Mei1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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155 records found for search term Mei1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405276772	CV3206800	single nucleotide variant	NM_152513.4(MEI1):c.174+9G>A	MEI1-related disorder [RCV003917229]	benign	22	41699721	41699721	Human		name , trait , alternate_id
405278548	CV3216665	single nucleotide variant	NM_152513.4(MEI1):c.529+9C>T	MEI1-related disorder [RCV003954559]	likely benign	22	41716155	41716155	Human		name , trait , alternate_id
156341567	CV1871289	single nucleotide variant	NM_152513.4(MEI1):c.3170-1G>C	not provided [RCV003064261]	likely pathogenic	22	41784607	41784607	Human		name
156353242	CV1893517	single nucleotide variant	NM_152513.4(MEI1):c.1097-1G>C	not provided [RCV003091143]	likely pathogenic	22	41732244	41732244	Human		name
155934777	CV2129438	single nucleotide variant	NM_152513.4(MEI1):c.1538+1G>A	not provided [RCV002970860]	likely pathogenic	22	41745065	41745065	Human		name
405292293	CV3192356	single nucleotide variant	NM_152513.4(MEI1):c.3346-6C>A	MEI1-related disorder [RCV003929633]	likely benign	22	41793823	41793823	Human		name , trait , alternate_id
405277342	CV3195432	single nucleotide variant	NM_152513.4(MEI1):c.2816-9C>T	MEI1-related disorder [RCV003904217]	likely benign	22	41781275	41781275	Human		name , trait , alternate_id
405280612	CV3200797	single nucleotide variant	NM_152513.4(MEI1):c.1332-6A>G	MEI1-related disorder [RCV003977422]	benign	22	41743074	41743074	Human		name , trait , alternate_id
405272240	CV3206450	deletion	NM_152513.4(MEI1):c.3346-7del	MEI1-related disorder [RCV003972054]	benign	22	41793807	41793807	Human		name , trait , alternate_id
405283822	CV3213415	single nucleotide variant	NM_152513.4(MEI1):c.2120+9A>G	MEI1-related disorder [RCV003922002]	benign	22	41758542	41758542	Human		name , trait , alternate_id
405265811	CV3215722	single nucleotide variant	NM_152513.4(MEI1):c.1197-5C>T	MEI1-related disorder [RCV003946889]	likely benign	22	41732464	41732464	Human		name , trait , alternate_id
598224497	CV3894133	single nucleotide variant	NM_152513.4(MEI1):c.2269-4C>G	not provided [RCV005257376]	uncertain significance	22	41770682	41770682	Human		name
14691463	CV615932	single nucleotide variant	NM_152513.4(MEI1):c.1196+1G>A	Hydatidiform mole, recurrent, 3 [RCV000770967]	pathogenic	22	41732345	41732345	Human	1	name
405291868	CV3207697	deletion	NM_152513.4(MEI1):c.864+9_864+13del	MEI1-related disorder [RCV003929391]	likely benign	22	41724078	41724082	Human		name , trait , alternate_id
405292372	CV3200061	duplication	NM_152513.4(MEI1):c.3346-8_3346-7dup	MEI1-related disorder [RCV003964479]	likely benign	22	41793806	41793807	Human		name , trait , alternate_id
405272088	CV3203079	deletion	NM_152513.4(MEI1):c.3346-8_3346-7del	MEI1-related disorder [RCV003914127]	benign	22	41793807	41793808	Human		name , trait , alternate_id
405292412	CV3192419	single nucleotide variant	NM_152513.4(MEI1):c.102C>T (p.Arg34=)	MEI1-related disorder [RCV003929685]	likely benign	22	41699640	41699640	Human		name , trait , alternate_id
405258052	CV3208124	single nucleotide variant	NM_152513.4(MEI1):c.615A>G (p.Leu205=)	MEI1-related disorder [RCV003941572]	likely benign	22	41718156	41718156	Human		name , trait , alternate_id
405283091	CV3216934	microsatellite	NM_152513.4(MEI1):c.-3GA[3] (p.Met1fs)	MEI1-related disorder [RCV003979095]	benign	22	41699535	41699536	Human		name , trait , alternate_id
405271017	CV3218842	single nucleotide variant	NM_152513.4(MEI1):c.303A>G (p.Leu101=)	MEI1-related disorder [RCV003971596]	likely benign	22	41705508	41705508	Human		name , trait , alternate_id
405693365	CV3281938	single nucleotide variant	NM_152513.4(MEI1):c.31A>C (p.Thr11Pro)	not specified [RCV004424090]	uncertain significance	22	41699569	41699569	Human		name
405693402	CV3281945	single nucleotide variant	NM_152513.4(MEI1):c.79G>T (p.Ala27Ser)	not specified [RCV004424097]	uncertain significance	22	41699617	41699617	Human		name
407502638	CV3449822	single nucleotide variant	NM_152513.4(MEI1):c.97C>T (p.Pro33Ser)	not specified [RCV004645213]	likely benign	22	41699635	41699635	Human		name
15104457	CV705961	single nucleotide variant	NM_152513.4(MEI1):c.61G>A (p.Ala21Thr)	MEI1-related disorder [RCV003926107]\|not provided [RCV000959690]	benign\|likely benign	22	41699599	41699599	Human	1	name , trait , alternate_id
15126394	CV758115	single nucleotide variant	NM_152513.4(MEI1):c.393C>T (p.Ile131=)	MEI1-related disorder [RCV003902985]\|not provided [RCV000919318]	benign\|likely benign	22	41714045	41714045	Human	1	name , trait , alternate_id
156009562	CV2290905	single nucleotide variant	NM_152513.4(MEI1):c.141C>G (p.Cys47Trp)	not specified [RCV004151470]	uncertain significance	22	41699679	41699679	Human		name
405265214	CV3190395	single nucleotide variant	NM_152513.4(MEI1):c.2667C>A (p.Ile889=)	MEI1-related disorder [RCV003897245]	likely benign	22	41776224	41776224	Human		name , trait , alternate_id
405279786	CV3191515	single nucleotide variant	NM_152513.4(MEI1):c.169G>C (p.Val57Leu)	MEI1-related disorder [RCV003919666]	benign	22	41699707	41699707	Human		name , trait , alternate_id
405286259	CV3192006	single nucleotide variant	NM_152513.4(MEI1):c.1992C>G (p.Pro664=)	MEI1-related disorder [RCV003923936]	likely benign	22	41758405	41758405	Human		name , trait , alternate_id
405288415	CV3197377	single nucleotide variant	NM_152513.4(MEI1):c.2172G>T (p.Ser724=)	MEI1-related disorder [RCV003982473]	benign	22	41763225	41763225	Human		name , trait , alternate_id
405274888	CV3199817	single nucleotide variant	NM_152513.4(MEI1):c.2013T>C (p.Pro671=)	MEI1-related disorder [RCV003973867]	benign	22	41758426	41758426	Human		name , trait , alternate_id
405289300	CV3205094	single nucleotide variant	NM_152513.4(MEI1):c.2535C>T (p.Leu845=)	MEI1-related disorder [RCV003961704]	likely benign	22	41770952	41770952	Human		name , trait , alternate_id
405274547	CV3208926	single nucleotide variant	NM_152513.4(MEI1):c.1101C>T (p.Ile367=)	MEI1-related disorder [RCV003951706]	likely benign	22	41732249	41732249	Human		name , trait , alternate_id
405271012	CV3209191	single nucleotide variant	NM_152513.4(MEI1):c.2805C>T (p.Leu935=)	MEI1-related disorder [RCV003949566]	likely benign	22	41778802	41778802	Human		name , trait , alternate_id
405693277	CV3281921	single nucleotide variant	NM_152513.4(MEI1):c.107T>A (p.Leu36Gln)	not specified [RCV004424073]	uncertain significance	22	41699645	41699645	Human		name
405693343	CV3281933	single nucleotide variant	NM_152513.4(MEI1):c.279C>G (p.His93Gln)	not specified [RCV004424085]	uncertain significance	22	41703435	41703435	Human		name
596926753	CV3542299	single nucleotide variant	NM_152513.4(MEI1):c.186G>C (p.Lys62Asn)	Hydatidiform mole, recurrent, 3 [RCV004796514]	uncertain significance	22	41703342	41703342	Human	1	name
597678082	CV3556563	single nucleotide variant	NM_152513.4(MEI1):c.125G>T (p.Arg42Leu)	not specified [RCV004830490]	uncertain significance	22	41699663	41699663	Human		name
598225532	CV3985762	single nucleotide variant	NM_152513.4(MEI1):c.242C>T (p.Thr81Met)	not specified [RCV005380418]	likely benign	22	41703398	41703398	Human		name
598241436	CV3985766	single nucleotide variant	NM_152513.4(MEI1):c.125G>C (p.Arg42Pro)	not specified [RCV005364813]	uncertain significance	22	41699663	41699663	Human		name
15104462	CV705962	single nucleotide variant	NM_152513.4(MEI1):c.1191G>C (p.Leu397=)	MEI1-related disorder [RCV003926108]\|not provided [RCV000959691]	benign	22	41732339	41732339	Human	1	name , trait , alternate_id
15181602	CV717480	single nucleotide variant	NM_152513.4(MEI1):c.2778A>G (p.Gln926=)	MEI1-related disorder [RCV003928587]\|not provided [RCV000974430]	benign	22	41778775	41778775	Human	1	name , trait , alternate_id
156190032	CV2206001	single nucleotide variant	NM_152513.4(MEI1):c.839C>T (p.Thr280Ile)	not specified [RCV004078419]	uncertain significance	22	41724048	41724048	Human		name
155922023	CV2284252	single nucleotide variant	NM_152513.4(MEI1):c.345T>G (p.Ile115Met)	not specified [RCV004146612]	uncertain significance	22	41705550	41705550	Human		name
156009575	CV2290906	single nucleotide variant	NM_152513.4(MEI1):c.931C>G (p.His311Asp)	not specified [RCV004151471]	uncertain significance	22	41729731	41729731	Human		name
156276552	CV2316544	single nucleotide variant	NM_152513.4(MEI1):c.367A>G (p.Thr123Ala)	not specified [RCV004170008]	uncertain significance	22	41714019	41714019	Human		name
155907073	CV2354361	single nucleotide variant	NM_152513.4(MEI1):c.455T>A (p.Leu152Gln)	not specified [RCV004200315]	uncertain significance	22	41716072	41716072	Human		name
401773830	CV2691422	single nucleotide variant	NM_152513.4(MEI1):c.394C>T (p.Arg132Cys)	not specified [RCV004305280]	uncertain significance	22	41714046	41714046	Human		name
401758856	CV2694315	single nucleotide variant	NM_152513.4(MEI1):c.913A>G (p.Ile305Val)	not specified [RCV004304511]	uncertain significance	22	41729713	41729713	Human		name
401748008	CV2698907	single nucleotide variant	NM_152513.4(MEI1):c.395G>A (p.Arg132His)	not specified [RCV004303450]	likely benign	22	41714047	41714047	Human		name
401771326	CV2711615	single nucleotide variant	NM_152513.4(MEI1):c.787C>G (p.Gln263Glu)	not specified [RCV004307257]	uncertain significance	22	41723996	41723996	Human		name
405285547	CV3212594	single nucleotide variant	NM_152513.4(MEI1):c.3435C>T (p.His1145=)	MEI1-related disorder [RCV003959160]	benign	22	41794378	41794378	Human		name , trait , alternate_id
405285947	CV3221628	single nucleotide variant	NM_152513.4(MEI1):c.3660C>T (p.Phe1220=)	MEI1-related disorder [RCV003981337]	benign	22	41795536	41795536	Human		name , trait , alternate_id
405278466	CV3221963	single nucleotide variant	NM_152513.4(MEI1):c.3054C>A (p.Ser1018=)	MEI1-related disorder [RCV003976504]	benign	22	41781812	41781812	Human		name , trait , alternate_id
405711109	CV3225780	single nucleotide variant	NM_152513.4(MEI1):c.567C>A (p.Tyr189Ter)	Hydatidiform mole, recurrent, 3 [RCV003990838]	uncertain significance	22	41718108	41718108	Human	1	name
405693376	CV3281940	single nucleotide variant	NM_152513.4(MEI1):c.410A>C (p.Glu137Ala)	not specified [RCV004424092]	uncertain significance	22	41714062	41714062	Human		name
405693380	CV3281941	single nucleotide variant	NM_152513.4(MEI1):c.514C>T (p.Leu172Phe)	not specified [RCV004424093]	uncertain significance	22	41716131	41716131	Human		name
405693384	CV3281942	single nucleotide variant	NM_152513.4(MEI1):c.543G>T (p.Glu181Asp)	not specified [RCV004424094]	uncertain significance	22	41718084	41718084	Human		name
405693391	CV3281943	single nucleotide variant	NM_152513.4(MEI1):c.650G>A (p.Gly217Glu)	not specified [RCV004424095]	uncertain significance	22	41718191	41718191	Human		name
405693397	CV3281944	single nucleotide variant	NM_152513.4(MEI1):c.658C>T (p.Arg220Cys)	not specified [RCV004424096]	uncertain significance	22	41718199	41718199	Human		name
405693406	CV3281946	single nucleotide variant	NM_152513.4(MEI1):c.815A>G (p.Asn272Ser)	not specified [RCV004424098]	likely benign	22	41724024	41724024	Human		name
407502629	CV3449818	single nucleotide variant	NM_152513.4(MEI1):c.307T>C (p.Cys103Arg)	not specified [RCV004645209]	uncertain significance	22	41705512	41705512	Human		name
407502641	CV3449823	single nucleotide variant	NM_152513.4(MEI1):c.380T>C (p.Leu127Pro)	not specified [RCV004645214]	uncertain significance	22	41714032	41714032	Human		name
597634731	CV3556550	single nucleotide variant	NM_152513.4(MEI1):c.977C>T (p.Pro326Leu)	not specified [RCV004824212]	uncertain significance	22	41729777	41729777	Human		name
597677473	CV3556555	single nucleotide variant	NM_152513.4(MEI1):c.961A>G (p.Ile321Val)	not specified [RCV004830484]	uncertain significance	22	41729761	41729761	Human		name
597677482	CV3556556	single nucleotide variant	NM_152513.4(MEI1):c.544C>T (p.His182Tyr)	not specified [RCV004830485]	uncertain significance	22	41718085	41718085	Human		name
597677501	CV3556559	single nucleotide variant	NM_152513.4(MEI1):c.920C>T (p.Ala307Val)	not specified [RCV004830487]	uncertain significance	22	41729720	41729720	Human		name
597677512	CV3556560	single nucleotide variant	NM_152513.4(MEI1):c.851T>C (p.Leu284Ser)	not specified [RCV004830488]	uncertain significance	22	41724060	41724060	Human		name
598225550	CV3985765	single nucleotide variant	NM_152513.4(MEI1):c.439T>C (p.Ser147Pro)	not specified [RCV005380421]	uncertain significance	22	41716056	41716056	Human		name
598225561	CV3985768	single nucleotide variant	NM_152513.4(MEI1):c.901A>T (p.Ser301Cys)	not specified [RCV005380423]	uncertain significance	22	41729701	41729701	Human		name
14691465	CV615933	deletion	NM_152513.4(MEI1):c.2206del (p.Val736fs)	Hydatidiform mole, recurrent, 3 [RCV000770968]	pathogenic	22	41763258	41763258	Human	1	name
15163384	CV758116	single nucleotide variant	NM_152513.4(MEI1):c.3060T>C (p.Ser1020=)	not provided [RCV000926115]	likely benign	22	41781818	41781818	Human		name
156080715	CV2195366	single nucleotide variant	NM_152513.4(MEI1):c.2263C>T (p.Arg755Cys)	not specified [RCV004080283]	uncertain significance	22	41763316	41763316	Human		name
155975240	CV2211259	single nucleotide variant	NM_152513.4(MEI1):c.1895A>G (p.Tyr632Cys)	not provided [RCV003434603]\|not specified [RCV004090194]	likely benign	22	41753990	41753990	Human		name
156172203	CV2247500	single nucleotide variant	NM_152513.4(MEI1):c.1403G>A (p.Arg468Gln)	not specified [RCV004108819]	uncertain significance	22	41743151	41743151	Human		name
156357566	CV2254054	single nucleotide variant	NM_152513.4(MEI1):c.1075T>A (p.Ser359Thr)	not specified [RCV004129503]	uncertain significance	22	41730616	41730616	Human		name
155991756	CV2255725	single nucleotide variant	NM_152513.4(MEI1):c.2449G>A (p.Asp817Asn)	not specified [RCV004120116]	uncertain significance	22	41770866	41770866	Human		name
155923368	CV2280285	single nucleotide variant	NM_152513.4(MEI1):c.2473G>A (p.Ala825Thr)	not specified [RCV004140486]	likely benign	22	41770890	41770890	Human		name
156086418	CV2289953	single nucleotide variant	NM_152513.4(MEI1):c.2562C>G (p.Ser854Arg)	not specified [RCV004150603]	uncertain significance	22	41776119	41776119	Human		name
156396456	CV2326283	single nucleotide variant	NM_152513.4(MEI1):c.2603C>A (p.Thr868Asn)	not specified [RCV004180529]	uncertain significance	22	41776160	41776160	Human		name
156220229	CV2345006	single nucleotide variant	NM_152513.4(MEI1):c.2308C>T (p.Pro770Ser)	not specified [RCV004193294]	uncertain significance	22	41770725	41770725	Human		name
156148102	CV2358061	single nucleotide variant	NM_152513.4(MEI1):c.2274G>A (p.Met758Ile)	not specified [RCV004209827]	uncertain significance	22	41770691	41770691	Human		name
156052492	CV2363445	single nucleotide variant	NM_152513.4(MEI1):c.2197C>T (p.Pro733Ser)	not specified [RCV004216022]	uncertain significance	22	41763250	41763250	Human		name
156003530	CV2400892	single nucleotide variant	NM_152513.4(MEI1):c.2570A>G (p.Asp857Gly)	not specified [RCV004244184]	uncertain significance	22	41776127	41776127	Human		name
329379070	CV2460134	single nucleotide variant	NM_152513.4(MEI1):c.1288G>A (p.Glu430Lys)	not specified [RCV004273239]	uncertain significance	22	41732560	41732560	Human		name
401745917	CV2678732	single nucleotide variant	NM_152513.4(MEI1):c.1412A>C (p.Glu471Ala)	not specified [RCV004292729]	uncertain significance	22	41743160	41743160	Human		name
401722011	CV2680784	single nucleotide variant	NM_152513.4(MEI1):c.2572A>G (p.Thr858Ala)	not specified [RCV004293434]	uncertain significance	22	41776129	41776129	Human		name
401781886	CV2689981	single nucleotide variant	NM_152513.4(MEI1):c.1531G>T (p.Ala511Ser)	not specified [RCV004297864]	uncertain significance	22	41745057	41745057	Human		name
401776556	CV2703278	single nucleotide variant	NM_152513.4(MEI1):c.2929G>T (p.Ala977Ser)	not specified [RCV004315638]	uncertain significance	22	41781687	41781687	Human		name
401749276	CV2708531	single nucleotide variant	NM_152513.4(MEI1):c.2851G>A (p.Val951Met)	not specified [RCV004313617]	uncertain significance	22	41781319	41781319	Human		name
401749454	CV2710745	single nucleotide variant	NM_152513.4(MEI1):c.2395C>T (p.Arg799Cys)	not specified [RCV004308682]	uncertain significance	22	41770812	41770812	Human		name
401764615	CV2721413	single nucleotide variant	NM_152513.4(MEI1):c.1040G>T (p.Cys347Phe)	not specified [RCV004322156]	uncertain significance	22	41730581	41730581	Human		name
401888499	CV2761561	single nucleotide variant	NM_152513.4(MEI1):c.2192G>A (p.Arg731His)	not specified [RCV004334728]	uncertain significance	22	41763245	41763245	Human		name
401876854	CV2767739	single nucleotide variant	NM_152513.4(MEI1):c.2465G>T (p.Gly822Val)	not specified [RCV004345868]	uncertain significance	22	41770882	41770882	Human		name
401897606	CV2776435	single nucleotide variant	NM_152513.4(MEI1):c.2225A>G (p.Tyr742Cys)	not specified [RCV004355555]	uncertain significance	22	41763278	41763278	Human		name
401890566	CV2778881	single nucleotide variant	NM_152513.4(MEI1):c.1562A>C (p.Glu521Ala)	not specified [RCV004346766]	uncertain significance	22	41745908	41745908	Human		name
401896639	CV2791853	single nucleotide variant	NM_152513.4(MEI1):c.2248A>G (p.Lys750Glu)	not specified [RCV004359297]	uncertain significance	22	41763301	41763301	Human		name
405266179	CV3186586	single nucleotide variant	NM_152513.4(MEI1):c.2672A>C (p.Gln891Pro)	not provided [RCV003886667]	uncertain significance	22	41776229	41776229	Human		name
405279822	CV3191530	single nucleotide variant	NM_152513.4(MEI1):c.2557T>A (p.Ser853Thr)	MEI1-related disorder [RCV003919681]	benign	22	41776114	41776114	Human		name , trait , alternate_id
405276240	CV3206605	single nucleotide variant	NM_152513.4(MEI1):c.2845A>G (p.Thr949Ala)	MEI1-related disorder [RCV003917050]	benign	22	41781313	41781313	Human		name , trait , alternate_id
405693280	CV3281922	single nucleotide variant	NM_152513.4(MEI1):c.1108G>T (p.Val370Leu)	not specified [RCV004424074]	uncertain significance	22	41732256	41732256	Human		name
405693287	CV3281923	single nucleotide variant	NM_152513.4(MEI1):c.1146C>A (p.Asn382Lys)	not specified [RCV004424075]	uncertain significance	22	41732294	41732294	Human		name
405693294	CV3281924	single nucleotide variant	NM_152513.4(MEI1):c.1253G>A (p.Arg418His)	not specified [RCV004424076]	uncertain significance	22	41732525	41732525	Human		name
405693298	CV3281925	single nucleotide variant	NM_152513.4(MEI1):c.1811G>A (p.Arg604Gln)	not specified [RCV004424077]	uncertain significance	22	41752609	41752609	Human		name
405693303	CV3281926	single nucleotide variant	NM_152513.4(MEI1):c.1873G>A (p.Val625Met)	not specified [RCV004424078]	uncertain significance	22	41753968	41753968	Human		name
405693307	CV3281927	single nucleotide variant	NM_152513.4(MEI1):c.2269A>G (p.Thr757Ala)	not specified [RCV004424079]	likely benign	22	41770686	41770686	Human		name
405693316	CV3281928	single nucleotide variant	NM_152513.4(MEI1):c.2458T>C (p.Ser820Pro)	not specified [RCV004424080]	uncertain significance	22	41770875	41770875	Human		name
405693319	CV3281929	single nucleotide variant	NM_152513.4(MEI1):c.2492T>A (p.Val831Glu)	not specified [RCV004424081]	uncertain significance	22	41770909	41770909	Human		name
405693332	CV3281931	single nucleotide variant	NM_152513.4(MEI1):c.2648G>A (p.Arg883Gln)	not specified [RCV004424083]	uncertain significance	22	41776205	41776205	Human		name
405693339	CV3281932	single nucleotide variant	NM_152513.4(MEI1):c.2714C>T (p.Ser905Leu)	not specified [RCV004424084]	uncertain significance	22	41778711	41778711	Human		name
405693348	CV3281934	single nucleotide variant	NM_152513.4(MEI1):c.2850C>G (p.Asp950Glu)	not specified [RCV004424086]	uncertain significance	22	41781318	41781318	Human		name
405693353	CV3281935	single nucleotide variant	NM_152513.4(MEI1):c.2903C>T (p.Thr968Ile)	not specified [RCV004424087]	uncertain significance	22	41781371	41781371	Human		name
407502631	CV3449819	single nucleotide variant	NM_152513.4(MEI1):c.1903C>T (p.Leu635Phe)	not specified [RCV004645210]	uncertain significance	22	41753998	41753998	Human		name
407502635	CV3449821	single nucleotide variant	NM_152513.4(MEI1):c.1270G>A (p.Val424Ile)	not specified [RCV004645212]	uncertain significance	22	41732542	41732542	Human		name
596926750	CV3542298	single nucleotide variant	NM_152513.4(MEI1):c.2647C>T (p.Arg883Ter)	Hydatidiform mole, recurrent, 3 [RCV004796513]	uncertain significance	22	41776204	41776204	Human	1	name
597677434	CV3556551	single nucleotide variant	NM_152513.4(MEI1):c.2014G>A (p.Glu672Lys)	not specified [RCV004830480]	uncertain significance	22	41758427	41758427	Human		name
597677441	CV3556552	single nucleotide variant	NM_152513.4(MEI1):c.1627T>G (p.Phe543Val)	not specified [RCV004830481]	uncertain significance	22	41745973	41745973	Human		name
597677452	CV3556553	single nucleotide variant	NM_152513.4(MEI1):c.1628T>C (p.Phe543Ser)	not specified [RCV004830482]	uncertain significance	22	41745974	41745974	Human		name
597677462	CV3556554	single nucleotide variant	NM_152513.4(MEI1):c.1756G>A (p.Val586Ile)	not specified [RCV004830483]	uncertain significance	22	41748182	41748182	Human		name
597677523	CV3556561	single nucleotide variant	NM_152513.4(MEI1):c.2555A>G (p.Tyr852Cys)	not specified [RCV004830489]	uncertain significance	22	41776112	41776112	Human		name
597634742	CV3556562	single nucleotide variant	NM_152513.4(MEI1):c.2798T>C (p.Met933Thr)	not specified [RCV004824214]	uncertain significance	22	41778795	41778795	Human		name
598241430	CV3985761	single nucleotide variant	NM_152513.4(MEI1):c.1709C>T (p.Ala570Val)	not specified [RCV005364812]	uncertain significance	22	41748135	41748135	Human		name
598225538	CV3985763	single nucleotide variant	NM_152513.4(MEI1):c.2866C>T (p.Pro956Ser)	not specified [RCV005380419]	uncertain significance	22	41781334	41781334	Human		name
598225544	CV3985764	single nucleotide variant	NM_152513.4(MEI1):c.2033C>G (p.Ser678Cys)	not specified [RCV005380420]	uncertain significance	22	41758446	41758446	Human		name
598225555	CV3985767	single nucleotide variant	NM_152513.4(MEI1):c.1658C>T (p.Ser553Leu)	not specified [RCV005380422]	uncertain significance	22	41746004	41746004	Human		name
598241443	CV3985769	single nucleotide variant	NM_152513.4(MEI1):c.2799G>A (p.Met933Ile)	not specified [RCV005364814]	uncertain significance	22	41778796	41778796	Human		name
598225567	CV3985770	single nucleotide variant	NM_152513.4(MEI1):c.1835G>C (p.Arg612Thr)	not specified [RCV005380424]	uncertain significance	22	41752633	41752633	Human		name
598225572	CV3985772	single nucleotide variant	NM_152513.4(MEI1):c.2618A>G (p.Asn873Ser)	not specified [RCV005380425]	uncertain significance	22	41776175	41776175	Human		name
15104466	CV705963	single nucleotide variant	NM_152513.4(MEI1):c.2303G>A (p.Gly768Asp)	MEI1-related disorder [RCV003916006]\|not provided [RCV000959692]	benign\|likely benign	22	41770720	41770720	Human	1	name , trait , alternate_id
15148655	CV717479	single nucleotide variant	NM_152513.4(MEI1):c.1969G>C (p.Glu657Gln)	MEI1-related disorder [RCV003928432]\|not provided [RCV000967590]	benign	22	41758382	41758382	Human	1	name , trait , alternate_id
8637659	CV92885	single nucleotide variant	NM_152513.3(MEI1):c.1520G>A (p.Gly507Glu)	Malignant melanoma [RCV000072983]	not provided	22	41745046	41745046	Human		name
155915752	CV2200499	single nucleotide variant	NM_152513.4(MEI1):c.3548G>A (p.Arg1183Gln)	not specified [RCV004078854]	likely benign	22	41795424	41795424	Human		name
156063891	CV2228857	single nucleotide variant	NM_152513.4(MEI1):c.3127A>G (p.Lys1043Glu)	not specified [RCV004095090]	uncertain significance	22	41784378	41784378	Human		name
155978999	CV2247163	single nucleotide variant	NM_152513.4(MEI1):c.3049G>A (p.Ala1017Thr)	not specified [RCV004114687]	uncertain significance	22	41781807	41781807	Human		name
156138462	CV2280674	single nucleotide variant	NM_152513.4(MEI1):c.3293G>A (p.Arg1098Gln)	not specified [RCV004143138]	uncertain significance	22	41784731	41784731	Human		name
156179305	CV2327651	single nucleotide variant	NM_152513.4(MEI1):c.3022C>G (p.Leu1008Val)	not specified [RCV004177231]	uncertain significance	22	41781780	41781780	Human		name
156154133	CV2328609	single nucleotide variant	NM_152513.4(MEI1):c.3569A>G (p.His1190Arg)	not specified [RCV004177865]	uncertain significance	22	41795445	41795445	Human		name
156179360	CV2331382	single nucleotide variant	NM_152513.4(MEI1):c.3530C>T (p.Thr1177Ile)	not specified [RCV004184020]	uncertain significance	22	41794473	41794473	Human		name
156199659	CV2331384	single nucleotide variant	NM_152513.4(MEI1):c.3782G>T (p.Cys1261Phe)	not specified [RCV004184022]	uncertain significance	22	41799256	41799256	Human		name
243052395	CV2416022	single nucleotide variant	NM_152513.4(MEI1):c.3772G>T (p.Asp1258Tyr)	Hydatidiform mole, recurrent, 3 [RCV003149079]\|MEI1-related disorder [RCV003936713]	likely pathogenic\|benign	22	41795840	41795840	Human	1	name , trait , alternate_id
401829691	CV2743923	single nucleotide variant	NM_152513.4(MEI1):c.3292C>T (p.Arg1098Ter)	not provided [RCV003327100]	uncertain significance	22	41784730	41784730	Human		name
405266561	CV3213146	single nucleotide variant	NM_152513.4(MEI1):c.3145A>G (p.Lys1049Glu)	MEI1-related disorder [RCV003969300]	likely benign	22	41784396	41784396	Human		name , trait , alternate_id
405693358	CV3281936	single nucleotide variant	NM_152513.4(MEI1):c.3098C>T (p.Thr1033Ile)	not specified [RCV004424088]	uncertain significance	22	41784349	41784349	Human		name
405693360	CV3281937	single nucleotide variant	NM_152513.4(MEI1):c.3196G>A (p.Ala1066Thr)	not specified [RCV004424089]	uncertain significance	22	41784634	41784634	Human		name
405693370	CV3281939	single nucleotide variant	NM_152513.4(MEI1):c.3299C>T (p.Ser1100Leu)	not specified [RCV004424091]	uncertain significance	22	41784737	41784737	Human		name
407518079	CV3449824	single nucleotide variant	NM_152513.4(MEI1):c.3506G>C (p.Arg1169Thr)	not specified [RCV004628746]	uncertain significance	22	41794449	41794449	Human		name
407502645	CV3449825	single nucleotide variant	NM_152513.4(MEI1):c.3703G>A (p.Ala1235Thr)	not specified [RCV004645215]	uncertain significance	22	41795771	41795771	Human		name
597677491	CV3556557	single nucleotide variant	NM_152513.4(MEI1):c.3133C>G (p.Leu1045Val)	not specified [RCV004830486]	uncertain significance	22	41784384	41784384	Human		name
597634736	CV3556558	single nucleotide variant	NM_152513.4(MEI1):c.3463T>A (p.Leu1155Met)	not specified [RCV004824213]	uncertain significance	22	41794406	41794406	Human		name
598241449	CV3985771	single nucleotide variant	NM_152513.4(MEI1):c.3458G>A (p.Arg1153Gln)	not specified [RCV005364815]	uncertain significance	22	41794401	41794401	Human		name
598225577	CV3985773	single nucleotide variant	NM_152513.4(MEI1):c.3154G>C (p.Ala1052Pro)	not specified [RCV005380426]	uncertain significance	22	41784405	41784405	Human		name
14689848	CV615931	single nucleotide variant	NM_152513.4(MEI1):c.3452G>A (p.Trp1151Ter)	Hydatidiform mole, recurrent, 3 [RCV000770966]	pathogenic\|likely pathogenic	22	41794395	41794395	Human	1	name
15171425	CV742944	single nucleotide variant	NM_152513.4(MEI1):c.3749C>T (p.Ser1250Phe)	not provided [RCV000905466]	likely benign	22	41795817	41795817	Human		name
243052052	CV2416021	microsatellite	NM_152513.4(MEI1):c.868CTC[1] (p.Leu291del)	Hydatidiform mole, recurrent, 3 [RCV003149078]	likely benign	22	41729668	41729670	Human		name
156153019	CV2131881	microsatellite	NM_152513.4(MEI1):c.1000_1003del (p.Ser334fs)	not provided [RCV002982720]	pathogenic	22	41730537	41730540	Human		name

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