Ebi3 Variant Search Result - Rat Genome Database

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32 records found for search term Ebi3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15150127	CV780008	single nucleotide variant	NM_005755.3(EBI3):c.200+3C>T	not provided [RCV000967884]	benign	19	4231326	4231326	Human		name
156191876	CV2206214	single nucleotide variant	NM_005755.3(EBI3):c.40A>G (p.Ser14Gly)	not specified [RCV004080650]	likely benign	19	4229590	4229590	Human		name
156206552	CV2307750	single nucleotide variant	NM_005755.3(EBI3):c.37G>A (p.Ala13Thr)	not specified [RCV004168440]	uncertain significance	19	4229587	4229587	Human		name
156196164	CV2367218	single nucleotide variant	NM_005755.3(EBI3):c.95G>A (p.Arg32Gln)	not specified [RCV004215644]	uncertain significance	19	4231218	4231218	Human		name
597803002	CV3667190	single nucleotide variant	NM_005755.3(EBI3):c.44G>A (p.Cys15Tyr)	not specified [RCV004906990]	uncertain significance	19	4229594	4229594	Human		name
15128130	CV716483	single nucleotide variant	NM_005755.3(EBI3):c.409C>T (p.Leu137=)	not provided [RCV000964028]	benign	19	4234696	4234696	Human		name
156332503	CV2214453	single nucleotide variant	NM_005755.3(EBI3):c.253A>G (p.Thr85Ala)	not specified [RCV004088514]	likely benign	19	4233181	4233181	Human		name
329361025	CV2436599	single nucleotide variant	NM_005755.3(EBI3):c.218G>A (p.Arg73Gln)	not specified [RCV004257980]	likely benign	19	4233146	4233146	Human		name
329368711	CV2453233	single nucleotide variant	NM_005755.3(EBI3):c.181T>G (p.Ser61Ala)	not specified [RCV004266879]	uncertain significance	19	4231304	4231304	Human		name
401777800	CV2718343	single nucleotide variant	NM_005755.3(EBI3):c.163A>G (p.Asn55Asp)	not specified [RCV004318177]	uncertain significance	19	4231286	4231286	Human		name
405753456	CV3238354	single nucleotide variant	NM_005755.3(EBI3):c.142T>C (p.Trp48Arg)	not specified [RCV004382230]	uncertain significance	19	4231265	4231265	Human		name
405753024	CV3238356	single nucleotide variant	NM_005755.3(EBI3):c.231G>T (p.Trp77Cys)	not specified [RCV004382232]	uncertain significance	19	4233159	4233159	Human		name
405752847	CV3238357	single nucleotide variant	NM_005755.3(EBI3):c.235T>C (p.Cys79Arg)	not specified [RCV004382233]	uncertain significance	19	4233163	4233163	Human		name
407478228	CV3441428	single nucleotide variant	NM_005755.3(EBI3):c.178G>A (p.Val60Met)	not specified [RCV004617476]	uncertain significance	19	4231301	4231301	Human		name
597803004	CV3667191	single nucleotide variant	NM_005755.3(EBI3):c.205G>T (p.Gly69Cys)	not specified [RCV004906991]	uncertain significance	19	4233133	4233133	Human		name
598268752	CV3953925	single nucleotide variant	NM_005755.3(EBI3):c.239T>C (p.Leu80Pro)	not specified [RCV005327166]	uncertain significance	19	4233167	4233167	Human		name
156213821	CV2257408	single nucleotide variant	NM_005755.3(EBI3):c.385C>T (p.Pro129Ser)	not specified [RCV004125493]	uncertain significance	19	4234672	4234672	Human		name
155987059	CV2275431	single nucleotide variant	NM_005755.3(EBI3):c.498G>T (p.Trp166Cys)	not specified [RCV004135307]	uncertain significance	19	4234785	4234785	Human		name
156140815	CV2280860	single nucleotide variant	NM_005755.3(EBI3):c.626C>G (p.Thr209Arg)	not specified [RCV004145113]	uncertain significance	19	4237024	4237024	Human		name
156153455	CV2307716	single nucleotide variant	NM_005755.3(EBI3):c.613G>T (p.Ala205Ser)	not specified [RCV004168125]	uncertain significance	19	4237011	4237011	Human		name
156284688	CV2317562	single nucleotide variant	NM_005755.3(EBI3):c.388G>A (p.Asp130Asn)	not specified [RCV004172515]	uncertain significance	19	4234675	4234675	Human		name
156276497	CV2351941	single nucleotide variant	NM_005755.3(EBI3):c.665C>G (p.Thr222Ser)	not specified [RCV004198077]	uncertain significance	19	4237063	4237063	Human		name
156105329	CV2352528	single nucleotide variant	NM_005755.3(EBI3):c.406C>T (p.Arg136Cys)	not specified [RCV004203030]	uncertain significance	19	4234693	4234693	Human		name
156050282	CV2367476	single nucleotide variant	NM_005755.3(EBI3):c.407G>A (p.Arg136His)	not specified [RCV004211414]	uncertain significance	19	4234694	4234694	Human		name
329351977	CV2455559	single nucleotide variant	NM_005755.3(EBI3):c.442C>G (p.Gln148Glu)	not specified [RCV004276811]	uncertain significance	19	4234729	4234729	Human		name
405752725	CV3238358	single nucleotide variant	NM_005755.3(EBI3):c.428G>A (p.Arg143His)	not specified [RCV004382234]	uncertain significance	19	4234715	4234715	Human		name
405752729	CV3238359	single nucleotide variant	NM_005755.3(EBI3):c.539T>G (p.Val180Gly)	not specified [RCV004382235]	uncertain significance	19	4236937	4236937	Human		name
407478218	CV3441426	single nucleotide variant	NM_005755.3(EBI3):c.403G>T (p.Val135Leu)	not specified [RCV004617474]	uncertain significance	19	4234690	4234690	Human		name
407478232	CV3441429	single nucleotide variant	NM_005755.3(EBI3):c.560C>T (p.Ser187Phe)	not specified [RCV004617477]	uncertain significance	19	4236958	4236958	Human		name
407478238	CV3441430	single nucleotide variant	NM_005755.3(EBI3):c.557C>T (p.Thr186Met)	not specified [RCV004617478]	uncertain significance	19	4236955	4236955	Human		name
407478242	CV3441431	single nucleotide variant	NM_005755.3(EBI3):c.671C>T (p.Thr224Ile)	not specified [RCV004617479]	uncertain significance	19	4237069	4237069	Human		name
598268762	CV3953927	single nucleotide variant	NM_005755.3(EBI3):c.388G>C (p.Asp130His)	not specified [RCV005327168]	uncertain significance	19	4234675	4234675	Human		name

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