Elovl3 Variant Search Result - Rat Genome Database

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32 records found for search term Elovl3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156075708	CV2230159	single nucleotide variant	NM_152310.3(ELOVL3):c.17A>G (p.Asn6Ser)	not specified [RCV004099799]	uncertain significance	10	102226565	102226565	Human		name
156171895	CV2312608	single nucleotide variant	NM_152310.3(ELOVL3):c.13A>G (p.Met5Val)	not specified [RCV004169346]	uncertain significance	10	102226561	102226561	Human		name
155925257	CV2348336	single nucleotide variant	NM_152310.3(ELOVL3):c.20T>G (p.Val7Gly)	not specified [RCV004193533]	uncertain significance	10	102226568	102226568	Human		name
329360853	CV2463050	single nucleotide variant	NM_152310.3(ELOVL3):c.19G>A (p.Val7Ile)	not specified [RCV004272865]	uncertain significance	10	102226567	102226567	Human		name
597667878	CV3667559	single nucleotide variant	NM_152310.3(ELOVL3):c.98A>G (p.Tyr33Cys)	not specified [RCV004912623]	uncertain significance	10	102226646	102226646	Human		name
156090655	CV2299982	single nucleotide variant	NM_152310.3(ELOVL3):c.202A>G (p.Ile68Val)	not specified [RCV004151198]	uncertain significance	10	102227726	102227726	Human		name
156012177	CV2358863	single nucleotide variant	NM_152310.3(ELOVL3):c.286G>A (p.Gly96Arg)	not specified [RCV004212208]	uncertain significance	10	102228469	102228469	Human		name
401780213	CV2725933	single nucleotide variant	NM_152310.3(ELOVL3):c.267G>A (p.Met89Ile)	not specified [RCV004324306]	uncertain significance	10	102228450	102228450	Human		name
405739789	CV3248674	single nucleotide variant	NM_152310.3(ELOVL3):c.164T>G (p.Met55Arg)	not specified [RCV004380377]	uncertain significance	10	102227688	102227688	Human		name
405739798	CV3248675	single nucleotide variant	NM_152310.3(ELOVL3):c.278T>C (p.Leu93Pro)	not specified [RCV004380378]	uncertain significance	10	102228461	102228461	Human		name
407506756	CV3434848	single nucleotide variant	NM_152310.3(ELOVL3):c.289G>A (p.Gly97Ser)	not specified [RCV004624823]	likely benign	10	102228472	102228472	Human		name
597747038	CV3667561	single nucleotide variant	NM_152310.3(ELOVL3):c.227T>A (p.Ile76Asn)	not specified [RCV004922821]	uncertain significance	10	102227751	102227751	Human		name
598191524	CV3957830	single nucleotide variant	NM_152310.3(ELOVL3):c.224C>A (p.Ala75Glu)	not specified [RCV005334849]	uncertain significance	10	102227748	102227748	Human		name
156339633	CV2225118	single nucleotide variant	NM_152310.3(ELOVL3):c.734C>T (p.Thr245Ile)	not specified [RCV004094932]	uncertain significance	10	102229173	102229173	Human		name
156062292	CV2277176	single nucleotide variant	NM_152310.3(ELOVL3):c.605T>A (p.Ile202Asn)	not specified [RCV004142817]	uncertain significance	10	102229044	102229044	Human		name
156028993	CV2278577	single nucleotide variant	NM_152310.3(ELOVL3):c.433C>T (p.His145Tyr)	not specified [RCV004133006]	uncertain significance	10	102228872	102228872	Human		name
156305784	CV2314741	single nucleotide variant	NM_152310.3(ELOVL3):c.449G>T (p.Ser150Ile)	not specified [RCV004170880]	uncertain significance	10	102228888	102228888	Human		name
156277005	CV2351995	single nucleotide variant	NM_152310.3(ELOVL3):c.460G>A (p.Val154Met)	not specified [RCV004191096]	uncertain significance	10	102228899	102228899	Human		name
156306773	CV2360043	single nucleotide variant	NM_152310.3(ELOVL3):c.721A>G (p.Ile241Val)	not specified [RCV004212878]	likely benign	10	102229160	102229160	Human		name
329360142	CV2446610	single nucleotide variant	NM_152310.3(ELOVL3):c.547A>G (p.Thr183Ala)	not specified [RCV004251501]	uncertain significance	10	102228986	102228986	Human		name
405739804	CV3248676	single nucleotide variant	NM_152310.3(ELOVL3):c.304G>A (p.Val102Met)	not specified [RCV004380379]	uncertain significance	10	102228487	102228487	Human		name
405739812	CV3248677	single nucleotide variant	NM_152310.3(ELOVL3):c.527G>C (p.Gly176Ala)	not specified [RCV004380380]	uncertain significance	10	102228966	102228966	Human		name
405739817	CV3248678	single nucleotide variant	NM_152310.3(ELOVL3):c.685T>C (p.Cys229Arg)	not specified [RCV004380381]	uncertain significance	10	102229124	102229124	Human		name
405739828	CV3248679	single nucleotide variant	NM_152310.3(ELOVL3):c.730A>G (p.Met244Val)	not specified [RCV004380382]	uncertain significance	10	102229169	102229169	Human		name
407506759	CV3434849	single nucleotide variant	NM_152310.3(ELOVL3):c.450C>A (p.Ser150Arg)	not specified [RCV004624824]	uncertain significance	10	102228889	102228889	Human		name
597667886	CV3667558	single nucleotide variant	NM_152310.3(ELOVL3):c.410G>A (p.Arg137His)	not specified [RCV004912622]	uncertain significance	10	102228849	102228849	Human		name
597747032	CV3667560	single nucleotide variant	NM_152310.3(ELOVL3):c.751G>T (p.Ala251Ser)	not specified [RCV004922820]	uncertain significance	10	102229190	102229190	Human		name
597667871	CV3667562	single nucleotide variant	NM_152310.3(ELOVL3):c.760T>C (p.Phe254Leu)	not specified [RCV004912624]	uncertain significance	10	102229199	102229199	Human		name
598191528	CV3957831	single nucleotide variant	NM_152310.3(ELOVL3):c.743T>G (p.Ile248Ser)	not specified [RCV005334850]	uncertain significance	10	102229182	102229182	Human		name
598191536	CV3957832	single nucleotide variant	NM_152310.3(ELOVL3):c.376A>G (p.Ile126Val)	not specified [RCV005334851]	likely benign	10	102228559	102228559	Human		name
598191543	CV3957833	single nucleotide variant	NM_152310.3(ELOVL3):c.319T>C (p.Phe107Leu)	not specified [RCV005334852]	uncertain significance	10	102228502	102228502	Human		name
598191554	CV3957835	single nucleotide variant	NM_152310.3(ELOVL3):c.365T>C (p.Leu122Pro)	not specified [RCV005334854]	uncertain significance	10	102228548	102228548	Human		name

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