Acly Variant Search Result - Rat Genome Database

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79 records found for search term Acly

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8621456	CV75430	single nucleotide variant	NM_001096.3(ACLY):c.-67C>T	not provided [RCV000054652]	uncertain significance	17	41918923	41918923	Human		name
15178578	CV731149	single nucleotide variant	NM_001096.3(ACLY):c.866+7G>A	not provided [RCV000885093]	benign	17	41906521	41906521	Human		name
156000880	CV2378751	single nucleotide variant	NM_001096.3(ACLY):c.29C>T (p.Thr10Met)	not specified [RCV004231206]	uncertain significance	17	41913845	41913845	Human		name
401935769	CV2811354	single nucleotide variant	NM_001096.3(ACLY):c.807G>C (p.Leu269=)	not provided [RCV003413230]	likely benign	17	41906587	41906587	Human		name
597717151	CV3646580	single nucleotide variant	NM_001096.3(ACLY):c.70G>A (p.Ala24Thr)	not specified [RCV004887375]	uncertain significance	17	41913804	41913804	Human		name
15189394	CV704143	single nucleotide variant	NM_001096.3(ACLY):c.942G>A (p.Gln314=)	not provided [RCV000954162]	benign	17	41905583	41905583	Human		name
15190825	CV727175	single nucleotide variant	NM_001096.3(ACLY):c.858C>T (p.Val286=)	not provided [RCV000888207]	benign	17	41906536	41906536	Human		name
8621463	CV75437	single nucleotide variant	NM_001096.3(ACLY):c.465C>A (p.Gly155=)	not provided [RCV000054659]	uncertain significance	17	41909581	41909581	Human		name
8621465	CV75439	single nucleotide variant	NM_001096.3(ACLY):c.789C>T (p.Ser263=)	not provided [RCV000054661]	uncertain significance	17	41906605	41906605	Human		name
155982548	CV2272979	single nucleotide variant	NM_001096.3(ACLY):c.193C>T (p.Arg65Cys)	not specified [RCV004137646]	uncertain significance	17	41912509	41912509	Human		name
156123911	CV2350064	single nucleotide variant	NM_001096.3(ACLY):c.281C>T (p.Thr94Ile)	not specified [RCV004199989]	uncertain significance	17	41912421	41912421	Human		name
405767803	CV3298737	single nucleotide variant	NM_001096.3(ACLY):c.224A>C (p.Asn75Thr)	not specified [RCV004434752]	uncertain significance	17	41912478	41912478	Human		name
15165956	CV715454	single nucleotide variant	NM_001096.3(ACLY):c.2412C>T (p.Leu804=)	not provided [RCV000971063]	benign	17	41878178	41878178	Human		name
8621457	CV75431	single nucleotide variant	NM_001096.3(ACLY):c.1122A>C (p.Thr374=)	not provided [RCV000054653]	uncertain significance	17	41901757	41901757	Human		name
8621458	CV75432	single nucleotide variant	NM_001096.3(ACLY):c.1395G>A (p.Ala465=)	not provided [RCV000054654]	uncertain significance	17	41897783	41897783	Human		name
8621462	CV75436	single nucleotide variant	NM_001096.3(ACLY):c.2895G>A (p.Lys965=)	not provided [RCV000054658]	uncertain significance	17	41871731	41871731	Human		name
15119874	CV755836	single nucleotide variant	NM_001096.3(ACLY):c.1650C>T (p.Ile550=)	not provided [RCV000918215]	benign	17	41892399	41892399	Human		name
155948442	CV2272145	single nucleotide variant	NM_001096.3(ACLY):c.709G>A (p.Glu237Lys)	not specified [RCV004124923]	uncertain significance	17	41907480	41907480	Human		name
156030866	CV2278759	single nucleotide variant	NM_001096.3(ACLY):c.385G>A (p.Gly129Arg)	not specified [RCV004134944]	uncertain significance	17	41909661	41909661	Human		name
156347372	CV2382884	single nucleotide variant	NM_001096.3(ACLY):c.517G>T (p.Ala173Ser)	not specified [RCV004217482]	uncertain significance	17	41909529	41909529	Human		name
329370833	CV2435701	single nucleotide variant	NM_001096.3(ACLY):c.517G>A (p.Ala173Thr)	not specified [RCV004254934]	uncertain significance	17	41909529	41909529	Human		name
329382117	CV2467512	single nucleotide variant	NM_001096.3(ACLY):c.714C>A (p.Phe238Leu)	not specified [RCV004287114]	uncertain significance	17	41907475	41907475	Human		name
401723714	CV2675052	single nucleotide variant	NM_001096.3(ACLY):c.371A>G (p.Tyr124Cys)	not specified [RCV004296349]	uncertain significance	17	41909675	41909675	Human		name
401762920	CV2710371	single nucleotide variant	NM_001096.3(ACLY):c.466G>A (p.Val156Met)	not specified [RCV004317536]	uncertain significance	17	41909580	41909580	Human		name
401774417	CV2713434	single nucleotide variant	NM_001096.3(ACLY):c.490G>T (p.Asp164Tyr)	not specified [RCV004319050]	uncertain significance	17	41909556	41909556	Human		name
405768020	CV3298773	single nucleotide variant	NM_001096.3(ACLY):c.409G>A (p.Glu137Lys)	not specified [RCV004434788]	uncertain significance	17	41909637	41909637	Human		name
405768037	CV3298776	single nucleotide variant	NM_001096.3(ACLY):c.451A>C (p.Lys151Gln)	not specified [RCV004434791]	uncertain significance	17	41909595	41909595	Human		name
405768162	CV3298797	single nucleotide variant	NM_001096.3(ACLY):c.985C>G (p.Arg329Gly)	not specified [RCV004434812]	uncertain significance	17	41905540	41905540	Human		name
597716710	CV3646535	single nucleotide variant	NM_001096.3(ACLY):c.661G>A (p.Val221Met)	not specified [RCV004887331]	uncertain significance	17	41907528	41907528	Human		name
597717269	CV3646591	single nucleotide variant	NM_001096.3(ACLY):c.721C>G (p.Pro241Ala)	not specified [RCV004887386]	uncertain significance	17	41907468	41907468	Human		name
597717382	CV3646602	single nucleotide variant	NM_001096.3(ACLY):c.897C>A (p.Asn299Lys)	not specified [RCV004887397]	uncertain significance	17	41905628	41905628	Human		name
597717600	CV3646623	single nucleotide variant	NM_001096.3(ACLY):c.703G>A (p.Asp235Asn)	not specified [RCV004887418]	uncertain significance	17	41907486	41907486	Human		name
598276643	CV3938696	single nucleotide variant	NM_001096.3(ACLY):c.569A>G (p.Asn190Ser)	not specified [RCV005305777]	uncertain significance	17	41909036	41909036	Human		name
598276670	CV3938744	single nucleotide variant	NM_001096.3(ACLY):c.512T>A (p.Val171Asp)	not specified [RCV005305804]	uncertain significance	17	41909534	41909534	Human		name
8621464	CV75438	single nucleotide variant	NM_001096.3(ACLY):c.652G>A (p.Ala218Thr)	not provided [RCV000054660]	uncertain significance	17	41907537	41907537	Human		name
156369717	CV2194062	single nucleotide variant	NM_001096.3(ACLY):c.1825C>A (p.Leu609Met)	not specified [RCV004076824]	uncertain significance	17	41887649	41887649	Human		name
156044500	CV2237684	single nucleotide variant	NM_001096.3(ACLY):c.1090T>G (p.Tyr364Asp)	not specified [RCV004106609]	uncertain significance	17	41901789	41901789	Human		name
155996451	CV2250456	single nucleotide variant	NM_001096.3(ACLY):c.1783G>A (p.Ala595Thr)	not specified [RCV004127325]	uncertain significance	17	41887691	41887691	Human		name
156195030	CV2251801	single nucleotide variant	NM_001096.3(ACLY):c.1859T>G (p.Ile620Ser)	not specified [RCV004119792]	uncertain significance	17	41887615	41887615	Human		name
156152805	CV2265942	single nucleotide variant	NM_001096.3(ACLY):c.2869A>G (p.Met957Val)	not specified [RCV004126787]	uncertain significance	17	41871757	41871757	Human		name
156111725	CV2267298	single nucleotide variant	NM_001096.3(ACLY):c.1948A>C (p.Lys650Gln)	not specified [RCV004133971]	uncertain significance	17	41886236	41886236	Human		name
156341047	CV2268212	single nucleotide variant	NM_001096.3(ACLY):c.1582G>A (p.Ala528Thr)	not specified [RCV004138518]	uncertain significance	17	41893052	41893052	Human		name
156022481	CV2273653	single nucleotide variant	NM_001096.3(ACLY):c.1670C>T (p.Ala557Val)	not specified [RCV004132319]	uncertain significance	17	41892379	41892379	Human		name
156075932	CV2291457	single nucleotide variant	NM_001096.3(ACLY):c.2420A>G (p.Asn807Ser)	not specified [RCV004155779]	uncertain significance	17	41878170	41878170	Human		name
156279216	CV2316739	single nucleotide variant	NM_001096.3(ACLY):c.2405A>G (p.Glu802Gly)	not specified [RCV004171961]	uncertain significance	17	41878185	41878185	Human		name
156305537	CV2338830	single nucleotide variant	NM_001096.3(ACLY):c.2186G>A (p.Arg729Gln)	not specified [RCV004182385]	uncertain significance	17	41883201	41883201	Human		name
155926904	CV2395889	single nucleotide variant	NM_001096.3(ACLY):c.1390G>A (p.Val464Met)	not specified [RCV004237448]	uncertain significance	17	41897788	41897788	Human		name
329366200	CV2438221	single nucleotide variant	NM_001096.3(ACLY):c.1337C>T (p.Ser446Leu)	not specified [RCV004256988]	uncertain significance	17	41898632	41898632	Human		name
329380165	CV2444249	single nucleotide variant	NM_001096.3(ACLY):c.1265G>A (p.Arg422Gln)	not specified [RCV004263018]	uncertain significance	17	41898704	41898704	Human		name
329401142	CV2446184	single nucleotide variant	NM_001096.3(ACLY):c.2786T>C (p.Leu929Pro)	not specified [RCV004264593]	uncertain significance	17	41872039	41872039	Human		name
401745269	CV2681231	single nucleotide variant	NM_001096.3(ACLY):c.1414C>G (p.Pro472Ala)	not specified [RCV004289369]	uncertain significance	17	41897764	41897764	Human		name
401752336	CV2682785	single nucleotide variant	NM_001096.3(ACLY):c.2559C>G (p.Ile853Met)	not specified [RCV004281758]	uncertain significance	17	41873894	41873894	Human		name
401772230	CV2687456	single nucleotide variant	NM_001096.3(ACLY):c.1844A>T (p.Gln615Leu)	not specified [RCV004300700]	uncertain significance	17	41887630	41887630	Human		name
401775484	CV2692390	single nucleotide variant	NM_001096.3(ACLY):c.1887C>G (p.Ile629Met)	not specified [RCV004310366]	uncertain significance	17	41886297	41886297	Human		name
401856850	CV2755113	single nucleotide variant	NM_001096.3(ACLY):c.2297A>G (p.Asn766Ser)	not specified [RCV004335263]	uncertain significance	17	41878893	41878893	Human		name
401860705	CV2758586	single nucleotide variant	NM_001096.3(ACLY):c.1081A>G (p.Ile361Val)	not specified [RCV004337671]	uncertain significance	17	41901798	41901798	Human		name
405767707	CV3298720	single nucleotide variant	NM_001096.3(ACLY):c.2078C>T (p.Pro693Leu)	not specified [RCV004434735]	uncertain significance	17	41884269	41884269	Human		name
405767735	CV3298725	single nucleotide variant	NM_001096.3(ACLY):c.2083T>C (p.Ser695Pro)	not specified [RCV004434740]	uncertain significance	17	41884264	41884264	Human		name
405767755	CV3298729	single nucleotide variant	NM_001096.3(ACLY):c.2144T>C (p.Val715Ala)	not specified [RCV004434744]	uncertain significance	17	41884203	41884203	Human		name
405767779	CV3298733	single nucleotide variant	NM_001096.3(ACLY):c.2221G>A (p.Val741Ile)	not specified [RCV004434748]	uncertain significance	17	41883166	41883166	Human		name
405767484	CV3302683	single nucleotide variant	NM_001096.3(ACLY):c.1294G>A (p.Ala432Thr)	not specified [RCV004434697]	uncertain significance	17	41898675	41898675	Human		name
407481631	CV3421437	single nucleotide variant	NM_001096.3(ACLY):c.1015A>G (p.Ile339Val)	not specified [RCV004602505]	uncertain significance	17	41904779	41904779	Human		name
407481637	CV3421438	single nucleotide variant	NM_001096.3(ACLY):c.1190C>T (p.Thr397Ile)	not specified [RCV004602506]	uncertain significance	17	41898779	41898779	Human		name
407481652	CV3421440	single nucleotide variant	NM_001096.3(ACLY):c.1370C>T (p.Ser457Phe)	not specified [RCV004602508]	uncertain significance	17	41897808	41897808	Human		name
597716429	CV3646517	single nucleotide variant	NM_001096.3(ACLY):c.1648A>G (p.Ile550Val)	not specified [RCV004887324]	uncertain significance	17	41892401	41892401	Human		name
597716774	CV3646543	single nucleotide variant	NM_001096.3(ACLY):c.1483C>T (p.Arg495Cys)	not specified [RCV004887338]	uncertain significance	17	41893151	41893151	Human		name
597716857	CV3646551	single nucleotide variant	NM_001096.3(ACLY):c.1525G>A (p.Val509Met)	not specified [RCV004887346]	uncertain significance	17	41893109	41893109	Human		name
597717065	CV3646571	single nucleotide variant	NM_001096.3(ACLY):c.2377C>T (p.Leu793Phe)	not specified [RCV004887366]	uncertain significance	17	41878813	41878813	Human		name
597717486	CV3646612	single nucleotide variant	NM_001096.3(ACLY):c.2288C>T (p.Ala763Val)	not specified [RCV004887407]	uncertain significance	17	41878902	41878902	Human		name
598276651	CV3938714	single nucleotide variant	NM_001096.3(ACLY):c.2499G>C (p.Leu833Phe)	not specified [RCV005305785]	uncertain significance	17	41873954	41873954	Human		name
598276658	CV3938724	single nucleotide variant	NM_001096.3(ACLY):c.1489A>G (p.Thr497Ala)	not specified [RCV005305792]	uncertain significance	17	41893145	41893145	Human		name
598201810	CV3938734	single nucleotide variant	NM_001096.3(ACLY):c.1433C>T (p.Ser478Leu)	not specified [RCV005314314]	uncertain significance	17	41896646	41896646	Human		name
15177861	CV740745	single nucleotide variant	NM_001096.3(ACLY):c.2045A>G (p.Tyr682Cys)	not provided [RCV000906746]	likely benign	17	41886139	41886139	Human		name
8621459	CV75433	single nucleotide variant	NM_001096.3(ACLY):c.1484G>A (p.Arg495His)	not provided [RCV000054655]	uncertain significance	17	41893150	41893150	Human		name
8621460	CV75434	single nucleotide variant	NM_001096.3(ACLY):c.1765G>A (p.Ala589Thr)	not provided [RCV000054656]	uncertain significance	17	41892284	41892284	Human		name
8621461	CV75435	single nucleotide variant	NM_001096.3(ACLY):c.2747C>T (p.Ala916Val)	not provided [RCV000054657]	uncertain significance	17	41872078	41872078	Human		name
329367377	CV2456784	single nucleotide variant	NM_001096.3(ACLY):c.3155T>C (p.Ile1052Thr)	not specified [RCV004270757]	uncertain significance	17	41868765	41868765	Human		name
405767968	CV3298764	single nucleotide variant	NM_001096.3(ACLY):c.3013G>A (p.Asp1005Asn)	not specified [RCV004434779]	uncertain significance	17	41869512	41869512	Human		name
407481644	CV3421439	single nucleotide variant	NM_001096.3(ACLY):c.3065T>C (p.Ile1022Thr)	not specified [RCV004602507]	uncertain significance	17	41869112	41869112	Human		name

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