Ccdc51 Variant Search Result - Rat Genome Database

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42 records found for search term Ccdc51

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15137520	CV708904	single nucleotide variant	NM_001256964.2(CCDC51):c.132C>T (p.Pro44=)	not provided [RCV000965634]	benign	3	48434997	48434997	Human		name
401718925	CV2679352	single nucleotide variant	NM_001256964.2(CCDC51):c.55G>A (p.Val19Ile)	not specified [RCV004285889]	likely benign	3	48435074	48435074	Human		name
401779320	CV2733324	single nucleotide variant	NM_001256964.2(CCDC51):c.88C>T (p.Leu30Phe)	not specified [RCV004332230]	uncertain significance	3	48435041	48435041	Human		name
405716035	CV3295819	single nucleotide variant	NM_001256964.2(CCDC51):c.64C>T (p.Arg22Trp)	not specified [RCV004427538]	uncertain significance	3	48435065	48435065	Human		name
405716043	CV3295820	single nucleotide variant	NM_001256964.2(CCDC51):c.65G>A (p.Arg22Gln)	not specified [RCV004427539]	uncertain significance	3	48435064	48435064	Human		name
329393336	CV2449662	single nucleotide variant	NM_001256964.2(CCDC51):c.176G>A (p.Arg59His)	not specified [RCV004268573]	uncertain significance	3	48434953	48434953	Human		name
401748847	CV2692815	single nucleotide variant	NM_001256964.2(CCDC51):c.272G>A (p.Gly91Glu)	not specified [RCV004306358]	uncertain significance	3	48434857	48434857	Human		name
401758747	CV2694257	single nucleotide variant	NM_001256964.2(CCDC51):c.142A>G (p.Arg48Gly)	not specified [RCV004302669]	uncertain significance	3	48434987	48434987	Human		name
596939730	CV3407977	single nucleotide variant	NM_001256964.2(CCDC51):c.278A>G (p.Asn93Ser)	Retinal dystrophy [RCV004814437]	uncertain significance	3	48434851	48434851	Human	2	name
597795119	CV3644513	single nucleotide variant	NM_001256964.2(CCDC51):c.181C>T (p.Pro61Ser)	not specified [RCV004903561]	uncertain significance	3	48434948	48434948	Human		name
598191116	CV3943289	single nucleotide variant	NM_001256964.2(CCDC51):c.232A>G (p.Thr78Ala)	not specified [RCV005312582]	uncertain significance	3	48434897	48434897	Human		name
598191130	CV3943291	single nucleotide variant	NM_001256964.2(CCDC51):c.182C>T (p.Pro61Leu)	not specified [RCV005312584]	uncertain significance	3	48434947	48434947	Human		name
156274711	CV2320079	single nucleotide variant	NM_001256964.2(CCDC51):c.662A>C (p.Tyr221Ser)	not specified [RCV004167930]	uncertain significance	3	48432982	48432982	Human		name
156344113	CV2384680	single nucleotide variant	NM_001256964.2(CCDC51):c.895C>T (p.Leu299Phe)	not specified [RCV004232455]	uncertain significance	3	48432749	48432749	Human		name
155903950	CV2386677	single nucleotide variant	NM_001256964.2(CCDC51):c.769C>T (p.Arg257Cys)	not specified [RCV004231014]	uncertain significance	3	48432875	48432875	Human		name
401872653	CV2779843	single nucleotide variant	NM_001256964.2(CCDC51):c.933G>T (p.Arg311Ser)	not specified [RCV004353463]	uncertain significance	3	48432711	48432711	Human		name
405715982	CV3295811	single nucleotide variant	NM_001256964.2(CCDC51):c.334G>T (p.Ala112Ser)	not specified [RCV004427530]	uncertain significance	3	48433850	48433850	Human		name
405715991	CV3295812	single nucleotide variant	NM_001256964.2(CCDC51):c.340G>C (p.Gly114Arg)	not specified [RCV004427531]	uncertain significance	3	48433844	48433844	Human		name
405715998	CV3295813	single nucleotide variant	NM_001256964.2(CCDC51):c.392A>G (p.Lys131Arg)	not specified [RCV004427532]	uncertain significance	3	48433792	48433792	Human		name
405716004	CV3295814	single nucleotide variant	NM_001256964.2(CCDC51):c.406C>T (p.Arg136Cys)	not specified [RCV004427533]	uncertain significance	3	48433778	48433778	Human		name
405716011	CV3295815	single nucleotide variant	NM_001256964.2(CCDC51):c.416G>A (p.Arg139His)	not specified [RCV004427534]	uncertain significance	3	48433768	48433768	Human		name
405716016	CV3295816	single nucleotide variant	NM_001256964.2(CCDC51):c.479A>G (p.Glu160Gly)	not specified [RCV004427535]	uncertain significance	3	48433165	48433165	Human		name
405716020	CV3295817	single nucleotide variant	NM_001256964.2(CCDC51):c.559C>T (p.Arg187Trp)	not specified [RCV004427536]	uncertain significance	3	48433085	48433085	Human		name
405716028	CV3295818	single nucleotide variant	NM_001256964.2(CCDC51):c.580C>T (p.Arg194Cys)	not specified [RCV004427537]	uncertain significance	3	48433064	48433064	Human		name
405716055	CV3295822	single nucleotide variant	NM_001256964.2(CCDC51):c.869C>T (p.Pro290Leu)	not specified [RCV004427541]	uncertain significance	3	48432775	48432775	Human		name
405716062	CV3295823	single nucleotide variant	NM_001256964.2(CCDC51):c.874A>G (p.Arg292Gly)	not specified [RCV004427542]	uncertain significance	3	48432770	48432770	Human		name
407490788	CV3418622	single nucleotide variant	NM_001256964.2(CCDC51):c.671G>A (p.Arg224His)	not specified [RCV004604542]	uncertain significance	3	48432973	48432973	Human		name
407454486	CV3418623	single nucleotide variant	NM_001256964.2(CCDC51):c.791A>G (p.Asn264Ser)	not specified [RCV004609872]	uncertain significance	3	48432853	48432853	Human		name
597795116	CV3644512	single nucleotide variant	NM_001256964.2(CCDC51):c.862A>C (p.Ser288Arg)	not specified [RCV004903560]	uncertain significance	3	48432782	48432782	Human		name
597795122	CV3644514	single nucleotide variant	NM_001256964.2(CCDC51):c.448C>A (p.Leu150Met)	not specified [RCV004903562]	uncertain significance	3	48433736	48433736	Human		name
597795125	CV3644515	single nucleotide variant	NM_001256964.2(CCDC51):c.449T>A (p.Leu150Gln)	not specified [RCV004903563]	uncertain significance	3	48433735	48433735	Human		name
597795128	CV3644516	single nucleotide variant	NM_001256964.2(CCDC51):c.755C>T (p.Ala252Val)	not specified [RCV004903564]	uncertain significance	3	48432889	48432889	Human		name
597761556	CV3644517	single nucleotide variant	NM_001256964.2(CCDC51):c.321A>C (p.Lys107Asn)	not specified [RCV004894980]	uncertain significance	3	48433863	48433863	Human		name
597761561	CV3644518	single nucleotide variant	NM_001256964.2(CCDC51):c.677G>C (p.Arg226Pro)	not specified [RCV004894981]	uncertain significance	3	48432967	48432967	Human		name
598191123	CV3943290	single nucleotide variant	NM_001256964.2(CCDC51):c.349C>G (p.Arg117Gly)	not specified [RCV005312583]	uncertain significance	3	48433835	48433835	Human		name
598227742	CV3943292	single nucleotide variant	NM_001256964.2(CCDC51):c.754G>A (p.Ala252Thr)	not specified [RCV005318972]	uncertain significance	3	48432890	48432890	Human		name
15137514	CV708903	single nucleotide variant	NM_001256964.2(CCDC51):c.968A>G (p.Gln323Arg)	not provided [RCV000965633]	benign	3	48432676	48432676	Human		name
15172081	CV720506	single nucleotide variant	NM_001256964.2(CCDC51):c.493C>T (p.Arg165Cys)	not provided [RCV000883772]	benign	3	48433151	48433151	Human		name
405715973	CV3295810	single nucleotide variant	NM_001256964.2(CCDC51):c.1007G>A (p.Gly336Glu)	Retinal dystrophy [RCV004818451]\|not specified [RCV004427529]	uncertain significance	3	48432637	48432637	Human	2	name
407490793	CV3418624	single nucleotide variant	NM_001256964.2(CCDC51):c.1031C>G (p.Ala344Gly)	not specified [RCV004604543]	uncertain significance	3	48432613	48432613	Human		name
597795131	CV3644519	single nucleotide variant	NM_001256964.2(CCDC51):c.1053A>T (p.Glu351Asp)	not specified [RCV004903565]	uncertain significance	3	48432591	48432591	Human		name
598227735	CV3943288	single nucleotide variant	NM_001256964.2(CCDC51):c.1099A>G (p.Met367Val)	not specified [RCV005318971]	likely benign	3	48432545	48432545	Human		name

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