Cdyl Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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99 records found for search term Cdyl

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
12896427	CV390509	duplication	NM_004824.4(CDYL):c.1332+31dup	not specified [RCV000455325]	benign	6	4943770	4943771	Human		name
8581944	CV116393	single nucleotide variant	NM_004824.3(CDYL):c.24+49747T>A	Lung cancer [RCV000096916]	uncertain significance	6	4826554	4826554	Human		name
156055807	CV2308823	single nucleotide variant	NM_004824.4(CDYL):c.260C>T (p.Thr87Ile)	not specified [RCV004169130]	uncertain significance	6	4891948	4891948	Human		name
405744404	CV3303661	single nucleotide variant	NM_004824.4(CDYL):c.172C>T (p.Arg58Cys)	not specified [RCV004431111]	uncertain significance	6	4891860	4891860	Human		name
405744396	CV3303662	single nucleotide variant	NM_004824.4(CDYL):c.188A>C (p.Gln63Pro)	not specified [RCV004431112]	uncertain significance	6	4891876	4891876	Human		name
597767504	CV3648823	single nucleotide variant	NM_004824.4(CDYL):c.244C>G (p.Gln82Glu)	not specified [RCV004896370]	uncertain significance	6	4891932	4891932	Human		name
156327997	CV2217392	single nucleotide variant	NM_004824.4(CDYL):c.725A>G (p.Asn242Ser)	not specified [RCV004087824]	uncertain significance	6	4935548	4935548	Human		name
155974533	CV2221126	single nucleotide variant	NM_004824.4(CDYL):c.562G>A (p.Gly188Arg)	not specified [RCV004094578]	uncertain significance	6	4892250	4892250	Human		name
156271826	CV2237285	single nucleotide variant	NM_004824.4(CDYL):c.652A>G (p.Thr218Ala)	not specified [RCV004115007]	uncertain significance	6	4892340	4892340	Human		name
156071510	CV2251421	single nucleotide variant	NM_004824.4(CDYL):c.412T>A (p.Ser138Thr)	not specified [RCV004117403]	uncertain significance	6	4892100	4892100	Human		name
156254284	CV2311525	single nucleotide variant	NM_004824.4(CDYL):c.445G>T (p.Val149Phe)	not specified [RCV004168353]	uncertain significance	6	4892133	4892133	Human		name
156054863	CV2344666	single nucleotide variant	NM_004824.4(CDYL):c.389G>A (p.Arg130Gln)	not specified [RCV004197433]	uncertain significance	6	4892077	4892077	Human		name
156171090	CV2380663	single nucleotide variant	NM_004824.4(CDYL):c.469G>A (p.Gly157Ser)	not specified [RCV004218249]	uncertain significance	6	4892157	4892157	Human		name
329373703	CV2434195	single nucleotide variant	NM_004824.4(CDYL):c.631C>T (p.Pro211Ser)	not specified [RCV004250085]	uncertain significance	6	4892319	4892319	Human		name
329378749	CV2447100	single nucleotide variant	NM_004824.4(CDYL):c.661A>G (p.Met221Val)	not specified [RCV004259973]	uncertain significance	6	4892349	4892349	Human		name
401733257	CV2685472	single nucleotide variant	NM_004824.4(CDYL):c.388C>T (p.Arg130Trp)	not specified [RCV004294496]	uncertain significance	6	4892076	4892076	Human		name
401871728	CV2760027	single nucleotide variant	NM_004824.4(CDYL):c.991G>A (p.Asp331Asn)	not specified [RCV004345439]	uncertain significance	6	4937607	4937607	Human		name
405744390	CV3303663	single nucleotide variant	NM_004824.4(CDYL):c.358A>G (p.Arg120Gly)	not specified [RCV004431113]	uncertain significance	6	4892046	4892046	Human		name
405744383	CV3303664	single nucleotide variant	NM_004824.4(CDYL):c.508G>A (p.Glu170Lys)	not specified [RCV004431114]	uncertain significance	6	4892196	4892196	Human		name
405744375	CV3303665	single nucleotide variant	NM_004824.4(CDYL):c.724A>G (p.Asn242Asp)	not specified [RCV004431115]	uncertain significance	6	4935547	4935547	Human		name
405744363	CV3303666	single nucleotide variant	NM_004824.4(CDYL):c.985G>A (p.Ala329Thr)	not specified [RCV004431116]	uncertain significance	6	4937601	4937601	Human		name
407460771	CV3418717	single nucleotide variant	NM_004824.4(CDYL):c.779A>G (p.Lys260Arg)	not specified [RCV004612418]	uncertain significance	6	4935602	4935602	Human		name
407460777	CV3418718	single nucleotide variant	NM_004824.4(CDYL):c.544G>T (p.Ala182Ser)	not specified [RCV004612419]	uncertain significance	6	4892232	4892232	Human		name
407460789	CV3418721	single nucleotide variant	NM_004824.4(CDYL):c.706A>C (p.Met236Leu)	not specified [RCV004612422]	uncertain significance	6	4935529	4935529	Human		name
407460793	CV3418722	single nucleotide variant	NM_004824.4(CDYL):c.538G>C (p.Glu180Gln)	not specified [RCV004612423]	uncertain significance	6	4892226	4892226	Human		name
407460798	CV3418723	single nucleotide variant	NM_004824.4(CDYL):c.307A>C (p.Lys103Gln)	not specified [RCV004612424]	uncertain significance	6	4891995	4891995	Human		name
597767494	CV3648821	single nucleotide variant	NM_004824.4(CDYL):c.460G>A (p.Ala154Thr)	not specified [RCV004896368]	uncertain significance	6	4892148	4892148	Human		name
597767510	CV3648824	single nucleotide variant	NM_004824.4(CDYL):c.379C>T (p.Leu127Phe)	not specified [RCV004896371]	uncertain significance	6	4892067	4892067	Human		name
597767515	CV3648825	single nucleotide variant	NM_004824.4(CDYL):c.479G>T (p.Ser160Ile)	not specified [RCV004896372]	uncertain significance	6	4892167	4892167	Human		name
597767527	CV3648827	single nucleotide variant	NM_004824.4(CDYL):c.741A>G (p.Ile247Met)	not specified [RCV004896374]	uncertain significance	6	4935564	4935564	Human		name
598240818	CV3940455	single nucleotide variant	NM_004824.4(CDYL):c.705C>A (p.Phe235Leu)	not specified [RCV005321447]	uncertain significance	6	4935528	4935528	Human		name
598193731	CV3940456	single nucleotide variant	NM_004824.4(CDYL):c.583G>A (p.Ala195Thr)	not specified [RCV005313041]	uncertain significance	6	4892271	4892271	Human		name
598193737	CV3940457	single nucleotide variant	NM_004824.4(CDYL):c.788A>G (p.Asp263Gly)	not specified [RCV005313042]	uncertain significance	6	4935611	4935611	Human		name
598193751	CV3940460	single nucleotide variant	NM_004824.4(CDYL):c.407C>T (p.Ala136Val)	not specified [RCV005313045]	uncertain significance	6	4892095	4892095	Human		name
156071825	CV2201288	single nucleotide variant	NM_004824.4(CDYL):c.1075A>G (p.Thr359Ala)	not specified [RCV004077422]	uncertain significance	6	4937691	4937691	Human		name
155919820	CV2279482	single nucleotide variant	NM_004824.4(CDYL):c.1584G>C (p.Gln528His)	not specified [RCV004142006]	uncertain significance	6	4954005	4954005	Human		name
156204395	CV2331663	single nucleotide variant	NM_004824.4(CDYL):c.1624G>A (p.Asp542Asn)	not specified [RCV004184293]	uncertain significance	6	4954045	4954045	Human		name
155970213	CV2335557	single nucleotide variant	NM_004824.4(CDYL):c.1021G>A (p.Val341Ile)	not specified [RCV004193769]	uncertain significance	6	4937637	4937637	Human		name
329377846	CV2436054	single nucleotide variant	NM_004824.4(CDYL):c.1474G>C (p.Val492Leu)	not specified [RCV004255272]	uncertain significance	6	4952407	4952407	Human		name
329353316	CV2469140	single nucleotide variant	NM_004824.4(CDYL):c.1351A>G (p.Ser451Gly)	not specified [RCV004274367]	uncertain significance	6	4952284	4952284	Human		name
329388874	CV2469518	single nucleotide variant	NM_004824.4(CDYL):c.1441G>A (p.Val481Ile)	not specified [RCV004282965]	uncertain significance	6	4952374	4952374	Human		name
405744420	CV3303659	single nucleotide variant	NM_004824.4(CDYL):c.1577C>T (p.Ser526Leu)	not specified [RCV004431109]	uncertain significance	6	4953998	4953998	Human		name
405744410	CV3303660	single nucleotide variant	NM_004824.4(CDYL):c.1595C>T (p.Ser532Phe)	not specified [RCV004431110]	uncertain significance	6	4954016	4954016	Human		name
597767489	CV3648819	single nucleotide variant	NM_004824.4(CDYL):c.1463C>T (p.Ser488Leu)	not specified [RCV004896367]	uncertain significance	6	4952396	4952396	Human		name
597767499	CV3648822	single nucleotide variant	NM_004824.4(CDYL):c.1505G>A (p.Arg502His)	not specified [RCV004896369]	uncertain significance	6	4953926	4953926	Human		name
597767522	CV3648826	single nucleotide variant	NM_004824.4(CDYL):c.1069C>T (p.Arg357Cys)	not specified [RCV004896373]	uncertain significance	6	4937685	4937685	Human		name
598193746	CV3940459	single nucleotide variant	NM_004824.4(CDYL):c.1540G>A (p.Glu514Lys)	not specified [RCV005313044]	uncertain significance	6	4953961	4953961	Human		name
598193756	CV3940461	single nucleotide variant	NM_004824.4(CDYL):c.1100C>T (p.Thr367Ile)	not specified [RCV005313046]	uncertain significance	6	4937716	4937716	Human		name
15141991	CV715096	single nucleotide variant	NM_152342.4(CDYL2):c.783G>A (p.Thr261=)	not provided [RCV000966401]	benign	16	80633070	80633070	Human		name
155996123	CV2375899	single nucleotide variant	NM_152342.4(CDYL2):c.122C>T (p.Pro41Leu)	not specified [RCV004217741]	uncertain significance	16	80685032	80685032	Human		name
329378363	CV2463653	single nucleotide variant	NM_152342.4(CDYL2):c.217A>G (p.Ser73Gly)	not specified [RCV004277447]	likely benign	16	80684937	80684937	Human		name
405744128	CV3303669	single nucleotide variant	NM_152342.4(CDYL2):c.251C>T (p.Pro84Leu)	not specified [RCV004431119]	uncertain significance	16	80684903	80684903	Human		name
405743952	CV3303670	single nucleotide variant	NM_152342.4(CDYL2):c.287C>T (p.Pro96Leu)	not specified [RCV004431120]	uncertain significance	16	80684867	80684867	Human		name
407460802	CV3418724	single nucleotide variant	NM_152342.4(CDYL2):c.184A>G (p.Lys62Glu)	not specified [RCV004612425]	uncertain significance	16	80684970	80684970	Human		name
597767573	CV3648837	single nucleotide variant	NM_152342.4(CDYL2):c.167A>G (p.Asn56Ser)	not specified [RCV004896383]	uncertain significance	16	80684987	80684987	Human		name
598193813	CV3940471	single nucleotide variant	NM_152342.4(CDYL2):c.245G>A (p.Arg82Gln)	not specified [RCV005313056]	uncertain significance	16	80684909	80684909	Human		name
15119513	CV715095	single nucleotide variant	NM_152342.4(CDYL2):c.1065G>T (p.Gly355=)	not provided [RCV000962563]	benign	16	80612779	80612779	Human		name
156142384	CV2208524	single nucleotide variant	NM_152342.4(CDYL2):c.598C>G (p.Leu200Val)	not specified [RCV004091055]	uncertain significance	16	80684556	80684556	Human		name
156301541	CV2245095	single nucleotide variant	NM_152342.4(CDYL2):c.931C>G (p.Leu311Val)	not specified [RCV004104808]	uncertain significance	16	80620839	80620839	Human		name
156362520	CV2265550	single nucleotide variant	NM_152342.4(CDYL2):c.806C>T (p.Thr269Ile)	not specified [RCV004124293]	uncertain significance	16	80633047	80633047	Human		name
156004436	CV2295937	single nucleotide variant	NM_152342.4(CDYL2):c.359A>G (p.Tyr120Cys)	not specified [RCV004151836]	uncertain significance	16	80684795	80684795	Human		name
156058867	CV2316927	single nucleotide variant	NM_152342.4(CDYL2):c.341C>G (p.Ala114Gly)	not specified [RCV004174438]	uncertain significance	16	80684813	80684813	Human		name
155982234	CV2337139	single nucleotide variant	NM_152342.4(CDYL2):c.680A>G (p.Glu227Gly)	not specified [RCV004192899]	uncertain significance	16	80633173	80633173	Human		name
155994421	CV2377511	single nucleotide variant	NM_152342.4(CDYL2):c.988C>T (p.Arg330Trp)	not specified [RCV004225672]	uncertain significance	16	80620782	80620782	Human		name
401757359	CV2675258	single nucleotide variant	NM_152342.4(CDYL2):c.488C>T (p.Ser163Phe)	not specified [RCV004290025]	uncertain significance	16	80684666	80684666	Human		name
401769648	CV2689871	single nucleotide variant	NM_152342.4(CDYL2):c.549T>A (p.Asp183Glu)	not specified [RCV004297768]	uncertain significance	16	80684605	80684605	Human		name
401757179	CV2692846	single nucleotide variant	NM_152342.4(CDYL2):c.850C>T (p.Arg284Trp)	not specified [RCV004306385]	uncertain significance	16	80620920	80620920	Human		name
401724657	CV2714915	single nucleotide variant	NM_152342.4(CDYL2):c.620C>A (p.Ser207Tyr)	not specified [RCV004322247]	uncertain significance	16	80633233	80633233	Human		name
401867162	CV2776674	single nucleotide variant	NM_152342.4(CDYL2):c.701A>G (p.Lys234Arg)	not specified [RCV004357839]	uncertain significance	16	80633152	80633152	Human		name
401879574	CV2785303	single nucleotide variant	NM_152342.4(CDYL2):c.659T>C (p.Val220Ala)	not specified [RCV004357061]	uncertain significance	16	80633194	80633194	Human		name
405743797	CV3303671	single nucleotide variant	NM_152342.4(CDYL2):c.353A>G (p.Lys118Arg)	not specified [RCV004431121]	uncertain significance	16	80684801	80684801	Human		name
405743694	CV3303672	single nucleotide variant	NM_152342.4(CDYL2):c.399G>C (p.Lys133Asn)	not specified [RCV004431122]	uncertain significance	16	80684755	80684755	Human		name
405743700	CV3303673	single nucleotide variant	NM_152342.4(CDYL2):c.804G>T (p.Gln268His)	not specified [RCV004431123]	uncertain significance	16	80633049	80633049	Human		name
405743705	CV3303674	single nucleotide variant	NM_152342.4(CDYL2):c.857C>T (p.Ala286Val)	not specified [RCV004431124]	uncertain significance	16	80620913	80620913	Human		name
405743721	CV3303676	single nucleotide variant	NM_152342.4(CDYL2):c.952G>A (p.Gly318Ser)	not specified [RCV004431126]	uncertain significance	16	80620818	80620818	Human		name
597767537	CV3648830	single nucleotide variant	NM_152342.4(CDYL2):c.301G>T (p.Gly101Trp)	not specified [RCV004896376]	uncertain significance	16	80684853	80684853	Human		name
597767552	CV3648833	single nucleotide variant	NM_152342.4(CDYL2):c.511G>A (p.Gly171Arg)	not specified [RCV004896379]	uncertain significance	16	80684643	80684643	Human		name
597767558	CV3648834	single nucleotide variant	NM_152342.4(CDYL2):c.989G>A (p.Arg330Gln)	not specified [RCV004896380]	uncertain significance	16	80620781	80620781	Human		name
597767563	CV3648835	single nucleotide variant	NM_152342.4(CDYL2):c.784C>T (p.His262Tyr)	not specified [RCV004896381]	uncertain significance	16	80633069	80633069	Human		name
597767584	CV3648839	single nucleotide variant	NM_152342.4(CDYL2):c.715A>C (p.Ser239Arg)	not specified [RCV004896385]	uncertain significance	16	80633138	80633138	Human		name
598193763	CV3940462	single nucleotide variant	NM_152342.4(CDYL2):c.484G>A (p.Gly162Ser)	not specified [RCV005313047]	uncertain significance	16	80684670	80684670	Human		name
598193774	CV3940464	single nucleotide variant	NM_152342.4(CDYL2):c.424A>C (p.Ser142Arg)	not specified [RCV005313049]	uncertain significance	16	80684730	80684730	Human		name
598193786	CV3940466	single nucleotide variant	NM_152342.4(CDYL2):c.498T>A (p.Asp166Glu)	not specified [RCV005313051]	uncertain significance	16	80684656	80684656	Human		name
598193792	CV3940467	single nucleotide variant	NM_152342.4(CDYL2):c.866A>G (p.Asn289Ser)	not specified [RCV005313052]	uncertain significance	16	80620904	80620904	Human		name
155939180	CV2225372	single nucleotide variant	NM_152342.4(CDYL2):c.1210G>T (p.Val404Phe)	not specified [RCV004100789]	uncertain significance	16	80612634	80612634	Human		name
156053297	CV2320372	single nucleotide variant	NM_152342.4(CDYL2):c.1243C>T (p.Arg415Trp)	not specified [RCV004178533]	uncertain significance	16	80608211	80608211	Human		name
156291865	CV2339949	single nucleotide variant	NM_152342.4(CDYL2):c.1391G>A (p.Arg464Gln)	not specified [RCV004192212]	uncertain significance	16	80604518	80604518	Human		name
405744357	CV3303667	single nucleotide variant	NM_152342.4(CDYL2):c.1051G>C (p.Val351Leu)	not specified [RCV004431117]	uncertain significance	16	80612793	80612793	Human		name
405744350	CV3303668	single nucleotide variant	NM_152342.4(CDYL2):c.1372G>A (p.Glu458Lys)	not specified [RCV004431118]	uncertain significance	16	80604537	80604537	Human		name
407460805	CV3418725	single nucleotide variant	NM_152342.4(CDYL2):c.1160G>A (p.Arg387His)	not specified [RCV004612426]	uncertain significance	16	80612684	80612684	Human		name
597767532	CV3648828	single nucleotide variant	NM_152342.4(CDYL2):c.1210G>A (p.Val404Ile)	not specified [RCV004896375]	uncertain significance	16	80612634	80612634	Human		name
597767543	CV3648831	single nucleotide variant	NM_152342.4(CDYL2):c.1159C>T (p.Arg387Cys)	not specified [RCV004896377]	uncertain significance	16	80612685	80612685	Human		name
597767547	CV3648832	single nucleotide variant	NM_152342.4(CDYL2):c.1198C>A (p.Gln400Lys)	not specified [RCV004896378]	uncertain significance	16	80612646	80612646	Human		name
597767567	CV3648836	single nucleotide variant	NM_152342.4(CDYL2):c.1452G>C (p.Gln484His)	not specified [RCV004896382]	uncertain significance	16	80604457	80604457	Human		name
597767580	CV3648838	single nucleotide variant	NM_152342.4(CDYL2):c.1024T>C (p.Phe342Leu)	not specified [RCV004896384]	uncertain significance	16	80612820	80612820	Human		name
598193768	CV3940463	single nucleotide variant	NM_152342.4(CDYL2):c.1022C>G (p.Ala341Gly)	not specified [RCV005313048]	uncertain significance	16	80612822	80612822	Human		name
598193779	CV3940465	single nucleotide variant	NM_152342.4(CDYL2):c.1108A>G (p.Ile370Val)	not specified [RCV005313050]	uncertain significance	16	80612736	80612736	Human		name
598193797	CV3940468	single nucleotide variant	NM_152342.4(CDYL2):c.1259A>G (p.Gln420Arg)	not specified [RCV005313053]	uncertain significance	16	80608195	80608195	Human		name
598193808	CV3940470	single nucleotide variant	NM_152342.4(CDYL2):c.1408G>T (p.Val470Leu)	not specified [RCV005313055]	uncertain significance	16	80604501	80604501	Human		name

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