Cdkl3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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52 records found for search term Cdkl3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401736741	CV2679137	single nucleotide variant	NM_001113575.2(CDKL3):c.23G>A (p.Gly8Glu)	not specified [RCV004283870]	uncertain significance	5	134366501	134366501	Human		name
155930217	CV2361088	single nucleotide variant	NM_001113575.2(CDKL3):c.94A>G (p.Ile32Val)	not specified [RCV004216283]	uncertain significance	5	134366430	134366430	Human		name
15178351	CV709627	single nucleotide variant	NM_001113575.2(CDKL3):c.891A>G (p.Pro297=)	not provided [RCV000973646]	benign	5	134308718	134308718	Human		name
329401215	CV2442170	single nucleotide variant	NM_001113575.2(CDKL3):c.177C>A (p.His59Gln)	not specified [RCV004264672]	uncertain significance	5	134360080	134360080	Human		name
405742643	CV3293049	single nucleotide variant	NM_001113575.2(CDKL3):c.226C>A (p.His76Asn)	not specified [RCV004430970]	uncertain significance	5	134360031	134360031	Human		name
597766818	CV3649537	single nucleotide variant	NM_001113575.2(CDKL3):c.293A>C (p.Glu98Ala)	not specified [RCV004896235]	uncertain significance	5	134359964	134359964	Human		name
597766823	CV3649538	single nucleotide variant	NM_001113575.2(CDKL3):c.136A>T (p.Ile46Phe)	not specified [RCV004896236]	uncertain significance	5	134366388	134366388	Human		name
15156914	CV709626	single nucleotide variant	NM_001113575.2(CDKL3):c.1428T>C (p.Asn476=)	not provided [RCV000969206]	benign	5	134306639	134306639	Human		name
155979262	CV2215166	single nucleotide variant	NM_001113575.2(CDKL3):c.785T>C (p.Ile262Thr)	not specified [RCV004086884]	uncertain significance	5	134319365	134319365	Human		name
155913744	CV2245948	single nucleotide variant	NM_001113575.2(CDKL3):c.355A>G (p.Asn119Asp)	not specified [RCV004113572]	uncertain significance	5	134359902	134359902	Human		name
156220331	CV2345018	single nucleotide variant	NM_001113575.2(CDKL3):c.599A>G (p.Tyr200Cys)	not specified [RCV004193304]	uncertain significance	5	134321844	134321844	Human		name
156183892	CV2349871	single nucleotide variant	NM_001113575.2(CDKL3):c.406T>A (p.Ser136Thr)	not specified [RCV004206293]	uncertain significance	5	134350382	134350382	Human		name
156191247	CV2385185	single nucleotide variant	NM_001113575.2(CDKL3):c.808G>A (p.Asp270Asn)	not specified [RCV004228436]	uncertain significance	5	134312365	134312365	Human		name
329373250	CV2439373	single nucleotide variant	NM_001113575.2(CDKL3):c.803A>C (p.Gln268Pro)	not specified [RCV004249670]	uncertain significance	5	134312370	134312370	Human		name
401737750	CV2679967	single nucleotide variant	NM_001113575.2(CDKL3):c.479A>G (p.Tyr160Cys)	not specified [RCV004284243]	uncertain significance	5	134350309	134350309	Human		name
401757863	CV2708003	single nucleotide variant	NM_001113575.2(CDKL3):c.827C>T (p.Ser276Leu)	not specified [RCV004309254]	uncertain significance	5	134312346	134312346	Human		name
401885456	CV2768177	single nucleotide variant	NM_001113575.2(CDKL3):c.418A>G (p.Lys140Glu)	not specified [RCV004350184]	uncertain significance	5	134350370	134350370	Human		name
405742651	CV3293050	single nucleotide variant	NM_001113575.2(CDKL3):c.443G>A (p.Arg148Gln)	not specified [RCV004430971]	uncertain significance	5	134350345	134350345	Human		name
405742659	CV3293051	single nucleotide variant	NM_001113575.2(CDKL3):c.491G>A (p.Arg164His)	not specified [RCV004430972]	uncertain significance	5	134350297	134350297	Human		name
407460390	CV3422539	single nucleotide variant	NM_001113575.2(CDKL3):c.769G>A (p.Gly257Arg)	not specified [RCV004612306]	uncertain significance	5	134319381	134319381	Human		name
407460405	CV3422543	single nucleotide variant	NM_001113575.2(CDKL3):c.332G>C (p.Arg111Pro)	not specified [RCV004612310]	uncertain significance	5	134359925	134359925	Human		name
407460410	CV3422544	single nucleotide variant	NM_001113575.2(CDKL3):c.949G>C (p.Glu317Gln)	not specified [RCV004612311]	uncertain significance	5	134308660	134308660	Human		name
597766803	CV3649534	single nucleotide variant	NM_001113575.2(CDKL3):c.337A>G (p.Ile113Val)	not specified [RCV004896232]	uncertain significance	5	134359920	134359920	Human		name
597766809	CV3649535	single nucleotide variant	NM_001113575.2(CDKL3):c.473C>T (p.Thr158Met)	not specified [RCV004896233]	uncertain significance	5	134350315	134350315	Human		name
597766813	CV3649536	single nucleotide variant	NM_001113575.2(CDKL3):c.697A>G (p.Ile233Val)	not specified [RCV004896234]	uncertain significance	5	134319453	134319453	Human		name
597766828	CV3649539	single nucleotide variant	NM_001113575.2(CDKL3):c.845A>G (p.His282Arg)	not specified [RCV004896237]	uncertain significance	5	134312328	134312328	Human		name
598240624	CV3940303	single nucleotide variant	NM_001113575.2(CDKL3):c.387G>T (p.Glu129Asp)	not specified [RCV005321411]	uncertain significance	5	134350401	134350401	Human		name
598193180	CV3940307	single nucleotide variant	NM_001113575.2(CDKL3):c.569T>A (p.Met190Lys)	not specified [RCV005312927]	uncertain significance	5	134321874	134321874	Human		name
598193185	CV3940308	single nucleotide variant	NM_001113575.2(CDKL3):c.469T>A (p.Tyr157Asn)	not specified [RCV005312928]	uncertain significance	5	134350319	134350319	Human		name
598193200	CV3940311	single nucleotide variant	NM_001113575.2(CDKL3):c.387G>C (p.Glu129Asp)	not specified [RCV005312931]	uncertain significance	5	134350401	134350401	Human		name
156242895	CV2246296	single nucleotide variant	NM_001113575.2(CDKL3):c.1060A>G (p.Lys354Glu)	not specified [RCV004107742]	uncertain significance	5	134308442	134308442	Human		name
155919535	CV2333214	single nucleotide variant	NM_001113575.2(CDKL3):c.1686A>T (p.Leu562Phe)	not specified [RCV004194500]	uncertain significance	5	134302623	134302623	Human		name
156109337	CV2355474	single nucleotide variant	NM_001113575.2(CDKL3):c.1390C>T (p.Arg464Cys)	not specified [RCV004205324]	uncertain significance	5	134306677	134306677	Human		name
156248179	CV2396986	single nucleotide variant	NM_001113575.2(CDKL3):c.1169A>G (p.Asn390Ser)	not specified [RCV004234094]	uncertain significance	5	134308333	134308333	Human		name
329393685	CV2449793	single nucleotide variant	NM_001113575.2(CDKL3):c.1030G>A (p.Gly344Arg)	not specified [RCV004268899]	uncertain significance	5	134308579	134308579	Human		name
329402608	CV2451161	single nucleotide variant	NM_001113575.2(CDKL3):c.1040T>C (p.Ile347Thr)	not specified [RCV004270089]	uncertain significance	5	134308462	134308462	Human		name
401768235	CV2675180	single nucleotide variant	NM_001113575.2(CDKL3):c.1125G>T (p.Lys375Asn)	not specified [RCV004289953]	uncertain significance	5	134308377	134308377	Human		name
401746232	CV2694817	single nucleotide variant	NM_001113575.2(CDKL3):c.1687C>G (p.Leu563Val)	not specified [RCV004300894]	uncertain significance	5	134302622	134302622	Human		name
401720068	CV2705637	single nucleotide variant	NM_001113575.2(CDKL3):c.1102G>C (p.Gly368Arg)	not specified [RCV004318495]	uncertain significance	5	134308400	134308400	Human		name
405742619	CV3293046	single nucleotide variant	NM_001113575.2(CDKL3):c.1180A>G (p.Met394Val)	not specified [RCV004430967]	uncertain significance	5	134308322	134308322	Human		name
405742626	CV3293047	single nucleotide variant	NM_001113575.2(CDKL3):c.1389A>T (p.Arg463Ser)	not specified [RCV004430968]	uncertain significance	5	134306678	134306678	Human		name
405742635	CV3293048	single nucleotide variant	NM_001113575.2(CDKL3):c.1415A>G (p.Gln472Arg)	not specified [RCV004430969]	uncertain significance	5	134306652	134306652	Human		name
407460379	CV3422536	single nucleotide variant	NM_001113575.2(CDKL3):c.1576G>A (p.Glu526Lys)	not specified [RCV004612303]	uncertain significance	5	134304450	134304450	Human		name
407460382	CV3422537	single nucleotide variant	NM_001113575.2(CDKL3):c.1183T>A (p.Ser395Thr)	not specified [RCV004612304]	uncertain significance	5	134308319	134308319	Human		name
407460386	CV3422538	single nucleotide variant	NM_001113575.2(CDKL3):c.1486G>A (p.Glu496Lys)	not specified [RCV004612305]	uncertain significance	5	134304540	134304540	Human		name
407460393	CV3422540	single nucleotide variant	NM_001113575.2(CDKL3):c.1501A>G (p.Ser501Gly)	not specified [RCV004612307]	uncertain significance	5	134304525	134304525	Human		name
407460415	CV3422545	single nucleotide variant	NM_001113575.2(CDKL3):c.1276G>A (p.Gly426Ser)	not specified [RCV004612312]	uncertain significance	5	134308226	134308226	Human		name
597766834	CV3649540	single nucleotide variant	NM_001113575.2(CDKL3):c.1311C>G (p.Asn437Lys)	not specified [RCV004896238]	uncertain significance	5	134308191	134308191	Human		name
598193166	CV3940305	single nucleotide variant	NM_001113575.2(CDKL3):c.1693G>A (p.Val565Met)	not specified [RCV005312925]	uncertain significance	5	134302616	134302616	Human		name
598193173	CV3940306	single nucleotide variant	NM_001113575.2(CDKL3):c.1229A>G (p.Asn410Ser)	not specified [RCV005312926]	uncertain significance	5	134308273	134308273	Human		name
598193190	CV3940309	single nucleotide variant	NM_001113575.2(CDKL3):c.1028T>G (p.Leu343Trp)	not specified [RCV005312929]	uncertain significance	5	134308581	134308581	Human		name
598193195	CV3940310	single nucleotide variant	NM_001113575.2(CDKL3):c.1058C>T (p.Pro353Leu)	not specified [RCV005312930]	uncertain significance	5	134308444	134308444	Human		name

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