Ccdc124 Variant Search Result - Rat Genome Database

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26 records found for search term Ccdc124

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156144071	CV2296466	single nucleotide variant	NM_001136203.2(CCDC124):c.23A>G (p.Glu8Gly)	not specified [RCV004148206]	uncertain significance	19	17936443	17936443	Human		name
401737630	CV2679930	single nucleotide variant	NM_001136203.2(CCDC124):c.76G>A (p.Ala26Thr)	not specified [RCV004284212]	uncertain significance	19	17936496	17936496	Human		name
401862740	CV2778987	single nucleotide variant	NM_001136203.2(CCDC124):c.89A>C (p.Lys30Thr)	not specified [RCV004348642]	uncertain significance	19	17936509	17936509	Human		name
405754974	CV3302829	single nucleotide variant	NM_001136203.2(CCDC124):c.95A>G (p.Lys32Arg)	not specified [RCV004432689]	uncertain significance	19	17936515	17936515	Human		name
598177099	CV3946685	single nucleotide variant	NM_001136203.2(CCDC124):c.35C>T (p.Ser12Leu)	not specified [RCV005310152]	uncertain significance	19	17936455	17936455	Human		name
598177110	CV3946687	single nucleotide variant	NM_001136203.2(CCDC124):c.80A>T (p.Asp27Val)	not specified [RCV005310154]	uncertain significance	19	17936500	17936500	Human		name
329360049	CV2462426	single nucleotide variant	NM_001136203.2(CCDC124):c.289C>T (p.Arg97Trp)	not specified [RCV004268181]	uncertain significance	19	17942785	17942785	Human		name
405754949	CV3302825	single nucleotide variant	NM_001136203.2(CCDC124):c.124G>A (p.Asp42Asn)	not specified [RCV004432685]	uncertain significance	19	17936544	17936544	Human		name
405754954	CV3302826	single nucleotide variant	NM_001136203.2(CCDC124):c.256G>A (p.Ala86Thr)	not specified [RCV004432686]	uncertain significance	19	17942752	17942752	Human		name
597786454	CV3638041	single nucleotide variant	NM_001136203.2(CCDC124):c.293C>T (p.Ala98Val)	not specified [RCV004900980]	uncertain significance	19	17942789	17942789	Human		name
597786814	CV3638042	single nucleotide variant	NM_001136203.2(CCDC124):c.246G>T (p.Lys82Asn)	not specified [RCV004900981]	uncertain significance	19	17942742	17942742	Human		name
156134463	CV2196028	single nucleotide variant	NM_001136203.2(CCDC124):c.570C>A (p.Asn190Lys)	not specified [RCV004072271]	uncertain significance	19	17943613	17943613	Human		name
156092843	CV2256704	single nucleotide variant	NM_001136203.2(CCDC124):c.380C>T (p.Pro127Leu)	not specified [RCV004118877]	uncertain significance	19	17943291	17943291	Human		name
156275128	CV2279910	single nucleotide variant	NM_001136203.2(CCDC124):c.547C>G (p.Arg183Gly)	not specified [RCV004144499]	uncertain significance	19	17943590	17943590	Human		name
155925626	CV2348453	single nucleotide variant	NM_001136203.2(CCDC124):c.659A>G (p.Asn220Ser)	not specified [RCV004193643]	uncertain significance	19	17943702	17943702	Human		name
156057393	CV2375869	single nucleotide variant	NM_001136203.2(CCDC124):c.649G>A (p.Val217Met)	not specified [RCV004217714]	uncertain significance	19	17943692	17943692	Human		name
156388434	CV2380416	single nucleotide variant	NM_001136203.2(CCDC124):c.476A>C (p.Glu159Ala)	not specified [RCV004218019]	uncertain significance	19	17943519	17943519	Human		name
329397903	CV2464114	single nucleotide variant	NM_001136203.2(CCDC124):c.352G>A (p.Glu118Lys)	not specified [RCV004273808]	uncertain significance	19	17943263	17943263	Human		name
401898191	CV2790932	single nucleotide variant	NM_001136203.2(CCDC124):c.570C>G (p.Asn190Lys)	not specified [RCV004354568]	uncertain significance	19	17943613	17943613	Human		name
405754961	CV3302827	single nucleotide variant	NM_001136203.2(CCDC124):c.326A>G (p.Gln109Arg)	not specified [RCV004432687]	uncertain significance	19	17942822	17942822	Human		name
405754966	CV3302828	single nucleotide variant	NM_001136203.2(CCDC124):c.422G>T (p.Ser141Ile)	not specified [RCV004432688]	uncertain significance	19	17943333	17943333	Human		name
597786427	CV3638035	single nucleotide variant	NM_001136203.2(CCDC124):c.479C>T (p.Ala160Val)	not specified [RCV004900974]	uncertain significance	19	17943522	17943522	Human		name
597786431	CV3638036	single nucleotide variant	NM_001136203.2(CCDC124):c.620C>T (p.Ser207Phe)	not specified [RCV004900975]	uncertain significance	19	17943663	17943663	Human		name
597786437	CV3638037	single nucleotide variant	NM_001136203.2(CCDC124):c.421A>G (p.Ser141Gly)	not specified [RCV004900976]	uncertain significance	19	17943332	17943332	Human		name
597786441	CV3638038	single nucleotide variant	NM_001136203.2(CCDC124):c.343G>T (p.Asp115Tyr)	not specified [RCV004900977]	uncertain significance	19	17942839	17942839	Human		name
598177116	CV3946688	single nucleotide variant	NM_001136203.2(CCDC124):c.585G>C (p.Gln195His)	not specified [RCV005310155]	uncertain significance	19	17943628	17943628	Human		name

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