Human		name
405142153	CV3155392	single nucleotide variant	NM_022765.4(MICAL1):c.1695T>C (p.Ala565=)	not provided [RCV003855630]	likely benign	6	109448363	109448363	Human		name
405167402	CV3156830	single nucleotide variant	NM_022765.4(MICAL1):c.1410C>T (p.Asn470=)	not provided [RCV003857534]	likely benign	6	109449681	109449681	Human		name
405221901	CV3158190	single nucleotide variant	NM_022765.4(MICAL1):c.112G>C (p.Gly38Arg)	not provided [RCV003863686]	uncertain significance	6	109454085	109454085	Human		name
405092899	CV3164109	single nucleotide variant	NM_022765.4(MICAL1):c.238C>T (p.Arg80Trp)	not provided [RCV003852424]	uncertain significance	6	109453959	109453959	Human		name
405242875	CV3164652	single nucleotide variant	NM_022765.4(MICAL1):c.1437A>T (p.Val479=)	not provided [RCV003867733]	likely benign	6	109449479	109449479	Human		name
405243516	CV3164850	single nucleotide variant	NM_022765.4(MICAL1):c.2517C>T (p.Ala839=)	not provided [RCV003867931]	likely benign	6	109446200	109446200	Human		name
405083555	CV3167198	single nucleotide variant	NM_022765.4(MICAL1):c.127G>A (p.Gly43Arg)	not provided [RCV003851779]	uncertain significance	6	109454070	109454070	Human		name
597852584	CV3737656	single nucleotide variant	NM_022765.4(MICAL1):c.160C>G (p.Gln54Glu)	not provided [RCV005066429]	uncertain significance	6	109454037	109454037	Human		name
597908450	CV3739001	single nucleotide variant	NM_022765.4(MICAL1):c.183G>C (p.Lys61Asn)	not provided [RCV005073236]	uncertain significance	6	109454014	109454014	Human		name
597831153	CV3739925	single nucleotide variant	NM_022765.4(MICAL1):c.2046G>C (p.Leu682=)	not provided [RCV005062623]	likely benign	6	109447381	109447381	Human		name
597885541	CV3741694	single nucleotide variant	NM_022765.4(MICAL1):c.1020T>C (p.Phe340=)	not provided [RCV005070413]	likely benign	6	109450471	109450471	Human		name
597864734	CV3742229	single nucleotide variant	NM_022765.4(MICAL1):c.2184G>A (p.Glu728=)	not provided [RCV005067845]	likely benign	6	109447116	109447116	Human		name
597878916	CV3744431	single nucleotide variant	NM_022765.4(MICAL1):c.2493C>G (p.Pro831=)	not provided [RCV005069645]	likely benign	6	109446224	109446224	Human		name
597859677	CV3744673	single nucleotide variant	NM_022765.4(MICAL1):c.2923C>T (p.Leu975=)	not provided [RCV005067218]	likely benign	6	109444954	109444954	Human		name
597928270	CV3749116	single nucleotide variant	NM_022765.4(MICAL1):c.2460C>T (p.Asn820=)	not provided [RCV005075572]	likely benign	6	109446257	109446257	Human		name
597868670	CV3749694	single nucleotide variant	NM_022765.4(MICAL1):c.1515C>T (p.Thr505=)	not provided [RCV005068375]	uncertain significance	6	109449401	109449401	Human		name
597965676	CV3751422	single nucleotide variant	NM_022765.4(MICAL1):c.2382T>C (p.Pro794=)	not provided [RCV005082791]	likely benign	6	109446335	109446335	Human		name
597960895	CV3753141	single nucleotide variant	NM_022765.4(MICAL1):c.1512C>T (p.Ala504=)	not provided [RCV005081641]	likely benign	6	109449404	109449404	Human		name
597963199	CV3753862	single nucleotide variant	NM_022765.4(MICAL1):c.1755G>A (p.Val585=)	not provided [RCV005082166]	likely benign	6	109448303	109448303	Human		name
597952657	CV3756670	single nucleotide variant	NM_022765.4(MICAL1):c.1629G>T (p.Leu543=)	not provided [RCV005079728]	likely benign	6	109448767	109448767	Human		name
597850922	CV3761791	single nucleotide variant	NM_022765.4(MICAL1):c.2409T>C (p.Arg803=)	not provided [RCV005087887]	likely benign	6	109446308	109446308	Human		name
597847954	CV3762049	single nucleotide variant	NM_022765.4(MICAL1):c.2676C>T (p.Ala892=)	not provided [RCV005087467]	likely benign	6	109445527	109445527	Human		name
597934445	CV3777051	single nucleotide variant	NM_022765.4(MICAL1):c.1204C>T (p.Leu402=)	not provided [RCV005117210]	likely benign	6	109450073	109450073	Human		name
597916495	CV3779378	single nucleotide variant	NM_022765.4(MICAL1):c.2457T>C (p.Leu819=)	not provided [RCV005129519]	likely benign	6	109446260	109446260	Human		name
597942583	CV3779950	single nucleotide variant	NM_022765.4(MICAL1):c.1620G>T (p.Gly540=)	not provided [RCV005118959]	likely benign	6	109448776	109448776	Human		name
597906909	CV3781402	single nucleotide variant	NM_022765.4(MICAL1):c.1566A>G (p.Thr522=)	not provided [RCV005128090]	likely benign	6	109448830	109448830	Human		name
597954135	CV3786623	single nucleotide variant	NM_022765.4(MICAL1):c.2553C>G (p.Gly851=)	not provided [RCV005121714]	likely benign	6	109446164	109446164	Human		name
597886417	CV3787410	single nucleotide variant	NM_022765.4(MICAL1):c.1593C>T (p.Ser531=)	not provided [RCV005124976]	uncertain significance	6	109448803	109448803	Human		name
597960844	CV3794773	single nucleotide variant	NM_022765.4(MICAL1):c.1209C>T (p.Gly403=)	not provided [RCV005138678]	likely benign	6	109450068	109450068	Human		name
597858826	CV3817077	single nucleotide variant	NM_022765.4(MICAL1):c.2118C>T (p.Val706=)	not provided [RCV005146458]	likely benign	6	109447182	109447182	Human		name
597947460	CV3841872	single nucleotide variant	NM_022765.4(MICAL1):c.2166C>T (p.Phe722=)	not provided [RCV005189306]	likely benign	6	109447134	109447134	Human		name
597911357	CV3850479	single nucleotide variant	NM_022765.4(MICAL1):c.2649G>A (p.Val883=)	not provided [RCV005203628]	likely benign	6	109445795	109445795	Human		name
597908905	CV3853803	single nucleotide variant	NM_022765.4(MICAL1):c.1830C>T (p.Ala610=)	not provided [RCV005203286]	likely benign	6	109448228	109448228	Human		name
598185786	CV3993011	single nucleotide variant	NM_022765.4(MICAL1):c.124G>C (p.Gly42Arg)	not specified [RCV005373313]	uncertain significance	6	109454073	109454073	Human		name
15153731	CV710108	single nucleotide variant	NM_022765.4(MICAL1):c.2274G>A (p.Ala758=)	not provided [RCV000968601]	benign	6	109446726	109446726	Human		name
15168034	CV710110	single nucleotide variant	NM_022765.4(MICAL1):c.1231C>T (p.Leu411=)	not provided [RCV000971528]	benign	6	109450046	109450046	Human		name
151782199	CV1341980	single nucleotide variant	NM_022765.4(MICAL1):c.905G>A (p.Cys302Tyr)	not provided [RCV001897349]	uncertain significance	6	109451628	109451628	Human		name
151710652	CV1365611	single nucleotide variant	NM_022765.4(MICAL1):c.966T>A (p.Ser322Arg)	not provided [RCV001907927]	uncertain significance	6	109450525	109450525	Human		name
151863006	CV1368257	single nucleotide variant	NM_022765.4(MICAL1):c.298G>A (p.Ala100Thr)	not provided [RCV001905540]\|not specified [RCV004041365]	uncertain significance	6	109453806	109453806	Human		name
151830308	CV1377766	single nucleotide variant	NM_022765.4(MICAL1):c.562C>T (p.Pro188Ser)	not provided [RCV002014248]	uncertain significance	6	109453272	109453272	Human		name
151833039	CV1388243	single nucleotide variant	NM_022765.4(MICAL1):c.868G>A (p.Asp290Asn)	not provided [RCV001955865]	uncertain significance	6	109451665	109451665	Human		name
151789990	CV1393002	single nucleotide variant	NM_022765.4(MICAL1):c.950A>G (p.Asn317Ser)	not provided [RCV001931321]\|not specified [RCV004041926]	uncertain significance	6	109450541	109450541	Human		name
151861317	CV1423257	duplication	NM_022765.4(MICAL1):c.2318dup (p.Ser774fs)	not provided [RCV001997166]	uncertain significance	6	109446398	109446399	Human		name
151794311	CV1434251	single nucleotide variant	NM_022765.4(MICAL1):c.953G>A (p.Arg318Gln)	not provided [RCV001866537]	uncertain significance	6	109450538	109450538	Human		name
151848788	CV1439918	single nucleotide variant	NM_022765.4(MICAL1):c.637G>A (p.Val213Ile)	not provided [RCV002016298]\|not specified [RCV004046253]	uncertain significance	6	109452550	109452550	Human		name
151766079	CV1469860	single nucleotide variant	NM_022765.4(MICAL1):c.604C>G (p.Pro202Ala)	not provided [RCV001914515]	uncertain significance	6	109452583	109452583	Human		name
151866377	CV1479022	single nucleotide variant	NM_022765.4(MICAL1):c.583C>T (p.Arg195Cys)	not provided [RCV002035103]	uncertain significance	6	109452604	109452604	Human		name
151778725	CV1493395	single nucleotide variant	NM_022765.4(MICAL1):c.679T>G (p.Phe227Val)	not provided [RCV001915676]	uncertain significance	6	109452399	109452399	Human		name
151786855	CV1495488	single nucleotide variant	NM_022765.4(MICAL1):c.662A>G (p.Lys221Arg)	not provided [RCV002026806]	uncertain significance	6	109452525	109452525	Human		name
152164641	CV1543562	single nucleotide variant	NM_022765.4(MICAL1):c.3100C>T (p.Leu1034=)	not provided [RCV002123843]	likely benign	6	109444295	109444295	Human		name
152081793	CV1548330	single nucleotide variant	NM_022765.4(MICAL1):c.322G>A (p.Ala108Thr)	not provided [RCV002076465]\|not specified [RCV004046432]	likely benign\|uncertain significance	6	109453782	109453782	Human		name
152103076	CV1656703	single nucleotide variant	NM_022765.4(MICAL1):c.347G>A (p.Arg116His)	not provided [RCV002115601]	benign\|likely benign	6	109453757	109453757	Human		name
329846729	CV1780680	single nucleotide variant	NM_022765.4(MICAL1):c.763G>T (p.Val255Leu)	Epilepsy, familial temporal lobe, 1 [RCV003226541]	likely pathogenic	6	109452315	109452315	Human	1	name
155999726	CV1872731	single nucleotide variant	NM_022765.4(MICAL1):c.994C>T (p.Arg332Cys)	not provided [RCV003076523]	uncertain significance	6	109450497	109450497	Human		name
156321367	CV1873156	single nucleotide variant	NM_022765.4(MICAL1):c.326G>A (p.Arg109Gln)	not provided [RCV003063091]\|not specified [RCV004070349]	uncertain significance	6	109453778	109453778	Human		name
156148844	CV1878831	single nucleotide variant	NM_022765.4(MICAL1):c.437G>A (p.Arg146His)	not provided [RCV003056460]	uncertain significance	6	109453667	109453667	Human		name
156323543	CV1882737	single nucleotide variant	NM_022765.4(MICAL1):c.667G>A (p.Val223Ile)	not provided [RCV003089331]	uncertain significance	6	109452520	109452520	Human		name
156126499	CV1889080	single nucleotide variant	NM_022765.4(MICAL1):c.911T>C (p.Leu304Pro)	not provided [RCV003081658]	likely benign	6	109451622	109451622	Human		name
155965970	CV1892093	single nucleotide variant	NM_022765.4(MICAL1):c.448G>A (p.Gly150Ser)	not provided [RCV003074933]	uncertain significance	6	109453656	109453656	Human		name
156399653	CV1897464	single nucleotide variant	NM_022765.4(MICAL1):c.367A>G (p.Asn123Asp)	not provided [RCV002584740]	uncertain significance	6	109453737	109453737	Human		name
156333182	CV1905739	single nucleotide variant	NM_022765.4(MICAL1):c.995G>A (p.Arg332His)	not provided [RCV003089918]	uncertain significance	6	109450496	109450496	Human		name
156414733	CV1909163	single nucleotide variant	NM_022765.4(MICAL1):c.361C>T (p.Arg121Cys)	not provided [RCV002588777]	uncertain significance	6	109453743	109453743	Human		name
156418234	CV1914602	single nucleotide variant	NM_022765.4(MICAL1):c.656G>T (p.Gly219Val)	not provided [RCV002611413]\|not specified [RCV004827940]	uncertain significance	6	109452531	109452531	Human		name
156407600	CV1918185	single nucleotide variant	NM_022765.4(MICAL1):c.767C>T (p.Pro256Leu)	not provided [RCV002606944]	uncertain significance	6	109452311	109452311	Human		name
156210067	CV1932450	single nucleotide variant	NM_022765.4(MICAL1):c.766C>T (p.Pro256Ser)	not provided [RCV002643960]\|not specified [RCV004070668]	uncertain significance	6	109452312	109452312	Human		name
156437344	CV1937485	single nucleotide variant	NM_022765.4(MICAL1):c.790A>G (p.Ile264Val)	not provided [RCV003106878]\|not specified [RCV005363067]	uncertain significance	6	109452288	109452288	Human		name
156440454	CV1943505	duplication	NM_022765.4(MICAL1):c.2239dup (p.Cys747fs)	not provided [RCV003110489]	uncertain significance	6	109446760	109446761	Human		name
156447337	CV1944981	single nucleotide variant	NM_022765.4(MICAL1):c.406C>T (p.Arg136Trp)	not provided [RCV003118864]	uncertain significance	6	109453698	109453698	Human		name
156445892	CV1952142	single nucleotide variant	NM_022765.4(MICAL1):c.991C>T (p.Gln331Ter)	not provided [RCV003116855]	uncertain significance	6	109450500	109450500	Human		name
156388091	CV1955057	single nucleotide variant	NM_022765.4(MICAL1):c.400G>A (p.Asp134Asn)	not provided [RCV002583641]\|not specified [RCV004064495]	likely benign\|uncertain significance	6	109453704	109453704	Human		name
156103977	CV1956774	single nucleotide variant	NM_022765.4(MICAL1):c.3183G>A (p.Leu1061=)	not provided [RCV002570951]	likely benign	6	109444212	109444212	Human		name
156219432	CV1960096	single nucleotide variant	NM_022765.4(MICAL1):c.952C>T (p.Arg318Trp)	not provided [RCV002575467]	uncertain significance	6	109450539	109450539	Human		name
156344400	CV1970430	single nucleotide variant	NM_022765.4(MICAL1):c.643A>G (p.Ile215Val)	not provided [RCV002601452]	uncertain significance	6	109452544	109452544	Human		name
156385104	CV1971899	single nucleotide variant	NM_022765.4(MICAL1):c.502G>A (p.Ala168Thr)	not provided [RCV002604241]\|not specified [RCV004065745]	uncertain significance	6	109453332	109453332	Human		name
155906165	CV1972142	single nucleotide variant	NM_022765.4(MICAL1):c.557C>T (p.Pro186Leu)	not provided [RCV002613686]	uncertain significance	6	109453277	109453277	Human		name
156042830	CV1977909	single nucleotide variant	NM_022765.4(MICAL1):c.485T>C (p.Leu162Pro)	not provided [RCV002590391]\|not specified [RCV004065659]	uncertain significance	6	109453349	109453349	Human		name
155924792	CV1987718	single nucleotide variant	NM_022765.4(MICAL1):c.459C>G (p.Asp153Glu)	not provided [RCV002614720]	uncertain significance	6	109453645	109453645	Human		name
156243661	CV1992667	single nucleotide variant	NM_022765.4(MICAL1):c.362G>A (p.Arg121His)	not provided [RCV002627220]	uncertain significance	6	109453742	109453742	Human		name
156403129	CV1993060	single nucleotide variant	NM_022765.4(MICAL1):c.867C>G (p.Asp289Glu)	not provided [RCV002657788]	uncertain significance	6	109451666	109451666	Human		name
156091311	CV1994353	single nucleotide variant	NM_022765.4(MICAL1):c.785C>T (p.Ala262Val)	not provided [RCV002639230]	uncertain significance	6	109452293	109452293	Human		name
156333043	CV2000736	single nucleotide variant	NM_022765.4(MICAL1):c.3180C>G (p.Ala1060=)	not provided [RCV002649926]	likely benign	6	109444215	109444215	Human		name
156210865	CV2000961	single nucleotide variant	NM_022765.4(MICAL1):c.806T>G (p.Phe269Cys)	not provided [RCV002666841]	uncertain significance	6	109452272	109452272	Human		name
156350462	CV2001294	single nucleotide variant	NM_022765.4(MICAL1):c.3171C>T (p.Ser1057=)	not provided [RCV002675555]	likely benign	6	109444224	109444224	Human		name
156179846	CV2001296	single nucleotide variant	NM_022765.4(MICAL1):c.3102G>A (p.Leu1034=)	not provided [RCV002642990]	likely benign	6	109444293	109444293	Human		name
156375209	CV2003994	single nucleotide variant	NM_022765.4(MICAL1):c.584G>C (p.Arg195Pro)	not provided [RCV002653239]	uncertain significance	6	109452603	109452603	Human		name
156275301	CV2014919	single nucleotide variant	NM_022765.4(MICAL1):c.971A>G (p.Asn324Ser)	not provided [RCV002715119]	uncertain significance	6	109450520	109450520	Human		name
156006255	CV2015045	single nucleotide variant	NM_022765.4(MICAL1):c.676G>A (p.Gly226Ser)	not provided [RCV002690284]	uncertain significance	6	109452511	109452511	Human		name
156208709	CV2018769	single nucleotide variant	NM_022765.4(MICAL1):c.599C>A (p.Pro200His)	not provided [RCV002700544]	uncertain significance	6	109452588	109452588	Human		name
156234545	CV2021459	deletion	NM_022765.4(MICAL1):c.2469del (p.Asp824fs)	not provided [RCV002745435]	uncertain significance	6	109446248	109446248	Human		name
156321843	CV2022149	single nucleotide variant	NM_022765.4(MICAL1):c.695T>C (p.Met232Thr)	not provided [RCV002717144]	uncertain significance	6	109452383	109452383	Human		name
156153929	CV2023197	single nucleotide variant	NM_022765.4(MICAL1):c.893C>A (p.Ala298Asp)	not provided [RCV002741311]	uncertain significance	6	109451640	109451640	Human		name
155988532	CV2026783	single nucleotide variant	NM_022765.4(MICAL1):c.853G>A (p.Val285Met)	not provided [RCV002755647]	uncertain significance	6	109451680	109451680	Human		name
155948381	CV2029101	single nucleotide variant	NM_022765.4(MICAL1):c.592C>G (p.Leu198Val)	not provided [RCV002730539]	uncertain significance	6	109452595	109452595	Human		name
156174911	CV2038110	single nucleotide variant	NM_022765.4(MICAL1):c.433G>A (p.Gly145Arg)	not provided [RCV002741976]	uncertain significance	6	109453671	109453671	Human		name
156102818	CV2038370	single nucleotide variant	NM_022765.4(MICAL1):c.359C>T (p.Ser120Phe)	not provided [RCV002761387]	uncertain significance	6	109453745	109453745	Human		name
156253055	CV2041145	single nucleotide variant	NM_022765.4(MICAL1):c.689G>A (p.Arg230Gln)	not provided [RCV002806077]	uncertain significance	6	109452389	109452389	Human		name
156016211	CV2046733	single nucleotide variant	NM_022765.4(MICAL1):c.929G>A (p.Arg310His)	not provided [RCV002756950]\|not specified [RCV004064709]	uncertain significance	6	109451604	109451604	Human		name
156147218	CV2052788	single nucleotide variant	NM_022765.4(MICAL1):c.872C>G (p.Thr291Ser)	not provided [RCV002801173]	uncertain significance	6	109451661	109451661	Human		name
155944870	CV2072531	single nucleotide variant	NM_022765.4(MICAL1):c.685G>A (p.Val229Ile)	not provided [RCV002862005]	uncertain significance	6	109452393	109452393	Human		name
156115013	CV2093132	single nucleotide variant	NM_022765.4(MICAL1):c.914G>A (p.Arg305Gln)	not provided [RCV002913932]	likely benign	6	109451619	109451619	Human		name
156237947	CV2115644	single nucleotide variant	NM_022765.4(MICAL1):c.913C>T (p.Arg305Trp)	not provided [RCV002919188]	uncertain significance	6	109451620	109451620	Human		name
156232217	CV2118237	single nucleotide variant	NM_022765.4(MICAL1):c.906C>A (p.Cys302Ter)	not provided [RCV002958553]	uncertain significance	6	109451627	109451627	Human		name
155994638	CV2122498	single nucleotide variant	NM_022765.4(MICAL1):c.415G>A (p.Gly139Ser)	not provided [RCV002974891]	uncertain significance	6	109453689	109453689	Human		name
156039437	CV2130349	single nucleotide variant	NM_022765.4(MICAL1):c.712A>G (p.Ile238Val)	not provided [RCV002949558]	likely benign	6	109452366	109452366	Human		name
155962522	CV2131986	single nucleotide variant	NM_022765.4(MICAL1):c.325C>T (p.Arg109Ter)	not provided [RCV002995227]	uncertain significance	6	109453779	109453779	Human		name
156097961	CV2132138	single nucleotide variant	NM_022765.4(MICAL1):c.698G>A (p.Arg233Gln)	not provided [RCV003002101]	benign	6	109452380	109452380	Human		name
155963832	CV2134643	deletion	NM_022765.4(MICAL1):c.1196del (p.Phe399fs)	not provided [RCV002972511]	likely benign\|uncertain significance	6	109450081	109450081	Human		name
156083543	CV2138359	single nucleotide variant	NM_022765.4(MICAL1):c.317T>C (p.Leu106Pro)	not provided [RCV002979343]	uncertain significance	6	109453787	109453787	Human		name
155935465	CV2138781	single nucleotide variant	NM_022765.4(MICAL1):c.3192G>C (p.Gly1064=)	not provided [RCV002993686]	likely benign	6	109444203	109444203	Human		name
156028785	CV2139338	single nucleotide variant	NM_022765.4(MICAL1):c.748G>A (p.Val250Met)	not provided [RCV002999047]	likely benign	6	109452330	109452330	Human		name
156316080	CV2140276	single nucleotide variant	NM_022765.4(MICAL1):c.649G>T (p.Ala217Ser)	not provided [RCV003011393]	likely benign	6	109452538	109452538	Human		name
156020882	CV2141268	single nucleotide variant	NM_022765.4(MICAL1):c.743G>A (p.Arg248His)	not provided [RCV002976147]\|not specified [RCV004065045]	likely benign\|uncertain significance	6	109452335	109452335	Human		name
155932230	CV2156796	single nucleotide variant	NM_022765.4(MICAL1):c.3066G>A (p.Lys1022=)	not provided [RCV003013699]	likely benign	6	109444329	109444329	Human		name
156074917	CV2160209	duplication	NM_022765.4(MICAL1):c.1686dup (p.Leu563fs)	not provided [RCV003020157]	uncertain significance	6	109448371	109448372	Human		name
156115798	CV2182913	single nucleotide variant	NM_022765.4(MICAL1):c.523A>C (p.Ile175Leu)	not provided [RCV003039120]	uncertain significance	6	109453311	109453311	Human		name
155915491	CV2243795	single nucleotide variant	NM_022765.4(MICAL1):c.713T>C (p.Ile238Thr)	not specified [RCV004114483]	uncertain significance	6	109452365	109452365	Human		name
156119776	CV2275851	single nucleotide variant	NM_022765.4(MICAL1):c.836T>C (p.Ile279Thr)	not specified [RCV004139513]	uncertain significance	6	109451697	109451697	Human		name
156173818	CV2284152	single nucleotide variant	NM_022765.4(MICAL1):c.602A>G (p.Asn201Ser)	not provided [RCV003720686]\|not specified [RCV004144742]	likely benign\|uncertain significance	6	109452585	109452585	Human		name
329847244	CV2534410	single nucleotide variant	NM_022765.4(MICAL1):c.922G>T (p.Val308Leu)	MICAL1-related Lateral temporal epilepsy [RCV003228618]\|not provided [RCV003779825]	uncertain significance	6	109451611	109451611	Human	1	name
401719000	CV2704909	single nucleotide variant	NM_022765.4(MICAL1):c.922G>C (p.Val308Leu)	not specified [RCV004307482]	uncertain significance	6	109451611	109451611	Human		name
401920841	CV2820616	single nucleotide variant	NM_022765.4(MICAL1):c.422A>C (p.Lys141Thr)	not provided [RCV003431989]	uncertain significance	6	109453682	109453682	Human		name
402511478	CV2858917	single nucleotide variant	NM_022765.4(MICAL1):c.518T>A (p.Val173Glu)	not provided [RCV003547060]	uncertain significance	6	109453316	109453316	Human		name
405045664	CV2859937	single nucleotide variant	NM_022765.4(MICAL1):c.3147C>A (p.Arg1049=)	not provided [RCV003579429]	likely benign	6	109444248	109444248	Human		name
405190804	CV2871311	single nucleotide variant	NM_022765.4(MICAL1):c.460C>T (p.His154Tyr)	not provided [RCV003550358]	uncertain significance	6	109453644	109453644	Human		name
405216947	CV2897246	single nucleotide variant	NM_022765.4(MICAL1):c.343A>G (p.Lys115Glu)	not provided [RCV003567901]	uncertain significance	6	109453761	109453761	Human		name
402471002	CV2904373	single nucleotide variant	NM_022765.4(MICAL1):c.3111G>A (p.Leu1037=)	not provided [RCV003570484]	likely benign	6	109444284	109444284	Human		name
405222678	CV2908484	single nucleotide variant	NM_022765.4(MICAL1):c.598C>G (p.Pro200Ala)	not provided [RCV003568673]	uncertain significance	6	109452589	109452589	Human		name
405189518	CV2924547	single nucleotide variant	NM_022765.4(MICAL1):c.766C>A (p.Pro256Thr)	not provided [RCV003564777]	uncertain significance	6	109452312	109452312	Human		name
402489132	CV2941688	single nucleotide variant	NM_022765.4(MICAL1):c.878A>G (p.Tyr293Cys)	not provided [RCV003660376]	uncertain significance	6	109451655	109451655	Human		name
405167881	CV2954674	single nucleotide variant	NM_022765.4(MICAL1):c.455T>C (p.Leu152Pro)	not provided [RCV003675073]	uncertain significance	6	109453649	109453649	Human		name
405144367	CV2955196	single nucleotide variant	NM_022765.4(MICAL1):c.697C>G (p.Arg233Gly)	not provided [RCV003673505]	uncertain significance	6	109452381	109452381	Human		name
402506609	CV2982347	single nucleotide variant	NM_022765.4(MICAL1):c.524T>C (p.Ile175Thr)	not provided [RCV003689115]	uncertain significance	6	109453310	109453310	Human		name
405254868	CV2985072	single nucleotide variant	NM_022765.4(MICAL1):c.508C>G (p.Leu170Val)	not provided [RCV003723072]	uncertain significance	6	109453326	109453326	Human		name
405020144	CV3001963	single nucleotide variant	NM_022765.4(MICAL1):c.418G>A (p.Ala140Thr)	not provided [RCV003694753]	uncertain significance	6	109453686	109453686	Human		name
405131111	CV3010906	single nucleotide variant	NM_022765.4(MICAL1):c.533G>T (p.Gly178Val)	not provided [RCV003701604]	uncertain significance	6	109453301	109453301	Human		name
402491350	CV3011943	deletion	NM_022765.4(MICAL1):c.2619del (p.Phe874fs)	not provided [RCV003687565]	likely benign	6	109445825	109445825	Human		name
405154204	CV3027981	single nucleotide variant	NM_022765.4(MICAL1):c.653C>A (p.Ala218Glu)	not provided [RCV003703500]	uncertain significance	6	109452534	109452534	Human		name
405085335	CV3028344	single nucleotide variant	NM_022765.4(MICAL1):c.589C>A (p.Gln197Lys)	not provided [RCV003699359]	uncertain significance	6	109452598	109452598	Human		name
405182738	CV3031875	single nucleotide variant	NM_022765.4(MICAL1):c.3024C>T (p.Asp1008=)	not provided [RCV003705703]	likely benign	6	109444756	109444756	Human		name
405224530	CV3035984	single nucleotide variant	NM_022765.4(MICAL1):c.3108G>A (p.Lys1036=)	not provided [RCV003710464]	likely benign	6	109444287	109444287	Human		name
405237816	CV3077782	single nucleotide variant	NM_022765.4(MICAL1):c.707T>C (p.Leu236Pro)	not provided [RCV003736240]	uncertain significance	6	109452371	109452371	Human		name
405236207	CV3079493	deletion	NM_022765.4(MICAL1):c.2649del (p.Pro884fs)	not provided [RCV003735850]	likely benign	6	109445795	109445795	Human		name
405210230	CV3117631	single nucleotide variant	NM_022765.4(MICAL1):c.304G>C (p.Glu102Gln)	not provided [RCV003823230]	uncertain significance	6	109453800	109453800	Human		name
405190390	CV3118009	single nucleotide variant	NM_022765.4(MICAL1):c.979C>T (p.Pro327Ser)	not provided [RCV003820919]	uncertain significance	6	109450512	109450512	Human		name
405091216	CV3118442	single nucleotide variant	NM_022765.4(MICAL1):c.982G>A (p.Glu328Lys)	not provided [RCV003811084]\|not specified [RCV004828000]	uncertain significance	6	109450509	109450509	Human		name
405112879	CV3118676	single nucleotide variant	NM_022765.4(MICAL1):c.986C>G (p.Ala329Gly)	not provided [RCV003813904]	uncertain significance	6	109450505	109450505	Human		name
405000070	CV3120235	single nucleotide variant	NM_022765.4(MICAL1):c.346C>T (p.Arg116Cys)	not provided [RCV003828025]	uncertain significance	6	109453758	109453758	Human		name
405163803	CV3125229	single nucleotide variant	NM_022765.4(MICAL1):c.965G>A (p.Ser322Asn)	not provided [RCV003818501]	uncertain significance	6	109450526	109450526	Human		name
405130669	CV3133389	single nucleotide variant	NM_022765.4(MICAL1):c.722C>T (p.Thr241Ile)	not provided [RCV003838359]	uncertain significance	6	109452356	109452356	Human		name
405108166	CV3136622	single nucleotide variant	NM_022765.4(MICAL1):c.3036A>C (p.Arg1012=)	not provided [RCV003835776]	likely benign	6	109444744	109444744	Human		name
405048111	CV3137873	deletion	NM_022765.4(MICAL1):c.1787del (p.Asp596fs)	not provided [RCV003831911]	likely benign	6	109448271	109448271	Human		name
405151830	CV3138258	single nucleotide variant	NM_022765.4(MICAL1):c.311C>T (p.Ala104Val)	not provided [RCV003840118]	uncertain significance	6	109453793	109453793	Human		name
405015941	CV3139050	single nucleotide variant	NM_022765.4(MICAL1):c.949A>G (p.Asn317Asp)	not provided [RCV003829387]	uncertain significance	6	109450542	109450542	Human		name
405037542	CV3140648	single nucleotide variant	NM_022765.4(MICAL1):c.407G>A (p.Arg136Gln)	not provided [RCV003831131]	uncertain significance	6	109453697	109453697	Human		name
405038973	CV3140871	single nucleotide variant	NM_022765.4(MICAL1):c.449G>A (p.Gly150Asp)	not provided [RCV003831164]	uncertain significance	6	109453655	109453655	Human		name
405225214	CV3142231	single nucleotide variant	NM_022765.4(MICAL1):c.928C>T (p.Arg310Cys)	not provided [RCV003847770]	uncertain significance	6	109451605	109451605	Human		name
405227669	CV3142868	single nucleotide variant	NM_022765.4(MICAL1):c.778G>A (p.Gly260Ser)	not provided [RCV003848211]	uncertain significance	6	109452300	109452300	Human		name
405217587	CV3143738	single nucleotide variant	NM_022765.4(MICAL1):c.812A>G (p.Gln271Arg)	not provided [RCV003846708]	uncertain significance	6	109452266	109452266	Human		name
405137613	CV3144724	single nucleotide variant	NM_022765.4(MICAL1):c.688C>T (p.Arg230Ter)	not provided [RCV003855241]	likely benign	6	109452390	109452390	Human		name
405071112	CV3145359	single nucleotide variant	NM_022765.4(MICAL1):c.310G>A (p.Ala104Thr)	not provided [RCV003850944]	uncertain significance	6	109453794	109453794	Human		name
405197980	CV3146809	single nucleotide variant	NM_022765.4(MICAL1):c.904T>C (p.Cys302Arg)	not provided [RCV003844164]	uncertain significance	6	109451629	109451629	Human		name
405173887	CV3150503	single nucleotide variant	NM_022765.4(MICAL1):c.900G>T (p.Lys300Asn)	not provided [RCV003841777]	uncertain significance	6	109451633	109451633	Human		name
405161748	CV3153080	single nucleotide variant	NM_022765.4(MICAL1):c.599C>G (p.Pro200Arg)	not provided [RCV003840815]	uncertain significance	6	109452588	109452588	Human		name
405167377	CV3153690	single nucleotide variant	NM_022765.4(MICAL1):c.647C>T (p.Ser216Leu)	not provided [RCV003841235]	uncertain significance	6	109452540	109452540	Human		name
405221843	CV3154686	single nucleotide variant	NM_022765.4(MICAL1):c.947C>T (p.Thr316Ile)	not provided [RCV003847181]	uncertain significance	6	109450544	109450544	Human		name
405139674	CV3155089	single nucleotide variant	NM_022765.4(MICAL1):c.763G>A (p.Val255Met)	not provided [RCV003855327]	uncertain significance	6	109452315	109452315	Human		name
405186415	CV3156391	single nucleotide variant	NM_022765.4(MICAL1):c.823A>G (p.Lys275Glu)	not provided [RCV003859269]	uncertain significance	6	109452255	109452255	Human		name
405182758	CV3159660	single nucleotide variant	NM_022765.4(MICAL1):c.370G>A (p.Val124Met)	not provided [RCV003858911]	uncertain significance	6	109453734	109453734	Human		name
405244794	CV3161606	single nucleotide variant	NM_022765.4(MICAL1):c.798C>A (p.Asn266Lys)	not provided [RCV003868319]	uncertain significance	6	109452280	109452280	Human		name
405203502	CV3165217	single nucleotide variant	NM_022765.4(MICAL1):c.452C>T (p.Thr151Ile)	not provided [RCV003861078]	uncertain significance	6	109453652	109453652	Human		name
405204904	CV3165606	single nucleotide variant	NM_022765.4(MICAL1):c.623A>G (p.Asn208Ser)	not provided [RCV003861272]	uncertain significance	6	109452564	109452564	Human		name
402492300	CV3182495	single nucleotide variant	NM_022765.4(MICAL1):c.361C>G (p.Arg121Gly)	not provided [RCV003876982]	uncertain significance	6	109453743	109453743	Human		name
405670988	CV3289329	single nucleotide variant	NM_022765.4(MICAL1):c.498G>C (p.Lys166Asn)	not provided [RCV005065071]\|not specified [RCV004419520]	uncertain significance	6	109453336	109453336	Human		name
405670994	CV3289330	single nucleotide variant	NM_022765.4(MICAL1):c.586G>A (p.Ala196Thr)	not provided [RCV005104548]\|not specified [RCV004419521]	uncertain significance	6	109452601	109452601	Human		name
405671000	CV3289331	single nucleotide variant	NM_022765.4(MICAL1):c.781G>A (p.Val261Ile)	not specified [RCV004419522]	uncertain significance	6	109452297	109452297	Human		name
407485107	CV3446880	single nucleotide variant	NM_022765.4(MICAL1):c.973G>A (p.Val325Met)	not specified [RCV004640657]	uncertain significance	6	109450518	109450518	Human		name
597645461	CV3563552	single nucleotide variant	NM_022765.4(MICAL1):c.625T>C (p.Tyr209His)	not specified [RCV004832913]	uncertain significance	6	109452562	109452562	Human		name
597645469	CV3563553	single nucleotide variant	NM_022765.4(MICAL1):c.974T>C (p.Val325Ala)	not specified [RCV004832914]	uncertain significance	6	109450517	109450517	Human		name
597645482	CV3563555	single nucleotide variant	NM_022765.4(MICAL1):c.613C>A (p.Gln205Lys)	not provided [RCV005061476]\|not specified [RCV004832916]	uncertain significance	6	109452574	109452574	Human		name
597862134	CV3745165	single nucleotide variant	NM_022765.4(MICAL1):c.851T>C (p.Ile284Thr)	not provided [RCV005067521]	uncertain significance	6	109451682	109451682	Human		name
597871540	CV3749893	deletion	NM_022765.4(MICAL1):c.1430del (p.Asn477fs)	not provided [RCV005068574]	likely benign	6	109449661	109449661	Human		name
597943264	CV3757946	single nucleotide variant	NM_022765.4(MICAL1):c.730T>G (p.Phe244Val)	not provided [RCV005077945]	uncertain significance	6	109452348	109452348	Human		name
597901005	CV3779037	single nucleotide variant	NM_022765.4(MICAL1):c.904T>G (p.Cys302Gly)	not provided [RCV005127114]	uncertain significance	6	109451629	109451629	Human		name
597924013	CV3808588	deletion	NM_022765.4(MICAL1):c.2967del (p.Glu990fs)	not provided [RCV005156102]	likely benign	6	109444910	109444910	Human		name
597941092	CV3819194	single nucleotide variant	NM_022765.4(MICAL1):c.320G>A (p.Gly107Glu)	not provided [RCV005159005]	uncertain significance	6	109453784	109453784	Human		name
597976091	CV3829092	single nucleotide variant	NM_022765.4(MICAL1):c.335T>C (p.Leu112Pro)	not provided [RCV005169541]	uncertain significance	6	109453769	109453769	Human		name
597971777	CV3833041	single nucleotide variant	NM_022765.4(MICAL1):c.545C>T (p.Thr182Ile)	not provided [RCV005166938]	uncertain significance	6	109453289	109453289	Human		name
597873291	CV3836276	single nucleotide variant	NM_022765.4(MICAL1):c.3181T>C (p.Leu1061=)	not provided [RCV005177073]	likely benign	6	109444214	109444214	Human		name
597926622	CV3855394	single nucleotide variant	NM_022765.4(MICAL1):c.866A>G (p.Asp289Gly)	not provided [RCV005205993]	uncertain significance	6	109451667	109451667	Human		name
597918388	CV3861533	single nucleotide variant	NM_022765.4(MICAL1):c.3003G>A (p.Glu1001=)	not provided [RCV005204690]	likely benign	6	109444777	109444777	Human		name
598185792	CV3993013	single nucleotide variant	NM_022765.4(MICAL1):c.452C>G (p.Thr151Ser)	not specified [RCV005373314]	uncertain significance	6	109453652	109453652	Human		name
15104120	CV699242	single nucleotide variant	NM_022765.4(MICAL1):c.3114G>A (p.Val1038=)	not provided [RCV000959620]	benign	6	109444281	109444281	Human		name
15175969	CV699244	single nucleotide variant	NM_022765.4(MICAL1):c.659G>A (p.Gly220Asp)	not provided [RCV000950714]	benign	6	109452528	109452528	Human		name
15177301	CV710112	single nucleotide variant	NM_022765.4(MICAL1):c.584G>A (p.Arg195His)	not provided [RCV000973391]	benign	6	109452603	109452603	Human		name
15182480	CV735328	single nucleotide variant	NM_022765.4(MICAL1):c.979C>A (p.Pro327Thr)	not provided [RCV000907830]	benign	6	109450512	109450512	Human		name
151874684	CV1466615	single nucleotide variant	NM_022765.4(MICAL1):c.2408G>A (p.Arg803His)	not provided [RCV001885709]\|not specified [RCV004041061]	uncertain significance	6	109446309	109446309	Human		name
156324566	CV1871064	single nucleotide variant	NM_022765.4(MICAL1):c.1063G>A (p.Ala355Thr)	not provided [RCV003063311]\|not specified [RCV004827928]	conflicting interpretations of pathogenicity\|uncertain significance	6	109450428	109450428	Human		name
156381168	CV1873644	single nucleotide variant	NM_022765.4(MICAL1):c.1627C>G (p.Leu543Val)	not provided [RCV003067181]	uncertain significance	6	109448769	109448769	Human		name
156328567	CV1881092	single nucleotide variant	NM_022765.4(MICAL1):c.1004G>A (p.Arg335Gln)	not provided [RCV003063557]\|not specified [RCV005362998]	conflicting interpretations of pathogenicity\|uncertain significance	6	109450487	109450487	Human		name
156327366	CV1887372	single nucleotide variant	NM_022765.4(MICAL1):c.2938A>C (p.Lys980Gln)	not provided [RCV003089574]\|not specified [RCV004071956]	uncertain significance	6	109444939	109444939	Human		name
156316041	CV1901231	single nucleotide variant	NM_022765.4(MICAL1):c.2744G>A (p.Arg915His)	not provided [RCV002578957]\|not specified [RCV004073420]	uncertain significance	6	109445459	109445459	Human		name
156295419	CV1904611	single nucleotide variant	NM_022765.4(MICAL1):c.2732G>A (p.Arg911Gln)	not provided [RCV002598927]\|not specified [RCV005377289]	uncertain significance	6	109445471	109445471	Human		name
156367147	CV1909416	single nucleotide variant	NM_022765.4(MICAL1):c.2444G>A (p.Arg815Gln)	not provided [RCV002602901]	uncertain significance	6	109446273	109446273	Human		name
156215597	CV1910576	single nucleotide variant	NM_022765.4(MICAL1):c.2729G>A (p.Arg910His)	not provided [RCV002596249]	uncertain significance	6	109445474	109445474	Human		name
156408630	CV1911704	single nucleotide variant	NM_022765.4(MICAL1):c.1235C>A (p.Ala412Glu)	not provided [RCV002607297]	uncertain significance	6	109450042	109450042	Human		name
156405684	CV1913208	single nucleotide variant	NM_022765.4(MICAL1):c.1603T>G (p.Ser535Ala)	not provided [RCV002606388]	uncertain significance	6	109448793	109448793	Human		name
155954217	CV1915252	single nucleotide variant	NM_022765.4(MICAL1):c.1358G>A (p.Arg453His)	not provided [RCV002616388]\|not specified [RCV004070544]	uncertain significance	6	109449733	109449733	Human		name
156304040	CV1916291	single nucleotide variant	NM_022765.4(MICAL1):c.2743C>T (p.Arg915Cys)	not provided [RCV002599311]	uncertain significance	6	109445460	109445460	Human		name
156405517	CV1919374	single nucleotide variant	NM_022765.4(MICAL1):c.2881A>C (p.Ser961Arg)	not provided [RCV002585666]	uncertain significance	6	109445197	109445197	Human		name
156372382	CV1920929	single nucleotide variant	NM_022765.4(MICAL1):c.2461C>G (p.Leu821Val)	not provided [RCV002603287]	uncertain significance	6	109446256	109446256	Human		name
156204997	CV1922677	single nucleotide variant	NM_022765.4(MICAL1):c.1463A>C (p.Lys488Thr)	not provided [RCV002643775]	uncertain significance	6	109449453	109449453	Human		name
156062450	CV1925711	single nucleotide variant	NM_022765.4(MICAL1):c.2036G>T (p.Gly679Val)	not provided [RCV002620993]	likely benign	6	109447391	109447391	Human		name
156446449	CV1937925	single nucleotide variant	NM_022765.4(MICAL1):c.1630T>C (p.Cys544Arg)	not provided [RCV003117954]	uncertain significance	6	109448766	109448766	Human		name
156442215	CV1938127	single nucleotide variant	NM_022765.4(MICAL1):c.2645A>C (p.Asp882Ala)	not provided [RCV003112554]	uncertain significance	6	109445799	109445799	Human		name
156444454	CV1938395	single nucleotide variant	NM_022765.4(MICAL1):c.1430A>G (p.Asn477Ser)	not provided [RCV003115378]	uncertain significance	6	109449661	109449661	Human		name
156434685	CV1940160	single nucleotide variant	NM_022765.4(MICAL1):c.2525G>A (p.Arg842His)	not provided [RCV003104574]	uncertain significance	6	109446192	109446192	Human		name
156443810	CV1941077	single nucleotide variant	NM_022765.4(MICAL1):c.2448G>C (p.Leu816Phe)	not provided [RCV003114719]	likely benign	6	109446269	109446269	Human		name
156449557	CV1941813	single nucleotide variant	NM_022765.4(MICAL1):c.2656G>A (p.Asp886Asn)	not provided [RCV003121681]	uncertain significance	6	109445788	109445788	Human		name
156446748	CV1948100	single nucleotide variant	NM_022765.4(MICAL1):c.2303C>T (p.Pro768Leu)	not provided [RCV003118264]	uncertain significance	6	109446697	109446697	Human		name
156444890	CV1948940	single nucleotide variant	NM_022765.4(MICAL1):c.1130G>A (p.Arg377His)	not provided [RCV003115821]	uncertain significance	6	109450361	109450361	Human		name
156445016	CV1949075	single nucleotide variant	NM_022765.4(MICAL1):c.2381C>G (p.Pro794Arg)	not provided [RCV003115950]	uncertain significance	6	109446336	109446336	Human		name
156446186	CV1951275	single nucleotide variant	NM_022765.4(MICAL1):c.1802T>C (p.Ile601Thr)	not provided [RCV003117152]	uncertain significance	6	109448256	109448256	Human		name
156443786	CV1952093	single nucleotide variant	NM_022765.4(MICAL1):c.1465G>C (p.Glu489Gln)	not provided [RCV003114166]\|not specified [RCV005377330]	uncertain significance	6	109449451	109449451	Human		name
156201535	CV1952431	single nucleotide variant	NM_022765.4(MICAL1):c.2432C>T (p.Pro811Leu)	not provided [RCV002574796]\|not specified [RCV004064304]	likely benign\|uncertain significance	6	109446285	109446285	Human		name
156107903	CV1953933	single nucleotide variant	NM_022765.4(MICAL1):c.2623T>G (p.Ser875Ala)	not provided [RCV002571088]	uncertain significance	6	109445821	109445821	Human		name
156303339	CV1955705	single nucleotide variant	NM_022765.4(MICAL1):c.2675C>T (p.Ala892Val)	not provided [RCV002578329]\|not specified [RCV004064538]	uncertain significance	6	109445528	109445528	Human		name
156382176	CV1960942	indel	NM_022765.4(MICAL1):c.832+12_832+13delinsAT	not provided [RCV002583253]	uncertain significance	6	109452233	109452234	Human		name
156415302	CV1962083	single nucleotide variant	NM_022765.4(MICAL1):c.1279G>A (p.Ala427Thr)	not provided [RCV002589089]\|not specified [RCV004641972]	uncertain significance	6	109449998	109449998	Human		name
156417437	CV1966951	single nucleotide variant	NM_022765.4(MICAL1):c.2815G>C (p.Glu939Gln)	not provided [RCV002590190]	uncertain significance	6	109445263	109445263	Human		name
156174009	CV1968493	single nucleotide variant	NM_022765.4(MICAL1):c.2146T>G (p.Phe716Val)	not provided [RCV002594857]	uncertain significance	6	109447154	109447154	Human		name
156412799	CV1968830	single nucleotide variant	NM_022765.4(MICAL1):c.1153C>T (p.Arg385Cys)	not provided [RCV002608646]	uncertain significance	6	109450338	109450338	Human		name
155976374	CV1971462	single nucleotide variant	NM_022765.4(MICAL1):c.2209G>A (p.Glu737Lys)	not provided [RCV002617406]	uncertain significance	6	109447091	109447091	Human		name
156073008	CV1972050	single nucleotide variant	NM_022765.4(MICAL1):c.2447T>C (p.Leu816Ser)	not provided [RCV002591327]	uncertain significance	6	109446270	109446270	Human		name
156353940	CV1974881	single nucleotide variant	NM_022765.4(MICAL1):c.2801G>A (p.Arg934Gln)	not provided [RCV002602027]	uncertain significance	6	109445277	109445277	Human		name
156177990	CV1978663	single nucleotide variant	NM_022765.4(MICAL1):c.1081G>A (p.Val361Ile)	not provided [RCV002594975]	uncertain significance	6	109450410	109450410	Human		name
156413609	CV1979073	single nucleotide variant	NM_022765.4(MICAL1):c.2242C>T (p.Leu748Phe)	not provided [RCV002608894]	uncertain significance	6	109446758	109446758	Human		name
156220364	CV1981263	single nucleotide variant	NM_022765.4(MICAL1):c.1393C>T (p.Arg465Cys)	not provided [RCV002626423]	uncertain significance	6	109449698	109449698	Human		name
156398849	CV1982064	single nucleotide variant	NM_022765.4(MICAL1):c.2171G>A (p.Cys724Tyr)	not provided [RCV002635776]	uncertain significance	6	109447129	109447129	Human		name
156394059	CV1984308	single nucleotide variant	NM_022765.4(MICAL1):c.2014G>A (p.Val672Met)	not provided [RCV002635283]	uncertain significance	6	109447413	109447413	Human		name
156218794	CV1984598	single nucleotide variant	NM_022765.4(MICAL1):c.1898T>A (p.Leu633Ter)	not provided [RCV002626368]	uncertain significance	6	109447921	109447921	Human		name
156342002	CV1984975	single nucleotide variant	NM_022765.4(MICAL1):c.1588G>A (p.Val530Ile)	not provided [RCV002631476]	uncertain significance	6	109448808	109448808	Human		name
156342313	CV1984999	single nucleotide variant	NM_022765.4(MICAL1):c.2051C>T (p.Pro684Leu)	not provided [RCV002631489]	uncertain significance	6	109447376	109447376	Human		name
156323623	CV1988630	single nucleotide variant	NM_022765.4(MICAL1):c.1279G>T (p.Ala427Ser)	not provided [RCV002649412]	uncertain significance	6	109449998	109449998	Human		name
156349586	CV1989356	single nucleotide variant	NM_022765.4(MICAL1):c.2956G>A (p.Ala986Thr)	not provided [RCV002631883]	uncertain significance	6	109444921	109444921	Human		name
156253183	CV1993617	single nucleotide variant	NM_022765.4(MICAL1):c.1661T>G (p.Leu554Arg)	not provided [RCV002627519]	uncertain significance	6	109448735	109448735	Human		name
156124936	CV1995282	single nucleotide variant	NM_022765.4(MICAL1):c.2314A>G (p.Thr772Ala)	not provided [RCV002662999]	uncertain significance	6	109446403	109446403	Human		name
156386832	CV1995845	single nucleotide variant	NM_022765.4(MICAL1):c.2173C>T (p.His725Tyr)	not provided [RCV002654048]	uncertain significance	6	109447127	109447127	Human		name
156261414	CV1996748	single nucleotide variant	NM_022765.4(MICAL1):c.1112G>A (p.Arg371Gln)	not provided [RCV002627777]	uncertain significance	6	109450379	109450379	Human		name
156183842	CV1997652	single nucleotide variant	NM_022765.4(MICAL1):c.1438C>T (p.Arg480Ter)	not provided [RCV002643109]	uncertain significance	6	109449478	109449478	Human		name
156188749	CV1997944	single nucleotide variant	NM_022765.4(MICAL1):c.1899A>C (p.Leu633Phe)	not provided [RCV002643249]	uncertain significance	6	109447920	109447920	Human		name
156234816	CV1999529	single nucleotide variant	NM_022765.4(MICAL1):c.2875C>T (p.Gln959Ter)	not provided [RCV002667717]	uncertain significance	6	109445203	109445203	Human		name
156236136	CV1999593	single nucleotide variant	NM_022765.4(MICAL1):c.1150G>A (p.Ala384Thr)	not provided [RCV002667763]\|not specified [RCV005370268]	uncertain significance	6	109450341	109450341	Human		name
156308728	CV1999962	single nucleotide variant	NM_022765.4(MICAL1):c.1517G>A (p.Gly506Glu)	not provided [RCV002671512]	uncertain significance	6	109448879	109448879	Human		name
156054289	CV2003171	single nucleotide variant	NM_022765.4(MICAL1):c.2303C>A (p.Pro768Gln)	not provided [RCV002659468]	uncertain significance	6	109446697	109446697	Human		name
156374744	CV2003924	single nucleotide variant	NM_022765.4(MICAL1):c.2473C>A (p.Pro825Thr)	not provided [RCV002653201]	likely benign	6	109446244	109446244	Human		name
156402763	CV2010117	single nucleotide variant	NM_022765.4(MICAL1):c.1843G>A (p.Ala615Thr)	not provided [RCV002726154]	uncertain significance	6	109448215	109448215	Human		name
156302876	CV2013554	single nucleotide variant	NM_022765.4(MICAL1):c.1798C>T (p.Leu600Phe)	not provided [RCV002716140]	uncertain significance	6	109448260	109448260	Human		name
156305317	CV2013695	single nucleotide variant	NM_022765.4(MICAL1):c.2405C>G (p.Thr802Ser)	not provided [RCV002716250]	uncertain significance	6	109446312	109446312	Human		name
156307196	CV2013810	single nucleotide variant	NM_022765.4(MICAL1):c.1688T>C (p.Leu563Pro)	not provided [RCV002716337]	uncertain significance	6	109448370	109448370	Human		name
156295896	CV2017051	single nucleotide variant	NM_022765.4(MICAL1):c.1717C>G (p.Leu573Val)	not provided [RCV002715841]	uncertain significance	6	109448341	109448341	Human		name
156316261	CV2018010	single nucleotide variant	NM_022765.4(MICAL1):c.2727G>T (p.Trp909Cys)	not provided [RCV002671918]	uncertain significance	6	109445476	109445476	Human		name
156167471	CV2019802	single nucleotide variant	NM_022765.4(MICAL1):c.1549T>C (p.Trp517Arg)	not provided [RCV002710382]\|not specified [RCV004067656]	uncertain significance	6	109448847	109448847	Human		name
156356610	CV2020062	single nucleotide variant	NM_022765.4(MICAL1):c.2411G>A (p.Arg804Gln)	not provided [RCV002720578]	uncertain significance	6	109446306	109446306	Human		name
156182996	CV2020559	single nucleotide variant	NM_022765.4(MICAL1):c.1735G>A (p.Glu579Lys)	not provided [RCV002710841]	uncertain significance	6	109448323	109448323	Human		name
156364839	CV2020791	single nucleotide variant	NM_022765.4(MICAL1):c.2237A>G (p.Tyr746Cys)	not provided [RCV002721113]\|not specified [RCV004067711]	uncertain significance	6	109446763	109446763	Human		name
156058341	CV2024052	single nucleotide variant	NM_022765.4(MICAL1):c.2489C>T (p.Pro830Leu)	not provided [RCV002736746]	uncertain significance	6	109446228	109446228	Human		name
156320827	CV2025345	single nucleotide variant	NM_022765.4(MICAL1):c.2444G>T (p.Arg815Leu)	not provided [RCV002717077]	uncertain significance	6	109446273	109446273	Human		name
155942736	CV2032393	single nucleotide variant	NM_022765.4(MICAL1):c.2901G>T (p.Lys967Asn)	not provided [RCV002730223]	uncertain significance	6	109444976	109444976	Human		name
156070647	CV2032638	single nucleotide variant	NM_022765.4(MICAL1):c.1567G>A (p.Ala523Thr)	not provided [RCV002760309]	uncertain significance	6	109448829	109448829	Human		name
156090514	CV2034387	single nucleotide variant	NM_022765.4(MICAL1):c.2141G>A (p.Gly714Asp)	not provided [RCV002760928]	uncertain significance	6	109447159	109447159	Human		name
156131406	CV2037467	single nucleotide variant	NM_022765.4(MICAL1):c.1612G>T (p.Ala538Ser)	not provided [RCV002800628]\|not specified [RCV004064805]	uncertain significance	6	109448784	109448784	Human		name
156258272	CV2041356	single nucleotide variant	NM_022765.4(MICAL1):c.2680C>T (p.Gln894Ter)	not provided [RCV002806240]	uncertain significance	6	109445523	109445523	Human		name
156207283	CV2042311	single nucleotide variant	NM_022765.4(MICAL1):c.2708T>C (p.Met903Thr)	not provided [RCV002766466]	uncertain significance	6	109445495	109445495	Human		name
156284955	CV2043073	single nucleotide variant	NM_022765.4(MICAL1):c.2273C>T (p.Ala758Val)	not provided [RCV002770524]	uncertain significance	6	109446727	109446727	Human		name
156164734	CV2045087	single nucleotide variant	NM_022765.4(MICAL1):c.1445T>G (p.Leu482Arg)	not provided [RCV002741673]	uncertain significance	6	109449471	109449471	Human		name
156001621	CV2045598	single nucleotide variant	NM_022765.4(MICAL1):c.2747G>A (p.Arg916His)	not provided [RCV002756235]	uncertain significance	6	109445456	109445456	Human		name
156214806	CV2047470	single nucleotide variant	NM_022765.4(MICAL1):c.1059G>C (p.Gln353His)	not provided [RCV002790390]	uncertain significance	6	109450432	109450432	Human		name
156370805	CV2048749	single nucleotide variant	NM_022765.4(MICAL1):c.1490A>G (p.Lys497Arg)	not provided [RCV002814267]\|not specified [RCV004064845]	uncertain significance	6	109449426	109449426	Human		name
155942399	CV2051229	single nucleotide variant	NM_022765.4(MICAL1):c.1522G>A (p.Ala508Thr)	not provided [RCV002815779]	uncertain significance	6	109448874	109448874	Human		name
156187779	CV2052140	single nucleotide variant	NM_022765.4(MICAL1):c.1976T>C (p.Leu659Pro)	not provided [RCV002828512]	uncertain significance	6	109447691	109447691	Human		name
155937920	CV2054697	single nucleotide variant	NM_022765.4(MICAL1):c.1349A>T (p.Asn450Ile)	not provided [RCV002815498]	uncertain significance	6	109449742	109449742	Human		name
156274793	CV2056151	single nucleotide variant	NM_022765.4(MICAL1):c.2624C>T (p.Ser875Phe)	not provided [RCV002806787]	uncertain significance	6	109445820	109445820	Human		name
156048873	CV2059961	single nucleotide variant	NM_022765.4(MICAL1):c.1093G>C (p.Asp365His)	not provided [RCV002796696]	uncertain significance	6	109450398	109450398	Human		name
156296241	CV2065331	single nucleotide variant	NM_022765.4(MICAL1):c.2696C>T (p.Thr899Ile)	not provided [RCV002856954]	likely benign	6	109445507	109445507	Human		name
156330986	CV2065356	single nucleotide variant	NM_022765.4(MICAL1):c.2557G>C (p.Gly853Arg)	not provided [RCV002835297]	uncertain significance	6	109446160	109446160	Human		name
156065267	CV2065546	single nucleotide variant	NM_022765.4(MICAL1):c.1314C>A (p.Ser438Arg)	not provided [RCV002846904]	uncertain significance	6	109449777	109449777	Human		name
156109336	CV2072603	single nucleotide variant	NM_022765.4(MICAL1):c.2974A>T (p.Met992Leu)	not provided [RCV002870831]	uncertain significance	6	109444903	109444903	Human		name
155954926	CV2077516	single nucleotide variant	NM_022765.4(MICAL1):c.1202C>T (p.Pro401Leu)	not provided [RCV002880710]	uncertain significance	6	109450075	109450075	Human		name
156312682	CV2078955	single nucleotide variant	NM_022765.4(MICAL1):c.2665G>A (p.Val889Met)	not provided [RCV002898810]	uncertain significance	6	109445779	109445779	Human		name
156212549	CV2080103	single nucleotide variant	NM_022765.4(MICAL1):c.2401C>G (p.Pro801Ala)	not provided [RCV002875539]	uncertain significance	6	109446316	109446316	Human		name
156138343	CV2082164	single nucleotide variant	NM_022765.4(MICAL1):c.2910G>A (p.Trp970Ter)	not provided [RCV002871892]	likely benign	6	109444967	109444967	Human		name
156192226	CV2082954	single nucleotide variant	NM_022765.4(MICAL1):c.1145A>T (p.His382Leu)	not provided [RCV002852176]	uncertain significance	6	109450346	109450346	Human		name
156077936	CV2083556	single nucleotide variant	NM_022765.4(MICAL1):c.2089T>A (p.Cys697Ser)	not provided [RCV002847289]	uncertain significance	6	109447211	109447211	Human		name
156114043	CV2084702	single nucleotide variant	NM_022765.4(MICAL1):c.2497C>T (p.Pro833Ser)	not provided [RCV002889305]	uncertain significance	6	109446220	109446220	Human		name
156079201	CV2098539	single nucleotide variant	NM_022765.4(MICAL1):c.1594G>A (p.Asp532Asn)	not provided [RCV002912642]\|not specified [RCV004066028]	uncertain significance	6	109448802	109448802	Human		name
156155480	CV2100498	single nucleotide variant	NM_022765.4(MICAL1):c.2822C>G (p.Ala941Gly)	not provided [RCV002872471]	uncertain significance	6	109445256	109445256	Human		name
156138289	CV2106041	single nucleotide variant	NM_022765.4(MICAL1):c.2932G>A (p.Val978Ile)	not provided [RCV002914807]	uncertain significance	6	109444945	109444945	Human		name
155996002	CV2109372	single nucleotide variant	NM_022765.4(MICAL1):c.1931G>T (p.Arg644Leu)	not provided [RCV002947563]\|not specified [RCV004824067]	likely benign\|uncertain significance	6	109447888	109447888	Human		name
155949807	CV2109675	single nucleotide variant	NM_022765.4(MICAL1):c.2084A>G (p.Asp695Gly)	not provided [RCV002905001]	likely benign	6	109447216	109447216	Human		name
156117478	CV2111233	single nucleotide variant	NM_022765.4(MICAL1):c.1299G>C (p.Leu433Phe)	not provided [RCV002914026]	uncertain significance	6	109449978	109449978	Human		name
155944326	CV2111362	single nucleotide variant	NM_022765.4(MICAL1):c.1153C>G (p.Arg385Gly)	not provided [RCV002904675]\|not specified [RCV004827909]	uncertain significance	6	109450338	109450338	Human		name
156132720	CV2113105	single nucleotide variant	NM_022765.4(MICAL1):c.1483A>G (p.Asn495Asp)	not provided [RCV002928263]	uncertain significance	6	109449433	109449433	Human		name
156327856	CV2116182	single nucleotide variant	NM_022765.4(MICAL1):c.1520C>T (p.Ser507Leu)	not provided [RCV002938190]\|not specified [RCV005362921]	uncertain significance	6	109448876	109448876	Human		name
156328101	CV2116207	single nucleotide variant	NM_022765.4(MICAL1):c.2594T>C (p.Met865Thr)	not provided [RCV002938204]	uncertain significance	6	109445850	109445850	Human		name
156313838	CV2120196	single nucleotide variant	NM_022765.4(MICAL1):c.2608A>G (p.Lys870Glu)	not provided [RCV002962775]	benign	6	109445836	109445836	Human		name
156393297	CV2120403	single nucleotide variant	NM_022765.4(MICAL1):c.1486G>A (p.Asp496Asn)	not provided [RCV002944139]\|not specified [RCV004068347]	uncertain significance	6	109449430	109449430	Human		name
156306852	CV2123162	single nucleotide variant	NM_022765.4(MICAL1):c.2150T>G (p.Phe717Cys)	not provided [RCV002962406]\|not specified [RCV004068287]	uncertain significance	6	109447150	109447150	Human		name
156360781	CV2126438	duplication	NM_022765.4(MICAL1):c.1308dup (p.Glu437Ter)	not provided [RCV002966968]	uncertain significance	6	109449782	109449783	Human		name
156340815	CV2127418	single nucleotide variant	NM_022765.4(MICAL1):c.1111C>T (p.Arg371Trp)	not provided [RCV002938890]	uncertain significance	6	109450380	109450380	Human		name
155963945	CV2134655	single nucleotide variant	NM_022765.4(MICAL1):c.1783A>G (p.Ser595Gly)	not provided [RCV002972516]\|not specified [RCV004065134]	uncertain significance	6	109448275	109448275	Human		name
155938021	CV2135150	single nucleotide variant	NM_022765.4(MICAL1):c.2321G>A (p.Ser774Asn)	not provided [RCV002993867]	uncertain significance	6	109446396	109446396	Human		name
156271338	CV2135342	single nucleotide variant	NM_022765.4(MICAL1):c.1414C>T (p.Arg472Trp)	not provided [RCV002988832]	likely benign	6	109449677	109449677	Human		name
156094241	CV2139416	single nucleotide variant	NM_022765.4(MICAL1):c.2746C>T (p.Arg916Cys)	not provided [RCV002979729]	benign	6	109445457	109445457	Human		name
156092833	CV2143064	single nucleotide variant	NM_022765.4(MICAL1):c.2443C>T (p.Arg815Trp)	not provided [RCV002979675]\|not specified [RCV004065272]	uncertain significance	6	109446274	109446274	Human		name
156309518	CV2150193	single nucleotide variant	NM_022765.4(MICAL1):c.2260A>G (p.Thr754Ala)	not provided [RCV003028495]	uncertain significance	6	109446740	109446740	Human		name
156303197	CV2156687	single nucleotide variant	NM_022765.4(MICAL1):c.2405C>T (p.Thr802Ile)	not provided [RCV003010484]	uncertain significance	6	109446312	109446312	Human		name
155941818	CV2158171	single nucleotide variant	NM_022765.4(MICAL1):c.1954G>A (p.Glu652Lys)	not provided [RCV003014317]	uncertain significance	6	109447713	109447713	Human		name
156187462	CV2160514	single nucleotide variant	NM_022765.4(MICAL1):c.2462T>G (p.Leu821Arg)	not provided [RCV003024023]	uncertain significance	6	109446255	109446255	Human		name
156072985	CV2163726	single nucleotide variant	NM_022765.4(MICAL1):c.2501C>T (p.Pro834Leu)	not provided [RCV003020095]	uncertain significance	6	109446216	109446216	Human		name
156102549	CV2164453	single nucleotide variant	NM_022765.4(MICAL1):c.1378C>G (p.Leu460Val)	not provided [RCV003038638]	uncertain significance	6	109449713	109449713	Human		name
156103862	CV2164560	single nucleotide variant	NM_022765.4(MICAL1):c.1285T>A (p.Ser429Thr)	not provided [RCV003038684]	uncertain significance	6	109449992	109449992	Human		name
156226538	CV2176463	single nucleotide variant	NM_022765.4(MICAL1):c.2224G>C (p.Asp742His)	not provided [RCV003059146]	uncertain significance	6	109447076	109447076	Human		name
156199240	CV2182726	single nucleotide variant	NM_022765.4(MICAL1):c.1238C>G (p.Ala413Gly)	not provided [RCV003024392]	uncertain significance	6	109450039	109450039	Human		name
156241466	CV2188910	single nucleotide variant	NM_022765.4(MICAL1):c.2975T>C (p.Met992Thr)	not provided [RCV003059671]	uncertain significance	6	109444902	109444902	Human		name
156377178	CV2189119	single nucleotide variant	NM_022765.4(MICAL1):c.1847A>C (p.His616Pro)	not provided [RCV003050201]	uncertain significance	6	109448211	109448211	Human		name
156164596	CV2189910	single nucleotide variant	NM_022765.4(MICAL1):c.2672A>C (p.Gln891Pro)	not provided [RCV003040834]	uncertain significance	6	109445772	109445772	Human		name
156290034	CV2192299	single nucleotide variant	NM_022765.4(MICAL1):c.2380C>G (p.Pro794Ala)	not provided [RCV003045104]	uncertain significance	6	109446337	109446337	Human		name
156325549	CV2195422	single nucleotide variant	NM_022765.4(MICAL1):c.1080T>A (p.Asp360Glu)	not specified [RCV004080332]	uncertain significance	6	109450411	109450411	Human		name
156272322	CV2247366	single nucleotide variant	NM_022765.4(MICAL1):c.1360A>C (p.Asn454His)	not specified [RCV004108703]	uncertain significance	6	109449731	109449731	Human		name
156159083	CV2262544	single nucleotide variant	NM_022765.4(MICAL1):c.2360C>T (p.Ala787Val)	not specified [RCV004130755]	uncertain significance	6	109446357	109446357	Human		name
155946164	CV2265997	single nucleotide variant	NM_022765.4(MICAL1):c.2939A>G (p.Lys980Arg)	not specified [RCV004126826]	uncertain significance	6	109444938	109444938	Human		name
156078055	CV2281709	single nucleotide variant	NM_022765.4(MICAL1):c.2848G>A (p.Val950Met)	not provided [RCV003777870]\|not specified [RCV004147858]	likely benign\|uncertain significance	6	109445230	109445230	Human		name
156059744	CV2305351	single nucleotide variant	NM_022765.4(MICAL1):c.1426C>T (p.Pro476Ser)	not specified [RCV004171259]	uncertain significance	6	109449665	109449665	Human		name
156301176	CV2307043	single nucleotide variant	NM_022765.4(MICAL1):c.1232T>C (p.Leu411Pro)	not specified [RCV004159539]	uncertain significance	6	109450045	109450045	Human		name
156254615	CV2311550	single nucleotide variant	NM_022765.4(MICAL1):c.2651C>T (p.Pro884Leu)	not specified [RCV004168370]	uncertain significance	6	109445793	109445793	Human		name
156071206	CV2337741	single nucleotide variant	NM_022765.4(MICAL1):c.2020C>A (p.Pro674Thr)	not specified [RCV004183762]	uncertain significance	6	109447407	109447407	Human		name
156139790	CV2350421	single nucleotide variant	NM_022765.4(MICAL1):c.1922C>A (p.Thr641Asn)	not specified [RCV004204798]	uncertain significance	6	109447897	109447897	Human		name
329389573	CV2445085	single nucleotide variant	NM_022765.4(MICAL1):c.2780A>G (p.Lys927Arg)	not specified [RCV004261689]	uncertain significance	6	109445423	109445423	Human		name
329396354	CV2459546	single nucleotide variant	NM_022765.4(MICAL1):c.2309T>G (p.Leu770Arg)	not specified [RCV004277003]	uncertain significance	6	109446408	109446408	Human		name
329370888	CV2461872	single nucleotide variant	NM_022765.4(MICAL1):c.1577C>T (p.Pro526Leu)	not provided [RCV003720797]\|not specified [RCV004271783]	uncertain significance	6	109448819	109448819	Human		name
401720550	CV2701955	single nucleotide variant	NM_022765.4(MICAL1):c.1890T>G (p.Ser630Arg)	not specified [RCV004320555]	uncertain significance	6	109447929	109447929	Human		name
401877445	CV2769457	single nucleotide variant	NM_022765.4(MICAL1):c.1030G>T (p.Gly344Cys)	not specified [RCV004357433]	uncertain significance	6	109450461	109450461	Human		name
401877448	CV2769458	single nucleotide variant	NM_022765.4(MICAL1):c.1031G>T (p.Gly344Val)	not specified [RCV004357434]	uncertain significance	6	109450460	109450460	Human		name
401882822	CV2775112	single nucleotide variant	NM_022765.4(MICAL1):c.1478G>A (p.Arg493Lys)	not provided [RCV003777548]\|not specified [RCV004346474]	uncertain significance	6	109449438	109449438	Human		name
401862165	CV2775178	single nucleotide variant	NM_022765.4(MICAL1):c.1714G>A (p.Ala572Thr)	not specified [RCV004346524]	uncertain significance	6	109448344	109448344	Human		name
405203658	CV2858408	single nucleotide variant	NM_022765.4(MICAL1):c.2971C>G (p.Leu991Val)	not provided [RCV003551668]	uncertain significance	6	109444906	109444906	Human		name
405086578	CV2862243	single nucleotide variant	NM_022765.4(MICAL1):c.2383G>A (p.Val795Ile)	not provided [RCV003549607]	uncertain significance	6	109446334	109446334	Human		name
405197112	CV2869784	single nucleotide variant	NM_022765.4(MICAL1):c.2694G>T (p.Lys898Asn)	not provided [RCV003550961]	uncertain significance	6	109445509	109445509	Human		name
405218359	CV2873693	single nucleotide variant	NM_022765.4(MICAL1):c.1075C>T (p.Pro359Ser)	not provided [RCV003553516]	uncertain significance	6	109450416	109450416	Human		name
402497147	CV2875450	single nucleotide variant	NM_022765.4(MICAL1):c.2162G>C (p.Cys721Ser)	not provided [RCV003545534]	uncertain significance	6	109447138	109447138	Human		name
405070265	CV2875779	single nucleotide variant	NM_022765.4(MICAL1):c.2989G>A (p.Glu997Lys)	not provided [RCV003548427]	uncertain significance	6	109444791	109444791	Human		name
405070517	CV2876467	single nucleotide variant	NM_022765.4(MICAL1):c.2284G>A (p.Asp762Asn)	not provided [RCV003548503]	uncertain significance	6	109446716	109446716	Human		name
405200366	CV2877161	single nucleotide variant	NM_022765.4(MICAL1):c.1706C>A (p.Thr569Asn)	not provided [RCV003551326]	uncertain significance	6	109448352	109448352	Human		name
402505955	CV2880635	single nucleotide variant	NM_022765.4(MICAL1):c.1087G>A (p.Ala363Thr)	not provided [RCV003546364]	uncertain significance	6	109450404	109450404	Human		name
405147033	CV2881597	single nucleotide variant	NM_022765.4(MICAL1):c.1930C>T (p.Arg644Ter)	not provided [RCV003561441]	uncertain significance	6	109447889	109447889	Human		name
405240582	CV2889208	single nucleotide variant	NM_022765.4(MICAL1):c.2036G>A (p.Gly679Asp)	not provided [RCV003557322]	uncertain significance	6	109447391	109447391	Human		name
405119303	CV2891477	single nucleotide variant	NM_022765.4(MICAL1):c.1369C>T (p.Gln457Ter)	not provided [RCV003558888]	likely benign	6	109449722	109449722	Human		name
405230179	CV2904684	single nucleotide variant	NM_022765.4(MICAL1):c.1944G>T (p.Lys648Asn)	not provided [RCV003555209]	uncertain significance	6	109447875	109447875	Human		name
405164155	CV2905633	single nucleotide variant	NM_022765.4(MICAL1):c.2789C>T (p.Thr930Ile)	not provided [RCV003562605]	uncertain significance	6	109445289	109445289	Human		name
402479749	CV2910793	single nucleotide variant	NM_022765.4(MICAL1):c.2608A>T (p.Lys870Ter)	not provided [RCV003571944]	likely benign	6	109445836	109445836	Human		name
405216019	CV2911296	single nucleotide variant	NM_022765.4(MICAL1):c.2498C>T (p.Pro833Leu)	not provided [RCV003567794]	uncertain significance	6	109446219	109446219	Human		name
405206911	CV2913474	single nucleotide variant	NM_022765.4(MICAL1):c.1969A>G (p.Lys657Glu)	not provided [RCV003566558]	uncertain significance	6	109447698	109447698	Human		name
405210945	CV2921028	single nucleotide variant	NM_022765.4(MICAL1):c.2377G>C (p.Gly793Arg)	not provided [RCV003567157]	uncertain significance	6	109446340	109446340	Human		name
405088699	CV2943446	single nucleotide variant	NM_022765.4(MICAL1):c.1637T>C (p.Leu546Pro)	not provided [RCV003665135]	uncertain significance	6	109448759	109448759	Human		name
402500458	CV2943584	single nucleotide variant	NM_022765.4(MICAL1):c.2249A>G (p.His750Arg)	not provided [RCV003661549]	uncertain significance	6	109446751	109446751	Human		name
405100361	CV2944192	single nucleotide variant	NM_022765.4(MICAL1):c.1366G>C (p.Ala456Pro)	not provided [RCV003665708]	uncertain significance	6	109449725	109449725	Human		name
402490163	CV2948960	single nucleotide variant	NM_022765.4(MICAL1):c.2030A>G (p.Glu677Gly)	not provided [RCV003660471]	uncertain significance	6	109447397	109447397	Human		name
405175634	CV2951849	single nucleotide variant	NM_022765.4(MICAL1):c.1396T>C (p.Tyr466His)	not provided [RCV003675805]	uncertain significance	6	109449695	109449695	Human		name
405246678	CV2966413	single nucleotide variant	NM_022765.4(MICAL1):c.2911G>T (p.Val971Leu)	not provided [RCV003685480]	uncertain significance	6	109444966	109444966	Human		name
405246890	CV2966493	single nucleotide variant	NM_022765.4(MICAL1):c.2815G>A (p.Glu939Lys)	not provided [RCV003685533]	uncertain significance	6	109445263	109445263	Human		name
405188570	CV2977868	single nucleotide variant	NM_022765.4(MICAL1):c.1166G>T (p.Gly389Val)	not provided [RCV003706253]	uncertain significance	6	109450325	109450325	Human		name
405010340	CV2987272	single nucleotide variant	NM_022765.4(MICAL1):c.1982T>C (p.Leu661Ser)	not provided [RCV003693926]	uncertain significance	6	109447685	109447685	Human		name
405204930	CV2990709	single nucleotide variant	NM_022765.4(MICAL1):c.1262A>C (p.Lys421Thr)	not provided [RCV003678610]	uncertain significance	6	109450015	109450015	Human		name
402484559	CV2998174	single nucleotide variant	NM_022765.4(MICAL1):c.2083G>A (p.Asp695Asn)	not provided [RCV003686875]	uncertain significance	6	109447217	109447217	Human		name
402484657	CV3002084	single nucleotide variant	NM_022765.4(MICAL1):c.1135C>T (p.Gln379Ter)	not provided [RCV003686940]	likely benign	6	109450356	109450356	Human		name
405240964	CV3004628	single nucleotide variant	NM_022765.4(MICAL1):c.2909G>A (p.Trp970Ter)	not provided [RCV003719197]	uncertain significance	6	109444968	109444968	Human		name
405001218	CV3005555	single nucleotide variant	NM_022765.4(MICAL1):c.1331C>T (p.Ser444Leu)	not provided [RCV003693196]	uncertain significance	6	109449760	109449760	Human		name
405007802	CV3006562	single nucleotide variant	NM_022765.4(MICAL1):c.1591T>C (p.Ser531Pro)	not provided [RCV003693731]	uncertain significance	6	109448805	109448805	Human		name
404978483	CV3013074	single nucleotide variant	NM_022765.4(MICAL1):c.2062C>T (p.His688Tyr)	not provided [RCV003690820]	uncertain significance	6	109447365	109447365	Human		name
404978967	CV3013242	single nucleotide variant	NM_022765.4(MICAL1):c.1963G>A (p.Gly655Ser)	not provided [RCV003690888]	uncertain significance	6	109447704	109447704	Human		name
405036680	CV3016838	single nucleotide variant	NM_022765.4(MICAL1):c.1007C>A (p.Ala336Glu)	not provided [RCV003695998]	uncertain significance	6	109450484	109450484	Human		name
405162683	CV3017925	single nucleotide variant	NM_022765.4(MICAL1):c.1145A>G (p.His382Arg)	not provided [RCV003704077]	uncertain significance	6	109450346	109450346	Human		name
405122480	CV3020905	single nucleotide variant	NM_022765.4(MICAL1):c.2288G>C (p.Arg763Thr)	not provided [RCV003700907]	uncertain significance	6	109446712	109446712	Human		name
405131735	CV3021869	single nucleotide variant	NM_022765.4(MICAL1):c.2110C>T (p.Leu704Phe)	not provided [RCV003701757]\|not specified [RCV004634323]	uncertain significance	6	109447190	109447190	Human		name
405181303	CV3024303	single nucleotide variant	NM_022765.4(MICAL1):c.2323G>A (p.Glu775Lys)	not provided [RCV003705557]	uncertain significance	6	109446394	109446394	Human		name
405087952	CV3024991	single nucleotide variant	NM_022765.4(MICAL1):c.1457T>C (p.Leu486Pro)	not provided [RCV003699534]	uncertain significance	6	109449459	109449459	Human		name
402480845	CV3033315	single nucleotide variant	NM_022765.4(MICAL1):c.2746C>A (p.Arg916Ser)	not provided [RCV003712771]	uncertain significance	6	109445457	109445457	Human		name
402485010	CV3033760	single nucleotide variant	NM_022765.4(MICAL1):c.2278G>T (p.Gly760Cys)	not provided [RCV003713210]	uncertain significance	6	109446722	109446722	Human		name
402506649	CV3039185	single nucleotide variant	NM_022765.4(MICAL1):c.1986G>T (p.Glu662Asp)	not provided [RCV003715264]	uncertain significance	6	109447681	109447681	Human		name
405094691	CV3045751	single nucleotide variant	NM_022765.4(MICAL1):c.1606T>C (p.Ser536Pro)	not provided [RCV003718077]	uncertain significance	6	109448790	109448790	Human		name
405244623	CV3050717	single nucleotide variant	NM_022765.4(MICAL1):c.2417T>C (p.Ile806Thr)	not provided [RCV003720040]\|not specified [RCV004636821]	uncertain significance	6	109446300	109446300	Human		name
405129339	CV3054502	single nucleotide variant	NM_022765.4(MICAL1):c.2538G>C (p.Glu846Asp)	not provided [RCV003724685]	uncertain significance	6	109446179	109446179	Human		name
405143382	CV3056141	single nucleotide variant	NM_022765.4(MICAL1):c.2882G>T (p.Ser961Ile)	not provided [RCV003725846]	uncertain significance	6	109444995	109444995	Human		name
405221973	CV3056866	single nucleotide variant	NM_022765.4(MICAL1):c.2800C>T (p.Arg934Ter)	not provided [RCV003733447]	likely benign	6	109445278	109445278	Human		name
405183121	CV3057747	single nucleotide variant	NM_022765.4(MICAL1):c.1110G>A (p.Met370Ile)	not provided [RCV003728991]\|not specified [RCV005363236]	uncertain significance	6	109450381	109450381	Human		name
405240704	CV3060739	single nucleotide variant	NM_022765.4(MICAL1):c.1771G>A (p.Val591Met)	not provided [RCV003737120]	uncertain significance	6	109448287	109448287	Human		name
405219866	CV3063430	single nucleotide variant	NM_022765.4(MICAL1):c.2263G>A (p.Asp755Asn)	not provided [RCV003733144]	uncertain significance	6	109446737	109446737	Human		name
405208239	CV3065363	single nucleotide variant	NM_022765.4(MICAL1):c.2639A>G (p.Glu880Gly)	not provided [RCV003731622]	uncertain significance	6	109445805	109445805	Human		name
405206052	CV3068306	single nucleotide variant	NM_022765.4(MICAL1):c.2437C>T (p.Arg813Cys)	not provided [RCV003731323]	uncertain significance	6	109446280	109446280	Human		name
405046823	CV3071477	single nucleotide variant	NM_022765.4(MICAL1):c.2303C>G (p.Pro768Arg)	not provided [RCV003740235]	uncertain significance	6	109446697	109446697	Human		name
405214351	CV3078445	single nucleotide variant	NM_022765.4(MICAL1):c.1979G>A (p.Arg660His)	not provided [RCV003732437]	uncertain significance	6	109447688	109447688	Human		name
405190526	CV3118020	single nucleotide variant	NM_022765.4(MICAL1):c.1964G>A (p.Gly655Asp)	not provided [RCV003820930]	uncertain significance	6	109447703	109447703	Human		name
405191305	CV3118113	single nucleotide variant	NM_022765.4(MICAL1):c.2929C>T (p.Leu977Phe)	not provided [RCV003821023]	uncertain significance	6	109444948	109444948	Human		name
405145026	CV3122701	single nucleotide variant	NM_022765.4(MICAL1):c.2196G>A (p.Trp732Ter)	not provided [RCV003817123]	likely benign	6	109447104	109447104	Human		name
405148148	CV3123151	single nucleotide variant	NM_022765.4(MICAL1):c.2365C>A (p.Gln789Lys)	not provided [RCV003817384]	uncertain significance	6	109446352	109446352	Human		name
405122190	CV3126234	single nucleotide variant	NM_022765.4(MICAL1):c.2254C>T (p.Pro752Ser)	not provided [RCV003814986]	uncertain significance	6	109446746	109446746	Human		name
405123781	CV3126406	single nucleotide variant	NM_022765.4(MICAL1):c.2581G>A (p.Ala861Thr)	not provided [RCV003815158]	uncertain significance	6	109446136	109446136	Human		name
405212559	CV3127518	single nucleotide variant	NM_022765.4(MICAL1):c.2978T>C (p.Ile993Thr)	not provided [RCV003823566]	uncertain significance	6	109444899	109444899	Human		name
405194365	CV3128578	single nucleotide variant	NM_022765.4(MICAL1):c.2144A>G (p.His715Arg)	not provided [RCV003821315]	uncertain significance	6	109447156	109447156	Human		name
405199743	CV3128851	single nucleotide variant	NM_022765.4(MICAL1):c.1931G>A (p.Arg644Gln)	not provided [RCV003821894]	uncertain significance	6	109447888	109447888	Human		name
405198566	CV3132183	single nucleotide variant	NM_022765.4(MICAL1):c.1264C>T (p.Arg422Trp)	not provided [RCV003821776]	uncertain significance	6	109450013	109450013	Human		name
405024426	CV3139484	single nucleotide variant	NM_022765.4(MICAL1):c.2077G>A (p.Ala693Thr)	not provided [RCV003830127]	uncertain significance	6	109447223	109447223	Human		name
405105044	CV3139822	single nucleotide variant	NM_022765.4(MICAL1):c.2731C>T (p.Arg911Trp)	not provided [RCV003835233]	uncertain significance	6	109445472	109445472	Human		name
405069721	CV3140236	single nucleotide variant	NM_022765.4(MICAL1):c.1415G>A (p.Arg472Gln)	not provided [RCV003833391]	uncertain significance	6	109449676	109449676	Human		name
405036433	CV3140499	single nucleotide variant	NM_022765.4(MICAL1):c.2621T>A (p.Phe874Tyr)	not provided [RCV003830981]	uncertain significance	6	109445823	109445823	Human		name
405143839	CV3141376	single nucleotide variant	NM_022765.4(MICAL1):c.1411C>T (p.Leu471Phe)	not provided [RCV003839492]	uncertain significance	6	109449680	109449680	Human		name
405146405	CV3141794	single nucleotide variant	NM_022765.4(MICAL1):c.1636C>G (p.Leu546Val)	not provided [RCV003839716]	uncertain significance	6	109448760	109448760	Human		name
405212929	CV3142734	single nucleotide variant	NM_022765.4(MICAL1):c.2547T>G (p.Phe849Leu)	not provided [RCV003846091]	uncertain significance	6	109446170	109446170	Human		name
405070281	CV3145285	single nucleotide variant	NM_022765.4(MICAL1):c.1895T>A (p.Val632Glu)	not provided [RCV003850870]\|not specified [RCV004369476]	uncertain significance	6	109447924	109447924	Human		name
405208894	CV3145772	single nucleotide variant	NM_022765.4(MICAL1):c.1908T>A (p.Ser636Arg)	not provided [RCV003845502]	uncertain significance	6	109447911	109447911	Human		name
405178396	CV3148697	single nucleotide variant	NM_022765.4(MICAL1):c.1649T>C (p.Leu550Pro)	not provided [RCV003858475]	uncertain significance	6	109448747	109448747	Human		name
405043835	CV3150268	single nucleotide variant	NM_022765.4(MICAL1):c.2932G>C (p.Val978Leu)	not provided [RCV003849062]	uncertain significance	6	109444945	109444945	Human		name
405048381	CV3150773	single nucleotide variant	NM_022765.4(MICAL1):c.2968G>A (p.Glu990Lys)	not provided [RCV003849376]\|not specified [RCV004828001]	uncertain significance	6	109444909	109444909	Human		name
405230536	CV3153896	single nucleotide variant	NM_022765.4(MICAL1):c.1817A>T (p.His606Leu)	not provided [RCV003848764]	uncertain significance	6	109448241	109448241	Human		name
405076495	CV3156200	single nucleotide variant	NM_022765.4(MICAL1):c.1429A>G (p.Asn477Asp)	not provided [RCV003851258]	uncertain significance	6	109449662	109449662	Human		name
405166962	CV3156798	single nucleotide variant	NM_022765.4(MICAL1):c.2953G>A (p.Val985Met)	not provided [RCV003857502]	uncertain significance	6	109444924	109444924	Human		name
405167710	CV3156856	single nucleotide variant	NM_022765.4(MICAL1):c.1295T>C (p.Val432Ala)	not provided [RCV003857560]\|not specified [RCV004369512]	likely benign\|uncertain significance	6	109449982	109449982	Human		name
405224785	CV3158842	single nucleotide variant	NM_022765.4(MICAL1):c.1837A>G (p.Ser613Gly)	not provided [RCV003864144]	uncertain significance	6	109448221	109448221	Human		name
405181376	CV3159509	single nucleotide variant	NM_022765.4(MICAL1):c.2252T>G (p.Leu751Arg)	not provided [RCV003858759]	uncertain significance	6	109446748	109446748	Human		name
405182984	CV3159684	single nucleotide variant	NM_022765.4(MICAL1):c.2375C>T (p.Ala792Val)	not provided [RCV003858935]\|not specified [RCV004824074]	likely benign\|uncertain significance	6	109446342	109446342	Human		name
405245365	CV3161800	single nucleotide variant	NM_022765.4(MICAL1):c.1624G>C (p.Ala542Pro)	not provided [RCV003868513]	uncertain significance	6	109448772	109448772	Human		name
405199168	CV3164457	single nucleotide variant	NM_022765.4(MICAL1):c.2002C>T (p.Pro668Ser)	not provided [RCV003860514]	uncertain significance	6	109447425	109447425	Human		name
405233182	CV3167988	single nucleotide variant	NM_022765.4(MICAL1):c.1361A>G (p.Asn454Ser)	not provided [RCV003865656]	uncertain significance	6	109449730	109449730	Human		name
405235893	CV3168933	single nucleotide variant	NM_022765.4(MICAL1):c.2599A>G (p.Lys867Glu)	not provided [RCV003866212]	uncertain significance	6	109445845	109445845	Human		name
402484066	CV3171227	single nucleotide variant	NM_022765.4(MICAL1):c.2872C>T (p.Arg958Cys)	not provided [RCV003876254]	uncertain significance	6	109445206	109445206	Human		name
402486353	CV3171438	single nucleotide variant	NM_022765.4(MICAL1):c.2504G>T (p.Arg835Leu)	not provided [RCV003876465]	uncertain significance	6	109446213	109446213	Human		name
402473743	CV3172143	single nucleotide variant	NM_022765.4(MICAL1):c.2836G>C (p.Glu946Gln)	not provided [RCV003874746]	uncertain significance	6	109445242	109445242	Human		name
402475666	CV3173674	single nucleotide variant	NM_022765.4(MICAL1):c.2380C>T (p.Pro794Ser)	not provided [RCV003875212]\|not specified [RCV005377603]	uncertain significance	6	109446337	109446337	Human		name
402467877	CV3174103	single nucleotide variant	NM_022765.4(MICAL1):c.2522C>T (p.Ala841Val)	not provided [RCV003873386]	uncertain significance	6	109446195	109446195	Human		name
404990880	CV3176258	single nucleotide variant	NM_022765.4(MICAL1):c.2185G>T (p.Ala729Ser)	not provided [RCV003881583]	uncertain significance	6	109447115	109447115	Human		name
405241355	CV3176933	single nucleotide variant	NM_022765.4(MICAL1):c.1357C>T (p.Arg453Cys)	not provided [RCV003867372]	uncertain significance	6	109449734	109449734	Human		name
402464449	CV3177045	single nucleotide variant	NM_022765.4(MICAL1):c.1216G>A (p.Val406Met)	not provided [RCV003872676]\|not specified [RCV004828004]	uncertain significance	6	109450061	109450061	Human		name
404984421	CV3180053	single nucleotide variant	NM_022765.4(MICAL1):c.2728C>T (p.Arg910Cys)	not provided [RCV003880855]	uncertain significance	6	109445475	109445475	Human		name
405270491	CV3187754	single nucleotide variant	NM_022765.4(MICAL1):c.2348C>G (p.Ser783Ter)	Epilepsy, familial temporal lobe, 1 [RCV003887837]\|not provided [RCV004546818]	likely pathogenic\|uncertain significance	6	109446369	109446369	Human	1	name
405670959	CV3289318	single nucleotide variant	NM_022765.4(MICAL1):c.1136A>C (p.Gln379Pro)	not specified [RCV004419509]	uncertain significance	6	109450355	109450355	Human		name
405670937	CV3289319	single nucleotide variant	NM_022765.4(MICAL1):c.1277G>A (p.Gly426Asp)	not specified [RCV004419510]	uncertain significance	6	109450000	109450000	Human		name
405670947	CV3289321	single nucleotide variant	NM_022765.4(MICAL1):c.1634C>A (p.Ala545Asp)	not specified [RCV004419512]	uncertain significance	6	109448762	109448762	Human		name
405670952	CV3289322	single nucleotide variant	NM_022765.4(MICAL1):c.1727C>T (p.Ala576Val)	not specified [RCV004419513]	uncertain significance	6	109448331	109448331	Human		name
405670964	CV3289324	single nucleotide variant	NM_022765.4(MICAL1):c.2168G>T (p.Arg723Leu)	not specified [RCV004419515]	uncertain significance	6	109447132	109447132	Human		name
405670974	CV3289326	single nucleotide variant	NM_022765.4(MICAL1):c.2374G>A (p.Ala792Thr)	not provided [RCV005104547]\|not specified [RCV004419517]	likely benign\|uncertain significance	6	109446343	109446343	Human		name
405670979	CV3289327	single nucleotide variant	NM_022765.4(MICAL1):c.2425T>C (p.Ser809Pro)	not specified [RCV004419518]	uncertain significance	6	109446292	109446292	Human		name
597645455	CV3563550	single nucleotide variant	NM_022765.4(MICAL1):c.1722G>C (p.Lys574Asn)	not specified [RCV004832912]	uncertain significance	6	109448336	109448336	Human		name
597635643	CV3563551	single nucleotide variant	NM_022765.4(MICAL1):c.2236T>C (p.Tyr746His)	not specified [RCV004824382]	uncertain significance	6	109446764	109446764	Human		name
597645477	CV3563554	single nucleotide variant	NM_022765.4(MICAL1):c.2500C>T (p.Pro834Ser)	not specified [RCV004832915]	uncertain significance	6	109446217	109446217	Human		name
597645491	CV3563556	single nucleotide variant	NM_022765.4(MICAL1):c.1639G>A (p.Val547Met)	not specified [RCV004832917]	uncertain significance	6	109448757	109448757	Human		name
597905547	CV3738647	single nucleotide variant	NM_022765.4(MICAL1):c.2674G>A (p.Ala892Thr)	not provided [RCV005072881]	uncertain significance	6	109445529	109445529	Human		name
597913660	CV3740513	single nucleotide variant	NM_022765.4(MICAL1):c.1852C>T (p.Pro618Ser)	not provided [RCV005073850]	uncertain significance	6	109448206	109448206	Human		name
597933397	CV3742786	single nucleotide variant	NM_022765.4(MICAL1):c.2838G>T (p.Glu946Asp)	not provided [RCV005076225]	uncertain significance	6	109445240	109445240	Human		name
597830892	CV3743625	single nucleotide variant	NM_022765.4(MICAL1):c.2636A>C (p.Glu879Ala)	not provided [RCV005062442]	uncertain significance	6	109445808	109445808	Human		name
597880593	CV3744838	single nucleotide variant	NM_022765.4(MICAL1):c.2293C>T (p.Pro765Ser)	not provided [RCV005069863]	uncertain significance	6	109446707	109446707	Human		name
597849882	CV3746820	single nucleotide variant	NM_022765.4(MICAL1):c.2042C>G (p.Pro681Arg)	not provided [RCV005060447]	uncertain significance	6	109447385	109447385	Human		name
597876903	CV3747916	single nucleotide variant	NM_022765.4(MICAL1):c.1507C>G (p.Pro503Ala)	not provided [RCV005069408]	uncertain significance	6	109449409	109449409	Human		name
597890231	CV3749264	single nucleotide variant	NM_022765.4(MICAL1):c.1823A>C (p.His608Pro)	not provided [RCV005071048]	uncertain significance	6	109448235	109448235	Human		name
597891555	CV3749393	single nucleotide variant	NM_022765.4(MICAL1):c.2109C>G (p.His703Gln)	not provided [RCV005071177]	uncertain significance	6	109447191	109447191	Human		name
597959200	CV3752056	single nucleotide variant	NM_022765.4(MICAL1):c.2000C>T (p.Thr667Ile)	not provided [RCV005081186]	uncertain significance	6	109447427	109447427	Human		name
597938365	CV3760087	single nucleotide variant	NM_022765.4(MICAL1):c.2177C>G (p.Thr726Ser)	not provided [RCV005077011]	uncertain significance	6	109447123	109447123	Human		name
597834013	CV3760505	single nucleotide variant	NM_022765.4(MICAL1):c.2392C>A (p.Pro798Thr)	not provided [RCV005085248]	uncertain significance	6	109446325	109446325	Human		name
597951815	CV3765488	single nucleotide variant	NM_022765.4(MICAL1):c.1072C>A (p.Gln358Lys)	not provided [RCV005121132]	uncertain significance	6	109450419	109450419	Human		name
597922037	CV3775011	single nucleotide variant	NM_022765.4(MICAL1):c.1489A>G (p.Lys497Glu)	not provided [RCV005115357]	uncertain significance	6	109449427	109449427	Human		name
597913629	CV3778735	single nucleotide variant	NM_022765.4(MICAL1):c.1069G>A (p.Gly357Arg)	not provided [RCV005129080]	uncertain significance	6	109450422	109450422	Human		name
597900995	CV3779036	single nucleotide variant	NM_022765.4(MICAL1):c.1313G>A (p.Ser438Asn)	not provided [RCV005127113]	uncertain significance	6	109449778	109449778	Human		name
597942445	CV3779918	single nucleotide variant	NM_022765.4(MICAL1):c.1121G>T (p.Ser374Ile)	not provided [RCV005118927]	uncertain significance	6	109450370	109450370	Human		name
597884654	CV3780631	single nucleotide variant	NM_022765.4(MICAL1):c.2912T>A (p.Val971Glu)	not provided [RCV005124759]	uncertain significance	6	109444965	109444965	Human		name
597878276	CV3783093	single nucleotide variant	NM_022765.4(MICAL1):c.1081G>T (p.Val361Phe)	not provided [RCV005123795]	uncertain significance	6	109450410	109450410	Human		name
597964466	CV3792276	single nucleotide variant	NM_022765.4(MICAL1):c.1303G>A (p.Glu435Lys)	not provided [RCV005139833]	uncertain significance	6	109449974	109449974	Human		name
597973742	CV3801558	single nucleotide variant	NM_022765.4(MICAL1):c.1126G>T (p.Ala376Ser)	not provided [RCV005143547]	uncertain significance	6	109450365	109450365	Human		name
597974250	CV3801851	single nucleotide variant	NM_022765.4(MICAL1):c.1050G>T (p.Glu350Asp)	not provided [RCV005143840]	uncertain significance	6	109450441	109450441	Human		name
597896852	CV3806734	single nucleotide variant	NM_022765.4(MICAL1):c.2401C>T (p.Pro801Ser)	not provided [RCV005152121]	uncertain significance	6	109446316	109446316	Human		name
597934875	CV3807148	single nucleotide variant	NM_022765.4(MICAL1):c.1250C>T (p.Ala417Val)	not provided [RCV005157719]	uncertain significance	6	109450027	109450027	Human		name
597945406	CV3807331	single nucleotide variant	NM_022765.4(MICAL1):c.1009G>A (p.Ala337Thr)	not provided [RCV005159966]	uncertain significance	6	109450482	109450482	Human		name
597938313	CV3808222	single nucleotide variant	NM_022765.4(MICAL1):c.2336C>T (p.Pro779Leu)	not provided [RCV005158410]	uncertain significance	6	109446381	109446381	Human		name
597917866	CV3811231	single nucleotide variant	NM_022765.4(MICAL1):c.2611G>A (p.Glu871Lys)	not provided [RCV005155266]	uncertain significance	6	109445833	109445833	Human		name
597952103	CV3815700	single nucleotide variant	NM_022765.4(MICAL1):c.2914G>A (p.Gly972Arg)	not provided [RCV005161453]	uncertain significance	6	109444963	109444963	Human		name
597913371	CV3817408	single nucleotide variant	NM_022765.4(MICAL1):c.2749G>A (p.Ala917Thr)	not provided [RCV005154610]	uncertain significance	6	109445454	109445454	Human		name
597852067	CV3821181	single nucleotide variant	NM_022765.4(MICAL1):c.2933T>C (p.Val978Ala)	not provided [RCV005173839]	uncertain significance	6	109444944	109444944	Human		name
597857515	CV3822263	single nucleotide variant	NM_022765.4(MICAL1):c.1127C>T (p.Ala376Val)	not provided [RCV005174561]	uncertain significance	6	109450364	109450364	Human		name
597880839	CV3826440	single nucleotide variant	NM_022765.4(MICAL1):c.1028A>G (p.His343Arg)	not provided [RCV005178137]	uncertain significance	6	109450463	109450463	Human		name
597972164	CV3829491	single nucleotide variant	NM_022765.4(MICAL1):c.2509T>C (p.Cys837Arg)	not provided [RCV005167278]	uncertain significance	6	109446208	109446208	Human		name
597908746	CV3829957	single nucleotide variant	NM_022765.4(MICAL1):c.1270G>A (p.Ala424Thr)	not provided [RCV005182526]	uncertain significance	6	109450007	109450007	Human		name
597936181	CV3845387	single nucleotide variant	NM_022765.4(MICAL1):c.1228T>C (p.Phe410Leu)	not provided [RCV005186700]	uncertain significance	6	109450049	109450049	Human		name
597965072	CV3848251	single nucleotide variant	NM_022765.4(MICAL1):c.2797C>T (p.Arg933Trp)	not provided [RCV005194131]	uncertain significance	6	109445281	109445281	Human		name
597902313	CV3851427	single nucleotide variant	NM_022765.4(MICAL1):c.2014G>T (p.Val672Leu)	not provided [RCV005202204]	uncertain significance	6	109447413	109447413	Human		name
597905416	CV3853119	single nucleotide variant	NM_022765.4(MICAL1):c.1751C>T (p.Pro584Leu)	not provided [RCV005202776]	uncertain significance	6	109448307	109448307	Human		name
597893752	CV3857125	single nucleotide variant	NM_022765.4(MICAL1):c.1661T>C (p.Leu554Pro)	not provided [RCV005200988]	uncertain significance	6	109448735	109448735	Human		name
597936281	CV3858988	single nucleotide variant	NM_022765.4(MICAL1):c.2712T>A (p.Asn904Lys)	not provided [RCV005207709]	uncertain significance	6	109445491	109445491	Human		name
598253914	CV3993012	single nucleotide variant	NM_022765.4(MICAL1):c.1580G>C (p.Gly527Ala)	not specified [RCV005367117]	uncertain significance	6	109448816	109448816	Human		name
156412405	CV1972093	indel	NM_022765.4(MICAL1):c.1308-14_1308-13delinsTG	not provided [RCV002608532]	uncertain significance	6	109449796	109449797	Human		name
156092465	CV2106224	indel	NM_022765.4(MICAL1):c.1435-18_1435-17delinsCC	not provided [RCV002952413]	likely benign	6	109449498	109449499	Human		name
405201319	CV3143464	indel	NM_022765.4(MICAL1):c.2228-14_2228-13delinsAT	not provided [RCV003844450]	uncertain significance	6	109446785	109446786	Human		name
151805455	CV1369127	insertion	NM_022765.4(MICAL1):c.2305-17_2305-16insCCACCCTGGGCAGGTGACTGACCAGA	not provided [RCV001991333]	uncertain significance	6	109446428	109446429	Human		name
151745852	CV1457266	insertion	NM_022765.4(MICAL1):c.2305-17_2305-16insCCACCCTGGGCACGTCACTGACCAGA	not provided [RCV001947579]	likely benign\|uncertain significance	6	109446428	109446429	Human		name
152158949	CV1544305	insertion	NM_022765.4(MICAL1):c.2305-17_2305-16insCCACCCTGGGCAGGTCACTGACCAGA	not provided [RCV002122851]	benign	6	109446428	109446429	Human		name
402524980	CV3175946	insertion	NM_022765.4(MICAL1):c.2305-20_2305-19insCTACCCTGGGCAGGTCACTGACCAGA	not provided [RCV003880046]	uncertain significance	6	109446431	109446432	Human		name
151821429	CV1449537	single nucleotide variant	NM_022765.4(MICAL1):c.2168G>A (p.Arg723His)	not provided [RCV002013418]\|not specified [RCV004046207]	likely benign\|uncertain significance	6	109447132	109447132	Human		name
156028537	CV1923043	single nucleotide variant	NM_022765.4(MICAL1):c.1894G>A (p.Val632Ile)	not provided [RCV002612458]\|not specified [RCV004070686]	likely benign\|uncertain significance	6	109447925	109447925	Human		name
156046733	CV2091245	single nucleotide variant	NM_022765.4(MICAL1):c.1645C>T (p.Arg549Trp)	not provided [RCV002886017]	uncertain significance	6	109448751	109448751	Human		name
155937462	CV2114290	single nucleotide variant	NM_022765.4(MICAL1):c.1547G>C (p.Arg516Pro)	not provided [RCV002904239]	uncertain significance	6	109448849	109448849	Human		name
156027855	CV2156185	single nucleotide variant	NM_022765.4(MICAL1):c.1070G>A (p.Gly357Glu)	not provided [RCV003018545]	uncertain significance	6	109450421	109450421	Human		name

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