Dcaf8 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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134 records found for search term Dcaf8

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155796505	CV1861883	single nucleotide variant	NM_015726.4(DCAF8):c.959+4A>C	not specified [RCV002470165]	uncertain significance	1	160237131	160237131	Human		name
152980450	CV1678619	single nucleotide variant	NM_015726.4(DCAF8):c.723+43G>T	not specified [RCV002247127]	uncertain significance	1	160239654	160239654	Human		name
401964104	CV2843493	single nucleotide variant	NM_015726.4(DCAF8):c.1561-12T>C	not specified [RCV003479835]	likely benign	1	160218452	160218452	Human		name
597800809	CV3651981	single nucleotide variant	NM_015726.4(DCAF8):c.25G>T (p.Asp9Tyr)	not specified [RCV004905880]	uncertain significance	1	160243984	160243984	Human		name
401933120	CV2806106	single nucleotide variant	NM_015726.4(DCAF8):c.612C>T (p.Arg204=)	not provided [RCV003409192]	likely benign	1	160239808	160239808	Human		name
405289010	CV3204921	single nucleotide variant	NM_015726.4(DCAF8):c.540G>T (p.Val180=)	DCAF8-related disorder [RCV003961565]	likely benign	1	160239880	160239880	Human		name , trait , alternate_id
15164339	CV706784	single nucleotide variant	NM_015726.4(DCAF8):c.822G>A (p.Lys274=)	DCAF8-related disorder [RCV003972900]\|Giant axonal neuropathy 2 [RCV002503067]\|not provided [RCV000970696]	benign\|likely benign	1	160238649	160238649	Human	1	name , trait , alternate_id
15164342	CV706785	single nucleotide variant	NM_015726.4(DCAF8):c.789A>G (p.Arg263=)	DCAF8-related disorder [RCV003962873]\|not provided [RCV000970697]	benign	1	160238682	160238682	Human	1	name , trait , alternate_id
15128147	CV731803	single nucleotide variant	NM_015726.4(DCAF8):c.444C>A (p.Pro148=)	not provided [RCV000897222]\|not specified [RCV005418399]	likely benign	1	160239976	160239976	Human		name
15103212	CV745779	single nucleotide variant	NM_015726.4(DCAF8):c.642C>T (p.Asp214=)	DCAF8-related disorder [RCV003950814]\|not provided [RCV000915120]	likely benign	1	160239778	160239778	Human	1	name , trait , alternate_id
15197919	CV761293	single nucleotide variant	NM_015726.4(DCAF8):c.777C>T (p.Asp259=)	not provided [RCV000934655]	likely benign	1	160238694	160238694	Human		name
8624766	CV79880	single nucleotide variant	NM_015726.3(DCAF8):c.549C>T (p.Phe183=)	Malignant melanoma [RCV000059956]	not provided	1	160239871	160239871	Human		name
152999928	CV1683471	single nucleotide variant	NM_015726.4(DCAF8):c.141T>A (p.Ser47Arg)	See cases [RCV002252655]	uncertain significance	1	160240279	160240279	Human		name
156038694	CV2313664	single nucleotide variant	NM_015726.4(DCAF8):c.283G>A (p.Val95Ile)	not specified [RCV004157594]	uncertain significance	1	160240137	160240137	Human		name
329401218	CV2442173	single nucleotide variant	NM_015726.4(DCAF8):c.154G>A (p.Gly52Arg)	not specified [RCV004264674]	uncertain significance	1	160240266	160240266	Human		name
405690275	CV3246591	single nucleotide variant	NM_015726.4(DCAF8):c.118G>A (p.Glu40Lys)	not specified [RCV004373161]	uncertain significance	1	160240302	160240302	Human		name
405690285	CV3246593	single nucleotide variant	NM_015726.4(DCAF8):c.287A>G (p.His96Arg)	not specified [RCV004373163]	uncertain significance	1	160240133	160240133	Human		name
407457284	CV3416096	single nucleotide variant	NM_015726.4(DCAF8):c.110C>T (p.Ser37Leu)	not provided [RCV004598974]	uncertain significance	1	160240310	160240310	Human		name
407457943	CV3430248	single nucleotide variant	NM_015726.4(DCAF8):c.218G>C (p.Gly73Ala)	not specified [RCV004611349]	uncertain significance	1	160240202	160240202	Human		name
12741030	CV359217	single nucleotide variant	NM_015726.4(DCAF8):c.152C>T (p.Thr51Ile)	not specified [RCV000413871]	uncertain significance	1	160240268	160240268	Human		name
597800813	CV3651983	single nucleotide variant	NM_015726.4(DCAF8):c.247G>A (p.Asp83Asn)	not specified [RCV004905882]	uncertain significance	1	160240173	160240173	Human		name
597800819	CV3651986	single nucleotide variant	NM_015726.4(DCAF8):c.133G>A (p.Asp45Asn)	not specified [RCV004905885]	uncertain significance	1	160240287	160240287	Human		name
15122207	CV780359	single nucleotide variant	NM_015726.4(DCAF8):c.1173C>T (p.Thr391=)	not provided [RCV000979608]	likely benign	1	160225090	160225090	Human		name
21071971	CV794461	single nucleotide variant	NM_015726.4(DCAF8):c.1233T>C (p.Ile411=)	DCAF8-related disorder [RCV003936257]\|not provided [RCV000994147]	likely benign\|uncertain significance	1	160224518	160224518	Human	1	name , trait , alternate_id
8689273	CV137087	single nucleotide variant	NM_015726.4(DCAF8):c.949C>T (p.Arg317Cys)	Giant axonal neuropathy 2 [RCV000119848]\|not provided [RCV005243116]	pathogenic\|likely pathogenic	1	160237145	160237145	Human	1	name
155641329	CV1709647	single nucleotide variant	NM_015726.4(DCAF8):c.437C>T (p.Ala146Val)	not provided [RCV002292747]	uncertain significance	1	160239983	160239983	Human		name
156275736	CV2255704	single nucleotide variant	NM_015726.4(DCAF8):c.359G>A (p.Arg120His)	not specified [RCV004120099]	uncertain significance	1	160240061	160240061	Human		name
156039335	CV2313724	single nucleotide variant	NM_015726.4(DCAF8):c.670C>T (p.Arg224Trp)	not specified [RCV004157638]	uncertain significance	1	160239750	160239750	Human		name
156155201	CV2371216	single nucleotide variant	NM_015726.4(DCAF8):c.400C>T (p.Arg134Trp)	not specified [RCV004220954]	uncertain significance	1	160240020	160240020	Human		name
243057319	CV2415069	single nucleotide variant	NM_015726.4(DCAF8):c.364C>T (p.Arg122Trp)	Giant axonal neuropathy 2 [RCV003146011]	uncertain significance	1	160240056	160240056	Human	1	name
401779752	CV2714741	single nucleotide variant	NM_015726.4(DCAF8):c.425C>T (p.Ser142Leu)	not specified [RCV004320313]	uncertain significance	1	160239995	160239995	Human		name
401899886	CV2755830	single nucleotide variant	NM_015726.4(DCAF8):c.551G>A (p.Arg184His)	not specified [RCV004342200]	uncertain significance	1	160239869	160239869	Human		name
401880410	CV2783200	single nucleotide variant	NM_015726.4(DCAF8):c.559C>A (p.His187Asn)	not specified [RCV004363540]	uncertain significance	1	160239861	160239861	Human		name
401931743	CV2801481	single nucleotide variant	NM_015726.4(DCAF8):c.959C>T (p.Ser320Leu)	DCAF8-related disorder [RCV003408462]	uncertain significance	1	160237135	160237135	Human		name , trait , alternate_id
401942863	CV2839884	single nucleotide variant	NM_015726.4(DCAF8):c.373C>T (p.Arg125Cys)	not provided [RCV003456671]	likely benign	1	160240047	160240047	Human		name
401942867	CV2839885	single nucleotide variant	NM_015726.4(DCAF8):c.347G>A (p.Arg116His)	not provided [RCV003456672]	likely benign	1	160240073	160240073	Human		name
405690292	CV3246594	single nucleotide variant	NM_015726.4(DCAF8):c.383A>T (p.Asp128Val)	not specified [RCV004373164]	uncertain significance	1	160240037	160240037	Human		name
407457935	CV3430245	single nucleotide variant	NM_015726.4(DCAF8):c.365G>A (p.Arg122Gln)	not specified [RCV004611346]	uncertain significance	1	160240055	160240055	Human		name
407457938	CV3430246	single nucleotide variant	NM_015726.4(DCAF8):c.674G>A (p.Arg225Gln)	not specified [RCV004611347]	uncertain significance	1	160239746	160239746	Human		name
407457940	CV3430247	single nucleotide variant	NM_015726.4(DCAF8):c.496A>G (p.Ser166Gly)	not specified [RCV004611348]	uncertain significance	1	160239924	160239924	Human		name
597800815	CV3651984	single nucleotide variant	NM_015726.4(DCAF8):c.707A>G (p.Lys236Arg)	not specified [RCV004905883]	uncertain significance	1	160239713	160239713	Human		name
597800821	CV3651987	single nucleotide variant	NM_015726.4(DCAF8):c.947A>G (p.Asp316Gly)	not specified [RCV004905886]	uncertain significance	1	160237147	160237147	Human		name
598122463	CV3884409	single nucleotide variant	NM_015726.4(DCAF8):c.370A>G (p.Asn124Asp)	not specified [RCV005237101]	uncertain significance	1	160240050	160240050	Human		name
598261879	CV3963604	single nucleotide variant	NM_015726.4(DCAF8):c.526G>T (p.Ala176Ser)	not specified [RCV005325265]	uncertain significance	1	160239894	160239894	Human		name
598261884	CV3963605	single nucleotide variant	NM_015726.4(DCAF8):c.571G>A (p.Gly191Ser)	not specified [RCV005325266]	uncertain significance	1	160239849	160239849	Human		name
598261890	CV3963606	single nucleotide variant	NM_015726.4(DCAF8):c.370A>C (p.Asn124His)	not specified [RCV005325267]	uncertain significance	1	160240050	160240050	Human		name
598261895	CV3963607	single nucleotide variant	NM_015726.4(DCAF8):c.499G>T (p.Ala167Ser)	not specified [RCV005325268]	uncertain significance	1	160239921	160239921	Human		name
617148343	CV4017146	single nucleotide variant	NM_015726.4(DCAF8):c.781C>A (p.Gln261Lys)	not provided [RCV005416311]	not provided	1	160238690	160238690	Human		name
617152922	CV4018492	single nucleotide variant	NM_015726.4(DCAF8):c.343C>T (p.Arg115Trp)	not specified [RCV005418753]	uncertain significance	1	160240077	160240077	Human		name
21071978	CV794463	single nucleotide variant	NM_015726.4(DCAF8):c.349C>T (p.Arg117Cys)	not provided [RCV000994149]\|not specified [RCV004030167]	uncertain significance	1	160240071	160240071	Human		name
8624765	CV79879	single nucleotide variant	NM_015726.3(DCAF8):c.550C>T (p.Arg184Cys)	Malignant melanoma [RCV000059955]	not provided	1	160239870	160239870	Human		name
38459448	CV918574	single nucleotide variant	NM_015726.4(DCAF8):c.451C>T (p.Arg151Cys)	Giant axonal neuropathy 2 [RCV001195846]	uncertain significance	1	160239969	160239969	Human	1	name
38491989	CV921707	single nucleotide variant	NM_015726.4(DCAF8):c.809C>T (p.Thr270Ile)	not provided [RCV001223235]	uncertain significance	1	160238662	160238662	Human		name
156276574	CV2230531	single nucleotide variant	NM_015726.4(DCAF8):c.1100A>G (p.Asn367Ser)	not specified [RCV004097504]	uncertain significance	1	160225634	160225634	Human		name
156199146	CV2365246	single nucleotide variant	NM_015726.4(DCAF8):c.1726T>C (p.Ser576Pro)	not specified [RCV003388166]	uncertain significance	1	160217660	160217660	Human		name
243051579	CV2415906	single nucleotide variant	NM_015726.4(DCAF8):c.1727C>T (p.Ser576Phe)	Giant axonal neuropathy 2 [RCV003148524]	uncertain significance	1	160217659	160217659	Human	1	name
401739302	CV2738527	single nucleotide variant	NM_015726.4(DCAF8):c.1684C>T (p.Arg562Ter)	not specified [RCV003317919]	uncertain significance	1	160217702	160217702	Human		name
405690280	CV3246592	single nucleotide variant	NM_015726.4(DCAF8):c.1381C>T (p.Leu461Phe)	not specified [RCV004373162]	uncertain significance	1	160222710	160222710	Human		name
405854280	CV3393858	single nucleotide variant	NM_015726.4(DCAF8):c.1162G>T (p.Ala388Ser)	not provided [RCV004547084]	uncertain significance	1	160225101	160225101	Human		name
405869364	CV3397763	single nucleotide variant	NM_015726.4(DCAF8):c.1679G>A (p.Arg560His)	Neurofibromatosis, type 1 [RCV004566514]	uncertain significance	1	160217707	160217707	Human	1	name
407457946	CV3430249	single nucleotide variant	NM_015726.4(DCAF8):c.1055G>A (p.Arg352Gln)	not specified [RCV004611350]	uncertain significance	1	160231312	160231312	Human		name
597800807	CV3651980	single nucleotide variant	NM_015726.4(DCAF8):c.1711G>A (p.Ala571Thr)	not specified [RCV004905879]	uncertain significance	1	160217675	160217675	Human		name
597800817	CV3651985	single nucleotide variant	NM_015726.4(DCAF8):c.1770C>A (p.Asp590Glu)	not specified [RCV004905884]	uncertain significance	1	160217616	160217616	Human		name
597800823	CV3651988	single nucleotide variant	NM_015726.4(DCAF8):c.1532C>T (p.Ala511Val)	not specified [RCV004905887]	uncertain significance	1	160218877	160218877	Human		name
598261905	CV3963609	single nucleotide variant	NM_015726.4(DCAF8):c.1256G>A (p.Ser419Asn)	not specified [RCV005325270]	uncertain significance	1	160224495	160224495	Human		name
616933444	CV4011506	single nucleotide variant	NM_015726.4(DCAF8):c.1430A>G (p.Lys477Arg)	not specified [RCV005407587]	uncertain significance	1	160222661	160222661	Human		name
21071975	CV794462	single nucleotide variant	NM_015726.4(DCAF8):c.1028A>G (p.Asn343Ser)	not provided [RCV000994148]\|not specified [RCV004030166]	uncertain significance	1	160231339	160231339	Human		name
150488040	CV1274264	microsatellite	NM_015726.4(DCAF8):c.297AGAGGA[2] (p.Glu111_Glu112del)	not provided [RCV001726626]\|not specified [RCV001699717]	benign\|likely benign	1	160240106	160240111	Human		name
15190802	CV696206	microsatellite	NM_015726.4(DCAF8):c.313GAGGAAGAAGAG[1] (p.Glu109_Glu112del)	not provided [RCV000954584]	benign	1	160240084	160240095	Human		name
401926583	CV2821409	single nucleotide variant	NM_001017930.2(DCAF8L1):c.93G>C (p.Ala31=)	not provided [RCV003437993]	likely benign	X	27981242	27981242	Human		name
401926576	CV2821404	single nucleotide variant	NM_001353450.2(DCAF8L2):c.435A>G (p.Glu145=)	not provided [RCV003437988]	likely benign	X	27747330	27747330	Human		name
597800827	CV3651990	single nucleotide variant	NM_001017930.2(DCAF8L1):c.97A>G (p.Thr33Ala)	not specified [RCV004905889]	uncertain significance	X	27981238	27981238	Human		name
156134753	CV2196046	single nucleotide variant	NM_001017930.2(DCAF8L1):c.155G>A (p.Gly52Asp)	not specified [RCV004072288]	uncertain significance	X	27981180	27981180	Human		name
156155380	CV2388780	single nucleotide variant	NM_001017930.2(DCAF8L1):c.200A>G (p.Asn67Ser)	not specified [RCV004239638]	uncertain significance	X	27981135	27981135	Human		name
329386904	CV2439481	single nucleotide variant	NM_001017930.2(DCAF8L1):c.116T>C (p.Ile39Thr)	not specified [RCV004249768]	likely benign	X	27981219	27981219	Human		name
401757892	CV2685618	single nucleotide variant	NM_001017930.2(DCAF8L1):c.208A>G (p.Thr70Ala)	not specified [RCV004294627]	uncertain significance	X	27981127	27981127	Human		name
401737652	CV2699872	single nucleotide variant	NM_001017930.2(DCAF8L1):c.292A>T (p.Thr98Ser)	not specified [RCV004308513]	uncertain significance	X	27981043	27981043	Human		name
401926579	CV2821406	single nucleotide variant	NM_001353450.2(DCAF8L2):c.1740T>G (p.Leu580=)	not provided [RCV003437990]	likely benign	X	27748635	27748635	Human		name
401926580	CV2821407	single nucleotide variant	NM_001017930.2(DCAF8L1):c.1200C>T (p.His400=)	not provided [RCV003437991]	likely benign	X	27980135	27980135	Human		name
405690325	CV3246601	single nucleotide variant	NM_001017930.2(DCAF8L1):c.275C>T (p.Pro92Leu)	not specified [RCV004373171]	uncertain significance	X	27981060	27981060	Human		name
407457951	CV3430251	single nucleotide variant	NM_001017930.2(DCAF8L1):c.145G>A (p.Gly49Arg)	not specified [RCV004611352]	uncertain significance	X	27981190	27981190	Human		name
407457955	CV3430252	single nucleotide variant	NM_001017930.2(DCAF8L1):c.120A>C (p.Glu40Asp)	not specified [RCV004611353]	uncertain significance	X	27981215	27981215	Human		name
407457957	CV3430253	single nucleotide variant	NM_001017930.2(DCAF8L1):c.123G>A (p.Met41Ile)	not specified [RCV004611354]	uncertain significance	X	27981212	27981212	Human		name
407457960	CV3430254	single nucleotide variant	NM_001017930.2(DCAF8L1):c.127G>A (p.Ala43Thr)	not specified [RCV004611355]	uncertain significance	X	27981208	27981208	Human		name
407457962	CV3430255	single nucleotide variant	NM_001017930.2(DCAF8L1):c.130A>T (p.Thr44Ser)	not specified [RCV004611356]	uncertain significance	X	27981205	27981205	Human		name
407457965	CV3430256	single nucleotide variant	NM_001017930.2(DCAF8L1):c.245A>C (p.Glu82Ala)	not specified [RCV004611357]	uncertain significance	X	27981090	27981090	Human		name
155917974	CV2195619	single nucleotide variant	NM_001017930.2(DCAF8L1):c.434C>T (p.Ser145Leu)	not specified [RCV004082827]	uncertain significance	X	27980901	27980901	Human		name
156259499	CV2204740	single nucleotide variant	NM_001017930.2(DCAF8L1):c.485G>A (p.Arg162His)	not specified [RCV004075000]	uncertain significance	X	27980850	27980850	Human		name
155973678	CV2211080	single nucleotide variant	NM_001017930.2(DCAF8L1):c.472C>G (p.Leu158Val)	not specified [RCV004088260]	uncertain significance	X	27980863	27980863	Human		name
156280003	CV2348403	single nucleotide variant	NM_001017930.2(DCAF8L1):c.476C>T (p.Thr159Ile)	not specified [RCV004193595]	uncertain significance	X	27980859	27980859	Human		name
156402333	CV2363823	single nucleotide variant	NM_001017930.2(DCAF8L1):c.377C>G (p.Thr126Ser)	not specified [RCV004218804]	uncertain significance	X	27980958	27980958	Human		name
155988025	CV2363921	single nucleotide variant	NM_001017930.2(DCAF8L1):c.376A>G (p.Thr126Ala)	not specified [RCV004218892]	likely benign	X	27980959	27980959	Human		name
329370114	CV2435479	single nucleotide variant	NM_001017930.2(DCAF8L1):c.559C>T (p.Arg187Cys)	not provided [RCV003435994]\|not specified [RCV004253125]	likely benign	X	27980776	27980776	Human		name
329365000	CV2443913	single nucleotide variant	NM_001017930.2(DCAF8L1):c.410A>C (p.Gln137Pro)	not specified [RCV004258243]	uncertain significance	X	27980925	27980925	Human		name
401726610	CV2677286	single nucleotide variant	NM_001017930.2(DCAF8L1):c.451C>A (p.Pro151Thr)	not specified [RCV004295905]	uncertain significance	X	27980884	27980884	Human		name
401774755	CV2688276	single nucleotide variant	NM_001017930.2(DCAF8L1):c.559C>A (p.Arg187Ser)	not specified [RCV004299286]	uncertain significance	X	27980776	27980776	Human		name
401926577	CV2821405	single nucleotide variant	NM_001353450.2(DCAF8L2):c.581A>G (p.His194Arg)	not provided [RCV003437989]	likely benign	X	27747476	27747476	Human		name
401926581	CV2821408	single nucleotide variant	NM_001017930.2(DCAF8L1):c.321G>A (p.Met107Ile)	not provided [RCV003437992]	likely benign	X	27981014	27981014	Human		name
405690330	CV3246602	single nucleotide variant	NM_001017930.2(DCAF8L1):c.505A>C (p.Ser169Arg)	not specified [RCV004373172]	uncertain significance	X	27980830	27980830	Human		name
405690341	CV3246604	single nucleotide variant	NM_001017930.2(DCAF8L1):c.586G>T (p.Ala196Ser)	not specified [RCV004373174]	uncertain significance	X	27980749	27980749	Human		name
405690348	CV3246605	single nucleotide variant	NM_001017930.2(DCAF8L1):c.657G>C (p.Arg219Ser)	not specified [RCV004373175]	uncertain significance	X	27980678	27980678	Human		name
405690353	CV3246606	single nucleotide variant	NM_001017930.2(DCAF8L1):c.770C>T (p.Ala257Val)	not specified [RCV004373176]	uncertain significance	X	27980565	27980565	Human		name
407457948	CV3430250	single nucleotide variant	NM_001017930.2(DCAF8L1):c.643G>A (p.Gly215Ser)	not specified [RCV004611351]	uncertain significance	X	27980692	27980692	Human		name
407457970	CV3430258	single nucleotide variant	NM_001353450.2(DCAF8L2):c.627T>G (p.Cys209Trp)	not specified [RCV004611359]	uncertain significance	X	27747522	27747522	Human		name
597800825	CV3651989	single nucleotide variant	NM_001017930.2(DCAF8L1):c.370G>A (p.Gly124Ser)	not specified [RCV004905888]	uncertain significance	X	27980965	27980965	Human		name
597800832	CV3651993	single nucleotide variant	NM_001017930.2(DCAF8L1):c.829G>A (p.Glu277Lys)	not specified [RCV004905892]	uncertain significance	X	27980506	27980506	Human		name
598261910	CV3963610	single nucleotide variant	NM_001017930.2(DCAF8L1):c.387T>A (p.Asp129Glu)	not specified [RCV005325271]	likely benign	X	27980948	27980948	Human		name
598261915	CV3963611	single nucleotide variant	NM_001017930.2(DCAF8L1):c.457T>C (p.Ser153Pro)	not specified [RCV005325272]	likely benign	X	27980878	27980878	Human		name
598261918	CV3963612	single nucleotide variant	NM_001017930.2(DCAF8L1):c.330A>C (p.Glu110Asp)	not specified [RCV005325273]	uncertain significance	X	27981005	27981005	Human		name
598261928	CV3963614	single nucleotide variant	NM_001017930.2(DCAF8L1):c.382C>T (p.His128Tyr)	not specified [RCV005325275]	uncertain significance	X	27980953	27980953	Human		name
598261933	CV3963615	single nucleotide variant	NM_001017930.2(DCAF8L1):c.995A>G (p.Asp332Gly)	not specified [RCV005325276]	uncertain significance	X	27980340	27980340	Human		name
8628733	CV83877	single nucleotide variant	NM_001017930.1(DCAF8L1):c.316G>A (p.Glu106Lys)	Malignant melanoma [RCV000063958]	not provided	X	27981019	27981019	Human		name
156331746	CV2218210	single nucleotide variant	NM_001017930.2(DCAF8L1):c.1556C>T (p.Thr519Ile)	not specified [RCV004088414]	uncertain significance	X	27979779	27979779	Human		name
155976968	CV2218659	single nucleotide variant	NM_001017930.2(DCAF8L1):c.1675G>A (p.Ala559Thr)	not specified [RCV004090910]	uncertain significance	X	27979660	27979660	Human		name
156169935	CV2273409	single nucleotide variant	NM_001017930.2(DCAF8L1):c.1772G>C (p.Gly591Ala)	not specified [RCV004132172]	uncertain significance	X	27979563	27979563	Human		name
156284872	CV2289014	single nucleotide variant	NM_001017930.2(DCAF8L1):c.1459C>T (p.Leu487Phe)	not specified [RCV004149964]	uncertain significance	X	27979876	27979876	Human		name
156402662	CV2371362	single nucleotide variant	NM_001353450.2(DCAF8L2):c.1332C>A (p.Asp444Glu)	not specified [RCV004223366]	likely benign	X	27748227	27748227	Human		name
156402663	CV2371363	single nucleotide variant	NM_001353450.2(DCAF8L2):c.1358A>T (p.His453Leu)	not specified [RCV004223367]	uncertain significance	X	27748253	27748253	Human		name
329377397	CV2457122	single nucleotide variant	NM_001017930.2(DCAF8L1):c.1646G>A (p.Arg549Gln)	not specified [RCV004264899]	uncertain significance	X	27979689	27979689	Human		name
401767525	CV2729723	single nucleotide variant	NM_001353450.2(DCAF8L2):c.1117A>T (p.Thr373Ser)	not specified [RCV004331977]	likely benign	X	27748012	27748012	Human		name
401728664	CV2729725	single nucleotide variant	NM_001353450.2(DCAF8L2):c.1120G>A (p.Val374Met)	not specified [RCV004331979]	uncertain significance	X	27748015	27748015	Human		name
401865676	CV2778874	single nucleotide variant	NM_001017930.2(DCAF8L1):c.1207A>G (p.Thr403Ala)	not specified [RCV004346761]	uncertain significance	X	27980128	27980128	Human		name
405690298	CV3246595	single nucleotide variant	NM_001017930.2(DCAF8L1):c.1015A>G (p.Thr339Ala)	not specified [RCV004373165]	uncertain significance	X	27980320	27980320	Human		name
405690302	CV3246596	single nucleotide variant	NM_001017930.2(DCAF8L1):c.1186G>A (p.Val396Ile)	not specified [RCV004373166]	likely benign	X	27980149	27980149	Human		name
405690305	CV3246597	single nucleotide variant	NM_001017930.2(DCAF8L1):c.1595G>T (p.Arg532Leu)	not specified [RCV004373167]	uncertain significance	X	27979740	27979740	Human		name
405690317	CV3246599	single nucleotide variant	NM_001017930.2(DCAF8L1):c.1683A>C (p.Gln561His)	not specified [RCV004373169]	likely benign	X	27979652	27979652	Human		name
405690320	CV3246600	single nucleotide variant	NM_001017930.2(DCAF8L1):c.1756A>G (p.Thr586Ala)	not specified [RCV004373170]	uncertain significance	X	27979579	27979579	Human		name
405690361	CV3246607	single nucleotide variant	NM_001353450.2(DCAF8L2):c.1243C>T (p.His415Tyr)	not specified [RCV004373177]	uncertain significance	X	27748138	27748138	Human		name
405690366	CV3246608	single nucleotide variant	NM_001353450.2(DCAF8L2):c.1385G>A (p.Arg462Lys)	not specified [RCV004373178]	uncertain significance	X	27748280	27748280	Human		name
405690370	CV3246609	single nucleotide variant	NM_001353450.2(DCAF8L2):c.1885A>T (p.Met629Leu)	not specified [RCV004373179]	likely benign	X	27748780	27748780	Human		name
407457968	CV3430257	single nucleotide variant	NM_001353450.2(DCAF8L2):c.1133A>G (p.Asn378Ser)	not specified [RCV004611358]	uncertain significance	X	27748028	27748028	Human		name
597800829	CV3651991	single nucleotide variant	NM_001017930.2(DCAF8L1):c.1658G>A (p.Arg553His)	not specified [RCV004905890]	uncertain significance	X	27979677	27979677	Human		name
597800834	CV3651994	single nucleotide variant	NM_001353450.2(DCAF8L2):c.1433A>G (p.Tyr478Cys)	not specified [RCV004905893]	uncertain significance	X	27748328	27748328	Human		name
598261923	CV3963613	single nucleotide variant	NM_001017930.2(DCAF8L1):c.1669C>G (p.Gln557Glu)	not specified [RCV005325274]	uncertain significance	X	27979666	27979666	Human		name

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