Baz2a Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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160 records found for search term Baz2a

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597759588	CV3642863	single nucleotide variant	NM_001300905.2(BAZ2A):c.13G>A (p.Asp5Asn)	not specified [RCV004894579]	uncertain significance	12	56617518	56617518	Human		name
8634800	CV90020	single nucleotide variant	NM_013449.3(BAZ2A):c.470C>T (p.Pro157Leu)	Malignant melanoma [RCV000070117]	not provided	12	56615280	56615280	Human		name
156167370	CV2279799	single nucleotide variant	NM_001300905.2(BAZ2A):c.95A>G (p.Tyr32Cys)	not specified [RCV004144406]	uncertain significance	12	56617436	56617436	Human		name
155917039	CV2366813	single nucleotide variant	NM_001300905.2(BAZ2A):c.92T>C (p.Leu31Pro)	not specified [RCV004210803]	uncertain significance	12	56617439	56617439	Human		name
401731291	CV2674324	single nucleotide variant	NM_001300905.2(BAZ2A):c.50C>T (p.Ala17Val)	not specified [RCV004289200]	uncertain significance	12	56617481	56617481	Human		name
597759618	CV3642870	single nucleotide variant	NM_001300905.2(BAZ2A):c.354A>G (p.Gln118=)	not specified [RCV004894586]	likely benign	12	56615390	56615390	Human		name
598245868	CV3934756	single nucleotide variant	NM_001300905.2(BAZ2A):c.38C>T (p.Pro13Leu)	not specified [RCV005297664]	uncertain significance	12	56617493	56617493	Human		name
156290016	CV2299436	single nucleotide variant	NM_001300905.2(BAZ2A):c.119T>A (p.Phe40Tyr)	not specified [RCV004154520]	uncertain significance	12	56617412	56617412	Human		name
156402079	CV2367949	single nucleotide variant	NM_001300905.2(BAZ2A):c.161A>G (p.Asn54Ser)	not specified [RCV004223042]	uncertain significance	12	56615583	56615583	Human		name
401932234	CV2807107	single nucleotide variant	NM_001300905.2(BAZ2A):c.1725C>T (p.Thr575=)	not provided [RCV003391900]	likely benign	12	56610463	56610463	Human		name
407494964	CV3417527	single nucleotide variant	NM_001300905.2(BAZ2A):c.253G>T (p.Val85Leu)	not specified [RCV004605709]	uncertain significance	12	56615491	56615491	Human		name
156187911	CV2195819	single nucleotide variant	NM_001300905.2(BAZ2A):c.418C>T (p.Leu140Phe)	not specified [RCV004076163]	uncertain significance	12	56615326	56615326	Human		name
156252920	CV2212493	single nucleotide variant	NM_001300905.2(BAZ2A):c.557C>G (p.Thr186Ser)	not specified [RCV004091379]	uncertain significance	12	56615187	56615187	Human		name
156033175	CV2259768	single nucleotide variant	NM_001300905.2(BAZ2A):c.821G>A (p.Ser274Asn)	not specified [RCV004116776]	uncertain significance	12	56614048	56614048	Human		name
156115068	CV2273269	single nucleotide variant	NM_001300905.2(BAZ2A):c.301C>T (p.Pro101Ser)	not specified [RCV004132062]	likely benign	12	56615443	56615443	Human		name
156232184	CV2273661	single nucleotide variant	NM_001300905.2(BAZ2A):c.817G>A (p.Val273Met)	not specified [RCV004132325]	uncertain significance	12	56614052	56614052	Human		name
156394943	CV2328340	single nucleotide variant	NM_001300905.2(BAZ2A):c.671T>C (p.Val224Ala)	not specified [RCV004175456]	uncertain significance	12	56615073	56615073	Human		name
156177727	CV2355875	single nucleotide variant	NM_001300905.2(BAZ2A):c.865A>G (p.Thr289Ala)	not specified [RCV004201265]	uncertain significance	12	56614004	56614004	Human		name
155906568	CV2357347	single nucleotide variant	NM_001300905.2(BAZ2A):c.557C>A (p.Thr186Asn)	not specified [RCV004200236]	uncertain significance	12	56615187	56615187	Human		name
401772119	CV2708137	single nucleotide variant	NM_001300905.2(BAZ2A):c.530T>A (p.Met177Lys)	not specified [RCV004311511]	uncertain significance	12	56615214	56615214	Human		name
401932232	CV2807105	single nucleotide variant	NM_001300905.2(BAZ2A):c.5613C>T (p.Asn1871=)	not provided [RCV003391898]	likely benign	12	56598717	56598717	Human		name
401932233	CV2807106	single nucleotide variant	NM_001300905.2(BAZ2A):c.4008G>A (p.Pro1336=)	not provided [RCV003391899]	likely benign	12	56601609	56601609	Human		name
405705164	CV3301545	single nucleotide variant	NM_001300905.2(BAZ2A):c.529A>G (p.Met177Val)	not specified [RCV004425972]	uncertain significance	12	56615215	56615215	Human		name
405705179	CV3301547	single nucleotide variant	NM_001300905.2(BAZ2A):c.871A>G (p.Ile291Val)	not specified [RCV004425974]	uncertain significance	12	56613998	56613998	Human		name
597759627	CV3642872	single nucleotide variant	NM_001300905.2(BAZ2A):c.748T>C (p.Tyr250His)	not specified [RCV004894588]	uncertain significance	12	56614121	56614121	Human		name
597759630	CV3642873	single nucleotide variant	NM_001300905.2(BAZ2A):c.521T>C (p.Phe174Ser)	not specified [RCV004894589]	uncertain significance	12	56615223	56615223	Human		name
598246228	CV3934839	single nucleotide variant	NM_001300905.2(BAZ2A):c.412A>G (p.Thr138Ala)	not specified [RCV005297713]	uncertain significance	12	56615332	56615332	Human		name
153349263	CV1694130	duplication	NM_001300905.2(BAZ2A):c.5041dup (p.Arg1681fs)	not provided [RCV002275655]	uncertain significance	12	56599832	56599833	Human		name
155924423	CV2211540	single nucleotide variant	NM_001300905.2(BAZ2A):c.2065C>T (p.Arg689Cys)	not specified [RCV004084447]	uncertain significance	12	56609763	56609763	Human		name
156129077	CV2238506	single nucleotide variant	NM_001300905.2(BAZ2A):c.2422C>T (p.Arg808Trp)	not specified [RCV004107129]	uncertain significance	12	56605901	56605901	Human		name
155901376	CV2241993	single nucleotide variant	NM_001300905.2(BAZ2A):c.1688G>A (p.Arg563His)	not specified [RCV004108940]	uncertain significance	12	56610500	56610500	Human		name
156056518	CV2243312	single nucleotide variant	NM_001300905.2(BAZ2A):c.1043C>G (p.Ala348Gly)	not specified [RCV004112012]	uncertain significance	12	56613107	56613107	Human		name
156314787	CV2253314	single nucleotide variant	NM_001300905.2(BAZ2A):c.1454C>T (p.Thr485Met)	not specified [RCV004123149]	uncertain significance	12	56611928	56611928	Human		name
156189358	CV2255049	single nucleotide variant	NM_001300905.2(BAZ2A):c.2990T>C (p.Met997Thr)	not specified [RCV004115690]	uncertain significance	12	56604265	56604265	Human		name
156368804	CV2267090	single nucleotide variant	NM_001300905.2(BAZ2A):c.2355G>C (p.Glu785Asp)	not specified [RCV004131715]	uncertain significance	12	56605968	56605968	Human		name
156144120	CV2268842	single nucleotide variant	NM_001300905.2(BAZ2A):c.1360G>A (p.Ala454Thr)	not specified [RCV004124217]	uncertain significance	12	56612022	56612022	Human		name
155904148	CV2275831	single nucleotide variant	NM_001300905.2(BAZ2A):c.1699G>A (p.Gly567Ser)	not specified [RCV004139497]	uncertain significance	12	56610489	56610489	Human		name
156126039	CV2283675	single nucleotide variant	NM_001300905.2(BAZ2A):c.1058C>T (p.Ala353Val)	not specified [RCV004142211]	uncertain significance	12	56613092	56613092	Human		name
156292874	CV2296874	single nucleotide variant	NM_001300905.2(BAZ2A):c.2401A>G (p.Thr801Ala)	not specified [RCV004148751]	uncertain significance	12	56605922	56605922	Human		name
156243040	CV2306701	single nucleotide variant	NM_001300905.2(BAZ2A):c.2986A>G (p.Ser996Gly)	not specified [RCV004159292]	uncertain significance	12	56604269	56604269	Human		name
156302078	CV2319470	single nucleotide variant	NM_001300905.2(BAZ2A):c.1997A>G (p.Lys666Arg)	not specified [RCV004185049]	uncertain significance	12	56609831	56609831	Human		name
155973219	CV2320982	single nucleotide variant	NM_001300905.2(BAZ2A):c.1369A>T (p.Thr457Ser)	not specified [RCV004172780]	uncertain significance	12	56612013	56612013	Human		name
156076730	CV2331829	single nucleotide variant	NM_001300905.2(BAZ2A):c.1694A>G (p.Lys565Arg)	not specified [RCV004184444]	uncertain significance	12	56610494	56610494	Human		name
155901969	CV2345903	single nucleotide variant	NM_001300905.2(BAZ2A):c.1226C>T (p.Pro409Leu)	not specified [RCV004198942]	uncertain significance	12	56612156	56612156	Human		name
156155584	CV2388797	single nucleotide variant	NM_001300905.2(BAZ2A):c.2206C>G (p.Arg736Gly)	not specified [RCV004239651]	uncertain significance	12	56606300	56606300	Human		name
156198616	CV2392182	single nucleotide variant	NM_001300905.2(BAZ2A):c.1898A>C (p.Gln633Pro)	not specified [RCV004242530]	uncertain significance	12	56609930	56609930	Human		name
329390280	CV2453848	single nucleotide variant	NM_001300905.2(BAZ2A):c.1499C>A (p.Ala500Glu)	not specified [RCV004271246]	uncertain significance	12	56611883	56611883	Human		name
329395469	CV2458401	single nucleotide variant	NM_001300905.2(BAZ2A):c.1610G>A (p.Gly537Asp)	not specified [RCV004266036]	uncertain significance	12	56611633	56611633	Human		name
401743328	CV2687923	single nucleotide variant	NM_001300905.2(BAZ2A):c.1895T>C (p.Val632Ala)	not specified [RCV004305013]	uncertain significance	12	56609933	56609933	Human		name
401762429	CV2723438	single nucleotide variant	NM_001300905.2(BAZ2A):c.2902C>A (p.Gln968Lys)	not specified [RCV004323513]	uncertain significance	12	56604646	56604646	Human		name
401893736	CV2760119	single nucleotide variant	NM_001300905.2(BAZ2A):c.2063A>G (p.Asn688Ser)	not specified [RCV004345523]	uncertain significance	12	56609765	56609765	Human		name
405705017	CV3301526	single nucleotide variant	NM_001300905.2(BAZ2A):c.1405C>G (p.Pro469Ala)	not specified [RCV004425953]	uncertain significance	12	56611977	56611977	Human		name
405705025	CV3301527	single nucleotide variant	NM_001300905.2(BAZ2A):c.1558A>C (p.Thr520Pro)	not specified [RCV004425954]	uncertain significance	12	56611824	56611824	Human		name
405705043	CV3301529	single nucleotide variant	NM_001300905.2(BAZ2A):c.1795G>C (p.Val599Leu)	not specified [RCV004425956]	uncertain significance	12	56610200	56610200	Human		name
405705049	CV3301530	single nucleotide variant	NM_001300905.2(BAZ2A):c.1810C>T (p.Arg604Cys)	not specified [RCV004425957]	uncertain significance	12	56610185	56610185	Human		name
405705055	CV3301531	single nucleotide variant	NM_001300905.2(BAZ2A):c.1854T>G (p.Asp618Glu)	not specified [RCV004425958]	uncertain significance	12	56610141	56610141	Human		name
405705071	CV3301533	single nucleotide variant	NM_001300905.2(BAZ2A):c.2588G>A (p.Gly863Asp)	not specified [RCV004425960]	uncertain significance	12	56605233	56605233	Human		name
405705080	CV3301534	single nucleotide variant	NM_001300905.2(BAZ2A):c.2626A>G (p.Ser876Gly)	not specified [RCV004425961]	uncertain significance	12	56605195	56605195	Human		name
407494949	CV3417522	single nucleotide variant	NM_001300905.2(BAZ2A):c.1345C>T (p.Pro449Ser)	not specified [RCV004605706]	uncertain significance	12	56612037	56612037	Human		name
407500323	CV3417523	single nucleotide variant	NM_001300905.2(BAZ2A):c.2345A>G (p.Glu782Gly)	not specified [RCV004606988]	uncertain significance	12	56605978	56605978	Human		name
407494954	CV3417525	single nucleotide variant	NM_001300905.2(BAZ2A):c.1795G>A (p.Val599Met)	not specified [RCV004605707]	uncertain significance	12	56610200	56610200	Human		name
407494959	CV3417526	single nucleotide variant	NM_001300905.2(BAZ2A):c.2246A>G (p.Lys749Arg)	not specified [RCV004605708]	uncertain significance	12	56606260	56606260	Human		name
597759595	CV3642865	single nucleotide variant	NM_001300905.2(BAZ2A):c.1595C>G (p.Thr532Ser)	not specified [RCV004894581]	uncertain significance	12	56611787	56611787	Human		name
597759605	CV3642867	single nucleotide variant	NM_001300905.2(BAZ2A):c.1556C>T (p.Thr519Ile)	not specified [RCV004894583]	uncertain significance	12	56611826	56611826	Human		name
597759610	CV3642868	single nucleotide variant	NM_001300905.2(BAZ2A):c.2958C>G (p.Ile986Met)	not specified [RCV004894584]	uncertain significance	12	56604590	56604590	Human		name
597759649	CV3642877	single nucleotide variant	NM_001300905.2(BAZ2A):c.1877C>T (p.Pro626Leu)	not specified [RCV004894593]	uncertain significance	12	56610118	56610118	Human		name
597759655	CV3642878	single nucleotide variant	NM_001300905.2(BAZ2A):c.1517C>G (p.Ala506Gly)	not specified [RCV004894594]	uncertain significance	12	56611865	56611865	Human		name
597759659	CV3642879	single nucleotide variant	NM_001300905.2(BAZ2A):c.2857T>C (p.Cys953Arg)	not specified [RCV004894595]	uncertain significance	12	56604691	56604691	Human		name
597759664	CV3642880	single nucleotide variant	NM_001300905.2(BAZ2A):c.2564T>C (p.Ile855Thr)	not specified [RCV004894596]	uncertain significance	12	56605257	56605257	Human		name
598172191	CV3931007	single nucleotide variant	NM_001300905.2(BAZ2A):c.2644G>C (p.Glu882Gln)	not specified [RCV005309352]	uncertain significance	12	56605177	56605177	Human		name
598246534	CV3931015	single nucleotide variant	NM_001300905.2(BAZ2A):c.1202A>G (p.Asp401Gly)	not specified [RCV005297758]	uncertain significance	12	56612180	56612180	Human		name
598245423	CV3934658	single nucleotide variant	NM_001300905.2(BAZ2A):c.1057G>T (p.Ala353Ser)	not specified [RCV005297601]	uncertain significance	12	56613093	56613093	Human		name
598245531	CV3934679	single nucleotide variant	NM_001300905.2(BAZ2A):c.1427C>T (p.Pro476Leu)	not specified [RCV005297614]	uncertain significance	12	56611955	56611955	Human		name
598171789	CV3934696	single nucleotide variant	NM_001300905.2(BAZ2A):c.1577T>A (p.Ile526Asn)	not specified [RCV005309277]	uncertain significance	12	56611805	56611805	Human		name
598171938	CV3934775	single nucleotide variant	NM_001300905.2(BAZ2A):c.2596C>G (p.Leu866Val)	not specified [RCV005309305]	uncertain significance	12	56605225	56605225	Human		name
598246052	CV3934802	single nucleotide variant	NM_001300905.2(BAZ2A):c.1421T>C (p.Val474Ala)	not specified [RCV005297689]	likely benign	12	56611961	56611961	Human		name
598246083	CV3934811	single nucleotide variant	NM_001300905.2(BAZ2A):c.1399G>C (p.Val467Leu)	not specified [RCV005297693]	uncertain significance	12	56611983	56611983	Human		name
598172057	CV3934819	single nucleotide variant	NM_001300905.2(BAZ2A):c.1435T>C (p.Ser479Pro)	not specified [RCV005309327]	uncertain significance	12	56611947	56611947	Human		name
598246280	CV3934849	single nucleotide variant	NM_001300905.2(BAZ2A):c.2222A>G (p.Lys741Arg)	not specified [RCV005297720]	uncertain significance	12	56606284	56606284	Human		name
598172161	CV3934880	single nucleotide variant	NM_001300905.2(BAZ2A):c.2301G>C (p.Lys767Asn)	not specified [RCV005309346]	uncertain significance	12	56606022	56606022	Human		name
156065033	CV2229099	single nucleotide variant	NM_001300905.2(BAZ2A):c.5702C>G (p.Ala1901Gly)	not specified [RCV004098868]	uncertain significance	12	56598628	56598628	Human		name
156296443	CV2233840	single nucleotide variant	NM_001300905.2(BAZ2A):c.5654G>A (p.Arg1885His)	not specified [RCV004102057]	uncertain significance	12	56598676	56598676	Human		name
156229790	CV2235004	single nucleotide variant	NM_001300905.2(BAZ2A):c.3217G>A (p.Glu1073Lys)	not specified [RCV004113195]	uncertain significance	12	56603522	56603522	Human		name
156169798	CV2247339	single nucleotide variant	NM_001300905.2(BAZ2A):c.5491A>G (p.Ile1831Val)	not specified [RCV004108683]	uncertain significance	12	56598923	56598923	Human		name
156074565	CV2248183	single nucleotide variant	NM_001300905.2(BAZ2A):c.3286C>G (p.Leu1096Val)	not specified [RCV004117577]	uncertain significance	12	56602851	56602851	Human		name
156035132	CV2252974	single nucleotide variant	NM_001300905.2(BAZ2A):c.3949C>G (p.Pro1317Ala)	not specified [RCV004120786]	uncertain significance	12	56601668	56601668	Human		name
155986934	CV2259421	single nucleotide variant	NM_001300905.2(BAZ2A):c.4939G>A (p.Glu1647Lys)	not specified [RCV004122639]	uncertain significance	12	56600050	56600050	Human		name
156319453	CV2260843	single nucleotide variant	NM_001300905.2(BAZ2A):c.5019C>G (p.Asn1673Lys)	not specified [RCV004125751]	uncertain significance	12	56599970	56599970	Human		name
156340336	CV2268096	single nucleotide variant	NM_001300905.2(BAZ2A):c.3257G>A (p.Arg1086His)	not specified [RCV004138422]	uncertain significance	12	56603381	56603381	Human		name
156258656	CV2274049	single nucleotide variant	NM_001300905.2(BAZ2A):c.3152T>C (p.Met1051Thr)	not specified [RCV004134704]	uncertain significance	12	56603587	56603587	Human		name
155984851	CV2274750	single nucleotide variant	NM_001300905.2(BAZ2A):c.4600C>T (p.Arg1534Trp)	not specified [RCV004139107]	uncertain significance	12	56600683	56600683	Human		name
156063034	CV2277332	single nucleotide variant	NM_001300905.2(BAZ2A):c.4724G>A (p.Arg1575His)	not specified [RCV004142941]	uncertain significance	12	56600369	56600369	Human		name
156085348	CV2289814	single nucleotide variant	NM_001300905.2(BAZ2A):c.4802G>A (p.Arg1601Gln)	not specified [RCV004150490]	uncertain significance	12	56600291	56600291	Human		name
156247472	CV2306948	single nucleotide variant	NM_001300905.2(BAZ2A):c.5210C>G (p.Pro1737Arg)	not specified [RCV004157467]	uncertain significance	12	56599321	56599321	Human		name
156247821	CV2307027	single nucleotide variant	NM_001300905.2(BAZ2A):c.3511A>G (p.Met1171Val)	not specified [RCV004159528]	uncertain significance	12	56602106	56602106	Human		name
155967063	CV2312670	single nucleotide variant	NM_001300905.2(BAZ2A):c.5494A>C (p.Ile1832Leu)	not specified [RCV004169402]	uncertain significance	12	56598920	56598920	Human		name
156198235	CV2312905	single nucleotide variant	NM_001300905.2(BAZ2A):c.4154G>T (p.Arg1385Leu)	not specified [RCV004159420]	uncertain significance	12	56601320	56601320	Human		name
156165101	CV2330021	single nucleotide variant	NM_001300905.2(BAZ2A):c.4084A>C (p.Ser1362Arg)	not specified [RCV004185514]	uncertain significance	12	56601390	56601390	Human		name
156069474	CV2353985	single nucleotide variant	NM_001300905.2(BAZ2A):c.4853G>A (p.Ser1618Asn)	not specified [RCV004204420]	uncertain significance	12	56600240	56600240	Human		name
156336741	CV2360804	single nucleotide variant	NM_001300905.2(BAZ2A):c.4055T>C (p.Leu1352Pro)	not specified [RCV004213580]	likely benign	12	56601562	56601562	Human		name
156196035	CV2367200	single nucleotide variant	NM_001300905.2(BAZ2A):c.4975C>G (p.Leu1659Val)	not specified [RCV004215627]	uncertain significance	12	56600014	56600014	Human		name
156060547	CV2380146	single nucleotide variant	NM_001300905.2(BAZ2A):c.3505A>G (p.Met1169Val)	not specified [RCV004224520]	likely benign	12	56602112	56602112	Human		name
155938299	CV2380682	single nucleotide variant	NM_001300905.2(BAZ2A):c.3112C>T (p.Arg1038Trp)	not specified [RCV004218265]	uncertain significance	12	56603627	56603627	Human		name
155999504	CV2396429	single nucleotide variant	NM_001300905.2(BAZ2A):c.3754C>G (p.Pro1252Ala)	not specified [RCV004242144]	uncertain significance	12	56601863	56601863	Human		name
156105833	CV2400400	single nucleotide variant	NM_001300905.2(BAZ2A):c.4403A>G (p.Asn1468Ser)	not specified [RCV004244449]	likely benign	12	56600990	56600990	Human		name
329367593	CV2427459	single nucleotide variant	NM_001300905.2(BAZ2A):c.5269C>T (p.Arg1757Cys)	not specified [RCV004248308]	uncertain significance	12	56599262	56599262	Human		name
329395958	CV2463114	single nucleotide variant	NM_001300905.2(BAZ2A):c.4915A>G (p.Ile1639Val)	not specified [RCV004274914]	likely benign	12	56600074	56600074	Human		name
329388629	CV2469431	single nucleotide variant	NM_001300905.2(BAZ2A):c.4898A>G (p.Tyr1633Cys)	not specified [RCV004282892]	uncertain significance	12	56600091	56600091	Human		name
401740110	CV2683261	single nucleotide variant	NM_001300905.2(BAZ2A):c.5452G>C (p.Glu1818Gln)	not specified [RCV004288046]	uncertain significance	12	56598962	56598962	Human		name
401759516	CV2690925	single nucleotide variant	NM_001300905.2(BAZ2A):c.5332G>A (p.Glu1778Lys)	not specified [RCV004298613]	uncertain significance	12	56599199	56599199	Human		name
401783241	CV2703905	single nucleotide variant	NM_001300905.2(BAZ2A):c.4242A>T (p.Lys1414Asn)	not specified [RCV004306763]	uncertain significance	12	56601232	56601232	Human		name
401742556	CV2715259	single nucleotide variant	NM_001300905.2(BAZ2A):c.3503C>T (p.Ser1168Phe)	not specified [RCV004324603]	uncertain significance	12	56602114	56602114	Human		name
401769978	CV2718977	single nucleotide variant	NM_001300905.2(BAZ2A):c.5705A>G (p.Asn1902Ser)	not specified [RCV004322567]	uncertain significance	12	56598625	56598625	Human		name
401890065	CV2762133	single nucleotide variant	NM_001300905.2(BAZ2A):c.3365G>A (p.Arg1122His)	not specified [RCV004341947]	uncertain significance	12	56602772	56602772	Human		name
401895720	CV2771731	single nucleotide variant	NM_001300905.2(BAZ2A):c.4100G>T (p.Cys1367Phe)	not specified [RCV004350515]	uncertain significance	12	56601374	56601374	Human		name
401874753	CV2781212	single nucleotide variant	NM_001300905.2(BAZ2A):c.3149G>C (p.Gly1050Ala)	not specified [RCV004352252]	uncertain significance	12	56603590	56603590	Human		name
401894762	CV2785122	single nucleotide variant	NM_001300905.2(BAZ2A):c.3737T>C (p.Leu1246Pro)	not specified [RCV004355128]	uncertain significance	12	56601880	56601880	Human		name
401865446	CV2786054	single nucleotide variant	NM_001300905.2(BAZ2A):c.3626G>A (p.Gly1209Asp)	not specified [RCV004359876]	uncertain significance	12	56601991	56601991	Human		name
401884386	CV2789668	single nucleotide variant	NM_001300905.2(BAZ2A):c.5366C>T (p.Ser1789Phe)	not specified [RCV004360261]	uncertain significance	12	56599165	56599165	Human		name
405705086	CV3301535	single nucleotide variant	NM_001300905.2(BAZ2A):c.3328C>T (p.Arg1110Trp)	not specified [RCV004425962]	uncertain significance	12	56602809	56602809	Human		name
405705092	CV3301536	single nucleotide variant	NM_001300905.2(BAZ2A):c.4045C>T (p.Pro1349Ser)	not specified [RCV004425963]	uncertain significance	12	56601572	56601572	Human		name
405705110	CV3301538	single nucleotide variant	NM_001300905.2(BAZ2A):c.4178C>T (p.Pro1393Leu)	not specified [RCV004425965]	uncertain significance	12	56601296	56601296	Human		name
405705119	CV3301539	single nucleotide variant	NM_001300905.2(BAZ2A):c.4367G>A (p.Arg1456Gln)	not specified [RCV004425966]	uncertain significance	12	56601026	56601026	Human		name
405705126	CV3301540	single nucleotide variant	NM_001300905.2(BAZ2A):c.4492G>T (p.Gly1498Trp)	not specified [RCV004425967]	uncertain significance	12	56600791	56600791	Human		name
405705134	CV3301541	single nucleotide variant	NM_001300905.2(BAZ2A):c.4570C>A (p.Gln1524Lys)	not specified [RCV004425968]	uncertain significance	12	56600713	56600713	Human		name
405705141	CV3301542	single nucleotide variant	NM_001300905.2(BAZ2A):c.4696C>T (p.Arg1566Trp)	not specified [RCV004425969]	uncertain significance	12	56600397	56600397	Human		name
405705150	CV3301543	single nucleotide variant	NM_001300905.2(BAZ2A):c.5275C>T (p.Arg1759Cys)	not specified [RCV004425970]	uncertain significance	12	56599256	56599256	Human		name
405705157	CV3301544	single nucleotide variant	NM_001300905.2(BAZ2A):c.5327C>T (p.Ser1776Leu)	not specified [RCV004425971]	uncertain significance	12	56599204	56599204	Human		name
405705171	CV3301546	single nucleotide variant	NM_001300905.2(BAZ2A):c.5671C>T (p.Arg1891Cys)	not specified [RCV004425973]	uncertain significance	12	56598659	56598659	Human		name
407500330	CV3417520	single nucleotide variant	NM_001300905.2(BAZ2A):c.4256G>A (p.Arg1419His)	not specified [RCV004606987]	uncertain significance	12	56601218	56601218	Human		name
407494945	CV3417521	single nucleotide variant	NM_001300905.2(BAZ2A):c.4325A>T (p.Asp1442Val)	not specified [RCV004605705]	uncertain significance	12	56601068	56601068	Human		name
407494968	CV3417528	single nucleotide variant	NM_001300905.2(BAZ2A):c.3134T>C (p.Met1045Thr)	not specified [RCV004605710]	uncertain significance	12	56603605	56603605	Human		name
407494972	CV3417529	single nucleotide variant	NM_001300905.2(BAZ2A):c.3383A>G (p.Tyr1128Cys)	not specified [RCV004605711]	uncertain significance	12	56602754	56602754	Human		name
407500315	CV3417530	single nucleotide variant	NM_001300905.2(BAZ2A):c.3668C>T (p.Ala1223Val)	not specified [RCV004606990]	uncertain significance	12	56601949	56601949	Human		name
407494978	CV3417531	single nucleotide variant	NM_001300905.2(BAZ2A):c.3992A>G (p.Asn1331Ser)	not specified [RCV004605712]	uncertain significance	12	56601625	56601625	Human		name
407494981	CV3417532	single nucleotide variant	NM_001300905.2(BAZ2A):c.3766G>A (p.Gly1256Ser)	not specified [RCV004605713]	uncertain significance	12	56601851	56601851	Human		name
407494985	CV3417533	single nucleotide variant	NM_001300905.2(BAZ2A):c.4458C>G (p.Ile1486Met)	not specified [RCV004605714]	uncertain significance	12	56600825	56600825	Human		name
597759574	CV3642860	single nucleotide variant	NM_001300905.2(BAZ2A):c.5320C>T (p.Arg1774Trp)	not specified [RCV004894576]	uncertain significance	12	56599211	56599211	Human		name
597759578	CV3642861	single nucleotide variant	NM_001300905.2(BAZ2A):c.5270G>A (p.Arg1757His)	not specified [RCV004894577]	uncertain significance	12	56599261	56599261	Human		name
597759582	CV3642862	single nucleotide variant	NM_001300905.2(BAZ2A):c.3062G>A (p.Arg1021Gln)	not specified [RCV004894578]	uncertain significance	12	56603677	56603677	Human		name
597759591	CV3642864	single nucleotide variant	NM_001300905.2(BAZ2A):c.3092G>C (p.Gly1031Ala)	not specified [RCV004894580]	uncertain significance	12	56603647	56603647	Human		name
597759600	CV3642866	single nucleotide variant	NM_001300905.2(BAZ2A):c.5353C>T (p.Arg1785Trp)	not specified [RCV004894582]	uncertain significance	12	56599178	56599178	Human		name
597759614	CV3642869	single nucleotide variant	NM_001300905.2(BAZ2A):c.4897T>A (p.Tyr1633Asn)	not specified [RCV004894585]	uncertain significance	12	56600092	56600092	Human		name
597759623	CV3642871	single nucleotide variant	NM_001300905.2(BAZ2A):c.3194G>T (p.Gly1065Val)	not specified [RCV004894587]	uncertain significance	12	56603545	56603545	Human		name
597759635	CV3642874	single nucleotide variant	NM_001300905.2(BAZ2A):c.5360G>A (p.Arg1787Gln)	not specified [RCV004894590]	uncertain significance	12	56599171	56599171	Human		name
597759640	CV3642875	single nucleotide variant	NM_001300905.2(BAZ2A):c.3145A>G (p.Ser1049Gly)	not specified [RCV004894591]	uncertain significance	12	56603594	56603594	Human		name
597759644	CV3642876	single nucleotide variant	NM_001300905.2(BAZ2A):c.4543G>T (p.Val1515Leu)	not specified [RCV004894592]	uncertain significance	12	56600740	56600740	Human		name
597760328	CV3642881	single nucleotide variant	NM_001300905.2(BAZ2A):c.3011A>G (p.Lys1004Arg)	not specified [RCV004894597]	uncertain significance	12	56604244	56604244	Human		name
598246566	CV3931026	single nucleotide variant	NM_001300905.2(BAZ2A):c.4651T>A (p.Cys1551Ser)	not specified [RCV005297763]	uncertain significance	12	56600442	56600442	Human		name
598245640	CV3934705	single nucleotide variant	NM_001300905.2(BAZ2A):c.4112A>T (p.Gln1371Leu)	not specified [RCV005297630]	uncertain significance	12	56601362	56601362	Human		name
598245685	CV3934715	single nucleotide variant	NM_001300905.2(BAZ2A):c.4148A>G (p.Lys1383Arg)	not specified [RCV005297637]	uncertain significance	12	56601326	56601326	Human		name
598171839	CV3934726	single nucleotide variant	NM_001300905.2(BAZ2A):c.3617C>T (p.Pro1206Leu)	not specified [RCV005309286]	uncertain significance	12	56602000	56602000	Human		name
598245815	CV3934745	single nucleotide variant	NM_001300905.2(BAZ2A):c.3364C>T (p.Arg1122Cys)	not specified [RCV005297656]	uncertain significance	12	56602773	56602773	Human		name
598171922	CV3934767	single nucleotide variant	NM_001300905.2(BAZ2A):c.3656T>C (p.Leu1219Pro)	not specified [RCV005309302]	uncertain significance	12	56601961	56601961	Human		name
598245977	CV3934784	single nucleotide variant	NM_001300905.2(BAZ2A):c.3331G>T (p.Ala1111Ser)	not specified [RCV005297679]	uncertain significance	12	56602806	56602806	Human		name
598246014	CV3934793	single nucleotide variant	NM_001300905.2(BAZ2A):c.4470G>T (p.Arg1490Ser)	not specified [RCV005297684]	likely benign	12	56600813	56600813	Human		name
598246173	CV3934829	single nucleotide variant	NM_001300905.2(BAZ2A):c.4144C>T (p.Pro1382Ser)	not specified [RCV005297706]	uncertain significance	12	56601330	56601330	Human		name
598246325	CV3934860	single nucleotide variant	NM_001300905.2(BAZ2A):c.5479G>C (p.Gly1827Arg)	not specified [RCV005297726]	uncertain significance	12	56598935	56598935	Human		name
598246377	CV3934870	single nucleotide variant	NM_001300905.2(BAZ2A):c.3181G>C (p.Ala1061Pro)	not specified [RCV005297733]	uncertain significance	12	56603558	56603558	Human		name
598246462	CV3934888	single nucleotide variant	NM_001300905.2(BAZ2A):c.3230C>T (p.Thr1077Ile)	not specified [RCV005297746]	uncertain significance	12	56603408	56603408	Human		name

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