Rcn3 Variant Search Result - Rat Genome Database

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40 records found for search term Rcn3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156225996	CV2352701	single nucleotide variant	NM_020650.3(RCN3):c.85C>G (p.His29Asp)	not specified [RCV004198727]	uncertain significance	19	49528557	49528557	Human		name
401910662	CV2818576	single nucleotide variant	NM_020650.3(RCN3):c.504C>T (p.Asp168=)	not provided [RCV003425331]	likely benign	19	49537091	49537091	Human		name
401937348	CV2818577	single nucleotide variant	NM_020650.3(RCN3):c.900G>A (p.Ala300=)	not provided [RCV003415357]	likely benign	19	49543126	49543126	Human		name
156335187	CV2228356	single nucleotide variant	NM_020650.3(RCN3):c.208C>A (p.Gln70Lys)	not specified [RCV004098341]	uncertain significance	19	49528680	49528680	Human		name
156362708	CV2265588	single nucleotide variant	NM_020650.3(RCN3):c.167A>G (p.His56Arg)	not specified [RCV004124324]	uncertain significance	19	49528639	49528639	Human		name
156002201	CV2353630	single nucleotide variant	NM_020650.3(RCN3):c.165C>A (p.Asp55Glu)	not specified [RCV004199602]	uncertain significance	19	49528637	49528637	Human		name
407507532	CV3465164	single nucleotide variant	NM_020650.3(RCN3):c.272G>A (p.Gly91Glu)	not specified [RCV004671755]	uncertain significance	19	49534222	49534222	Human		name
597764535	CV3582894	single nucleotide variant	NM_020650.3(RCN3):c.274G>A (p.Asp92Asn)	not specified [RCV004849802]	uncertain significance	19	49534224	49534224	Human		name
598255430	CV3899023	single nucleotide variant	NM_020650.3(RCN3):c.265C>A (p.Arg89Ser)	not specified [RCV005259892]	uncertain significance	19	49534215	49534215	Human		name
156134176	CV2235502	single nucleotide variant	NM_020650.3(RCN3):c.868G>A (p.Asp290Asn)	not specified [RCV004109543]	uncertain significance	19	49542741	49542741	Human		name
155919240	CV2254832	single nucleotide variant	NM_020650.3(RCN3):c.401G>C (p.Gly134Ala)	not specified [RCV004115293]	uncertain significance	19	49534351	49534351	Human		name
155906643	CV2279347	single nucleotide variant	NM_020650.3(RCN3):c.583G>A (p.Glu195Lys)	not specified [RCV004139861]	uncertain significance	19	49537170	49537170	Human		name
156278387	CV2284931	single nucleotide variant	NM_020650.3(RCN3):c.856C>G (p.Leu286Val)	not specified [RCV004143377]	uncertain significance	19	49542729	49542729	Human		name
156103674	CV2291631	single nucleotide variant	NM_020650.3(RCN3):c.470A>G (p.Asp157Gly)	not specified [RCV004155921]	uncertain significance	19	49537057	49537057	Human		name
156143223	CV2358557	single nucleotide variant	NM_020650.3(RCN3):c.508C>T (p.Arg170Trp)	not specified [RCV004207439]	uncertain significance	19	49537095	49537095	Human		name
156255168	CV2358961	single nucleotide variant	NM_020650.3(RCN3):c.862G>A (p.Glu288Lys)	not specified [RCV004212291]	uncertain significance	19	49542735	49542735	Human		name
156304265	CV2359572	single nucleotide variant	NM_020650.3(RCN3):c.623C>T (p.Thr208Ile)	not specified [RCV004214875]	uncertain significance	19	49539123	49539123	Human		name
156383133	CV2361423	single nucleotide variant	NM_020650.3(RCN3):c.886C>T (p.Arg296Trp)	not specified [RCV004221068]	uncertain significance	19	49543112	49543112	Human		name
155996231	CV2393158	single nucleotide variant	NM_020650.3(RCN3):c.409G>A (p.Glu137Lys)	not specified [RCV004226635]	uncertain significance	19	49534359	49534359	Human		name
329365119	CV2440053	single nucleotide variant	NM_020650.3(RCN3):c.971A>G (p.His324Arg)	not specified [RCV004260523]	uncertain significance	19	49543197	49543197	Human		name
401744161	CV2680904	single nucleotide variant	NM_020650.3(RCN3):c.499C>T (p.Arg167Trp)	not specified [RCV004295979]	uncertain significance	19	49537086	49537086	Human		name
401744641	CV2681094	single nucleotide variant	NM_020650.3(RCN3):c.512G>A (p.Arg171His)	not specified [RCV004296153]	uncertain significance	19	49537099	49537099	Human		name
401720875	CV2702170	single nucleotide variant	NM_020650.3(RCN3):c.793G>A (p.Glu265Lys)	not specified [RCV004314520]	uncertain significance	19	49542666	49542666	Human		name
401859956	CV2765222	single nucleotide variant	NM_020650.3(RCN3):c.757C>T (p.Arg253Trp)	not specified [RCV004339749]	uncertain significance	19	49542630	49542630	Human		name
405682661	CV3319386	single nucleotide variant	NM_020650.3(RCN3):c.301G>A (p.Glu101Lys)	not specified [RCV004443654]	uncertain significance	19	49534251	49534251	Human		name
405682665	CV3319387	single nucleotide variant	NM_020650.3(RCN3):c.311C>T (p.Ala104Val)	not specified [RCV004443655]	uncertain significance	19	49534261	49534261	Human		name
405682668	CV3319388	single nucleotide variant	NM_020650.3(RCN3):c.551C>T (p.Thr184Ile)	not specified [RCV004443656]	uncertain significance	19	49537138	49537138	Human		name
405682672	CV3319389	single nucleotide variant	NM_020650.3(RCN3):c.602G>A (p.Arg201Gln)	not specified [RCV004443657]	uncertain significance	19	49537189	49537189	Human		name
405682674	CV3319390	single nucleotide variant	NM_020650.3(RCN3):c.692C>T (p.Ser231Leu)	not specified [RCV004443658]	uncertain significance	19	49542565	49542565	Human		name
405682680	CV3319391	single nucleotide variant	NM_020650.3(RCN3):c.695C>A (p.Ala232Asp)	not specified [RCV004443659]	uncertain significance	19	49542568	49542568	Human		name
407532201	CV3465160	single nucleotide variant	NM_020650.3(RCN3):c.872C>T (p.Thr291Met)	not specified [RCV004657987]	uncertain significance	19	49542745	49542745	Human		name
407532204	CV3465161	single nucleotide variant	NM_020650.3(RCN3):c.716C>T (p.Pro239Leu)	not specified [RCV004657988]	uncertain significance	19	49542589	49542589	Human		name
407507529	CV3465162	single nucleotide variant	NM_020650.3(RCN3):c.559G>A (p.Glu187Lys)	not specified [RCV004671754]	uncertain significance	19	49537146	49537146	Human		name
407532206	CV3465163	single nucleotide variant	NM_020650.3(RCN3):c.560A>T (p.Glu187Val)	not specified [RCV004657989]	uncertain significance	19	49537147	49537147	Human		name
597764540	CV3582896	single nucleotide variant	NM_020650.3(RCN3):c.359C>T (p.Ala120Val)	not specified [RCV004849803]	uncertain significance	19	49534309	49534309	Human		name
597729409	CV3582897	single nucleotide variant	NM_020650.3(RCN3):c.493C>G (p.Leu165Val)	not specified [RCV004862915]	uncertain significance	19	49537080	49537080	Human		name
597764544	CV3582898	single nucleotide variant	NM_020650.3(RCN3):c.814C>T (p.Pro272Ser)	not specified [RCV004849804]	uncertain significance	19	49542687	49542687	Human		name
597764548	CV3582899	single nucleotide variant	NM_020650.3(RCN3):c.955G>A (p.Glu319Lys)	not specified [RCV004849805]	uncertain significance	19	49543181	49543181	Human		name
598255425	CV3899022	single nucleotide variant	NM_020650.3(RCN3):c.536G>A (p.Gly179Glu)	not specified [RCV005259891]	uncertain significance	19	49537123	49537123	Human		name
598255435	CV3899024	single nucleotide variant	NM_020650.3(RCN3):c.771G>T (p.Lys257Asn)	not specified [RCV005259893]	uncertain significance	19	49542644	49542644	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
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