Slc27a1 Variant Search Result - Rat Genome Database

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68 records found for search term Slc27a1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15153594	CV745380	single nucleotide variant	NM_198580.3(SLC27A1):c.794+8G>A	not provided [RCV000901790]	benign	19	17487537	17487537	Human		name
15120295	CV780072	single nucleotide variant	NM_198580.3(SLC27A1):c.887-6C>A	not provided [RCV000962699]	benign	19	17489002	17489002	Human		name
15130159	CV716280	single nucleotide variant	NM_198580.3(SLC27A1):c.453G>A (p.Ala151=)	not provided [RCV000964387]	benign	19	17486848	17486848	Human		name
15159815	CV728020	single nucleotide variant	NM_198580.3(SLC27A1):c.702G>A (p.Gln234=)	not provided [RCV000881264]	benign	19	17487313	17487313	Human		name
401725807	CV2687275	single nucleotide variant	NM_198580.3(SLC27A1):c.179T>C (p.Val60Ala)	not specified [RCV004298213]	uncertain significance	19	17486574	17486574	Human		name
405769601	CV3321926	single nucleotide variant	NM_198580.3(SLC27A1):c.218G>T (p.Arg73Leu)	not specified [RCV004456745]	uncertain significance	19	17486613	17486613	Human		name
405769606	CV3321927	single nucleotide variant	NM_198580.3(SLC27A1):c.241A>G (p.Ile81Val)	not specified [RCV004456746]	uncertain significance	19	17486636	17486636	Human		name
597755158	CV3606572	single nucleotide variant	NM_198580.3(SLC27A1):c.275G>A (p.Arg92His)	not specified [RCV004868076]	uncertain significance	19	17486670	17486670	Human		name
597755162	CV3606573	single nucleotide variant	NM_198580.3(SLC27A1):c.163C>T (p.Leu55Phe)	not specified [RCV004868077]	uncertain significance	19	17470703	17470703	Human		name
597701049	CV3606576	single nucleotide variant	NM_198580.3(SLC27A1):c.272A>C (p.Glu91Ala)	not specified [RCV004859937]	uncertain significance	19	17486667	17486667	Human		name
598169577	CV3918384	single nucleotide variant	NM_198580.3(SLC27A1):c.106G>A (p.Val36Met)	not specified [RCV005284309]	uncertain significance	19	17470646	17470646	Human		name
15101693	CV728021	single nucleotide variant	NM_198580.3(SLC27A1):c.1614C>T (p.Ala538=)	not provided [RCV000892329]	benign	19	17500854	17500854	Human		name
156226166	CV2203112	single nucleotide variant	NM_198580.3(SLC27A1):c.385G>A (p.Asp129Asn)	not specified [RCV004069354]	uncertain significance	19	17486780	17486780	Human		name
156030344	CV2278711	single nucleotide variant	NM_198580.3(SLC27A1):c.967T>C (p.Trp323Arg)	not specified [RCV004134905]	uncertain significance	19	17489088	17489088	Human		name
156165277	CV2315154	single nucleotide variant	NM_198580.3(SLC27A1):c.487C>T (p.Arg163Trp)	not specified [RCV004165332]	uncertain significance	19	17486882	17486882	Human		name
401721252	CV2709887	single nucleotide variant	NM_198580.3(SLC27A1):c.643C>T (p.Pro215Ser)	not specified [RCV004321179]	uncertain significance	19	17487254	17487254	Human		name
401783518	CV2723662	single nucleotide variant	NM_198580.3(SLC27A1):c.839A>G (p.Gln280Arg)	not specified [RCV004325840]	likely benign	19	17488892	17488892	Human		name
405769612	CV3321928	single nucleotide variant	NM_198580.3(SLC27A1):c.412C>T (p.Arg138Trp)	not specified [RCV004456747]	uncertain significance	19	17486807	17486807	Human		name
405769616	CV3321929	single nucleotide variant	NM_198580.3(SLC27A1):c.459G>A (p.Met153Ile)	not specified [RCV004456748]	uncertain significance	19	17486854	17486854	Human		name
405769623	CV3321930	single nucleotide variant	NM_198580.3(SLC27A1):c.600G>C (p.Leu200Phe)	not specified [RCV004456749]	uncertain significance	19	17487211	17487211	Human		name
405769630	CV3321931	single nucleotide variant	NM_198580.3(SLC27A1):c.613T>C (p.Ser205Pro)	not specified [RCV004456750]	uncertain significance	19	17487224	17487224	Human		name
405769636	CV3321932	single nucleotide variant	NM_198580.3(SLC27A1):c.781G>A (p.Val261Ile)	not specified [RCV004456751]	uncertain significance	19	17487516	17487516	Human		name
407509611	CV3474112	single nucleotide variant	NM_198580.3(SLC27A1):c.728G>A (p.Arg243His)	not specified [RCV004672413]	uncertain significance	19	17487463	17487463	Human		name
407509487	CV3474115	single nucleotide variant	NM_198580.3(SLC27A1):c.994A>G (p.Thr332Ala)	not specified [RCV004672416]	uncertain significance	19	17489115	17489115	Human		name
407509494	CV3474117	single nucleotide variant	NM_198580.3(SLC27A1):c.380C>G (p.Pro127Arg)	not specified [RCV004672418]	uncertain significance	19	17486775	17486775	Human		name
407451349	CV3474118	single nucleotide variant	NM_198580.3(SLC27A1):c.896T>A (p.Ile299Asn)	not specified [RCV004683636]	uncertain significance	19	17489017	17489017	Human		name
407509498	CV3474119	single nucleotide variant	NM_198580.3(SLC27A1):c.718A>C (p.Met240Leu)	not specified [RCV004672419]	uncertain significance	19	17487329	17487329	Human		name
597701075	CV3606579	single nucleotide variant	NM_198580.3(SLC27A1):c.816C>A (p.Phe272Leu)	not specified [RCV004859940]	uncertain significance	19	17488869	17488869	Human		name
598169555	CV3918377	single nucleotide variant	NM_198580.3(SLC27A1):c.563C>T (p.Ala188Val)	not specified [RCV005284304]	uncertain significance	19	17487174	17487174	Human		name
598169580	CV3918385	single nucleotide variant	NM_198580.3(SLC27A1):c.821A>G (p.His274Arg)	not specified [RCV005284310]	uncertain significance	19	17488874	17488874	Human		name
156314155	CV2196602	single nucleotide variant	NM_198580.3(SLC27A1):c.1532C>T (p.Thr511Ile)	not specified [RCV004073876]	uncertain significance	19	17500772	17500772	Human		name
156247694	CV2221914	single nucleotide variant	NM_198580.3(SLC27A1):c.1093G>C (p.Gly365Arg)	not specified [RCV004102926]	uncertain significance	19	17497351	17497351	Human		name
155945167	CV2269506	single nucleotide variant	NM_198580.3(SLC27A1):c.1597G>A (p.Gly533Ser)	not specified [RCV004124616]	uncertain significance	19	17500837	17500837	Human		name
155915817	CV2274404	single nucleotide variant	NM_198580.3(SLC27A1):c.1579G>A (p.Val527Met)	not specified [RCV004136776]	uncertain significance	19	17500819	17500819	Human		name
156132236	CV2280034	single nucleotide variant	NM_198580.3(SLC27A1):c.1000G>A (p.Val334Ile)	not specified [RCV004146395]	uncertain significance	19	17497258	17497258	Human		name
156183600	CV2294811	single nucleotide variant	NM_198580.3(SLC27A1):c.1742G>A (p.Arg581Gln)	not specified [RCV004162322]	uncertain significance	19	17501378	17501378	Human		name
156396291	CV2326197	single nucleotide variant	NM_198580.3(SLC27A1):c.1547G>A (p.Gly516Glu)	not specified [RCV004180464]	uncertain significance	19	17500787	17500787	Human		name
156065696	CV2348885	single nucleotide variant	NM_198580.3(SLC27A1):c.1666G>A (p.Val556Ile)	not specified [RCV004203321]	likely benign	19	17501302	17501302	Human		name
156259665	CV2381006	single nucleotide variant	NM_198580.3(SLC27A1):c.1835G>A (p.Arg612His)	not specified [RCV004225047]	uncertain significance	19	17504506	17504506	Human		name
401756198	CV2686332	single nucleotide variant	NM_198580.3(SLC27A1):c.1805C>T (p.Thr602Met)	not specified [RCV004297408]	uncertain significance	19	17504476	17504476	Human		name
401762458	CV2696133	single nucleotide variant	NM_198580.3(SLC27A1):c.1477G>A (p.Val493Met)	not specified [RCV004310193]	uncertain significance	19	17500717	17500717	Human		name
405769555	CV3321918	single nucleotide variant	NM_198580.3(SLC27A1):c.1055C>T (p.Ala352Val)	not specified [RCV004456737]	uncertain significance	19	17497313	17497313	Human		name
405769559	CV3321919	single nucleotide variant	NM_198580.3(SLC27A1):c.1135G>C (p.Gly379Arg)	not specified [RCV004456738]	uncertain significance	19	17497393	17497393	Human		name
405769565	CV3321920	single nucleotide variant	NM_198580.3(SLC27A1):c.1258C>G (p.Arg420Gly)	not specified [RCV004456739]	uncertain significance	19	17500329	17500329	Human		name
405769570	CV3321921	single nucleotide variant	NM_198580.3(SLC27A1):c.1312C>T (p.Leu438Phe)	not specified [RCV004456740]	uncertain significance	19	17500383	17500383	Human		name
405769577	CV3321922	single nucleotide variant	NM_198580.3(SLC27A1):c.1376C>T (p.Pro459Leu)	not specified [RCV004456741]	uncertain significance	19	17500537	17500537	Human		name
405769583	CV3321923	single nucleotide variant	NM_198580.3(SLC27A1):c.1538G>A (p.Arg513His)	not specified [RCV004456742]	uncertain significance	19	17500778	17500778	Human		name
405769588	CV3321924	single nucleotide variant	NM_198580.3(SLC27A1):c.1741C>T (p.Arg581Trp)	not specified [RCV004456743]	uncertain significance	19	17501377	17501377	Human		name
405769594	CV3321925	single nucleotide variant	NM_198580.3(SLC27A1):c.1817G>A (p.Arg606Gln)	not specified [RCV004456744]	uncertain significance	19	17504488	17504488	Human		name
407509617	CV3474110	single nucleotide variant	NM_198580.3(SLC27A1):c.1797C>G (p.Ile599Met)	not specified [RCV004672411]	uncertain significance	19	17504468	17504468	Human		name
407509614	CV3474111	single nucleotide variant	NM_198580.3(SLC27A1):c.1051G>A (p.Glu351Lys)	not specified [RCV004672412]	uncertain significance	19	17497309	17497309	Human		name
407509483	CV3474114	single nucleotide variant	NM_198580.3(SLC27A1):c.1382G>A (p.Arg461His)	not specified [RCV004672415]	uncertain significance	19	17500543	17500543	Human		name
407509490	CV3474116	single nucleotide variant	NM_198580.3(SLC27A1):c.1909A>G (p.Thr637Ala)	not specified [RCV004672417]	uncertain significance	19	17504580	17504580	Human		name
597755146	CV3606568	single nucleotide variant	NM_198580.3(SLC27A1):c.1736A>C (p.Tyr579Ser)	not specified [RCV004868073]	uncertain significance	19	17501372	17501372	Human		name
597755150	CV3606569	single nucleotide variant	NM_198580.3(SLC27A1):c.1589G>A (p.Arg530His)	not specified [RCV004868074]	uncertain significance	19	17500829	17500829	Human		name
597701023	CV3606571	single nucleotide variant	NM_198580.3(SLC27A1):c.1262T>C (p.Leu421Pro)	not specified [RCV004859934]	uncertain significance	19	17500333	17500333	Human		name
597701032	CV3606574	single nucleotide variant	NM_198580.3(SLC27A1):c.1115A>G (p.Glu372Gly)	not specified [RCV004859935]	uncertain significance	19	17497373	17497373	Human		name
597701040	CV3606575	single nucleotide variant	NM_198580.3(SLC27A1):c.1201G>C (p.Gly401Arg)	not specified [RCV004859936]	uncertain significance	19	17497459	17497459	Human		name
597701058	CV3606577	single nucleotide variant	NM_198580.3(SLC27A1):c.1585A>G (p.Ser529Gly)	not specified [RCV004859938]	uncertain significance	19	17500825	17500825	Human		name
597701067	CV3606578	single nucleotide variant	NM_198580.3(SLC27A1):c.1693C>T (p.Pro565Ser)	not specified [RCV004859939]	uncertain significance	19	17501329	17501329	Human		name
598169547	CV3918375	single nucleotide variant	NM_198580.3(SLC27A1):c.1555G>T (p.Val519Phe)	not specified [RCV005284302]	uncertain significance	19	17500795	17500795	Human		name
598169551	CV3918376	single nucleotide variant	NM_198580.3(SLC27A1):c.1871A>G (p.Lys624Arg)	not specified [RCV005284303]	uncertain significance	19	17504542	17504542	Human		name
598169559	CV3918378	single nucleotide variant	NM_198580.3(SLC27A1):c.1927G>A (p.Ala643Thr)	not specified [RCV005284305]	uncertain significance	19	17504598	17504598	Human		name
598236963	CV3918380	single nucleotide variant	NM_198580.3(SLC27A1):c.1505T>C (p.Met502Thr)	not specified [RCV005275557]	uncertain significance	19	17500745	17500745	Human		name
598169563	CV3918381	single nucleotide variant	NM_198580.3(SLC27A1):c.1231C>T (p.Arg411Cys)	not specified [RCV005284306]	uncertain significance	19	17500302	17500302	Human		name
598169567	CV3918382	single nucleotide variant	NM_198580.3(SLC27A1):c.1285A>G (p.Met429Val)	not specified [RCV005284307]	uncertain significance	19	17500356	17500356	Human		name
598169572	CV3918383	single nucleotide variant	NM_198580.3(SLC27A1):c.1634C>T (p.Pro545Leu)	not specified [RCV005284308]	uncertain significance	19	17500874	17500874	Human		name
15187493	CV728022	single nucleotide variant	NM_198580.3(SLC27A1):c.1934C>T (p.Ala645Val)	not provided [RCV000887269]	benign	19	17504605	17504605	Human		name

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