Cep68 Variant Search Result - Rat Genome Database

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117 records found for search term Cep68

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15103706	CV777332	single nucleotide variant	NM_015147.3(CEP68):c.2007+9C>G	not provided [RCV000959534]	benign	2	65074413	65074413	Human		name
401912068	CV2811974	single nucleotide variant	NM_015147.3(CEP68):c.1884+21G>A	not provided [RCV003427000]	likely benign	2	65073001	65073001	Human		name
405777547	CV3296976	single nucleotide variant	NM_015147.3(CEP68):c.10G>T (p.Gly4Cys)	not specified [RCV004436369]	uncertain significance	2	65069454	65069454	Human		name
401749582	CV2710815	single nucleotide variant	NM_015147.3(CEP68):c.38C>G (p.Ser13Cys)	not specified [RCV004308738]	uncertain significance	2	65069482	65069482	Human		name
405722860	CV3297000	single nucleotide variant	NM_015147.3(CEP68):c.56A>T (p.Gln19Leu)	not specified [RCV004428377]	uncertain significance	2	65069500	65069500	Human		name
405722874	CV3297002	single nucleotide variant	NM_015147.3(CEP68):c.59C>T (p.Ser20Phe)	not specified [RCV004428379]	uncertain significance	2	65069503	65069503	Human		name
597789287	CV3653014	single nucleotide variant	NM_015147.3(CEP68):c.86G>A (p.Arg29Gln)	not specified [RCV004901727]	likely benign	2	65069530	65069530	Human		name
598241984	CV3947977	single nucleotide variant	NM_015147.3(CEP68):c.29C>T (p.Ala10Val)	not specified [RCV005321646]	likely benign	2	65069473	65069473	Human		name
598209898	CV3947981	single nucleotide variant	NM_015147.3(CEP68):c.64G>A (p.Gly22Arg)	not specified [RCV005315776]	uncertain significance	2	65069508	65069508	Human		name
15143719	CV781423	single nucleotide variant	NM_015147.3(CEP68):c.693C>T (p.Val231=)	not provided [RCV000983375]	likely benign	2	65071789	65071789	Human		name
155995148	CV2250316	single nucleotide variant	NM_015147.3(CEP68):c.265G>A (p.Glu89Lys)	not specified [RCV004127212]	uncertain significance	2	65069709	65069709	Human		name
155924411	CV2358145	single nucleotide variant	NM_015147.3(CEP68):c.157T>G (p.Ser53Ala)	not specified [RCV004211950]	uncertain significance	2	65069601	65069601	Human		name
156000056	CV2373489	single nucleotide variant	NM_015147.3(CEP68):c.131G>T (p.Arg44Leu)	not specified [RCV004220178]	uncertain significance	2	65069575	65069575	Human		name
156228142	CV2392886	single nucleotide variant	NM_015147.3(CEP68):c.224C>T (p.Pro75Leu)	not specified [RCV004247237]	likely benign	2	65069668	65069668	Human		name
329352628	CV2470242	single nucleotide variant	NM_015147.3(CEP68):c.265G>C (p.Glu89Gln)	not specified [RCV004279652]	uncertain significance	2	65069709	65069709	Human		name
401912067	CV2811973	single nucleotide variant	NM_015147.3(CEP68):c.1230T>C (p.Arg410=)	not provided [RCV003426999]	likely benign	2	65072326	65072326	Human		name
405722707	CV3296979	single nucleotide variant	NM_015147.3(CEP68):c.122A>G (p.Gln41Arg)	not specified [RCV004428356]	uncertain significance	2	65069566	65069566	Human		name
405722741	CV3296984	single nucleotide variant	NM_015147.3(CEP68):c.130C>T (p.Arg44Cys)	not specified [RCV004428361]	uncertain significance	2	65069574	65069574	Human		name
405722770	CV3296988	single nucleotide variant	NM_015147.3(CEP68):c.154A>G (p.Ile52Val)	not specified [RCV004428365]	uncertain significance	2	65069598	65069598	Human		name
407469332	CV3429002	single nucleotide variant	NM_015147.3(CEP68):c.149G>A (p.Gly50Glu)	not specified [RCV004615000]	uncertain significance	2	65069593	65069593	Human		name
597789249	CV3653003	single nucleotide variant	NM_015147.3(CEP68):c.205G>A (p.Gly69Arg)	not specified [RCV004901717]	uncertain significance	2	65069649	65069649	Human		name
15144203	CV708332	single nucleotide variant	NM_015147.3(CEP68):c.1341G>A (p.Ser447=)	not provided [RCV000966799]	benign	2	65072437	65072437	Human		name
15154897	CV719938	single nucleotide variant	NM_015147.3(CEP68):c.1698C>T (p.His566=)	not provided [RCV000880308]	benign\|likely benign	2	65072794	65072794	Human		name
15110179	CV719939	single nucleotide variant	NM_015147.3(CEP68):c.1758G>A (p.Leu586=)	not provided [RCV000894009]	benign	2	65072854	65072854	Human		name
15119516	CV747741	single nucleotide variant	NM_015147.3(CEP68):c.1734G>A (p.Gln578=)	not provided [RCV000918156]	benign	2	65072830	65072830	Human		name
155963737	CV2198007	single nucleotide variant	NM_015147.3(CEP68):c.974C>T (p.Ala325Val)	not specified [RCV004077214]	uncertain significance	2	65072070	65072070	Human		name
156272634	CV2247475	single nucleotide variant	NM_015147.3(CEP68):c.922C>G (p.Pro308Ala)	not specified [RCV004108799]	uncertain significance	2	65072018	65072018	Human		name
156369986	CV2263453	single nucleotide variant	NM_015147.3(CEP68):c.962G>A (p.Ser321Asn)	not specified [RCV004133699]	uncertain significance	2	65072058	65072058	Human		name
155997292	CV2288606	single nucleotide variant	NM_015147.3(CEP68):c.865C>G (p.His289Asp)	not specified [RCV004152123]	uncertain significance	2	65071961	65071961	Human		name
155970294	CV2309172	single nucleotide variant	NM_015147.3(CEP68):c.964C>T (p.Arg322Cys)	not specified [RCV004171523]	uncertain significance	2	65072060	65072060	Human		name
156249404	CV2314151	single nucleotide variant	NM_015147.3(CEP68):c.887A>G (p.Asn296Ser)	not specified [RCV004166236]	uncertain significance	2	65071983	65071983	Human		name
156306501	CV2314972	single nucleotide variant	NM_015147.3(CEP68):c.845T>C (p.Leu282Pro)	not specified [RCV004164898]	uncertain significance	2	65071941	65071941	Human		name
156396635	CV2323266	single nucleotide variant	NM_015147.3(CEP68):c.958G>A (p.Asp320Asn)	not specified [RCV004187651]	uncertain significance	2	65072054	65072054	Human		name
155902053	CV2345920	single nucleotide variant	NM_015147.3(CEP68):c.385G>A (p.Glu129Lys)	not specified [RCV004198958]	uncertain significance	2	65071481	65071481	Human		name
156386978	CV2364906	single nucleotide variant	NM_015147.3(CEP68):c.346G>A (p.Gly116Arg)	not specified [RCV004221806]	uncertain significance	2	65069790	65069790	Human		name
156073378	CV2376898	single nucleotide variant	NM_015147.3(CEP68):c.596C>T (p.Ser199Phe)	not specified [RCV004229593]	uncertain significance	2	65071692	65071692	Human		name
156157586	CV2378774	single nucleotide variant	NM_015147.3(CEP68):c.641C>T (p.Ala214Val)	not specified [RCV004231225]	uncertain significance	2	65071737	65071737	Human		name
329357204	CV2431277	single nucleotide variant	NM_015147.3(CEP68):c.956T>C (p.Leu319Pro)	not specified [RCV004250610]	uncertain significance	2	65072052	65072052	Human		name
329400965	CV2445964	single nucleotide variant	NM_015147.3(CEP68):c.344C>A (p.Ser115Tyr)	not specified [RCV004270555]	uncertain significance	2	65069788	65069788	Human		name
401744513	CV2697016	single nucleotide variant	NM_015147.3(CEP68):c.790A>G (p.Arg264Gly)	not specified [RCV004293006]	uncertain significance	2	65071886	65071886	Human		name
405722829	CV3296996	single nucleotide variant	NM_015147.3(CEP68):c.299G>C (p.Ser100Thr)	not specified [RCV004428373]	uncertain significance	2	65069743	65069743	Human		name
405722835	CV3296997	single nucleotide variant	NM_015147.3(CEP68):c.302G>T (p.Gly101Val)	not specified [RCV004428374]	uncertain significance	2	65069746	65069746	Human		name
405722846	CV3296998	single nucleotide variant	NM_015147.3(CEP68):c.365A>C (p.Lys122Thr)	not specified [RCV004428375]	uncertain significance	2	65071461	65071461	Human		name
405722853	CV3296999	single nucleotide variant	NM_015147.3(CEP68):c.518C>T (p.Ser173Leu)	not specified [RCV004428376]	uncertain significance	2	65071614	65071614	Human		name
405722867	CV3297001	single nucleotide variant	NM_015147.3(CEP68):c.590G>A (p.Ser197Asn)	not specified [RCV004428378]	uncertain significance	2	65071686	65071686	Human		name
405722886	CV3297003	single nucleotide variant	NM_015147.3(CEP68):c.602C>G (p.Ser201Cys)	not specified [RCV004428380]	uncertain significance	2	65071698	65071698	Human		name
405722900	CV3297005	single nucleotide variant	NM_015147.3(CEP68):c.954C>A (p.His318Gln)	not specified [RCV004428382]	likely benign	2	65072050	65072050	Human		name
407469313	CV3428996	single nucleotide variant	NM_015147.3(CEP68):c.935G>C (p.Gly312Ala)	not specified [RCV004614994]	uncertain significance	2	65072031	65072031	Human		name
597789245	CV3653002	single nucleotide variant	NM_015147.3(CEP68):c.796C>T (p.Arg266Cys)	not specified [RCV004901716]	uncertain significance	2	65071892	65071892	Human		name
597789264	CV3653007	single nucleotide variant	NM_015147.3(CEP68):c.770G>C (p.Gly257Ala)	not specified [RCV004901721]	uncertain significance	2	65071866	65071866	Human		name
597789267	CV3653008	single nucleotide variant	NM_015147.3(CEP68):c.965G>A (p.Arg322His)	not specified [RCV004901722]	likely benign	2	65072061	65072061	Human		name
597789271	CV3653009	single nucleotide variant	NM_015147.3(CEP68):c.451A>T (p.Thr151Ser)	not specified [RCV004901723]	uncertain significance	2	65071547	65071547	Human		name
597789294	CV3653016	single nucleotide variant	NM_015147.3(CEP68):c.452C>T (p.Thr151Ile)	not specified [RCV004901729]	uncertain significance	2	65071548	65071548	Human		name
598209865	CV3947975	single nucleotide variant	NM_015147.3(CEP68):c.797G>A (p.Arg266His)	not specified [RCV005315771]	uncertain significance	2	65071893	65071893	Human		name
598209878	CV3947978	single nucleotide variant	NM_015147.3(CEP68):c.689C>T (p.Pro230Leu)	not specified [RCV005315773]	likely benign	2	65071785	65071785	Human		name
15121736	CV708330	single nucleotide variant	NM_015147.3(CEP68):c.650G>A (p.Arg217His)	not provided [RCV000962948]	benign	2	65071746	65071746	Human		name
8625395	CV80518	single nucleotide variant	NM_015147.2(CEP68):c.647C>T (p.Pro216Leu)	Malignant melanoma [RCV000060595]	not provided	2	65071743	65071743	Human		name
155973898	CV2224796	single nucleotide variant	NM_015147.3(CEP68):c.2097C>G (p.Asn699Lys)	not specified [RCV004092611]	uncertain significance	2	65077957	65077957	Human		name
156032913	CV2236129	single nucleotide variant	NM_015147.3(CEP68):c.1660C>A (p.Gln554Lys)	not specified [RCV004114275]	uncertain significance	2	65072756	65072756	Human		name
155979454	CV2247254	single nucleotide variant	NM_015147.3(CEP68):c.1459G>C (p.Ala487Pro)	not specified [RCV004114763]	uncertain significance	2	65072555	65072555	Human		name
156136897	CV2253361	single nucleotide variant	NM_015147.3(CEP68):c.1421A>G (p.Glu474Gly)	not specified [RCV004123188]	uncertain significance	2	65072517	65072517	Human		name
156269474	CV2293269	single nucleotide variant	NM_015147.3(CEP68):c.1619C>G (p.Pro540Arg)	not specified [RCV004150766]	uncertain significance	2	65072715	65072715	Human		name
156354910	CV2324375	single nucleotide variant	NM_015147.3(CEP68):c.2245G>T (p.Ala749Ser)	not specified [RCV004178875]	uncertain significance	2	65082676	65082676	Human		name
155963779	CV2330366	single nucleotide variant	NM_015147.3(CEP68):c.1222G>A (p.Asp408Asn)	not specified [RCV004180942]	uncertain significance	2	65072318	65072318	Human		name
156062905	CV2330970	single nucleotide variant	NM_015147.3(CEP68):c.1925A>G (p.Tyr642Cys)	not specified [RCV004188014]	uncertain significance	2	65074322	65074322	Human		name
156333019	CV2335918	single nucleotide variant	NM_015147.3(CEP68):c.1796G>A (p.Arg599Gln)	not specified [RCV004189531]	uncertain significance	2	65072892	65072892	Human		name
155913905	CV2341883	single nucleotide variant	NM_015147.3(CEP68):c.1304C>G (p.Ser435Cys)	not specified [RCV004184831]	uncertain significance	2	65072400	65072400	Human		name
156075948	CV2350917	single nucleotide variant	NM_015147.3(CEP68):c.1774T>G (p.Ser592Ala)	not specified [RCV004211750]	uncertain significance	2	65072870	65072870	Human		name
155926188	CV2365710	single nucleotide variant	NM_015147.3(CEP68):c.1805T>G (p.Phe602Cys)	not specified [RCV004214256]	uncertain significance	2	65072901	65072901	Human		name
155998388	CV2393420	single nucleotide variant	NM_015147.3(CEP68):c.1238G>A (p.Arg413His)	not specified [RCV004228917]	uncertain significance	2	65072334	65072334	Human		name
329358397	CV2425243	single nucleotide variant	NM_015147.3(CEP68):c.1795C>T (p.Arg599Trp)	not specified [RCV004250915]	uncertain significance	2	65072891	65072891	Human		name
329367597	CV2427461	single nucleotide variant	NM_015147.3(CEP68):c.1741G>A (p.Gly581Arg)	not specified [RCV004248310]	uncertain significance	2	65072837	65072837	Human		name
329375897	CV2441190	single nucleotide variant	NM_015147.3(CEP68):c.1572T>G (p.Ser524Arg)	not specified [RCV004263586]	uncertain significance	2	65072668	65072668	Human		name
329366822	CV2441914	single nucleotide variant	NM_015147.3(CEP68):c.1418A>T (p.Glu473Val)	not specified [RCV004262095]	uncertain significance	2	65072514	65072514	Human		name
401856131	CV2764392	single nucleotide variant	NM_015147.3(CEP68):c.1742G>T (p.Gly581Val)	not specified [RCV004338963]	uncertain significance	2	65072838	65072838	Human		name
401897742	CV2772890	single nucleotide variant	NM_015147.3(CEP68):c.1588T>C (p.Phe530Leu)	not specified [RCV004357664]	likely benign	2	65072684	65072684	Human		name
401888149	CV2791289	single nucleotide variant	NM_015147.3(CEP68):c.1507T>A (p.Ser503Thr)	not specified [RCV004356914]	uncertain significance	2	65072603	65072603	Human		name
405777542	CV3296975	single nucleotide variant	NM_015147.3(CEP68):c.1069T>C (p.Cys357Arg)	not specified [RCV004436368]	uncertain significance	2	65072165	65072165	Human		name
405722693	CV3296977	single nucleotide variant	NM_015147.3(CEP68):c.1135C>A (p.Pro379Thr)	not specified [RCV004428354]	uncertain significance	2	65072231	65072231	Human		name
405722701	CV3296978	single nucleotide variant	NM_015147.3(CEP68):c.1202C>T (p.Pro401Leu)	not specified [RCV004428355]	uncertain significance	2	65072298	65072298	Human		name
405722714	CV3296980	single nucleotide variant	NM_015147.3(CEP68):c.1237C>T (p.Arg413Cys)	not specified [RCV004428357]	uncertain significance	2	65072333	65072333	Human		name
405722723	CV3296981	single nucleotide variant	NM_015147.3(CEP68):c.1270C>T (p.Arg424Trp)	not specified [RCV004428358]	likely benign	2	65072366	65072366	Human		name
405722727	CV3296982	single nucleotide variant	NM_015147.3(CEP68):c.1271G>A (p.Arg424Gln)	not specified [RCV004428359]	uncertain significance	2	65072367	65072367	Human		name
405722735	CV3296983	single nucleotide variant	NM_015147.3(CEP68):c.1306C>T (p.Pro436Ser)	not specified [RCV004428360]	uncertain significance	2	65072402	65072402	Human		name
405722748	CV3296985	single nucleotide variant	NM_015147.3(CEP68):c.1322G>A (p.Arg441Gln)	not specified [RCV004428362]	likely benign	2	65072418	65072418	Human		name
405722756	CV3296986	single nucleotide variant	NM_015147.3(CEP68):c.1459G>A (p.Ala487Thr)	not specified [RCV004428363]	likely benign	2	65072555	65072555	Human		name
405722764	CV3296987	single nucleotide variant	NM_015147.3(CEP68):c.1542A>C (p.Lys514Asn)	not specified [RCV004428364]	uncertain significance	2	65072638	65072638	Human		name
405722779	CV3296989	single nucleotide variant	NM_015147.3(CEP68):c.1748C>T (p.Ser583Phe)	not specified [RCV004428366]	uncertain significance	2	65072844	65072844	Human		name
405722784	CV3296990	single nucleotide variant	NM_015147.3(CEP68):c.1822G>A (p.Glu608Lys)	not specified [RCV004428367]	uncertain significance	2	65072918	65072918	Human		name
405722794	CV3296991	single nucleotide variant	NM_015147.3(CEP68):c.1970A>G (p.Asn657Ser)	not specified [RCV004428368]	likely benign	2	65074367	65074367	Human		name
405722803	CV3296992	single nucleotide variant	NM_015147.3(CEP68):c.2141C>G (p.Ser714Cys)	not specified [RCV004428369]	uncertain significance	2	65082572	65082572	Human		name
405722811	CV3296993	single nucleotide variant	NM_015147.3(CEP68):c.2161G>A (p.Ala721Thr)	not specified [RCV004428370]	uncertain significance	2	65082592	65082592	Human		name
405722815	CV3296994	single nucleotide variant	NM_015147.3(CEP68):c.2168G>A (p.Arg723His)	not specified [RCV004428371]	likely benign	2	65082599	65082599	Human		name
405722821	CV3296995	single nucleotide variant	NM_015147.3(CEP68):c.2188G>A (p.Ala730Thr)	not specified [RCV004428372]	uncertain significance	2	65082619	65082619	Human		name
407469317	CV3428997	single nucleotide variant	NM_015147.3(CEP68):c.1658G>T (p.Gly553Val)	not specified [RCV004614995]	uncertain significance	2	65072754	65072754	Human		name
407469320	CV3428998	single nucleotide variant	NM_015147.3(CEP68):c.1690C>T (p.Arg564Cys)	not specified [RCV004614996]	uncertain significance	2	65072786	65072786	Human		name
407469323	CV3428999	single nucleotide variant	NM_015147.3(CEP68):c.1951G>A (p.Gly651Arg)	not specified [RCV004614997]	uncertain significance	2	65074348	65074348	Human		name
407469326	CV3429000	single nucleotide variant	NM_015147.3(CEP68):c.1445A>C (p.Tyr482Ser)	not specified [RCV004614998]	uncertain significance	2	65072541	65072541	Human		name
407469329	CV3429001	single nucleotide variant	NM_015147.3(CEP68):c.1669T>C (p.Cys557Arg)	not specified [RCV004614999]	uncertain significance	2	65072765	65072765	Human		name
407469335	CV3429003	single nucleotide variant	NM_015147.3(CEP68):c.1987T>A (p.Ser663Thr)	not specified [RCV004615001]	uncertain significance	2	65074384	65074384	Human		name
407469338	CV3429004	single nucleotide variant	NM_015147.3(CEP68):c.1874A>G (p.Gln625Arg)	not specified [RCV004615002]	uncertain significance	2	65072970	65072970	Human		name
407469340	CV3429005	single nucleotide variant	NM_015147.3(CEP68):c.1934C>T (p.Ala645Val)	not specified [RCV004615003]	uncertain significance	2	65074331	65074331	Human		name
597789242	CV3653001	single nucleotide variant	NM_015147.3(CEP68):c.2102C>T (p.Pro701Leu)	not specified [RCV004901715]	uncertain significance	2	65077962	65077962	Human		name
597789253	CV3653004	single nucleotide variant	NM_015147.3(CEP68):c.1229G>A (p.Arg410His)	not specified [RCV004901718]	uncertain significance	2	65072325	65072325	Human		name
597789257	CV3653005	single nucleotide variant	NM_015147.3(CEP68):c.1249G>A (p.Ala417Thr)	not specified [RCV004901719]	uncertain significance	2	65072345	65072345	Human		name
597789260	CV3653006	single nucleotide variant	NM_015147.3(CEP68):c.1721T>C (p.Leu574Pro)	not specified [RCV004901720]	uncertain significance	2	65072817	65072817	Human		name
597789275	CV3653011	single nucleotide variant	NM_015147.3(CEP68):c.2006G>A (p.Arg669Gln)	not specified [RCV004901724]	uncertain significance	2	65074403	65074403	Human		name
597789279	CV3653012	single nucleotide variant	NM_015147.3(CEP68):c.1436A>G (p.Asp479Gly)	not specified [RCV004901725]	uncertain significance	2	65072532	65072532	Human		name
597789283	CV3653013	single nucleotide variant	NM_015147.3(CEP68):c.1364G>A (p.Arg455Lys)	not specified [RCV004901726]	uncertain significance	2	65072460	65072460	Human		name
597789291	CV3653015	single nucleotide variant	NM_015147.3(CEP68):c.1031C>T (p.Ala344Val)	not specified [RCV004901728]	uncertain significance	2	65072127	65072127	Human		name
597789297	CV3653017	single nucleotide variant	NM_015147.3(CEP68):c.1311G>C (p.Gln437His)	not specified [RCV004901730]	uncertain significance	2	65072407	65072407	Human		name
598209872	CV3947976	single nucleotide variant	NM_015147.3(CEP68):c.2216C>T (p.Thr739Ile)	not specified [RCV005315772]	uncertain significance	2	65082647	65082647	Human		name
598209885	CV3947979	single nucleotide variant	NM_015147.3(CEP68):c.1898A>G (p.Gln633Arg)	not specified [RCV005315774]	uncertain significance	2	65074295	65074295	Human		name
598209893	CV3947980	single nucleotide variant	NM_015147.3(CEP68):c.1940T>A (p.Val647Asp)	not specified [RCV005315775]	uncertain significance	2	65074337	65074337	Human		name
15166572	CV708331	single nucleotide variant	NM_015147.3(CEP68):c.1100T>A (p.Phe367Tyr)	not provided [RCV000971210]	benign	2	65072196	65072196	Human		name
15183589	CV708333	single nucleotide variant	NM_015147.3(CEP68):c.1820T>C (p.Val607Ala)	not provided [RCV000974911]	benign	2	65072916	65072916	Human		name
15103700	CV697618	microsatellite	NM_015147.3(CEP68):c.1844GAG[1] (p.Gly616del)	not provided [RCV000959533]	benign	2	65072938	65072940	Human		name

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