Zxdb Variant Search Result - Rat Genome Database

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8587522	CV122153	single nucleotide variant	NM_007157.3(ZXDB):c.-1634C>A	Lung cancer [RCV000102673]	uncertain significance	X	57590415	57590415	Human		name
401919123	CV2829119	single nucleotide variant	NM_007157.4(ZXDB):c.267C>T (p.Gly89=)	not provided [RCV003430570]	likely benign	X	57592315	57592315	Human		name
405689661	CV3351549	single nucleotide variant	NM_007157.4(ZXDB):c.19C>T (p.Leu7Phe)	not specified [RCV004490499]	uncertain significance	X	57592067	57592067	Human		name
156247579	CV2276890	single nucleotide variant	NM_007157.4(ZXDB):c.70G>A (p.Gly24Ser)	not specified [RCV004140232]	uncertain significance	X	57592118	57592118	Human		name
401919125	CV2829120	single nucleotide variant	NM_007157.4(ZXDB):c.498G>A (p.Ala166=)	not provided [RCV003430571]	likely benign	X	57592546	57592546	Human		name
401919127	CV2829121	single nucleotide variant	NM_007157.4(ZXDB):c.792C>T (p.Ser264=)	not provided [RCV003430572]	likely benign	X	57592840	57592840	Human		name
401919129	CV2829122	single nucleotide variant	NM_007157.4(ZXDB):c.795C>T (p.Gly265=)	not provided [RCV003430573]	likely benign	X	57592843	57592843	Human		name
156219294	CV2254036	single nucleotide variant	NM_007157.4(ZXDB):c.203G>A (p.Gly68Asp)	not specified [RCV004129489]	uncertain significance	X	57592251	57592251	Human		name
155971199	CV2334186	single nucleotide variant	NM_007157.4(ZXDB):c.257G>T (p.Gly86Val)	not specified [RCV004186173]	uncertain significance	X	57592305	57592305	Human		name
156281428	CV2338461	single nucleotide variant	NM_007157.4(ZXDB):c.222G>C (p.Leu74Phe)	not provided [RCV003434636]\|not specified [RCV004186503]	likely benign\|uncertain significance	X	57592270	57592270	Human		name
329368843	CV2450435	single nucleotide variant	NM_007157.4(ZXDB):c.119C>T (p.Pro40Leu)	not specified [RCV004265361]	uncertain significance	X	57592167	57592167	Human		name
401780101	CV2725873	single nucleotide variant	NM_007157.4(ZXDB):c.125G>A (p.Arg42His)	not specified [RCV004324257]	uncertain significance	X	57592173	57592173	Human		name
401868404	CV2767228	single nucleotide variant	NM_007157.4(ZXDB):c.200G>C (p.Arg67Pro)	not specified [RCV004349407]	uncertain significance	X	57592248	57592248	Human		name
401919116	CV2829116	single nucleotide variant	NM_007157.4(ZXDB):c.232A>C (p.Thr78Pro)	not provided [RCV003430567]	likely benign	X	57592280	57592280	Human		name
401919118	CV2829117	single nucleotide variant	NM_007157.4(ZXDB):c.235G>C (p.Asp79His)	not provided [RCV003430568]	likely benign	X	57592283	57592283	Human		name
401919131	CV2829123	single nucleotide variant	NM_007157.4(ZXDB):c.1284T>C (p.Phe428=)	not provided [RCV003430574]	likely benign	X	57593332	57593332	Human		name
401919133	CV2829124	single nucleotide variant	NM_007157.4(ZXDB):c.1299A>G (p.Lys433=)	not provided [RCV003430575]	likely benign	X	57593347	57593347	Human		name
401919136	CV2829125	single nucleotide variant	NM_007157.4(ZXDB):c.2220G>A (p.Ser740=)	not provided [RCV003430576]	likely benign	X	57594268	57594268	Human		name
405689638	CV3351544	single nucleotide variant	NM_007157.4(ZXDB):c.121A>C (p.Thr41Pro)	not specified [RCV004490494]	uncertain significance	X	57592169	57592169	Human		name
405689643	CV3351545	single nucleotide variant	NM_007157.4(ZXDB):c.151C>G (p.Gln51Glu)	not specified [RCV004490495]	uncertain significance	X	57592199	57592199	Human		name
407493839	CV3421174	single nucleotide variant	NM_007157.4(ZXDB):c.244A>G (p.Ser82Gly)	not specified [RCV004605447]	likely benign	X	57592292	57592292	Human		name
597758866	CV3642631	single nucleotide variant	NM_007157.4(ZXDB):c.118C>T (p.Pro40Ser)	not specified [RCV004894400]	uncertain significance	X	57592166	57592166	Human		name
598201268	CV3938474	single nucleotide variant	NM_007157.4(ZXDB):c.200G>T (p.Arg67Leu)	not specified [RCV005314198]	uncertain significance	X	57592248	57592248	Human		name
156169348	CV2276734	single nucleotide variant	NM_007157.4(ZXDB):c.371G>T (p.Gly124Val)	not specified [RCV004146520]	uncertain significance	X	57592419	57592419	Human		name
156280929	CV2295077	single nucleotide variant	NM_007157.4(ZXDB):c.323G>C (p.Gly108Ala)	not specified [RCV004156190]	uncertain significance	X	57592371	57592371	Human		name
156098285	CV2306447	single nucleotide variant	NM_007157.4(ZXDB):c.665G>A (p.Gly222Asp)	not specified [RCV004157071]	uncertain significance	X	57592713	57592713	Human		name
156086758	CV2336797	single nucleotide variant	NM_007157.4(ZXDB):c.659A>C (p.His220Pro)	not specified [RCV004190420]	uncertain significance	X	57592707	57592707	Human		name
155978139	CV2338934	single nucleotide variant	NM_007157.4(ZXDB):c.799G>T (p.Gly267Cys)	not specified [RCV004184524]	uncertain significance	X	57592847	57592847	Human		name
156274942	CV2351767	single nucleotide variant	NM_007157.4(ZXDB):c.434G>A (p.Arg145His)	not specified [RCV004197925]	uncertain significance	X	57592482	57592482	Human		name
155908036	CV2354554	single nucleotide variant	NM_007157.4(ZXDB):c.580G>C (p.Ala194Pro)	not specified [RCV004202531]	uncertain significance	X	57592628	57592628	Human		name
156179697	CV2356031	single nucleotide variant	NM_007157.4(ZXDB):c.547G>C (p.Gly183Arg)	not specified [RCV004201405]	uncertain significance	X	57592595	57592595	Human		name
155936527	CV2379845	single nucleotide variant	NM_007157.4(ZXDB):c.425T>A (p.Leu142Gln)	not specified [RCV004219955]	uncertain significance	X	57592473	57592473	Human		name
156109934	CV2387572	single nucleotide variant	NM_007157.4(ZXDB):c.401C>T (p.Ala134Val)	not specified [RCV004234126]	uncertain significance	X	57592449	57592449	Human		name
156218566	CV2393500	single nucleotide variant	NM_007157.4(ZXDB):c.351G>T (p.Leu117Phe)	not specified [RCV004229277]	uncertain significance	X	57592399	57592399	Human		name
156158837	CV2398069	single nucleotide variant	NM_007157.4(ZXDB):c.418A>T (p.Thr140Ser)	not specified [RCV004241658]	uncertain significance	X	57592466	57592466	Human		name
401735542	CV2672679	single nucleotide variant	NM_007157.4(ZXDB):c.895C>A (p.Gln299Lys)	not specified [RCV004287694]	uncertain significance	X	57592943	57592943	Human		name
401773243	CV2698145	single nucleotide variant	NM_007157.4(ZXDB):c.725C>T (p.Ala242Val)	not specified [RCV004302928]	uncertain significance	X	57592773	57592773	Human		name
401752954	CV2703599	single nucleotide variant	NM_007157.4(ZXDB):c.328G>A (p.Gly110Ser)	not specified [RCV004317765]	uncertain significance	X	57592376	57592376	Human		name
401752957	CV2703600	single nucleotide variant	NM_007157.4(ZXDB):c.337G>A (p.Ala113Thr)	not specified [RCV004317766]	likely benign	X	57592385	57592385	Human		name
401772548	CV2712790	single nucleotide variant	NM_007157.4(ZXDB):c.683C>G (p.Pro228Arg)	not specified [RCV004314219]	uncertain significance	X	57592731	57592731	Human		name
401859003	CV2775038	single nucleotide variant	NM_007157.4(ZXDB):c.836G>C (p.Gly279Ala)	not specified [RCV004346419]	uncertain significance	X	57592884	57592884	Human		name
405689675	CV3351552	single nucleotide variant	NM_007157.4(ZXDB):c.540T>G (p.Phe180Leu)	not specified [RCV004490502]	uncertain significance	X	57592588	57592588	Human		name
405689680	CV3351553	single nucleotide variant	NM_007157.4(ZXDB):c.590C>T (p.Pro197Leu)	not specified [RCV004490503]	uncertain significance	X	57592638	57592638	Human		name
405689686	CV3351554	single nucleotide variant	NM_007157.4(ZXDB):c.616G>A (p.Gly206Arg)	not specified [RCV004490504]	uncertain significance	X	57592664	57592664	Human		name
405689691	CV3351555	single nucleotide variant	NM_007157.4(ZXDB):c.662C>T (p.Pro221Leu)	not specified [RCV004490505]	uncertain significance	X	57592710	57592710	Human		name
405689698	CV3351556	single nucleotide variant	NM_007157.4(ZXDB):c.755C>T (p.Pro252Leu)	not specified [RCV004490506]	uncertain significance	X	57592803	57592803	Human		name
405689703	CV3351557	single nucleotide variant	NM_007157.4(ZXDB):c.782C>T (p.Pro261Leu)	not specified [RCV004490507]	uncertain significance	X	57592830	57592830	Human		name
407493829	CV3421170	single nucleotide variant	NM_007157.4(ZXDB):c.541G>C (p.Glu181Gln)	not specified [RCV004605444]	uncertain significance	X	57592589	57592589	Human		name
407493846	CV3421176	single nucleotide variant	NM_007157.4(ZXDB):c.796C>T (p.Pro266Ser)	not specified [RCV004605449]	uncertain significance	X	57592844	57592844	Human		name
597758828	CV3642624	single nucleotide variant	NM_007157.4(ZXDB):c.547G>A (p.Gly183Ser)	not specified [RCV004894393]	uncertain significance	X	57592595	57592595	Human		name
597758834	CV3642625	single nucleotide variant	NM_007157.4(ZXDB):c.410C>T (p.Ala137Val)	not specified [RCV004894394]	uncertain significance	X	57592458	57592458	Human		name
597758856	CV3642629	single nucleotide variant	NM_007157.4(ZXDB):c.793G>C (p.Gly265Arg)	not specified [RCV004894398]	uncertain significance	X	57592841	57592841	Human		name
597758861	CV3642630	single nucleotide variant	NM_007157.4(ZXDB):c.398G>T (p.Gly133Val)	not specified [RCV004894399]	uncertain significance	X	57592446	57592446	Human		name
598276519	CV3938470	single nucleotide variant	NM_007157.4(ZXDB):c.571C>T (p.Pro191Ser)	not specified [RCV005305653]	uncertain significance	X	57592619	57592619	Human		name
598201248	CV3938471	single nucleotide variant	NM_007157.4(ZXDB):c.578A>C (p.His193Pro)	not specified [RCV005314195]	likely benign	X	57592626	57592626	Human		name
598201255	CV3938472	single nucleotide variant	NM_007157.4(ZXDB):c.384G>C (p.Gln128His)	not specified [RCV005314196]	uncertain significance	X	57592432	57592432	Human		name
598201277	CV3938476	single nucleotide variant	NM_007157.4(ZXDB):c.461C>T (p.Ala154Val)	not specified [RCV005314200]	uncertain significance	X	57592509	57592509	Human		name
598201283	CV3938477	single nucleotide variant	NM_007157.4(ZXDB):c.310G>T (p.Val104Leu)	not specified [RCV005314201]	uncertain significance	X	57592358	57592358	Human		name
598201296	CV3938479	single nucleotide variant	NM_007157.4(ZXDB):c.515A>C (p.His172Pro)	not specified [RCV005314203]	uncertain significance	X	57592563	57592563	Human		name
156238914	CV2217115	single nucleotide variant	NM_007157.4(ZXDB):c.1543G>A (p.Val515Met)	not specified [RCV004085790]	uncertain significance	X	57593591	57593591	Human		name
156400766	CV2217151	single nucleotide variant	NM_007157.4(ZXDB):c.1556C>T (p.Ala519Val)	not specified [RCV004085821]	uncertain significance	X	57593604	57593604	Human		name
156237302	CV2224198	single nucleotide variant	NM_007157.4(ZXDB):c.1912G>A (p.Ala638Thr)	not specified [RCV004096041]	uncertain significance	X	57593960	57593960	Human		name
156043817	CV2237554	single nucleotide variant	NM_007157.4(ZXDB):c.1922G>A (p.Ser641Asn)	not specified [RCV004106495]	uncertain significance	X	57593970	57593970	Human		name
155906789	CV2279428	single nucleotide variant	NM_007157.4(ZXDB):c.2101G>T (p.Val701Leu)	not specified [RCV004141969]	uncertain significance	X	57594149	57594149	Human		name
156193120	CV2296931	single nucleotide variant	NM_007157.4(ZXDB):c.1113G>C (p.Glu371Asp)	not specified [RCV004149078]	uncertain significance	X	57593161	57593161	Human		name
156301491	CV2322774	single nucleotide variant	NM_007157.4(ZXDB):c.1721T>C (p.Val574Ala)	not specified [RCV004182881]	uncertain significance	X	57593769	57593769	Human		name
156279901	CV2348395	single nucleotide variant	NM_007157.4(ZXDB):c.2035C>G (p.Leu679Val)	not specified [RCV004193588]	uncertain significance	X	57594083	57594083	Human		name
155966126	CV2396030	single nucleotide variant	NM_007157.4(ZXDB):c.2270C>T (p.Ala757Val)	not specified [RCV004237572]	uncertain significance	X	57594318	57594318	Human		name
329383699	CV2434849	single nucleotide variant	NM_007157.4(ZXDB):c.1714C>A (p.His572Asn)	not specified [RCV004250726]	uncertain significance	X	57593762	57593762	Human		name
329360958	CV2439703	single nucleotide variant	NM_007157.4(ZXDB):c.2329G>A (p.Gly777Arg)	not specified [RCV004255715]	uncertain significance	X	57594377	57594377	Human		name
405689616	CV3351540	single nucleotide variant	NM_007157.4(ZXDB):c.1010C>A (p.Pro337Gln)	not specified [RCV004490490]	uncertain significance	X	57593058	57593058	Human		name
405689623	CV3351541	single nucleotide variant	NM_007157.4(ZXDB):c.1069G>A (p.Gly357Ser)	not specified [RCV004490491]	uncertain significance	X	57593117	57593117	Human		name
405689632	CV3351543	single nucleotide variant	NM_007157.4(ZXDB):c.1138A>G (p.Ser380Gly)	not specified [RCV004490493]	uncertain significance	X	57593186	57593186	Human		name
405689648	CV3351546	single nucleotide variant	NM_007157.4(ZXDB):c.1702A>G (p.Met568Val)	not specified [RCV004490496]	uncertain significance	X	57593750	57593750	Human		name
405689651	CV3351547	single nucleotide variant	NM_007157.4(ZXDB):c.1754C>A (p.Ala585Glu)	not specified [RCV004490497]	uncertain significance	X	57593802	57593802	Human		name
405689657	CV3351548	single nucleotide variant	NM_007157.4(ZXDB):c.1819A>G (p.Ile607Val)	not specified [RCV004490498]	uncertain significance	X	57593867	57593867	Human		name
405689666	CV3351550	single nucleotide variant	NM_007157.4(ZXDB):c.2369A>C (p.Glu790Ala)	not specified [RCV004490500]	uncertain significance	X	57594417	57594417	Human		name
407499761	CV3421168	single nucleotide variant	NM_007157.4(ZXDB):c.2098A>G (p.Ser700Gly)	not specified [RCV004606954]	uncertain significance	X	57594146	57594146	Human		name
407493824	CV3421169	single nucleotide variant	NM_007157.4(ZXDB):c.2126T>C (p.Leu709Pro)	not specified [RCV004605443]	uncertain significance	X	57594174	57594174	Human		name
407493832	CV3421171	single nucleotide variant	NM_007157.4(ZXDB):c.2281G>A (p.Val761Ile)	not specified [RCV004605445]	uncertain significance	X	57594329	57594329	Human		name
407493836	CV3421172	single nucleotide variant	NM_007157.4(ZXDB):c.1810G>A (p.Asp604Asn)	not specified [RCV004605446]	uncertain significance	X	57593858	57593858	Human		name
407499765	CV3421173	single nucleotide variant	NM_007157.4(ZXDB):c.1348G>A (p.Gly450Ser)	not specified [RCV004606955]	uncertain significance	X	57593396	57593396	Human		name
597758840	CV3642626	single nucleotide variant	NM_007157.4(ZXDB):c.2207C>T (p.Ala736Val)	not specified [RCV004894395]	uncertain significance	X	57594255	57594255	Human		name
597758845	CV3642627	single nucleotide variant	NM_007157.4(ZXDB):c.2281G>T (p.Val761Leu)	not specified [RCV004894396]	uncertain significance	X	57594329	57594329	Human		name
597758850	CV3642628	single nucleotide variant	NM_007157.4(ZXDB):c.1385G>A (p.Gly462Asp)	not specified [RCV004894397]	uncertain significance	X	57593433	57593433	Human		name
597758871	CV3642632	single nucleotide variant	NM_007157.4(ZXDB):c.2375A>C (p.Asp792Ala)	not specified [RCV004894401]	uncertain significance	X	57594423	57594423	Human		name
597758876	CV3642633	single nucleotide variant	NM_007157.4(ZXDB):c.1682A>G (p.Lys561Arg)	not specified [RCV004894402]	uncertain significance	X	57593730	57593730	Human		name
598201262	CV3938473	single nucleotide variant	NM_007157.4(ZXDB):c.1121C>T (p.Pro374Leu)	not specified [RCV005314197]	uncertain significance	X	57593169	57593169	Human		name
598201273	CV3938475	single nucleotide variant	NM_007157.4(ZXDB):c.1966G>A (p.Val656Ile)	not specified [RCV005314199]	uncertain significance	X	57594014	57594014	Human		name
401919121	CV2829118	microsatellite	NM_007157.4(ZXDB):c.245GCG[4] (p.Gly86_Gly89del)	not provided [RCV003430569]	likely benign	X	57592293	57592304	Human		name

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