Nfatc2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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144 records found for search term Nfatc2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
153000405	CV1685551	single nucleotide variant	NM_012340.5(NFATC2):c.*71T>G	Dilated cardiomyopathy 1A [RCV002259538]	likely pathogenic	20	51391425	51391425	Human	2	name
156178132	CV2201569	single nucleotide variant	NM_012340.5(NFATC2):c.*96C>T	not specified [RCV004080058]	uncertain significance	20	51391400	51391400	Human		name
156050379	CV2304574	single nucleotide variant	NM_012340.5(NFATC2):c.*57T>C	not specified [RCV004166471]	uncertain significance	20	51391439	51391439	Human		name
401919805	CV2824493	single nucleotide variant	NM_012340.5(NFATC2):c.*52A>G	not provided [RCV003431363]	likely benign	20	51391444	51391444	Human		name
405080141	CV3137155	duplication	NM_012340.5(NFATC2):c.*45-19dup	not provided [RCV003834054]	benign	20	51391469	51391470	Human		name
8586525	CV121128	single nucleotide variant	NM_001136021.2(NFATC2):c.1100+2786G>T	Lung cancer [RCV000101648]	uncertain significance	20	51520295	51520295	Human		name
155961376	CV2285522	single nucleotide variant	NM_012340.5(NFATC2):c.40G>C (p.Asp14His)	not specified [RCV004139365]	uncertain significance	20	51542460	51542460	Human		name
156259609	CV2322244	single nucleotide variant	NM_012340.5(NFATC2):c.31G>A (p.Asp11Asn)	not specified [RCV004176015]	uncertain significance	20	51542469	51542469	Human		name
407489974	CV3451184	single nucleotide variant	NM_012340.5(NFATC2):c.92C>T (p.Ser31Phe)	not specified [RCV004641580]	uncertain significance	20	51542408	51542408	Human		name
597641003	CV3562883	single nucleotide variant	NM_012340.5(NFATC2):c.64G>C (p.Gly22Arg)	not specified [RCV004832193]	uncertain significance	20	51542436	51542436	Human		name
15112874	CV757609	single nucleotide variant	NM_012340.5(NFATC2):c.759G>A (p.Arg253=)	not provided [RCV000916992]	likely benign	20	51523482	51523482	Human		name
155920840	CV2211982	single nucleotide variant	NM_012340.5(NFATC2):c.266C>A (p.Pro89Gln)	not specified [RCV004088899]	uncertain significance	20	51523975	51523975	Human		name
155990011	CV2258888	single nucleotide variant	NM_012340.5(NFATC2):c.265C>T (p.Pro89Ser)	not specified [RCV004118094]	uncertain significance	20	51523976	51523976	Human		name
155911311	CV2303793	single nucleotide variant	NM_012340.5(NFATC2):c.277G>A (p.Gly93Arg)	not specified [RCV004163634]	uncertain significance	20	51523964	51523964	Human		name
155924873	CV2348229	single nucleotide variant	NM_012340.5(NFATC2):c.236C>T (p.Ser79Phe)	not specified [RCV004191272]	uncertain significance	20	51524005	51524005	Human		name
407526719	CV3451182	single nucleotide variant	NM_012340.5(NFATC2):c.126C>A (p.Asn42Lys)	not specified [RCV004654917]	uncertain significance	20	51542374	51542374	Human		name
407489984	CV3451190	single nucleotide variant	NM_012340.5(NFATC2):c.266C>T (p.Pro89Leu)	not specified [RCV004641582]	uncertain significance	20	51523975	51523975	Human		name
597640993	CV3562881	single nucleotide variant	NM_012340.5(NFATC2):c.244C>A (p.Pro82Thr)	not specified [RCV004832191]	uncertain significance	20	51523997	51523997	Human		name
15202861	CV705546	single nucleotide variant	NM_012340.5(NFATC2):c.2631C>T (p.Asn877=)	not provided [RCV000958075]	benign	20	51432158	51432158	Human		name
15099560	CV705548	single nucleotide variant	NM_012340.5(NFATC2):c.151G>C (p.Val51Leu)	not provided [RCV000958780]	benign	20	51524090	51524090	Human		name
15178813	CV717040	single nucleotide variant	NM_012340.5(NFATC2):c.2247C>T (p.Ala749=)	not provided [RCV000973756]	benign	20	51432542	51432542	Human		name
15162924	CV717041	single nucleotide variant	NM_012340.5(NFATC2):c.1089G>A (p.Ser363=)	not provided [RCV000970371]	benign	20	51523152	51523152	Human		name
15191412	CV728729	single nucleotide variant	NM_012340.5(NFATC2):c.1224C>T (p.Tyr408=)	not provided [RCV000888372]	benign\|likely benign	20	51516892	51516892	Human		name
15102690	CV757607	single nucleotide variant	NM_012340.5(NFATC2):c.2067T>C (p.Tyr689=)	not provided [RCV000915014]	likely benign	20	51432722	51432722	Human		name
15172063	CV773162	single nucleotide variant	NM_012340.5(NFATC2):c.1131G>A (p.Lys377=)	not provided [RCV000928033]	likely benign	20	51523110	51523110	Human		name
156389791	CV2222731	single nucleotide variant	NM_012340.5(NFATC2):c.818G>A (p.Arg273Gln)	not specified [RCV004101577]	uncertain significance	20	51523423	51523423	Human		name
156300421	CV2248809	single nucleotide variant	NM_012340.5(NFATC2):c.317C>A (p.Ala106Asp)	not specified [RCV004121958]	uncertain significance	20	51523924	51523924	Human		name
155915009	CV2264825	single nucleotide variant	NM_012340.5(NFATC2):c.586G>A (p.Gly196Ser)	not specified [RCV004134583]	uncertain significance	20	51523655	51523655	Human		name
329402257	CV2454099	single nucleotide variant	NM_012340.5(NFATC2):c.593C>A (p.Pro198His)	not specified [RCV004265602]	uncertain significance	20	51523648	51523648	Human		name
401751266	CV2696280	single nucleotide variant	NM_012340.5(NFATC2):c.773A>G (p.Glu258Gly)	not specified [RCV004310616]	likely benign	20	51523468	51523468	Human		name
401751272	CV2696282	single nucleotide variant	NM_012340.5(NFATC2):c.788T>C (p.Leu263Pro)	not specified [RCV004310618]	likely benign	20	51523453	51523453	Human		name
401752145	CV2710337	single nucleotide variant	NM_012340.5(NFATC2):c.317C>T (p.Ala106Val)	not specified [RCV004317509]	uncertain significance	20	51523924	51523924	Human		name
401729078	CV2730010	single nucleotide variant	NM_012340.5(NFATC2):c.673A>G (p.Ser225Gly)	not specified [RCV004332989]	uncertain significance	20	51523568	51523568	Human		name
401884060	CV2765014	single nucleotide variant	NM_012340.5(NFATC2):c.722C>T (p.Pro241Leu)	not specified [RCV004337137]	uncertain significance	20	51523519	51523519	Human		name
401870902	CV2788940	single nucleotide variant	NM_012340.5(NFATC2):c.691T>C (p.Cys231Arg)	not specified [RCV004363262]	uncertain significance	20	51523550	51523550	Human		name
405715221	CV3361098	single nucleotide variant	NM_012340.5(NFATC2):c.325C>A (p.Leu109Met)	not specified [RCV004494453]	uncertain significance	20	51523916	51523916	Human		name
405715611	CV3361122	single nucleotide variant	NM_012340.5(NFATC2):c.682G>A (p.Glu228Lys)	not specified [RCV004494477]	uncertain significance	20	51523559	51523559	Human		name
405715310	CV3361135	single nucleotide variant	NM_012340.5(NFATC2):c.959C>G (p.Pro320Arg)	not specified [RCV004494490]	uncertain significance	20	51523282	51523282	Human		name
405715323	CV3361137	single nucleotide variant	NM_012340.5(NFATC2):c.977G>A (p.Ser326Asn)	not specified [RCV004494492]	uncertain significance	20	51523264	51523264	Human		name
407489980	CV3451186	single nucleotide variant	NM_012340.5(NFATC2):c.422C>T (p.Pro141Leu)	not specified [RCV004641581]	uncertain significance	20	51523819	51523819	Human		name
597640977	CV3562878	single nucleotide variant	NM_012340.5(NFATC2):c.436G>A (p.Ala146Thr)	not specified [RCV004832188]	uncertain significance	20	51523805	51523805	Human		name
597640982	CV3562879	single nucleotide variant	NM_012340.5(NFATC2):c.571G>C (p.Val191Leu)	not specified [RCV004832189]	uncertain significance	20	51523670	51523670	Human		name
597641031	CV3562888	single nucleotide variant	NM_012340.5(NFATC2):c.737C>T (p.Ser246Leu)	not specified [RCV004832198]	uncertain significance	20	51523504	51523504	Human		name
598191830	CV3997593	single nucleotide variant	NM_012340.5(NFATC2):c.320C>T (p.Ser107Leu)	not specified [RCV005374261]	uncertain significance	20	51523921	51523921	Human		name
598191835	CV3997594	single nucleotide variant	NM_012340.5(NFATC2):c.830C>T (p.Pro277Leu)	not specified [RCV005374262]	uncertain significance	20	51523411	51523411	Human		name
598191860	CV3997599	single nucleotide variant	NM_012340.5(NFATC2):c.533T>A (p.Phe178Tyr)	not specified [RCV005374266]	uncertain significance	20	51523708	51523708	Human		name
598191868	CV3997600	single nucleotide variant	NM_012340.5(NFATC2):c.877G>A (p.Gly293Arg)	not specified [RCV005374267]	uncertain significance	20	51523364	51523364	Human		name
598238073	CV3997603	single nucleotide variant	NM_012340.5(NFATC2):c.785C>A (p.Ala262Asp)	not specified [RCV005382689]	uncertain significance	20	51523456	51523456	Human		name
156232318	CV2199730	single nucleotide variant	NM_012340.5(NFATC2):c.1937G>A (p.Arg646Gln)	not specified [RCV004072459]	uncertain significance	20	51435283	51435283	Human		name
155926856	CV2230694	single nucleotide variant	NM_012340.5(NFATC2):c.2638C>G (p.Pro880Ala)	not specified [RCV004097639]	uncertain significance	20	51432151	51432151	Human		name
156308832	CV2249566	single nucleotide variant	NM_012340.5(NFATC2):c.2221C>G (p.Arg741Gly)	not specified [RCV004120591]	uncertain significance	20	51432568	51432568	Human		name
156113848	CV2268431	single nucleotide variant	NM_012340.5(NFATC2):c.2636C>T (p.Pro879Leu)	not specified [RCV004130136]	uncertain significance	20	51432153	51432153	Human		name
156193520	CV2296986	single nucleotide variant	NM_012340.5(NFATC2):c.2438A>G (p.Tyr813Cys)	not specified [RCV004150915]	uncertain significance	20	51432351	51432351	Human		name
156090539	CV2302574	single nucleotide variant	NM_012340.5(NFATC2):c.1976A>G (p.Tyr659Cys)	not specified [RCV004160742]	uncertain significance	20	51435244	51435244	Human		name
156285605	CV2317649	single nucleotide variant	NM_012340.5(NFATC2):c.2045A>G (p.Lys682Arg)	not specified [RCV004172584]	uncertain significance	20	51432744	51432744	Human		name
156396198	CV2326147	single nucleotide variant	NM_012340.5(NFATC2):c.2284C>G (p.Leu762Val)	not specified [RCV004180419]	uncertain significance	20	51432505	51432505	Human		name
156178978	CV2327579	single nucleotide variant	NM_012340.5(NFATC2):c.2093C>T (p.Thr698Ile)	not specified [RCV004176876]	uncertain significance	20	51432696	51432696	Human		name
156221222	CV2343814	single nucleotide variant	NM_012340.5(NFATC2):c.2218G>A (p.Ala740Thr)	not provided [RCV004695625]\|not specified [RCV004193400]	uncertain significance	20	51432571	51432571	Human		name
155981343	CV2351307	single nucleotide variant	NM_012340.5(NFATC2):c.1487C>T (p.Thr496Ile)	not specified [RCV004193011]	uncertain significance	20	51475506	51475506	Human		name
156110347	CV2353250	single nucleotide variant	NM_012340.5(NFATC2):c.1208G>A (p.Ser403Asn)	not specified [RCV004203715]	uncertain significance	20	51516908	51516908	Human		name
156189475	CV2356619	single nucleotide variant	NM_012340.5(NFATC2):c.2512G>C (p.Ala838Pro)	not specified [RCV004201983]	uncertain significance	20	51432277	51432277	Human		name
156255262	CV2358981	single nucleotide variant	NM_012340.5(NFATC2):c.2537C>T (p.Pro846Leu)	not specified [RCV004212310]	uncertain significance	20	51432252	51432252	Human		name
156346659	CV2382780	single nucleotide variant	NM_012340.5(NFATC2):c.1505C>T (p.Pro502Leu)	not specified [RCV004224125]	uncertain significance	20	51475488	51475488	Human		name
156052429	CV2386603	single nucleotide variant	NM_012340.5(NFATC2):c.1582C>A (p.Leu528Met)	not specified [RCV004230949]	uncertain significance	20	51474106	51474106	Human		name
329370894	CV2461874	single nucleotide variant	NM_012340.5(NFATC2):c.2057C>T (p.Thr686Met)	not specified [RCV004271785]	uncertain significance	20	51432732	51432732	Human		name
329393505	CV2467040	single nucleotide variant	NM_012340.5(NFATC2):c.2180C>T (p.Pro727Leu)	not specified [RCV004282781]	uncertain significance	20	51432609	51432609	Human		name
401729209	CV2673191	single nucleotide variant	NM_012340.5(NFATC2):c.1183C>T (p.Pro395Ser)	not specified [RCV004286002]	uncertain significance	20	51516933	51516933	Human		name
401744659	CV2697045	single nucleotide variant	NM_012340.5(NFATC2):c.2164G>C (p.Val722Leu)	not specified [RCV004293032]	uncertain significance	20	51432625	51432625	Human		name
401773544	CV2709364	single nucleotide variant	NM_012340.5(NFATC2):c.2248G>A (p.Val750Ile)	not specified [RCV004316505]	uncertain significance	20	51432541	51432541	Human		name
401889796	CV2755000	single nucleotide variant	NM_012340.5(NFATC2):c.2500T>C (p.Cys834Arg)	not specified [RCV004335157]	uncertain significance	20	51432289	51432289	Human		name
401884475	CV2761754	single nucleotide variant	NM_012340.5(NFATC2):c.1952G>A (p.Arg651His)	not specified [RCV004339407]	uncertain significance	20	51435268	51435268	Human		name
401891159	CV2769099	single nucleotide variant	NM_012340.5(NFATC2):c.1715G>A (p.Arg572Gln)	not specified [RCV004348955]	uncertain significance	20	51454682	51454682	Human		name
401887063	CV2771364	single nucleotide variant	NM_012340.5(NFATC2):c.2413C>A (p.Gln805Lys)	not specified [RCV004348123]	uncertain significance	20	51432376	51432376	Human		name
401930481	CV2824494	single nucleotide variant	NM_012340.5(NFATC2):c.1151C>G (p.Pro384Arg)	not provided [RCV003440443]	uncertain significance	20	51523090	51523090	Human		name
405700314	CV3350956	single nucleotide variant	NM_012340.5(NFATC2):c.1378A>C (p.Ile460Leu)	not specified [RCV004492357]	uncertain significance	20	51475615	51475615	Human		name
405700413	CV3350972	single nucleotide variant	NM_012340.5(NFATC2):c.1733C>G (p.Pro578Arg)	not specified [RCV004492373]	uncertain significance	20	51454664	51454664	Human		name
405700484	CV3350986	single nucleotide variant	NM_012340.5(NFATC2):c.2000G>A (p.Arg667Gln)	not specified [RCV004492387]	uncertain significance	20	51435220	51435220	Human		name
405700513	CV3350991	single nucleotide variant	NM_012340.5(NFATC2):c.2135C>T (p.Pro712Leu)	not specified [RCV004492392]	uncertain significance	20	51432654	51432654	Human		name
405700568	CV3361029	single nucleotide variant	NM_012340.5(NFATC2):c.2173A>G (p.Met725Val)	not specified [RCV004492401]	uncertain significance	20	51432616	51432616	Human		name
405714872	CV3361047	single nucleotide variant	NM_012340.5(NFATC2):c.2374G>A (p.Gly792Ser)	not specified [RCV004494402]	uncertain significance	20	51432415	51432415	Human		name
407526715	CV3451180	single nucleotide variant	NM_012340.5(NFATC2):c.1147A>C (p.Ile383Leu)	not specified [RCV004654916]	uncertain significance	20	51523094	51523094	Human		name
407489970	CV3451181	single nucleotide variant	NM_012340.5(NFATC2):c.2096A>G (p.His699Arg)	not specified [RCV004641579]	uncertain significance	20	51432693	51432693	Human		name
407526721	CV3451183	single nucleotide variant	NM_012340.5(NFATC2):c.1379T>C (p.Ile460Thr)	not specified [RCV004654918]	uncertain significance	20	51475614	51475614	Human		name
407526724	CV3451185	single nucleotide variant	NM_012340.5(NFATC2):c.2243C>T (p.Ala748Val)	not specified [RCV004654919]	uncertain significance	20	51432546	51432546	Human		name
407526727	CV3451187	single nucleotide variant	NM_012340.5(NFATC2):c.2462G>A (p.Arg821His)	not specified [RCV004654920]	uncertain significance	20	51432327	51432327	Human		name
407526732	CV3451189	single nucleotide variant	NM_012340.5(NFATC2):c.2028C>G (p.His676Gln)	not specified [RCV004654922]	uncertain significance	20	51435192	51435192	Human		name
407489988	CV3451191	single nucleotide variant	NM_012340.5(NFATC2):c.1657T>C (p.Ser553Pro)	not specified [RCV004641583]	uncertain significance	20	51474031	51474031	Human		name
597640965	CV3562876	single nucleotide variant	NM_012340.5(NFATC2):c.2512G>A (p.Ala838Thr)	not specified [RCV004832186]	uncertain significance	20	51432277	51432277	Human		name
597640971	CV3562877	single nucleotide variant	NM_012340.5(NFATC2):c.1828G>T (p.Val610Leu)	not specified [RCV004832187]	uncertain significance	20	51454569	51454569	Human		name
597640987	CV3562880	single nucleotide variant	NM_012340.5(NFATC2):c.2194C>T (p.Arg732Cys)	not specified [RCV004832190]	uncertain significance	20	51432595	51432595	Human		name
597640998	CV3562882	single nucleotide variant	NM_012340.5(NFATC2):c.1039C>T (p.Pro347Ser)	not specified [RCV004832192]	uncertain significance	20	51523202	51523202	Human		name
597641008	CV3562884	single nucleotide variant	NM_012340.5(NFATC2):c.2471G>A (p.Ser824Asn)	not specified [RCV004832194]	uncertain significance	20	51432318	51432318	Human		name
597641013	CV3562885	single nucleotide variant	NM_012340.5(NFATC2):c.1466A>G (p.Tyr489Cys)	not specified [RCV004832195]	uncertain significance	20	51475527	51475527	Human		name
597641025	CV3562887	single nucleotide variant	NM_012340.5(NFATC2):c.2534G>A (p.Gly845Asp)	not specified [RCV004832197]	uncertain significance	20	51432255	51432255	Human		name
597641037	CV3562889	single nucleotide variant	NM_012340.5(NFATC2):c.2201G>A (p.Gly734Glu)	not specified [RCV004832199]	uncertain significance	20	51432588	51432588	Human		name
598123866	CV3890477	single nucleotide variant	NM_012340.5(NFATC2):c.1322C>G (p.Pro441Arg)	Joint contractures, osteochondromas, and B-cell lymphoma [RCV005250996]	uncertain significance	20	51516794	51516794	Human	1	name
598238066	CV3997595	single nucleotide variant	NM_012340.5(NFATC2):c.2680A>G (p.Ile894Val)	not specified [RCV005382688]	uncertain significance	20	51432109	51432109	Human		name
598191842	CV3997596	single nucleotide variant	NM_012340.5(NFATC2):c.1225G>A (p.Glu409Lys)	not specified [RCV005374263]	uncertain significance	20	51516891	51516891	Human		name
598191847	CV3997597	single nucleotide variant	NM_012340.5(NFATC2):c.1315G>A (p.Gly439Ser)	not specified [RCV005374264]	uncertain significance	20	51516801	51516801	Human		name
598191853	CV3997598	single nucleotide variant	NM_012340.5(NFATC2):c.1478T>C (p.Val493Ala)	not specified [RCV005374265]	uncertain significance	20	51475515	51475515	Human		name
598191875	CV3997601	single nucleotide variant	NM_012340.5(NFATC2):c.1687G>C (p.Ala563Pro)	not specified [RCV005374268]	uncertain significance	20	51474001	51474001	Human		name
598191881	CV3997602	single nucleotide variant	NM_012340.5(NFATC2):c.2579A>G (p.Tyr860Cys)	not specified [RCV005374269]	uncertain significance	20	51432210	51432210	Human		name
598191888	CV3997604	single nucleotide variant	NM_012340.5(NFATC2):c.2251C>G (p.Leu751Val)	not specified [RCV005374270]	uncertain significance	20	51432538	51432538	Human		name
15176602	CV705547	single nucleotide variant	NM_012340.5(NFATC2):c.1337A>G (p.His446Arg)	not provided [RCV000950862]	benign	20	51475656	51475656	Human		name
15120995	CV717039	single nucleotide variant	NM_012340.5(NFATC2):c.2543C>T (p.Pro848Leu)	not provided [RCV000962813]	likely benign	20	51432246	51432246	Human		name
15135355	CV757608	single nucleotide variant	NM_012340.5(NFATC2):c.1453A>T (p.Thr485Ser)	not provided [RCV000920838]	likely benign	20	51475540	51475540	Human		name
8637368	CV92594	single nucleotide variant	NM_001136021.2(NFATC2):c.1119C>T (p.Ser373=)	Malignant melanoma [RCV000072692]	not provided	20	51516937	51516937	Human		name
243050871	CV2417581	microsatellite	NM_012340.5(NFATC2):c.2023_2026del (p.Tyr675fs)	Joint contractures, osteochondromas, and B-cell lymphoma [RCV003152453]	pathogenic	20	51435194	51435197	Human		name
156267692	CV2305680	single nucleotide variant	NM_032815.4(NFATC2IP):c.11C>T (p.Pro4Leu)	not specified [RCV004167505]	uncertain significance	16	28951022	28951022	Human		name
156088998	CV2295553	single nucleotide variant	NM_032815.4(NFATC2IP):c.80G>C (p.Gly27Ala)	not specified [RCV004160648]	uncertain significance	16	28951091	28951091	Human		name
598238087	CV3997607	single nucleotide variant	NM_032815.4(NFATC2IP):c.61G>A (p.Gly21Ser)	not specified [RCV005382691]	uncertain significance	16	28951072	28951072	Human		name
156077573	CV2230295	single nucleotide variant	NM_032815.4(NFATC2IP):c.242C>T (p.Pro81Leu)	not specified [RCV004099907]	uncertain significance	16	28951253	28951253	Human		name
156100316	CV2306611	single nucleotide variant	NM_032815.4(NFATC2IP):c.116C>T (p.Ser39Phe)	not specified [RCV004157211]	uncertain significance	16	28951127	28951127	Human		name
401898609	CV2782538	single nucleotide variant	NM_032815.4(NFATC2IP):c.173T>G (p.Ile58Ser)	not specified [RCV004359575]	uncertain significance	16	28951184	28951184	Human		name
405715420	CV3361151	single nucleotide variant	NM_032815.4(NFATC2IP):c.142G>A (p.Val48Met)	not specified [RCV004494506]	uncertain significance	16	28951153	28951153	Human		name
405715459	CV3361157	single nucleotide variant	NM_032815.4(NFATC2IP):c.224C>G (p.Pro75Arg)	not specified [RCV004494512]	uncertain significance	16	28951235	28951235	Human		name
407489992	CV3451192	single nucleotide variant	NM_032815.4(NFATC2IP):c.125C>T (p.Thr42Met)	not specified [RCV004641584]	uncertain significance	16	28951136	28951136	Human		name
597641043	CV3562890	single nucleotide variant	NM_032815.4(NFATC2IP):c.207C>A (p.Asp69Glu)	not specified [RCV004832200]	uncertain significance	16	28951218	28951218	Human		name
597641056	CV3562893	single nucleotide variant	NM_032815.4(NFATC2IP):c.227C>G (p.Pro76Arg)	not specified [RCV004832203]	uncertain significance	16	28951238	28951238	Human		name
597641067	CV3562895	single nucleotide variant	NM_032815.4(NFATC2IP):c.140C>G (p.Ser47Cys)	not specified [RCV004832205]	uncertain significance	16	28951151	28951151	Human		name
597641079	CV3562897	single nucleotide variant	NM_032815.4(NFATC2IP):c.106C>G (p.Arg36Gly)	not specified [RCV004832207]	uncertain significance	16	28951117	28951117	Human		name
598191925	CV3997612	single nucleotide variant	NM_032815.4(NFATC2IP):c.271G>A (p.Asp91Asn)	not specified [RCV005374276]	uncertain significance	16	28951282	28951282	Human		name
598238095	CV3997613	single nucleotide variant	NM_032815.4(NFATC2IP):c.257A>C (p.Asp86Ala)	not specified [RCV005382692]	uncertain significance	16	28951268	28951268	Human		name
156032692	CV2214498	single nucleotide variant	NM_032815.4(NFATC2IP):c.815G>A (p.Arg272Gln)	not specified [RCV004088552]	uncertain significance	16	28956306	28956306	Human		name
156067378	CV2221819	single nucleotide variant	NM_032815.4(NFATC2IP):c.383G>A (p.Gly128Glu)	not specified [RCV004102848]	likely benign	16	28951394	28951394	Human		name
156053943	CV2326470	single nucleotide variant	NM_032815.4(NFATC2IP):c.973G>A (p.Gly325Arg)	not specified [RCV004183032]	uncertain significance	16	28958843	28958843	Human		name
155965929	CV2330621	single nucleotide variant	NM_032815.4(NFATC2IP):c.784C>T (p.Pro262Ser)	not specified [RCV004183216]	uncertain significance	16	28956275	28956275	Human		name
155936595	CV2375938	single nucleotide variant	NM_032815.4(NFATC2IP):c.329G>T (p.Arg110Leu)	not specified [RCV004218148]	uncertain significance	16	28951340	28951340	Human		name
156172315	CV2380802	single nucleotide variant	NM_032815.4(NFATC2IP):c.632C>T (p.Thr211Met)	not specified [RCV004218363]	uncertain significance	16	28956031	28956031	Human		name
401766888	CV2680182	single nucleotide variant	NM_032815.4(NFATC2IP):c.455A>C (p.Glu152Ala)	not specified [RCV004286661]	uncertain significance	16	28952199	28952199	Human		name
401721797	CV2680681	single nucleotide variant	NM_032815.4(NFATC2IP):c.640C>T (p.Arg214Trp)	not specified [RCV004291295]	uncertain significance	16	28956039	28956039	Human		name
405715700	CV3361170	single nucleotide variant	NM_032815.4(NFATC2IP):c.479C>T (p.Ser160Leu)	not specified [RCV004494525]	uncertain significance	16	28954583	28954583	Human		name
405715778	CV3361181	single nucleotide variant	NM_032815.4(NFATC2IP):c.808C>T (p.Arg270Cys)	not specified [RCV004494536]	uncertain significance	16	28956299	28956299	Human		name
597641049	CV3562891	single nucleotide variant	NM_032815.4(NFATC2IP):c.503C>T (p.Ser168Phe)	not specified [RCV004832201]	uncertain significance	16	28954607	28954607	Human		name
597641052	CV3562892	single nucleotide variant	NM_032815.4(NFATC2IP):c.931A>T (p.Thr311Ser)	not specified [RCV004832202]	uncertain significance	16	28958801	28958801	Human		name
597641062	CV3562894	single nucleotide variant	NM_032815.4(NFATC2IP):c.356A>T (p.Glu119Val)	not specified [RCV004832204]	uncertain significance	16	28951367	28951367	Human		name
597641073	CV3562896	single nucleotide variant	NM_032815.4(NFATC2IP):c.909G>C (p.Arg303Ser)	not specified [RCV004832206]	uncertain significance	16	28958779	28958779	Human		name
598238080	CV3997605	single nucleotide variant	NM_032815.4(NFATC2IP):c.674G>A (p.Arg225His)	not specified [RCV005382690]	uncertain significance	16	28956165	28956165	Human		name
598191895	CV3997606	single nucleotide variant	NM_032815.4(NFATC2IP):c.899C>A (p.Ser300Tyr)	not specified [RCV005374271]	uncertain significance	16	28958769	28958769	Human		name
598191901	CV3997608	single nucleotide variant	NM_032815.4(NFATC2IP):c.892G>C (p.Gly298Arg)	not specified [RCV005374272]	uncertain significance	16	28958762	28958762	Human		name
598191913	CV3997610	single nucleotide variant	NM_032815.4(NFATC2IP):c.913C>T (p.Leu305Phe)	not specified [RCV005374274]	uncertain significance	16	28958783	28958783	Human		name
598191919	CV3997611	single nucleotide variant	NM_032815.4(NFATC2IP):c.763G>A (p.Gly255Arg)	not specified [RCV005374275]	uncertain significance	16	28956254	28956254	Human		name
156061972	CV2323213	single nucleotide variant	NM_032815.4(NFATC2IP):c.1124T>G (p.Met375Arg)	not specified [RCV004187608]	uncertain significance	16	28963727	28963727	Human		name
598191907	CV3997609	single nucleotide variant	NM_032815.4(NFATC2IP):c.1054G>A (p.Val352Met)	not specified [RCV005374273]	uncertain significance	16	28959053	28959053	Human		name

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