Dlec1 Variant Search Result - Rat Genome Database

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224 records found for search term Dlec1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156224247	CV2229738	single nucleotide variant	NM_007335.4(DLEC1):c.*1G>C	not specified [RCV004103538]	uncertain significance	3	38122413	38122413	Human		name
156191969	CV2388580	single nucleotide variant	NM_007335.4(DLEC1):c.*6C>T	not specified [RCV004237426]	likely benign	3	38122418	38122418	Human		name
156134868	CV2235591	single nucleotide variant	NM_007335.4(DLEC1):c.*45A>G	not specified [RCV004109618]	uncertain significance	3	38122457	38122457	Human		name
156166835	CV2373637	single nucleotide variant	NM_007335.4(DLEC1):c.*71C>A	not specified [RCV004222726]	uncertain significance	3	38122483	38122483	Human		name
401733181	CV2685450	single nucleotide variant	NM_007335.4(DLEC1):c.*117G>C	not specified [RCV004294478]	uncertain significance	3	38122529	38122529	Human		name
126744183	CV1016240	single nucleotide variant	NM_007335.4(DLEC1):c.1919+1G>A	Malignant tumor of esophagus [RCV001330381]	pathogenic	3	38093768	38093768	Human		name
126731177	CV1019818	single nucleotide variant	NM_007335.4(DLEC1):c.1919+2T>G	Malignant tumor of esophagus [RCV001333645]	pathogenic	3	38093769	38093769	Human		name
401922185	CV2827254	single nucleotide variant	NM_007335.4(DLEC1):c.1757-6T>G	not provided [RCV003433517]	likely benign	3	38093599	38093599	Human		name
401926307	CV2827255	single nucleotide variant	NM_007335.4(DLEC1):c.2112+6G>C	not provided [RCV003437754]	likely benign	3	38095077	38095077	Human		name
15144589	CV778984	single nucleotide variant	NM_007335.4(DLEC1):c.3666+8T>C	not provided [RCV000966857]	benign	3	38112369	38112369	Human		name
401867479	CV2770410	single nucleotide variant	NM_007335.4(DLEC1):c.25C>T (p.Arg9Trp)	not specified [RCV004358056]	uncertain significance	3	38039250	38039250	Human		name
407474737	CV3430586	single nucleotide variant	NM_007335.4(DLEC1):c.13A>G (p.Ser5Gly)	not specified [RCV004616517]	uncertain significance	3	38039238	38039238	Human		name
156296460	CV2233841	single nucleotide variant	NM_007335.4(DLEC1):c.74C>T (p.Ala25Val)	not specified [RCV004102058]	uncertain significance	3	38039299	38039299	Human		name
156164485	CV2319713	single nucleotide variant	NM_007335.4(DLEC1):c.59A>G (p.Gln20Arg)	not specified [RCV004187251]	uncertain significance	3	38039284	38039284	Human		name
401880606	CV2780274	single nucleotide variant	NM_007335.4(DLEC1):c.44G>A (p.Arg15Gln)	not specified [RCV004355905]	uncertain significance	3	38039269	38039269	Human		name
401880835	CV2789397	single nucleotide variant	NM_007335.4(DLEC1):c.50A>G (p.Asn17Ser)	not specified [RCV004360041]	uncertain significance	3	38039275	38039275	Human		name
15172773	CV698051	single nucleotide variant	NM_007335.4(DLEC1):c.543C>T (p.Ser181=)	not provided [RCV000950100]	benign	3	38045674	38045674	Human		name
15165583	CV720418	single nucleotide variant	NM_007335.4(DLEC1):c.47C>T (p.Thr16Ile)	not provided [RCV000882445]	likely benign	3	38039272	38039272	Human		name
401922183	CV2827251	single nucleotide variant	NM_007335.4(DLEC1):c.250C>T (p.Pro84Ser)	not provided [RCV003433515]	likely benign	3	38039475	38039475	Human		name
401926305	CV2827253	single nucleotide variant	NM_007335.4(DLEC1):c.1203G>C (p.Thr401=)	not provided [RCV003437753]	likely benign	3	38084187	38084187	Human		name
405706764	CV3240267	single nucleotide variant	NM_007335.4(DLEC1):c.226G>A (p.Glu76Lys)	not specified [RCV004376023]	uncertain significance	3	38039451	38039451	Human		name
405706770	CV3240268	single nucleotide variant	NM_007335.4(DLEC1):c.227A>T (p.Glu76Val)	not specified [RCV004376024]	uncertain significance	3	38039452	38039452	Human		name
597679936	CV3662598	single nucleotide variant	NM_007335.4(DLEC1):c.254C>T (p.Ser85Phe)	not specified [RCV004914148]	uncertain significance	3	38039479	38039479	Human		name
597801367	CV3662622	single nucleotide variant	NM_007335.4(DLEC1):c.139T>A (p.Ser47Thr)	not specified [RCV004906166]	uncertain significance	3	38039364	38039364	Human		name
15196012	CV698053	single nucleotide variant	NM_007335.4(DLEC1):c.2181G>A (p.Ala727=)	not provided [RCV000956080]	benign	3	38096578	38096578	Human		name
15168830	CV708808	single nucleotide variant	NM_007335.4(DLEC1):c.152A>G (p.Tyr51Cys)	not provided [RCV000971694]	likely benign	3	38039377	38039377	Human		name
15178441	CV720419	single nucleotide variant	NM_007335.4(DLEC1):c.2613C>T (p.Leu871=)	not provided [RCV000885062]	benign\|likely benign	3	38097791	38097791	Human		name
15099368	CV720420	single nucleotide variant	NM_007335.4(DLEC1):c.2655C>T (p.Asn885=)	not provided [RCV000891934]	benign	3	38097833	38097833	Human		name
15129380	CV734037	single nucleotide variant	NM_007335.4(DLEC1):c.1185G>A (p.Ala395=)	not provided [RCV000897431]	benign	3	38084169	38084169	Human		name
15137278	CV763845	single nucleotide variant	NM_007335.4(DLEC1):c.1530C>T (p.Phe510=)	not provided [RCV000943213]	likely benign	3	38086335	38086335	Human		name
126731180	CV1019817	single nucleotide variant	NM_007335.4(DLEC1):c.865C>A (p.Pro289Thr)	Malignant tumor of esophagus [RCV001333646]	uncertain significance	3	38062360	38062360	Human	1	name
156066394	CV2225532	single nucleotide variant	NM_007335.4(DLEC1):c.850G>C (p.Glu284Gln)	not specified [RCV004100917]	likely benign	3	38062345	38062345	Human		name
156080701	CV2255945	single nucleotide variant	NM_007335.4(DLEC1):c.538G>A (p.Glu180Lys)	not specified [RCV004122398]	uncertain significance	3	38045669	38045669	Human		name
156290028	CV2299445	single nucleotide variant	NM_007335.4(DLEC1):c.412A>T (p.Ile138Phe)	not specified [RCV004154528]	uncertain significance	3	38045543	38045543	Human		name
156305613	CV2369526	single nucleotide variant	NM_007335.4(DLEC1):c.5190C>G (p.Leu1730=)	not specified [RCV004210460]	uncertain significance	3	38122334	38122334	Human		name
156154016	CV2395039	single nucleotide variant	NM_007335.4(DLEC1):c.5232C>T (p.Ser1744=)	not specified [RCV004236726]	likely benign	3	38122376	38122376	Human		name
329399279	CV2436547	single nucleotide variant	NM_007335.4(DLEC1):c.914T>C (p.Leu305Ser)	not specified [RCV004253705]	uncertain significance	3	38062621	38062621	Human		name
329378416	CV2463723	single nucleotide variant	NM_007335.4(DLEC1):c.653C>T (p.Pro218Leu)	not specified [RCV004279289]	uncertain significance	3	38059832	38059832	Human		name
401768815	CV2735441	single nucleotide variant	NM_007335.4(DLEC1):c.5190C>T (p.Leu1730=)	not specified [RCV004331001]	likely benign	3	38122334	38122334	Human		name
401860778	CV2758623	single nucleotide variant	NM_007335.4(DLEC1):c.416G>A (p.Arg139Gln)	not specified [RCV004337698]	uncertain significance	3	38045547	38045547	Human		name
401872815	CV2764349	single nucleotide variant	NM_007335.4(DLEC1):c.461G>A (p.Arg154Lys)	not specified [RCV004338922]	uncertain significance	3	38045592	38045592	Human		name
401863677	CV2773151	single nucleotide variant	NM_007335.4(DLEC1):c.485G>T (p.Arg162Leu)	not specified [RCV004351879]	uncertain significance	3	38045616	38045616	Human		name
401878300	CV2774156	single nucleotide variant	NM_007335.4(DLEC1):c.446T>C (p.Phe149Ser)	not specified [RCV004345746]	uncertain significance	3	38045577	38045577	Human		name
401894678	CV2785168	single nucleotide variant	NM_007335.4(DLEC1):c.305A>G (p.Asn102Ser)	not specified [RCV004355163]	uncertain significance	3	38039530	38039530	Human		name
401882778	CV2788587	single nucleotide variant	NM_007335.4(DLEC1):c.872A>G (p.Lys291Arg)	not specified [RCV004361084]	uncertain significance	3	38062367	38062367	Human		name
401922184	CV2827252	single nucleotide variant	NM_007335.4(DLEC1):c.578G>A (p.Arg193Lys)	not provided [RCV003433516]	likely benign	3	38059757	38059757	Human		name
405706841	CV3240278	single nucleotide variant	NM_007335.4(DLEC1):c.355A>G (p.Lys119Glu)	not specified [RCV004376034]	uncertain significance	3	38039580	38039580	Human		name
405706848	CV3240279	single nucleotide variant	NM_007335.4(DLEC1):c.367A>G (p.Ser123Gly)	not specified [RCV004376035]	uncertain significance	3	38039592	38039592	Human		name
405706910	CV3240287	single nucleotide variant	NM_007335.4(DLEC1):c.395T>C (p.Val132Ala)	not specified [RCV004376043]	uncertain significance	3	38039620	38039620	Human		name
405706978	CV3240296	single nucleotide variant	NM_007335.4(DLEC1):c.506G>A (p.Arg169Gln)	not specified [RCV004376052]	uncertain significance	3	38045637	38045637	Human		name
405707007	CV3240300	single nucleotide variant	NM_007335.4(DLEC1):c.925C>G (p.Gln309Glu)	not specified [RCV004376056]	uncertain significance	3	38062632	38062632	Human		name
405707014	CV3240301	single nucleotide variant	NM_007335.4(DLEC1):c.988C>A (p.Pro330Thr)	not specified [RCV004376057]	uncertain significance	3	38062695	38062695	Human		name
407474723	CV3430583	single nucleotide variant	NM_007335.4(DLEC1):c.715G>A (p.Glu239Lys)	not specified [RCV004616514]	uncertain significance	3	38062210	38062210	Human		name
597679882	CV3662591	single nucleotide variant	NM_007335.4(DLEC1):c.868C>T (p.Leu290Phe)	not specified [RCV004914141]	uncertain significance	3	38062363	38062363	Human		name
597679985	CV3662604	single nucleotide variant	NM_007335.4(DLEC1):c.804C>G (p.Asp268Glu)	not specified [RCV004914154]	uncertain significance	3	38062299	38062299	Human		name
597680000	CV3662606	single nucleotide variant	NM_007335.4(DLEC1):c.5262G>A (p.Gln1754=)	not specified [RCV004914156]	uncertain significance	3	38122406	38122406	Human		name
597801354	CV3662616	single nucleotide variant	NM_007335.4(DLEC1):c.762T>G (p.Asp254Glu)	not specified [RCV004906160]	uncertain significance	3	38062257	38062257	Human		name
597801357	CV3662617	single nucleotide variant	NM_007335.4(DLEC1):c.692G>A (p.Cys231Tyr)	not specified [RCV004906161]	likely benign	3	38062187	38062187	Human		name
597801361	CV3662619	single nucleotide variant	NM_007335.4(DLEC1):c.646A>T (p.Thr216Ser)	not specified [RCV004906163]	uncertain significance	3	38059825	38059825	Human		name
598173715	CV3964097	single nucleotide variant	NM_007335.4(DLEC1):c.968G>A (p.Arg323Gln)	not specified [RCV005331583]	uncertain significance	3	38062675	38062675	Human		name
598173757	CV3964104	single nucleotide variant	NM_007335.4(DLEC1):c.992G>C (p.Arg331Pro)	not specified [RCV005331590]	uncertain significance	3	38062699	38062699	Human		name
598173814	CV3964113	single nucleotide variant	NM_007335.4(DLEC1):c.5205C>T (p.Cys1735=)	not specified [RCV005331599]	uncertain significance	3	38122349	38122349	Human		name
15164115	CV698052	single nucleotide variant	NM_007335.4(DLEC1):c.575C>T (p.Ser192Phe)	not provided [RCV000948259]	benign	3	38059754	38059754	Human		name
15196016	CV698054	single nucleotide variant	NM_007335.4(DLEC1):c.3657C>A (p.Leu1219=)	not provided [RCV000956081]	likely benign	3	38112352	38112352	Human		name
15103823	CV698055	single nucleotide variant	NM_007335.4(DLEC1):c.3702C>T (p.His1234=)	not provided [RCV000959558]	likely benign	3	38114377	38114377	Human		name
15150710	CV708814	single nucleotide variant	NM_007335.4(DLEC1):c.3804C>T (p.Ser1268=)	not provided [RCV000967997]	benign	3	38115001	38115001	Human		name
15150717	CV708815	single nucleotide variant	NM_007335.4(DLEC1):c.5014C>T (p.Leu1672=)	not provided [RCV000967998]	benign	3	38121775	38121775	Human		name
15155800	CV748219	single nucleotide variant	NM_007335.4(DLEC1):c.4494T>C (p.Ser1498=)	not provided [RCV000924537]	likely benign	3	38117814	38117814	Human		name
8630784	CV85939	single nucleotide variant	NM_007335.2(DLEC1):c.643G>A (p.Asp215Asn)	Malignant melanoma [RCV000066023]	not provided	3	38059822	38059822	Human		name
42722986	CV985204	single nucleotide variant	NM_007335.4(DLEC1):c.5212C>A (p.Arg1738=)	Malignant tumor of esophagus [RCV001292980]	pathogenic	3	38122356	38122356	Human		name
156400205	CV2199033	single nucleotide variant	NM_007335.4(DLEC1):c.1879C>T (p.Arg627Trp)	not specified [RCV004080438]	uncertain significance	3	38093727	38093727	Human		name
156229667	CV2199510	single nucleotide variant	NM_007335.4(DLEC1):c.1723G>A (p.Asp575Asn)	not specified [RCV004071062]	uncertain significance	3	38092847	38092847	Human		name
156096877	CV2206687	single nucleotide variant	NM_007335.4(DLEC1):c.2866T>C (p.Tyr956His)	not specified [RCV004083381]	uncertain significance	3	38107585	38107585	Human		name
156293704	CV2233569	single nucleotide variant	NM_007335.4(DLEC1):c.2945T>G (p.Leu982Arg)	not specified [RCV004100044]	uncertain significance	3	38107664	38107664	Human		name
156051884	CV2238113	single nucleotide variant	NM_007335.4(DLEC1):c.1656A>G (p.Ile552Met)	not specified [RCV004111128]	uncertain significance	3	38088379	38088379	Human		name
156094257	CV2252936	single nucleotide variant	NM_007335.4(DLEC1):c.1214A>G (p.Tyr405Cys)	not specified [RCV004120758]	uncertain significance	3	38084198	38084198	Human		name
155962753	CV2254455	single nucleotide variant	NM_007335.4(DLEC1):c.2479G>A (p.Val827Ile)	not specified [RCV004123830]	uncertain significance	3	38097551	38097551	Human		name
156112447	CV2261096	single nucleotide variant	NM_007335.4(DLEC1):c.1505A>T (p.Asn502Ile)	not specified [RCV004128000]	uncertain significance	3	38086310	38086310	Human		name
155974623	CV2269978	single nucleotide variant	NM_007335.4(DLEC1):c.2736C>A (p.Phe912Leu)	not specified [RCV004128971]	uncertain significance	3	38100297	38100297	Human		name
156145684	CV2292532	single nucleotide variant	NM_007335.4(DLEC1):c.2297C>T (p.Pro766Leu)	not specified [RCV004150306]	uncertain significance	3	38096694	38096694	Human		name
156341411	CV2344791	single nucleotide variant	NM_007335.4(DLEC1):c.1924G>T (p.Val642Leu)	not specified [RCV004190938]	uncertain significance	3	38094883	38094883	Human		name
156165699	CV2348617	single nucleotide variant	NM_007335.4(DLEC1):c.2528C>G (p.Pro843Arg)	not specified [RCV004195842]	uncertain significance	3	38097600	38097600	Human		name
156129887	CV2364771	single nucleotide variant	NM_007335.4(DLEC1):c.2651G>A (p.Arg884Gln)	not specified [RCV004219642]	likely benign	3	38097829	38097829	Human		name
156080475	CV2384648	single nucleotide variant	NM_007335.4(DLEC1):c.1291G>T (p.Ala431Ser)	not specified [RCV004232426]	uncertain significance	3	38085303	38085303	Human		name
329366284	CV2438319	single nucleotide variant	NM_007335.4(DLEC1):c.1649A>G (p.His550Arg)	not specified [RCV004257072]	uncertain significance	3	38088372	38088372	Human		name
329399657	CV2444088	single nucleotide variant	NM_007335.4(DLEC1):c.2615G>A (p.Arg872His)	not specified [RCV004260831]	uncertain significance	3	38097793	38097793	Human		name
329393296	CV2449635	single nucleotide variant	NM_007335.4(DLEC1):c.2845G>A (p.Val949Met)	not specified [RCV004268552]	uncertain significance	3	38100406	38100406	Human		name
329395799	CV2454576	single nucleotide variant	NM_007335.4(DLEC1):c.1145C>A (p.Thr382Lys)	not specified [RCV004268050]	uncertain significance	3	38063891	38063891	Human		name
329362067	CV2456709	single nucleotide variant	NM_007335.4(DLEC1):c.1250C>A (p.Ala417Asp)	not specified [RCV004277876]	uncertain significance	3	38084234	38084234	Human		name
329401755	CV2457372	single nucleotide variant	NM_007335.4(DLEC1):c.1201A>G (p.Thr401Ala)	not specified [RCV004267205]	likely benign	3	38084185	38084185	Human		name
401738713	CV2676356	single nucleotide variant	NM_007335.4(DLEC1):c.2741T>C (p.Ile914Thr)	not specified [RCV004286383]	uncertain significance	3	38100302	38100302	Human		name
401739948	CV2684221	single nucleotide variant	NM_007335.4(DLEC1):c.2539G>T (p.Val847Leu)	not specified [RCV004288885]	uncertain significance	3	38097611	38097611	Human		name
401744972	CV2693152	single nucleotide variant	NM_007335.4(DLEC1):c.1918A>T (p.Thr640Ser)	not specified [RCV004293087]	uncertain significance	3	38093766	38093766	Human		name
401779048	CV2702079	single nucleotide variant	NM_007335.4(DLEC1):c.2275G>A (p.Glu759Lys)	not specified [RCV004320651]	uncertain significance	3	38096672	38096672	Human		name
401770010	CV2710810	single nucleotide variant	NM_007335.4(DLEC1):c.1457G>A (p.Gly486Asp)	not specified [RCV004308734]	uncertain significance	3	38086262	38086262	Human		name
401777601	CV2718263	single nucleotide variant	NM_007335.4(DLEC1):c.2080C>T (p.His694Tyr)	not specified [RCV004316250]	uncertain significance	3	38095039	38095039	Human		name
401776352	CV2724668	single nucleotide variant	NM_007335.4(DLEC1):c.2441G>A (p.Ser814Asn)	not specified [RCV004331467]	likely benign	3	38097513	38097513	Human		name
401763700	CV2725262	single nucleotide variant	NM_007335.4(DLEC1):c.1856T>C (p.Ile619Thr)	not specified [RCV004319931]	uncertain significance	3	38093704	38093704	Human		name
401872222	CV2754307	single nucleotide variant	NM_007335.4(DLEC1):c.2476G>T (p.Gly826Cys)	not specified [RCV004334483]	uncertain significance	3	38097548	38097548	Human		name
401871571	CV2759900	single nucleotide variant	NM_007335.4(DLEC1):c.1643C>T (p.Pro548Leu)	not specified [RCV004345327]	uncertain significance	3	38088366	38088366	Human		name
401873306	CV2761419	single nucleotide variant	NM_007335.4(DLEC1):c.1759A>G (p.Ile587Val)	not specified [RCV004334598]	uncertain significance	3	38093607	38093607	Human		name
401889005	CV2761648	single nucleotide variant	NM_007335.4(DLEC1):c.2557G>A (p.Val853Ile)	not provided [RCV005425139]\|not specified [RCV004337268]	likely benign\|uncertain significance	3	38097629	38097629	Human		name
401894384	CV2780871	single nucleotide variant	NM_007335.4(DLEC1):c.1335C>G (p.Asp445Glu)	not specified [RCV004352182]	uncertain significance	3	38085347	38085347	Human		name
401868283	CV2784906	single nucleotide variant	NM_007335.4(DLEC1):c.2097C>G (p.Ser699Arg)	not specified [RCV004352682]	uncertain significance	3	38095056	38095056	Human		name
405262839	CV3185043	single nucleotide variant	NM_007335.4(DLEC1):c.2026G>A (p.Glu676Lys)	not provided [RCV003885607]	likely benign	3	38094985	38094985	Human		name
405706724	CV3240261	single nucleotide variant	NM_007335.4(DLEC1):c.1238C>T (p.Thr413Met)	not specified [RCV004376017]	uncertain significance	3	38084222	38084222	Human		name
405706733	CV3240262	single nucleotide variant	NM_007335.4(DLEC1):c.1551C>G (p.Ser517Arg)	not specified [RCV004376018]	uncertain significance	3	38086356	38086356	Human		name
405706745	CV3240264	single nucleotide variant	NM_007335.4(DLEC1):c.1880G>A (p.Arg627Gln)	not specified [RCV004376020]	likely benign	3	38093728	38093728	Human		name
405706752	CV3240265	single nucleotide variant	NM_007335.4(DLEC1):c.2003G>C (p.Ser668Thr)	not specified [RCV004376021]	uncertain significance	3	38094962	38094962	Human		name
405706759	CV3240266	single nucleotide variant	NM_007335.4(DLEC1):c.2266G>T (p.Val756Phe)	not specified [RCV004376022]	uncertain significance	3	38096663	38096663	Human		name
405706776	CV3240269	single nucleotide variant	NM_007335.4(DLEC1):c.2332G>A (p.Ala778Thr)	not specified [RCV004376025]	likely benign	3	38096729	38096729	Human		name
405706787	CV3240270	single nucleotide variant	NM_007335.4(DLEC1):c.2384A>G (p.Lys795Arg)	not specified [RCV004376026]	uncertain significance	3	38097225	38097225	Human		name
405706793	CV3240271	single nucleotide variant	NM_007335.4(DLEC1):c.2392G>A (p.Asp798Asn)	not specified [RCV004376027]	uncertain significance	3	38097233	38097233	Human		name
405706799	CV3240272	single nucleotide variant	NM_007335.4(DLEC1):c.2646G>T (p.Gln882His)	not specified [RCV004376028]	uncertain significance	3	38097824	38097824	Human		name
405706805	CV3240273	single nucleotide variant	NM_007335.4(DLEC1):c.2797T>G (p.Leu933Val)	not specified [RCV004376029]	uncertain significance	3	38100358	38100358	Human		name
405706814	CV3240274	single nucleotide variant	NM_007335.4(DLEC1):c.2852A>T (p.Asn951Ile)	not specified [RCV004376030]	uncertain significance	3	38100413	38100413	Human		name
405706820	CV3240275	single nucleotide variant	NM_007335.4(DLEC1):c.2887G>T (p.Val963Leu)	not specified [RCV004376031]	uncertain significance	3	38107606	38107606	Human		name
407474728	CV3430584	single nucleotide variant	NM_007335.4(DLEC1):c.1876C>G (p.Leu626Val)	not specified [RCV004616515]	uncertain significance	3	38093724	38093724	Human		name
407474744	CV3430588	single nucleotide variant	NM_007335.4(DLEC1):c.2265G>C (p.Gln755His)	not specified [RCV004616519]	uncertain significance	3	38096662	38096662	Human		name
407474749	CV3430589	single nucleotide variant	NM_007335.4(DLEC1):c.1766A>T (p.Gln589Leu)	not specified [RCV004616520]	uncertain significance	3	38093614	38093614	Human		name
407474753	CV3430590	single nucleotide variant	NM_007335.4(DLEC1):c.2731C>G (p.Pro911Ala)	not specified [RCV004616521]	uncertain significance	3	38100292	38100292	Human		name
597679813	CV3662582	single nucleotide variant	NM_007335.4(DLEC1):c.2246G>C (p.Gly749Ala)	not specified [RCV004914133]	uncertain significance	3	38096643	38096643	Human		name
597679822	CV3662583	single nucleotide variant	NM_007335.4(DLEC1):c.2083G>A (p.Glu695Lys)	not specified [RCV004914134]	uncertain significance	3	38095042	38095042	Human		name
597679831	CV3662584	single nucleotide variant	NM_007335.4(DLEC1):c.1399C>G (p.Pro467Ala)	not specified [RCV004914135]	uncertain significance	3	38085411	38085411	Human		name
597679839	CV3662585	single nucleotide variant	NM_007335.4(DLEC1):c.2635A>G (p.Asn879Asp)	not specified [RCV004914136]	uncertain significance	3	38097813	38097813	Human		name
597679854	CV3662587	single nucleotide variant	NM_007335.4(DLEC1):c.2525C>T (p.Ser842Leu)	not specified [RCV004914138]	uncertain significance	3	38097597	38097597	Human		name
597783387	CV3662589	single nucleotide variant	NM_007335.4(DLEC1):c.1400C>G (p.Pro467Arg)	not specified [RCV004900193]	uncertain significance	3	38085412	38085412	Human		name
597679914	CV3662595	single nucleotide variant	NM_007335.4(DLEC1):c.1831A>G (p.Thr611Ala)	not specified [RCV004914145]	uncertain significance	3	38093679	38093679	Human		name
597679993	CV3662605	single nucleotide variant	NM_007335.4(DLEC1):c.2312T>C (p.Ile771Thr)	not specified [RCV004914155]	uncertain significance	3	38096709	38096709	Human		name
597680025	CV3662609	single nucleotide variant	NM_007335.4(DLEC1):c.2759A>G (p.Gln920Arg)	not specified [RCV004914159]	uncertain significance	3	38100320	38100320	Human		name
597801350	CV3662614	single nucleotide variant	NM_007335.4(DLEC1):c.2290A>G (p.Ile764Val)	not specified [RCV004906158]	uncertain significance	3	38096687	38096687	Human		name
597801365	CV3662621	single nucleotide variant	NM_007335.4(DLEC1):c.1483A>T (p.Met495Leu)	not specified [RCV004906165]	uncertain significance	3	38086288	38086288	Human		name
597801369	CV3662623	single nucleotide variant	NM_007335.4(DLEC1):c.2989C>T (p.Leu997Phe)	not specified [RCV004906167]	uncertain significance	3	38107708	38107708	Human		name
598173719	CV3964098	single nucleotide variant	NM_007335.4(DLEC1):c.1487C>T (p.Thr496Ile)	not specified [RCV005331584]	uncertain significance	3	38086292	38086292	Human		name
598173725	CV3964099	single nucleotide variant	NM_007335.4(DLEC1):c.1229C>T (p.Pro410Leu)	not specified [RCV005331585]	uncertain significance	3	38084213	38084213	Human		name
598173794	CV3964110	single nucleotide variant	NM_007335.4(DLEC1):c.1681A>G (p.Lys561Glu)	not specified [RCV005331596]	uncertain significance	3	38092805	38092805	Human		name
598173821	CV3964114	single nucleotide variant	NM_007335.4(DLEC1):c.2674A>T (p.Thr892Ser)	not specified [RCV005331600]	uncertain significance	3	38097852	38097852	Human		name
598173828	CV3964115	single nucleotide variant	NM_007335.4(DLEC1):c.2838G>C (p.Glu946Asp)	not specified [RCV005331601]	uncertain significance	3	38100399	38100399	Human		name
15110100	CV708809	single nucleotide variant	NM_007335.4(DLEC1):c.1129C>G (p.Pro377Ala)	not provided [RCV000960834]	benign	3	38063875	38063875	Human		name
15168835	CV708810	single nucleotide variant	NM_007335.4(DLEC1):c.1184C>T (p.Ala395Val)	not provided [RCV000971695]	likely benign	3	38084168	38084168	Human		name
156179408	CV2201656	single nucleotide variant	NM_007335.4(DLEC1):c.3118G>A (p.Ala1040Thr)	not specified [RCV004082114]	uncertain significance	3	38108504	38108504	Human		name
156329979	CV2216532	single nucleotide variant	NM_007335.4(DLEC1):c.4196G>A (p.Gly1399Asp)	not specified [RCV004097322]	uncertain significance	3	38116991	38116991	Human		name
156137596	CV2253489	single nucleotide variant	NM_007335.4(DLEC1):c.4879C>T (p.Arg1627Trp)	not specified [RCV004125202]	uncertain significance	3	38121640	38121640	Human		name
156276487	CV2255799	single nucleotide variant	NM_007335.4(DLEC1):c.4951C>A (p.Gln1651Lys)	not specified [RCV004120172]	uncertain significance	3	38121712	38121712	Human		name
156338710	CV2271321	single nucleotide variant	NM_007335.4(DLEC1):c.4052C>G (p.Thr1351Ser)	not specified [RCV004136440]	uncertain significance	3	38116648	38116648	Human		name
155905831	CV2283193	single nucleotide variant	NM_007335.4(DLEC1):c.4598C>T (p.Ala1533Val)	not specified [RCV004145872]	uncertain significance	3	38117918	38117918	Human		name
155994560	CV2286426	single nucleotide variant	NM_007335.4(DLEC1):c.4975C>G (p.Leu1659Val)	not specified [RCV004139946]	uncertain significance	3	38121736	38121736	Human		name
156082104	CV2292883	single nucleotide variant	NM_007335.4(DLEC1):c.4115T>C (p.Val1372Ala)	not specified [RCV004148386]	uncertain significance	3	38116825	38116825	Human		name
155931435	CV2293514	single nucleotide variant	NM_007335.4(DLEC1):c.3862C>G (p.Arg1288Gly)	not specified [RCV004153049]	uncertain significance	3	38116458	38116458	Human		name
156259495	CV2304960	single nucleotide variant	NM_007335.4(DLEC1):c.4384T>C (p.Tyr1462His)	not specified [RCV004168859]	uncertain significance	3	38117286	38117286	Human		name
156051908	CV2328986	single nucleotide variant	NM_007335.4(DLEC1):c.4456G>A (p.Asp1486Asn)	not specified [RCV004180278]	uncertain significance	3	38117582	38117582	Human		name
156176271	CV2331155	single nucleotide variant	NM_007335.4(DLEC1):c.3373C>T (p.Arg1125Trp)	not specified [RCV004181763]	uncertain significance	3	38110211	38110211	Human		name
156332148	CV2339740	single nucleotide variant	NM_007335.4(DLEC1):c.3805G>A (p.Gly1269Arg)	not specified [RCV004196441]	uncertain significance	3	38115002	38115002	Human		name
156065519	CV2340840	single nucleotide variant	NM_007335.4(DLEC1):c.4147G>A (p.Gly1383Ser)	not specified [RCV004188197]	uncertain significance	3	38116857	38116857	Human		name
156219052	CV2344844	single nucleotide variant	NM_007335.4(DLEC1):c.4886T>C (p.Val1629Ala)	not specified [RCV004190985]	uncertain significance	3	38121647	38121647	Human		name
155990459	CV2352462	single nucleotide variant	NM_007335.4(DLEC1):c.3575A>G (p.Gln1192Arg)	not specified [RCV004202970]	uncertain significance	3	38112270	38112270	Human		name
155929585	CV2356910	single nucleotide variant	NM_007335.4(DLEC1):c.3406G>A (p.Gly1136Arg)	not specified [RCV004204285]	uncertain significance	3	38110244	38110244	Human		name
155989824	CV2374537	single nucleotide variant	NM_007335.4(DLEC1):c.4745A>G (p.Tyr1582Cys)	not specified [RCV004232037]	uncertain significance	3	38120488	38120488	Human		name
156062269	CV2380348	single nucleotide variant	NM_007335.4(DLEC1):c.3640G>A (p.Glu1214Lys)	not specified [RCV004217962]	uncertain significance	3	38112335	38112335	Human		name
329362590	CV2438948	single nucleotide variant	NM_007335.4(DLEC1):c.5245T>G (p.Tyr1749Asp)	not specified [RCV004264464]	uncertain significance	3	38122389	38122389	Human		name
329371280	CV2458061	single nucleotide variant	NM_007335.4(DLEC1):c.3767A>G (p.Gln1256Arg)	not specified [RCV004271893]	uncertain significance	3	38114442	38114442	Human		name
329396706	CV2458957	single nucleotide variant	NM_007335.4(DLEC1):c.3847A>T (p.Ser1283Cys)	not specified [RCV004272446]	uncertain significance	3	38115044	38115044	Human		name
401749328	CV2694619	single nucleotide variant	NM_007335.4(DLEC1):c.4033T>C (p.Ser1345Pro)	not specified [RCV004298734]	uncertain significance	3	38116629	38116629	Human		name
401747807	CV2696797	single nucleotide variant	NM_007335.4(DLEC1):c.3580A>G (p.Met1194Val)	not specified [RCV004290768]	uncertain significance	3	38112275	38112275	Human		name
401782624	CV2719909	single nucleotide variant	NM_007335.4(DLEC1):c.4250T>C (p.Leu1417Pro)	not specified [RCV004329310]	uncertain significance	3	38117045	38117045	Human		name
401884994	CV2786642	single nucleotide variant	NM_007335.4(DLEC1):c.4563G>A (p.Met1521Ile)	not specified [RCV004363778]	uncertain significance	3	38117883	38117883	Human		name
401926308	CV2827256	single nucleotide variant	NM_007335.4(DLEC1):c.3331C>T (p.Arg1111Cys)	not provided [RCV003437755]	likely benign	3	38110169	38110169	Human		name
401926309	CV2827257	single nucleotide variant	NM_007335.4(DLEC1):c.5150G>A (p.Ser1717Asn)	not provided [RCV003437756]	likely benign	3	38122294	38122294	Human		name
405706825	CV3240276	single nucleotide variant	NM_007335.4(DLEC1):c.3025G>A (p.Gly1009Arg)	not specified [RCV004376032]	uncertain significance	3	38108411	38108411	Human		name
405706835	CV3240277	single nucleotide variant	NM_007335.4(DLEC1):c.3128A>G (p.Gln1043Arg)	not specified [RCV004376033]	uncertain significance	3	38108514	38108514	Human		name
405706855	CV3240280	single nucleotide variant	NM_007335.4(DLEC1):c.3705G>A (p.Met1235Ile)	not specified [RCV004376036]	uncertain significance	3	38114380	38114380	Human		name
405706862	CV3240281	single nucleotide variant	NM_007335.4(DLEC1):c.3790G>A (p.Gly1264Ser)	not specified [RCV004376037]	uncertain significance	3	38114987	38114987	Human		name
405706868	CV3240282	single nucleotide variant	NM_007335.4(DLEC1):c.3793A>G (p.Thr1265Ala)	not specified [RCV004376038]	uncertain significance	3	38114990	38114990	Human		name
405706874	CV3240283	single nucleotide variant	NM_007335.4(DLEC1):c.3794C>G (p.Thr1265Ser)	not specified [RCV004376039]	uncertain significance	3	38114991	38114991	Human		name
405706885	CV3240284	single nucleotide variant	NM_007335.4(DLEC1):c.3809G>T (p.Gly1270Val)	not specified [RCV004376040]	uncertain significance	3	38115006	38115006	Human		name
405706892	CV3240285	single nucleotide variant	NM_007335.4(DLEC1):c.3813C>G (p.Asp1271Glu)	not specified [RCV004376041]	uncertain significance	3	38115010	38115010	Human		name
405706900	CV3240286	single nucleotide variant	NM_007335.4(DLEC1):c.3827C>T (p.Thr1276Ile)	not specified [RCV004376042]	uncertain significance	3	38115024	38115024	Human		name
405706929	CV3240289	single nucleotide variant	NM_007335.4(DLEC1):c.4121T>C (p.Leu1374Pro)	not specified [RCV004376045]	uncertain significance	3	38116831	38116831	Human		name
405706933	CV3240290	single nucleotide variant	NM_007335.4(DLEC1):c.4134G>C (p.Glu1378Asp)	not specified [RCV004376046]	uncertain significance	3	38116844	38116844	Human		name
405706939	CV3240291	single nucleotide variant	NM_007335.4(DLEC1):c.4430G>A (p.Ser1477Asn)	not specified [RCV004376047]	uncertain significance	3	38117556	38117556	Human		name
405706948	CV3240292	single nucleotide variant	NM_007335.4(DLEC1):c.4468G>A (p.Glu1490Lys)	not specified [RCV004376048]	uncertain significance	3	38117594	38117594	Human		name
405706953	CV3240293	single nucleotide variant	NM_007335.4(DLEC1):c.4771C>G (p.Leu1591Val)	not specified [RCV004376049]	uncertain significance	3	38120514	38120514	Human		name
405706958	CV3240294	single nucleotide variant	NM_007335.4(DLEC1):c.4931T>G (p.Phe1644Cys)	not specified [RCV004376050]	uncertain significance	3	38121692	38121692	Human		name
405706969	CV3240295	single nucleotide variant	NM_007335.4(DLEC1):c.4997G>C (p.Arg1666Pro)	not specified [RCV004376051]	uncertain significance	3	38121758	38121758	Human		name
405706985	CV3240297	single nucleotide variant	NM_007335.4(DLEC1):c.5196G>T (p.Glu1732Asp)	not specified [RCV004376053]	uncertain significance	3	38122340	38122340	Human		name
407474719	CV3430582	single nucleotide variant	NM_007335.4(DLEC1):c.3379C>T (p.Arg1127Cys)	not specified [RCV004616513]	uncertain significance	3	38110217	38110217	Human		name
407474732	CV3430585	single nucleotide variant	NM_007335.4(DLEC1):c.4300A>C (p.Ser1434Arg)	not specified [RCV004616516]	uncertain significance	3	38117095	38117095	Human		name
597679865	CV3662588	single nucleotide variant	NM_007335.4(DLEC1):c.5191G>A (p.Gly1731Ser)	not specified [RCV004914139]	likely benign	3	38122335	38122335	Human		name
597679874	CV3662590	single nucleotide variant	NM_007335.4(DLEC1):c.3341G>A (p.Arg1114His)	not specified [RCV004914140]	uncertain significance	3	38110179	38110179	Human		name
597679891	CV3662592	single nucleotide variant	NM_007335.4(DLEC1):c.4582G>A (p.Val1528Ile)	not specified [RCV004914142]	uncertain significance	3	38117902	38117902	Human		name
597679899	CV3662593	single nucleotide variant	NM_007335.4(DLEC1):c.3361C>T (p.Arg1121Cys)	not specified [RCV004914143]	likely benign	3	38110199	38110199	Human		name
597679907	CV3662594	single nucleotide variant	NM_007335.4(DLEC1):c.3862C>T (p.Arg1288Cys)	not specified [RCV004914144]	uncertain significance	3	38116458	38116458	Human		name
597679923	CV3662596	single nucleotide variant	NM_007335.4(DLEC1):c.3961G>A (p.Gly1321Arg)	not specified [RCV004914146]	uncertain significance	3	38116557	38116557	Human		name
597679944	CV3662599	single nucleotide variant	NM_007335.4(DLEC1):c.3332G>A (p.Arg1111His)	not specified [RCV004914149]	uncertain significance	3	38110170	38110170	Human		name
597679952	CV3662600	single nucleotide variant	NM_007335.4(DLEC1):c.5012T>C (p.Met1671Thr)	not specified [RCV004914150]	uncertain significance	3	38121773	38121773	Human		name
597679960	CV3662601	single nucleotide variant	NM_007335.4(DLEC1):c.3928T>C (p.Tyr1310His)	not specified [RCV004914151]	uncertain significance	3	38116524	38116524	Human		name
597679968	CV3662602	single nucleotide variant	NM_007335.4(DLEC1):c.3385T>C (p.Ser1129Pro)	not specified [RCV004914152]	uncertain significance	3	38110223	38110223	Human		name
597679977	CV3662603	single nucleotide variant	NM_007335.4(DLEC1):c.3092A>T (p.Glu1031Val)	not specified [RCV004914153]	uncertain significance	3	38108478	38108478	Human		name
597680017	CV3662608	single nucleotide variant	NM_007335.4(DLEC1):c.5248A>G (p.Met1750Val)	not specified [RCV004914158]	likely benign	3	38122392	38122392	Human		name
597801342	CV3662610	single nucleotide variant	NM_007335.4(DLEC1):c.4265G>T (p.Cys1422Phe)	not specified [RCV004906154]	uncertain significance	3	38117060	38117060	Human		name
597801344	CV3662611	single nucleotide variant	NM_007335.4(DLEC1):c.4289T>C (p.Met1430Thr)	not specified [RCV004906155]	uncertain significance	3	38117084	38117084	Human		name
597801346	CV3662612	single nucleotide variant	NM_007335.4(DLEC1):c.3397G>C (p.Glu1133Gln)	not specified [RCV004906156]	uncertain significance	3	38110235	38110235	Human		name
597801348	CV3662613	single nucleotide variant	NM_007335.4(DLEC1):c.4034C>T (p.Ser1345Leu)	not specified [RCV004906157]	uncertain significance	3	38116630	38116630	Human		name
597801352	CV3662615	single nucleotide variant	NM_007335.4(DLEC1):c.4973A>G (p.Tyr1658Cys)	not specified [RCV004906159]	uncertain significance	3	38121734	38121734	Human		name
597801363	CV3662620	single nucleotide variant	NM_007335.4(DLEC1):c.3328A>G (p.Thr1110Ala)	not specified [RCV004906164]	uncertain significance	3	38110166	38110166	Human		name
597801371	CV3662624	single nucleotide variant	NM_007335.4(DLEC1):c.3958G>A (p.Ala1320Thr)	not specified [RCV004906168]	uncertain significance	3	38116554	38116554	Human		name
598173708	CV3964096	single nucleotide variant	NM_007335.4(DLEC1):c.3380G>A (p.Arg1127His)	not specified [RCV005331582]	uncertain significance	3	38110218	38110218	Human		name
598173732	CV3964100	single nucleotide variant	NM_007335.4(DLEC1):c.3479G>A (p.Arg1160Gln)	not specified [RCV005331586]	uncertain significance	3	38111712	38111712	Human		name
598173744	CV3964102	single nucleotide variant	NM_007335.4(DLEC1):c.4172A>G (p.Lys1391Arg)	not specified [RCV005331588]	uncertain significance	3	38116882	38116882	Human		name
598173751	CV3964103	single nucleotide variant	NM_007335.4(DLEC1):c.4861A>C (p.Thr1621Pro)	not specified [RCV005331589]	uncertain significance	3	38120604	38120604	Human		name
598173764	CV3964105	single nucleotide variant	NM_007335.4(DLEC1):c.3503G>A (p.Arg1168Gln)	not specified [RCV005331591]	uncertain significance	3	38111736	38111736	Human		name
598173770	CV3964106	single nucleotide variant	NM_007335.4(DLEC1):c.3493C>A (p.Leu1165Met)	not specified [RCV005331592]	uncertain significance	3	38111726	38111726	Human		name
598173777	CV3964107	single nucleotide variant	NM_007335.4(DLEC1):c.3938C>T (p.Pro1313Leu)	not specified [RCV005331593]	uncertain significance	3	38116534	38116534	Human		name
598173784	CV3964108	single nucleotide variant	NM_007335.4(DLEC1):c.5234A>G (p.Tyr1745Cys)	not specified [RCV005331594]	uncertain significance	3	38122378	38122378	Human		name
598173790	CV3964109	single nucleotide variant	NM_007335.4(DLEC1):c.4558C>T (p.Leu1520Phe)	not specified [RCV005331595]	uncertain significance	3	38117878	38117878	Human		name
598173802	CV3964111	single nucleotide variant	NM_007335.4(DLEC1):c.4832A>C (p.Asn1611Thr)	not specified [RCV005331597]	uncertain significance	3	38120575	38120575	Human		name
598173834	CV3964116	single nucleotide variant	NM_007335.4(DLEC1):c.5243G>A (p.Arg1748Lys)	not specified [RCV005331602]	uncertain significance	3	38122387	38122387	Human		name
598173839	CV3964117	single nucleotide variant	NM_007335.4(DLEC1):c.4276G>A (p.Ala1426Thr)	not specified [RCV005331603]	uncertain significance	3	38117071	38117071	Human		name
598173845	CV3964118	single nucleotide variant	NM_007335.4(DLEC1):c.3737G>A (p.Arg1246Lys)	not specified [RCV005331604]	uncertain significance	3	38114412	38114412	Human		name
598173851	CV3964119	single nucleotide variant	NM_007335.4(DLEC1):c.4195G>C (p.Gly1399Arg)	not specified [RCV005331605]	uncertain significance	3	38116990	38116990	Human		name
15150704	CV708811	single nucleotide variant	NM_007335.4(DLEC1):c.3066A>T (p.Lys1022Asn)	not provided [RCV000967996]	benign	3	38108452	38108452	Human		name
15144583	CV708812	single nucleotide variant	NM_007335.4(DLEC1):c.3448A>G (p.Asn1150Asp)	not provided [RCV000966856]	benign	3	38111681	38111681	Human		name
15144598	CV708813	single nucleotide variant	NM_007335.4(DLEC1):c.3680T>C (p.Leu1227Pro)	not provided [RCV000966858]	benign	3	38114355	38114355	Human		name
8625608	CV80732	single nucleotide variant	NM_007335.2(DLEC1):c.3283C>T (p.Pro1095Ser)	Malignant melanoma [RCV000060809]	not provided	3	38110121	38110121	Human		name

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