Art3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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38 records found for search term Art3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405664863	CV3286558	single nucleotide variant	NM_001130016.3(ART3):c.16T>C (p.Phe6Leu)	not specified [RCV004418296]	uncertain significance	4	76075905	76075905	Human		name
405664873	CV3286560	single nucleotide variant	NM_001130016.3(ART3):c.20A>C (p.Glu7Ala)	not specified [RCV004418298]	uncertain significance	4	76075909	76075909	Human		name
401875118	CV2791100	single nucleotide variant	NM_001130016.3(ART3):c.40G>T (p.Ala14Ser)	not specified [RCV004356479]	uncertain significance	4	76075929	76075929	Human		name
597776003	CV3586453	single nucleotide variant	NM_001130016.3(ART3):c.55G>C (p.Val19Leu)	not specified [RCV004852402]	uncertain significance	4	76075944	76075944	Human		name
597788293	CV3586485	single nucleotide variant	NM_001130016.3(ART3):c.309C>T (p.Ser103=)	not specified [RCV004855459]	likely benign	4	76082063	76082063	Human		name
329373522	CV2447287	single nucleotide variant	NM_001130016.3(ART3):c.163C>A (p.Leu55Met)	not specified [RCV004262575]	uncertain significance	4	76081917	76081917	Human		name
401878323	CV2774184	single nucleotide variant	NM_001130016.3(ART3):c.296T>A (p.Met99Lys)	not specified [RCV004345772]	uncertain significance	4	76082050	76082050	Human		name
405664868	CV3286559	single nucleotide variant	NM_001130016.3(ART3):c.186C>G (p.Ser62Arg)	not specified [RCV004418297]	uncertain significance	4	76081940	76081940	Human		name
597788201	CV3586435	single nucleotide variant	NM_001130016.3(ART3):c.256C>A (p.Leu86Ile)	not specified [RCV004855436]	uncertain significance	4	76082010	76082010	Human		name
156231887	CV2227636	single nucleotide variant	NM_001130016.3(ART3):c.353C>T (p.Ala118Val)	not specified [RCV004094044]	uncertain significance	4	76082107	76082107	Human		name
155941964	CV2229393	single nucleotide variant	NM_001130016.3(ART3):c.724C>T (p.Leu242Phe)	not specified [RCV004101172]	uncertain significance	4	76082478	76082478	Human		name
156292995	CV2233503	single nucleotide variant	NM_001130016.3(ART3):c.560A>G (p.Tyr187Cys)	not specified [RCV004099987]	uncertain significance	4	76082314	76082314	Human		name
156038279	CV2278915	single nucleotide variant	NM_001130016.3(ART3):c.898G>C (p.Glu300Gln)	not specified [RCV004145613]	uncertain significance	4	76100815	76100815	Human		name
156168510	CV2299433	single nucleotide variant	NM_001130016.3(ART3):c.414C>G (p.Phe138Leu)	not specified [RCV004154517]	uncertain significance	4	76082168	76082168	Human		name
155995367	CV2375812	single nucleotide variant	NM_001130016.3(ART3):c.872A>G (p.Asp291Gly)	not specified [RCV004224395]	uncertain significance	4	76100315	76100315	Human		name
329368855	CV2424675	single nucleotide variant	NM_001130016.3(ART3):c.613A>C (p.Thr205Pro)	not specified [RCV004254543]	uncertain significance	4	76082367	76082367	Human		name
329392980	CV2469136	single nucleotide variant	NM_001130016.3(ART3):c.920A>G (p.Gln307Arg)	not specified [RCV004274363]	uncertain significance	4	76101002	76101002	Human		name
401768338	CV2675256	single nucleotide variant	NM_001130016.3(ART3):c.454C>A (p.Pro152Thr)	not specified [RCV004290023]	uncertain significance	4	76082208	76082208	Human		name
401768342	CV2675257	single nucleotide variant	NM_001130016.3(ART3):c.908G>A (p.Gly303Asp)	not specified [RCV004290024]	uncertain significance	4	76100990	76100990	Human		name
401723738	CV2684850	single nucleotide variant	NM_001130016.3(ART3):c.903C>A (p.Asp301Glu)	not specified [RCV004296356]	uncertain significance	4	76100820	76100820	Human		name
401753591	CV2684993	single nucleotide variant	NM_001130016.3(ART3):c.577G>A (p.Ala193Thr)	not specified [RCV004289578]	uncertain significance	4	76082331	76082331	Human		name
405664878	CV3286561	single nucleotide variant	NM_001130016.3(ART3):c.399C>G (p.Phe133Leu)	not specified [RCV004418299]	uncertain significance	4	76082153	76082153	Human		name
405664884	CV3286562	single nucleotide variant	NM_001130016.3(ART3):c.402G>T (p.Gln134His)	not specified [RCV004418300]	uncertain significance	4	76082156	76082156	Human		name
405664889	CV3286563	single nucleotide variant	NM_001130016.3(ART3):c.419T>A (p.Phe140Tyr)	not specified [RCV004418301]	uncertain significance	4	76082173	76082173	Human		name
405664895	CV3286564	single nucleotide variant	NM_001130016.3(ART3):c.521G>A (p.Gly174Glu)	not specified [RCV004418302]	uncertain significance	4	76082275	76082275	Human		name
405664899	CV3286565	single nucleotide variant	NM_001130016.3(ART3):c.872A>T (p.Asp291Val)	not specified [RCV004418303]	uncertain significance	4	76100315	76100315	Human		name
407461982	CV3480304	single nucleotide variant	NM_001130016.3(ART3):c.308C>G (p.Ser103Cys)	not specified [RCV004658908]	uncertain significance	4	76082062	76082062	Human		name
407491589	CV3480315	single nucleotide variant	NM_001130016.3(ART3):c.966A>G (p.Ile322Met)	not specified [RCV004666929]	uncertain significance	4	76103965	76103965	Human		name
597775942	CV3586427	single nucleotide variant	NM_001130016.3(ART3):c.898G>A (p.Glu300Lys)	not specified [RCV004852388]	uncertain significance	4	76100815	76100815	Human		name
597776028	CV3586463	single nucleotide variant	NM_001130016.3(ART3):c.463G>A (p.Ala155Thr)	not specified [RCV004852408]	uncertain significance	4	76082217	76082217	Human		name
597788269	CV3586474	single nucleotide variant	NM_001130016.3(ART3):c.570A>C (p.Lys190Asn)	not specified [RCV004855453]	uncertain significance	4	76082324	76082324	Human		name
597776104	CV3586496	single nucleotide variant	NM_001130016.3(ART3):c.593T>G (p.Leu198Arg)	not specified [RCV004852427]	uncertain significance	4	76082347	76082347	Human		name
597776108	CV3586502	single nucleotide variant	NM_001130016.3(ART3):c.320A>G (p.Glu107Gly)	not specified [RCV004852428]	uncertain significance	4	76082074	76082074	Human		name
598255464	CV3899030	single nucleotide variant	NM_001130016.3(ART3):c.773T>C (p.Phe258Ser)	not specified [RCV005259899]	uncertain significance	4	76082527	76082527	Human		name
598255511	CV3908981	single nucleotide variant	NM_001130016.3(ART3):c.836T>C (p.Val279Ala)	not specified [RCV005259909]	uncertain significance	4	76098976	76098976	Human		name
598255546	CV3908990	single nucleotide variant	NM_001130016.3(ART3):c.628G>T (p.Asp210Tyr)	not specified [RCV005259918]	uncertain significance	4	76082382	76082382	Human		name
156374663	CV2194715	single nucleotide variant	NM_001130016.3(ART3):c.1049T>C (p.Val350Ala)	not specified [RCV004075270]	uncertain significance	4	76112398	76112398	Human		name
329376960	CV2435758	single nucleotide variant	NM_001130016.3(ART3):c.1145C>A (p.Ala382Asp)	not specified [RCV004253387]	uncertain significance	4	76112494	76112494	Human		name

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