Znf536 Variant Search Result - Rat Genome Database

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135 records found for search term Znf536

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15152984	CV731267	single nucleotide variant	NM_014717.3(ZNF536):c.2171-7G>A	not provided [RCV000879919]	benign\|likely benign	19	30534840	30534840	Human		name
8586081	CV120676	single nucleotide variant	NM_014717.1(ZNF536):c.-2-20526A>G	Lung cancer [RCV000101196]	uncertain significance	19	30423035	30423035	Human		name
8586082	CV120677	single nucleotide variant	NM_014717.1(ZNF536):c.-2-20470A>G	Lung cancer [RCV000101197]	uncertain significance	19	30423091	30423091	Human		name
8586083	CV120678	single nucleotide variant	NM_014717.1(ZNF536):c.2170+28510G>A	Lung cancer [RCV000101198]	uncertain significance	19	30474242	30474242	Human		name
156176766	CV2317540	single nucleotide variant	NM_014717.3(ZNF536):c.10G>A (p.Ala4Thr)	not specified [RCV004172496]	uncertain significance	19	30443572	30443572	Human		name
329375569	CV2440994	single nucleotide variant	NM_014717.3(ZNF536):c.14G>A (p.Ser5Asn)	not specified [RCV004261370]	uncertain significance	19	30443576	30443576	Human		name
156198725	CV2365162	single nucleotide variant	NM_014717.3(ZNF536):c.44C>T (p.Pro15Leu)	not specified [RCV004205179]	uncertain significance	19	30443606	30443606	Human		name
598172391	CV3931100	single nucleotide variant	NM_014717.3(ZNF536):c.46G>A (p.Glu16Lys)	not specified [RCV005309387]	uncertain significance	19	30443608	30443608	Human		name
329390425	CV2459209	single nucleotide variant	NM_014717.3(ZNF536):c.253G>A (p.Ala85Thr)	not specified [RCV004274650]	uncertain significance	19	30443815	30443815	Human		name
329390427	CV2459210	single nucleotide variant	NM_014717.3(ZNF536):c.254C>A (p.Ala85Asp)	not specified [RCV004274651]	uncertain significance	19	30443816	30443816	Human		name
401757060	CV2692787	single nucleotide variant	NM_014717.3(ZNF536):c.273G>C (p.Glu91Asp)	not specified [RCV004306332]	likely benign	19	30443835	30443835	Human		name
401763164	CV2720218	single nucleotide variant	NM_014717.3(ZNF536):c.200A>G (p.Lys67Arg)	not specified [RCV004325556]	uncertain significance	19	30443762	30443762	Human		name
401928639	CV2811939	single nucleotide variant	NM_014717.3(ZNF536):c.1962G>A (p.Lys654=)	not provided [RCV003406920]	likely benign	19	30445524	30445524	Human		name
401910454	CV2811940	single nucleotide variant	NM_014717.3(ZNF536):c.2421C>T (p.Asn807=)	not provided [RCV003425086]	likely benign	19	30548040	30548040	Human		name
405714855	CV3361044	single nucleotide variant	NM_014717.3(ZNF536):c.220G>C (p.Gly74Arg)	not specified [RCV004494399]	uncertain significance	19	30443782	30443782	Human		name
407470654	CV3416917	single nucleotide variant	NM_014717.3(ZNF536):c.165C>G (p.Asn55Lys)	not specified [RCV004599708]	uncertain significance	19	30443727	30443727	Human		name
407470659	CV3416918	single nucleotide variant	NM_014717.3(ZNF536):c.261G>C (p.Gln87His)	not specified [RCV004599709]	uncertain significance	19	30443823	30443823	Human		name
15168731	CV716342	single nucleotide variant	NM_014717.3(ZNF536):c.1440C>T (p.Val480=)	not provided [RCV000971674]	benign	19	30445002	30445002	Human		name
15109795	CV728089	single nucleotide variant	NM_014717.3(ZNF536):c.2085C>T (p.Thr695=)	not provided [RCV000893937]	benign	19	30445647	30445647	Human		name
15179665	CV728090	single nucleotide variant	NM_014717.3(ZNF536):c.2262G>A (p.Pro754=)	not provided [RCV000885342]	benign	19	30534938	30534938	Human		name
15192033	CV728091	single nucleotide variant	NM_014717.3(ZNF536):c.2964G>A (p.Pro988=)	not provided [RCV000888548]	benign	19	30548583	30548583	Human		name
156271494	CV2237216	single nucleotide variant	NM_014717.3(ZNF536):c.400C>A (p.Leu134Ile)	not specified [RCV004114950]	uncertain significance	19	30443962	30443962	Human		name
156196219	CV2259162	single nucleotide variant	NM_014717.3(ZNF536):c.590G>C (p.Arg197Pro)	not specified [RCV004120405]	uncertain significance	19	30444152	30444152	Human		name
401770247	CV2711015	single nucleotide variant	NM_014717.3(ZNF536):c.803T>G (p.Val268Gly)	not specified [RCV004310715]	uncertain significance	19	30444365	30444365	Human		name
401894250	CV2780492	single nucleotide variant	NM_014717.3(ZNF536):c.998G>A (p.Gly333Asp)	not specified [RCV004358185]	uncertain significance	19	30444560	30444560	Human		name
401937158	CV2811941	single nucleotide variant	NM_014717.3(ZNF536):c.3105C>T (p.Ile1035=)	not provided [RCV003415179]	likely benign	19	30548724	30548724	Human		name
401928641	CV2811942	single nucleotide variant	NM_014717.3(ZNF536):c.3534C>T (p.Asn1178=)	not provided [RCV003406921]	likely benign	19	30549153	30549153	Human		name
405261557	CV3186201	single nucleotide variant	NM_014717.3(ZNF536):c.3186C>T (p.Asp1062=)	not provided [RCV003885277]	likely benign	19	30548805	30548805	Human		name
405714868	CV3361046	single nucleotide variant	NM_014717.3(ZNF536):c.3279C>T (p.Ser1093=)	not specified [RCV004494401]	likely benign	19	30548898	30548898	Human		name
405714900	CV3361051	single nucleotide variant	NM_014717.3(ZNF536):c.616G>T (p.Ala206Ser)	not specified [RCV004494406]	uncertain significance	19	30444178	30444178	Human		name
405714906	CV3361052	single nucleotide variant	NM_014717.3(ZNF536):c.775A>G (p.Lys259Glu)	not specified [RCV004494407]	uncertain significance	19	30444337	30444337	Human		name
407470633	CV3416911	single nucleotide variant	NM_014717.3(ZNF536):c.727C>A (p.Gln243Lys)	not specified [RCV004599702]	uncertain significance	19	30444289	30444289	Human		name
407470648	CV3416915	single nucleotide variant	NM_014717.3(ZNF536):c.722C>A (p.Ala241Asp)	not specified [RCV004599706]	uncertain significance	19	30444284	30444284	Human		name
407470666	CV3416920	single nucleotide variant	NM_014717.3(ZNF536):c.636G>C (p.Gln212His)	not specified [RCV004599711]	uncertain significance	19	30444198	30444198	Human		name
597743786	CV3638906	single nucleotide variant	NM_014717.3(ZNF536):c.786C>G (p.Ser262Arg)	not specified [RCV004891204]	uncertain significance	19	30444348	30444348	Human		name
597743822	CV3638912	single nucleotide variant	NM_014717.3(ZNF536):c.823C>T (p.Arg275Cys)	not specified [RCV004891210]	uncertain significance	19	30444385	30444385	Human		name
597744431	CV3638916	single nucleotide variant	NM_014717.3(ZNF536):c.750C>G (p.Asp250Glu)	not specified [RCV004891214]	uncertain significance	19	30444312	30444312	Human		name
598172398	CV3931104	single nucleotide variant	NM_014717.3(ZNF536):c.373C>G (p.Arg125Gly)	not specified [RCV005309388]	uncertain significance	19	30443935	30443935	Human		name
598172427	CV3931109	single nucleotide variant	NM_014717.3(ZNF536):c.676C>T (p.Pro226Ser)	not specified [RCV005309392]	uncertain significance	19	30444238	30444238	Human		name
15182635	CV772566	single nucleotide variant	NM_014717.3(ZNF536):c.3798G>T (p.Ser1266=)	not provided [RCV000930405]	likely benign	19	30549417	30549417	Human		name
150410131	CV1196218	single nucleotide variant	NM_014717.3(ZNF536):c.2091G>C (p.Glu697Asp)	not provided [RCV001572924]\|not specified [RCV004039390]	uncertain significance	19	30445653	30445653	Human		name
153346865	CV1694244	single nucleotide variant	NM_014717.3(ZNF536):c.1015G>T (p.Glu339Ter)	Neurodevelopmental disorder [RCV002277660]	uncertain significance	19	30444577	30444577	Human	1	name
156183724	CV2198532	single nucleotide variant	NM_014717.3(ZNF536):c.1663G>T (p.Ala555Ser)	not specified [RCV004075559]	uncertain significance	19	30445225	30445225	Human		name
156398129	CV2204281	single nucleotide variant	NM_014717.3(ZNF536):c.1852T>G (p.Tyr618Asp)	not specified [RCV004079109]	uncertain significance	19	30445414	30445414	Human		name
156334065	CV2230861	single nucleotide variant	NM_014717.3(ZNF536):c.1784C>T (p.Pro595Leu)	not specified [RCV004092341]	uncertain significance	19	30445346	30445346	Human		name
156301191	CV2248941	single nucleotide variant	NM_014717.3(ZNF536):c.1298G>T (p.Cys433Phe)	not specified [RCV004115941]	uncertain significance	19	30444860	30444860	Human		name
156313098	CV2256962	single nucleotide variant	NM_014717.3(ZNF536):c.2980G>A (p.Val994Met)	not specified [RCV004121155]	likely benign	19	30548599	30548599	Human		name
156000400	CV2287377	single nucleotide variant	NM_014717.3(ZNF536):c.1939G>T (p.Val647Phe)	not specified [RCV004146987]	uncertain significance	19	30445501	30445501	Human		name
156186059	CV2294996	single nucleotide variant	NM_014717.3(ZNF536):c.2098G>T (p.Val700Phe)	not specified [RCV004156133]	uncertain significance	19	30445660	30445660	Human		name
156016881	CV2295443	single nucleotide variant	NM_014717.3(ZNF536):c.2734G>C (p.Val912Leu)	not specified [RCV004160563]	uncertain significance	19	30548353	30548353	Human		name
156270160	CV2305973	single nucleotide variant	NM_014717.3(ZNF536):c.2942G>A (p.Arg981Gln)	not specified [RCV004169533]	uncertain significance	19	30548561	30548561	Human		name
156159881	CV2311623	single nucleotide variant	NM_014717.3(ZNF536):c.1442C>T (p.Pro481Leu)	not specified [RCV004168723]	uncertain significance	19	30445004	30445004	Human		name
156101220	CV2313467	single nucleotide variant	NM_014717.3(ZNF536):c.2216C>T (p.Ala739Val)	not specified [RCV004163779]	uncertain significance	19	30534892	30534892	Human		name
156179378	CV2324222	single nucleotide variant	NM_014717.3(ZNF536):c.2335T>C (p.Tyr779His)	not specified [RCV004176961]	uncertain significance	19	30547954	30547954	Human		name
156299578	CV2326105	single nucleotide variant	NM_014717.3(ZNF536):c.1510G>A (p.Glu504Lys)	not specified [RCV004180386]	uncertain significance	19	30445072	30445072	Human		name
156052344	CV2329015	single nucleotide variant	NM_014717.3(ZNF536):c.1483G>A (p.Val495Met)	not specified [RCV004180303]	uncertain significance	19	30445045	30445045	Human		name
155921144	CV2340405	single nucleotide variant	NM_014717.3(ZNF536):c.1000C>T (p.Pro334Ser)	not specified [RCV004197135]	uncertain significance	19	30444562	30444562	Human		name
156253156	CV2390126	single nucleotide variant	NM_014717.3(ZNF536):c.2173A>G (p.Ile725Val)	not specified [RCV004240515]	uncertain significance	19	30534849	30534849	Human		name
156061066	CV2391951	single nucleotide variant	NM_014717.3(ZNF536):c.2203G>A (p.Val735Ile)	not specified [RCV004235815]	uncertain significance	19	30534879	30534879	Human		name
329378521	CV2447013	single nucleotide variant	NM_014717.3(ZNF536):c.2858A>G (p.Asp953Gly)	not specified [RCV004257849]	uncertain significance	19	30548477	30548477	Human		name
329390514	CV2459359	single nucleotide variant	NM_014717.3(ZNF536):c.1487C>T (p.Pro496Leu)	not specified [RCV004274766]	uncertain significance	19	30445049	30445049	Human		name
401866998	CV2472783	single nucleotide variant	NM_014717.3(ZNF536):c.1571G>A (p.Trp524Ter)	not provided [RCV003331480]	uncertain significance	19	30445133	30445133	Human		name
401757058	CV2692786	single nucleotide variant	NM_014717.3(ZNF536):c.1769G>A (p.Ser590Asn)	not specified [RCV004306331]	likely benign	19	30445331	30445331	Human		name
401771590	CV2711776	single nucleotide variant	NM_014717.3(ZNF536):c.1328A>G (p.Lys443Arg)	not specified [RCV004309425]	uncertain significance	19	30444890	30444890	Human		name
401854355	CV2766881	single nucleotide variant	NM_014717.3(ZNF536):c.1993C>T (p.His665Tyr)	not specified [RCV004343278]	uncertain significance	19	30445555	30445555	Human		name
405714801	CV3361035	single nucleotide variant	NM_014717.3(ZNF536):c.1010G>T (p.Gly337Val)	not specified [RCV004494390]	uncertain significance	19	30444572	30444572	Human		name
405714808	CV3361036	single nucleotide variant	NM_014717.3(ZNF536):c.1240C>T (p.Pro414Ser)	not specified [RCV004494391]	uncertain significance	19	30444802	30444802	Human		name
405714814	CV3361037	single nucleotide variant	NM_014717.3(ZNF536):c.1458C>G (p.His486Gln)	not specified [RCV004494392]	uncertain significance	19	30445020	30445020	Human		name
405714821	CV3361038	single nucleotide variant	NM_014717.3(ZNF536):c.1552G>T (p.Val518Leu)	not specified [RCV004494393]	uncertain significance	19	30445114	30445114	Human		name
405714827	CV3361039	single nucleotide variant	NM_014717.3(ZNF536):c.1690C>T (p.Arg564Trp)	not specified [RCV004494394]	uncertain significance	19	30445252	30445252	Human		name
405714833	CV3361040	single nucleotide variant	NM_014717.3(ZNF536):c.1769G>T (p.Ser590Ile)	not specified [RCV004494395]	uncertain significance	19	30445331	30445331	Human		name
405714840	CV3361041	single nucleotide variant	NM_014717.3(ZNF536):c.1789A>G (p.Lys597Glu)	not specified [RCV004494396]	uncertain significance	19	30445351	30445351	Human		name
405714847	CV3361042	single nucleotide variant	NM_014717.3(ZNF536):c.2048T>C (p.Val683Ala)	not specified [RCV004494397]	uncertain significance	19	30445610	30445610	Human		name
405714851	CV3361043	single nucleotide variant	NM_014717.3(ZNF536):c.2201G>C (p.Gly734Ala)	not specified [RCV004494398]	uncertain significance	19	30534877	30534877	Human		name
405714861	CV3361045	single nucleotide variant	NM_014717.3(ZNF536):c.2484A>C (p.Lys828Asn)	not specified [RCV004494400]	uncertain significance	19	30548103	30548103	Human		name
407470637	CV3416912	single nucleotide variant	NM_014717.3(ZNF536):c.2018G>A (p.Gly673Asp)	not specified [RCV004599703]	uncertain significance	19	30445580	30445580	Human		name
407470652	CV3416916	single nucleotide variant	NM_014717.3(ZNF536):c.1025C>T (p.Ala342Val)	not specified [RCV004599707]	uncertain significance	19	30444587	30444587	Human		name
407470674	CV3416922	single nucleotide variant	NM_014717.3(ZNF536):c.1762G>A (p.Val588Met)	not specified [RCV004599713]	uncertain significance	19	30445324	30445324	Human		name
597710423	CV3638901	single nucleotide variant	NM_014717.3(ZNF536):c.2587G>T (p.Val863Phe)	not specified [RCV004886660]	uncertain significance	19	30548206	30548206	Human		name
597710205	CV3638902	single nucleotide variant	NM_014717.3(ZNF536):c.2770A>G (p.Ser924Gly)	not specified [RCV004886661]	uncertain significance	19	30548389	30548389	Human		name
597743778	CV3638905	single nucleotide variant	NM_014717.3(ZNF536):c.2197G>T (p.Ala733Ser)	not specified [RCV004891203]	uncertain significance	19	30534873	30534873	Human		name
597743792	CV3638907	single nucleotide variant	NM_014717.3(ZNF536):c.2864G>T (p.Gly955Val)	not specified [RCV004891205]	uncertain significance	19	30548483	30548483	Human		name
597743804	CV3638909	single nucleotide variant	NM_014717.3(ZNF536):c.2833C>G (p.Pro945Ala)	not specified [RCV004891207]	uncertain significance	19	30548452	30548452	Human		name
597743810	CV3638910	single nucleotide variant	NM_014717.3(ZNF536):c.1309G>A (p.Gly437Ser)	not specified [RCV004891208]	uncertain significance	19	30444871	30444871	Human		name
597743816	CV3638911	single nucleotide variant	NM_014717.3(ZNF536):c.2963C>A (p.Pro988Gln)	not specified [RCV004891209]	uncertain significance	19	30548582	30548582	Human		name
597743828	CV3638913	single nucleotide variant	NM_014717.3(ZNF536):c.1969C>T (p.Arg657Cys)	not specified [RCV004891211]	uncertain significance	19	30445531	30445531	Human		name
597743836	CV3638914	single nucleotide variant	NM_014717.3(ZNF536):c.1275C>A (p.Asn425Lys)	not specified [RCV004891212]	uncertain significance	19	30444837	30444837	Human		name
597744436	CV3638915	single nucleotide variant	NM_014717.3(ZNF536):c.1438G>C (p.Val480Leu)	not specified [RCV004891213]	uncertain significance	19	30445000	30445000	Human		name
597744427	CV3638917	single nucleotide variant	NM_014717.3(ZNF536):c.2186C>T (p.Ala729Val)	not specified [RCV004891215]	uncertain significance	19	30534862	30534862	Human		name
598246877	CV3931096	single nucleotide variant	NM_014717.3(ZNF536):c.1747G>A (p.Val583Ile)	not specified [RCV005297806]	uncertain significance	19	30445309	30445309	Human		name
598246888	CV3931098	single nucleotide variant	NM_014717.3(ZNF536):c.1379T>A (p.Met460Lys)	not specified [RCV005297808]	uncertain significance	19	30444941	30444941	Human		name
598246895	CV3931099	single nucleotide variant	NM_014717.3(ZNF536):c.1742A>T (p.Asp581Val)	not specified [RCV005297809]	uncertain significance	19	30445304	30445304	Human		name
598246903	CV3931101	single nucleotide variant	NM_014717.3(ZNF536):c.2773T>G (p.Phe925Val)	not specified [RCV005297810]	uncertain significance	19	30548392	30548392	Human		name
598246915	CV3931102	single nucleotide variant	NM_014717.3(ZNF536):c.1319C>G (p.Thr440Ser)	not specified [RCV005297811]	uncertain significance	19	30444881	30444881	Human		name
598246924	CV3931103	single nucleotide variant	NM_014717.3(ZNF536):c.2537C>T (p.Pro846Leu)	not specified [RCV005297812]	uncertain significance	19	30548156	30548156	Human		name
598172407	CV3931105	single nucleotide variant	NM_014717.3(ZNF536):c.2128G>C (p.Ala710Pro)	not specified [RCV005309389]	uncertain significance	19	30445690	30445690	Human		name
598246934	CV3931106	single nucleotide variant	NM_014717.3(ZNF536):c.1628C>T (p.Pro543Leu)	not specified [RCV005297813]	uncertain significance	19	30445190	30445190	Human		name
14696131	CV612416	single nucleotide variant	NM_014717.3(ZNF536):c.1312T>C (p.Phe438Leu)	High myopia [RCV000785677]	uncertain significance	19	30444874	30444874	Human	2	name
15105837	CV716343	single nucleotide variant	NM_014717.3(ZNF536):c.2831C>A (p.Pro944His)	not provided [RCV000959962]	benign	19	30548450	30548450	Human		name
15165020	CV741760	single nucleotide variant	NM_014717.3(ZNF536):c.2731G>A (p.Gly911Ser)	not provided [RCV000904131]	likely benign	19	30548350	30548350	Human		name
15111279	CV772565	single nucleotide variant	NM_014717.3(ZNF536):c.1390G>A (p.Glu464Lys)	not provided [RCV000938718]	likely benign	19	30444952	30444952	Human		name
8628267	CV83411	single nucleotide variant	NM_014717.1(ZNF536):c.2767G>A (p.Asp923Asn)	Malignant melanoma [RCV000063491]	not provided	19	30548386	30548386	Human		name
8628268	CV83412	single nucleotide variant	NM_014717.1(ZNF536):c.2800A>T (p.Lys934Ter)	Malignant melanoma [RCV000063492]	not provided	19	30548419	30548419	Human		name
8636737	CV91962	single nucleotide variant	NM_014717.1(ZNF536):c.2333C>T (p.Pro778Leu)	Malignant melanoma [RCV000072060]	not provided	19	30547952	30547952	Human		name
8636738	CV91963	single nucleotide variant	NM_014717.1(ZNF536):c.2518G>A (p.Gly840Arg)	Malignant melanoma [RCV000072061]	not provided	19	30548137	30548137	Human		name
8636739	CV91964	single nucleotide variant	NM_014717.1(ZNF536):c.2920G>A (p.Glu974Lys)	Malignant melanoma [RCV000072062]	not provided	19	30548539	30548539	Human		name
155911778	CV2235418	single nucleotide variant	NM_014717.3(ZNF536):c.3668C>T (p.Ser1223Leu)	not specified [RCV004109475]	uncertain significance	19	30549287	30549287	Human		name
156038817	CV2260094	single nucleotide variant	NM_014717.3(ZNF536):c.3400G>A (p.Glu1134Lys)	not specified [RCV004119098]	uncertain significance	19	30549019	30549019	Human		name
156272756	CV2297277	single nucleotide variant	NM_014717.3(ZNF536):c.3296A>C (p.His1099Pro)	not specified [RCV004152940]	uncertain significance	19	30548915	30548915	Human		name
156176005	CV2299739	single nucleotide variant	NM_014717.3(ZNF536):c.3392C>G (p.Pro1131Arg)	not specified [RCV004148900]	uncertain significance	19	30549011	30549011	Human		name
156175138	CV2326995	single nucleotide variant	NM_014717.3(ZNF536):c.3434T>A (p.Val1145Asp)	not specified [RCV004178590]	uncertain significance	19	30549053	30549053	Human		name
156166134	CV2330103	single nucleotide variant	NM_014717.3(ZNF536):c.3088C>T (p.Arg1030Cys)	not specified [RCV004185593]	uncertain significance	19	30548707	30548707	Human		name
156339225	CV2351554	single nucleotide variant	NM_014717.3(ZNF536):c.3004G>A (p.Gly1002Ser)	not specified [RCV004195277]	uncertain significance	19	30548623	30548623	Human		name
155938333	CV2380696	single nucleotide variant	NM_014717.3(ZNF536):c.3287G>C (p.Trp1096Ser)	not specified [RCV004218276]	uncertain significance	19	30548906	30548906	Human		name
329364832	CV2443945	single nucleotide variant	NM_014717.3(ZNF536):c.3458C>T (p.Thr1153Met)	not specified [RCV004258274]	uncertain significance	19	30549077	30549077	Human		name
329398186	CV2466611	single nucleotide variant	NM_014717.3(ZNF536):c.3841G>A (p.Gly1281Arg)	not specified [RCV004274135]	uncertain significance	19	30549460	30549460	Human		name
401780086	CV2676811	single nucleotide variant	NM_014717.3(ZNF536):c.3137G>A (p.Arg1046Gln)	not specified [RCV004290980]	uncertain significance	19	30548756	30548756	Human		name
401759979	CV2701819	single nucleotide variant	NM_014717.3(ZNF536):c.3610G>T (p.Asp1204Tyr)	not specified [RCV004314208]	uncertain significance	19	30549229	30549229	Human		name
401779341	CV2718505	single nucleotide variant	NM_014717.3(ZNF536):c.3693G>T (p.Lys1231Asn)	not specified [RCV004318312]	uncertain significance	19	30549312	30549312	Human		name
405714881	CV3361048	single nucleotide variant	NM_014717.3(ZNF536):c.3368G>A (p.Gly1123Asp)	not specified [RCV004494403]	uncertain significance	19	30548987	30548987	Human		name
405714886	CV3361049	single nucleotide variant	NM_014717.3(ZNF536):c.3686C>T (p.Pro1229Leu)	not specified [RCV004494404]	uncertain significance	19	30549305	30549305	Human		name
405714893	CV3361050	single nucleotide variant	NM_014717.3(ZNF536):c.3757C>T (p.Arg1253Trp)	not specified [RCV004494405]	uncertain significance	19	30549376	30549376	Human		name
407470641	CV3416913	single nucleotide variant	NM_014717.3(ZNF536):c.3560C>T (p.Pro1187Leu)	not specified [RCV004599704]	uncertain significance	19	30549179	30549179	Human		name
407470662	CV3416919	single nucleotide variant	NM_014717.3(ZNF536):c.3050C>A (p.Ala1017Asp)	not specified [RCV004599710]	uncertain significance	19	30548669	30548669	Human		name
407470670	CV3416921	single nucleotide variant	NM_014717.3(ZNF536):c.3851G>A (p.Ser1284Asn)	not specified [RCV004599712]	uncertain significance	19	30549470	30549470	Human		name
407470679	CV3416923	single nucleotide variant	NM_014717.3(ZNF536):c.3523G>A (p.Gly1175Arg)	not specified [RCV004599714]	uncertain significance	19	30549142	30549142	Human		name
407470684	CV3416924	single nucleotide variant	NM_014717.3(ZNF536):c.3167C>T (p.Ser1056Leu)	not specified [RCV004599715]	uncertain significance	19	30548786	30548786	Human		name
597710431	CV3638900	single nucleotide variant	NM_014717.3(ZNF536):c.3567G>C (p.Met1189Ile)	not specified [RCV004886659]	uncertain significance	19	30549186	30549186	Human		name
597710042	CV3638903	single nucleotide variant	NM_014717.3(ZNF536):c.3760G>C (p.Gly1254Arg)	not specified [RCV004886662]	uncertain significance	19	30549379	30549379	Human		name
597743797	CV3638908	single nucleotide variant	NM_014717.3(ZNF536):c.3577C>G (p.Pro1193Ala)	not specified [RCV004891206]	uncertain significance	19	30549196	30549196	Human		name
12896675	CV390267	single nucleotide variant	NM_014717.3(ZNF536):c.3143C>T (p.Ala1048Val)	not provided [RCV004717629]\|not specified [RCV000455670]	benign	19	30548762	30548762	Human		name
598246869	CV3931095	single nucleotide variant	NM_014717.3(ZNF536):c.3610G>A (p.Asp1204Asn)	not specified [RCV005297805]	uncertain significance	19	30549229	30549229	Human		name
598172414	CV3931107	single nucleotide variant	NM_014717.3(ZNF536):c.3389G>A (p.Cys1130Tyr)	not specified [RCV005309390]	uncertain significance	19	30549008	30549008	Human		name
15178163	CV716344	single nucleotide variant	NM_014717.3(ZNF536):c.3700C>G (p.His1234Asp)	not provided [RCV000973597]	likely benign	19	30549319	30549319	Human		name
38460365	CV919846	deletion	NM_014717.3(ZNF536):c.1617_1627del (p.Lys540fs)	See cases [RCV001196574]	uncertain significance	19	30445177	30445187	Human		name

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