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83 records found for search term Elmo3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155984226CV2247739single nucleotide variantNM_024712.5(ELMO3):c.-11C>Tnot specified [RCV004121211]uncertain significance166719931667199316Humanname
329351640CV2459219single nucleotide variantNM_024712.5(ELMO3):c.-77G>Anot specified [RCV004274658]uncertain significance166719925067199250Humanname
597746979CV3670981single nucleotide variantNM_024712.5(ELMO3):c.-78G>Anot specified [RCV004922809]uncertain significance166719924967199249Humanname
597666506CV3670983single nucleotide variantNM_024712.5(ELMO3):c.-69G>Anot specified [RCV004912562]likely benign166719925867199258Humanname
598191153CV3957778single nucleotide variantNM_024712.5(ELMO3):c.-98G>Anot specified [RCV005334797]uncertain significance166719922967199229Humanname
156003633CV2290043single nucleotide variantNM_024712.5(ELMO3):c.-119C>Gnot specified [RCV004152734]likely benign166719920867199208Humanname
28877496CV860275single nucleotide variantNM_024712.5(ELMO3):c.1780+1G>Anot provided [RCV001090440]uncertain significance166720322467203224Humanname
155919344CV2360230single nucleotide variantNM_024712.5(ELMO3):c.4G>A (p.Ala2Thr)not specified [RCV004208578]likely benign166719933067199330Humanname
156015157CV2360231single nucleotide variantNM_024712.5(ELMO3):c.20T>C (p.Val7Ala)not specified [RCV004208579]uncertain significance166719934667199346Humanname
405738888CV3248546single nucleotide variantNM_024712.5(ELMO3):c.23T>C (p.Val8Ala)not specified [RCV004380249]uncertain significance166719934967199349Humanname
156113753CV2349148single nucleotide variantNM_024712.5(ELMO3):c.86C>T (p.Pro29Leu)not specified [RCV004205986]uncertain significance166719956067199560Humanname
401872785CV2764339single nucleotide variantNM_024712.5(ELMO3):c.43C>T (p.Arg15Cys)not specified [RCV004338912]uncertain significance166719936967199369Humanname
401911725CV2808029single nucleotide variantNM_024712.5(ELMO3):c.981G>A (p.Ser327=)not provided [RCV003426740]likely benign166720180467201804Humanname
407506675CV3438307single nucleotide variantNM_024712.5(ELMO3):c.52A>G (p.Ile18Val)not specified [RCV004624777]uncertain significance166719937867199378Humanname
598191113CV3957773single nucleotide variantNM_024712.5(ELMO3):c.92C>T (p.Ala31Val)not specified [RCV005334792]uncertain significance166719956667199566Humanname
156184473CV2349939single nucleotide variantNM_024712.5(ELMO3):c.191A>G (p.Asn64Ser)not specified [RCV004206351]uncertain significance166719975567199755Humanname
329359631CV2461581single nucleotide variantNM_024712.5(ELMO3):c.185C>T (p.Thr62Ile)not specified [RCV004269762]uncertain significance166719974967199749Humanname
401761700CV2726869single nucleotide variantNM_024712.5(ELMO3):c.241C>T (p.Pro81Ser)not specified [RCV004323163]uncertain significance166719999967199999Humanname
405738897CV3248547single nucleotide variantNM_024712.5(ELMO3):c.116A>G (p.Asp39Gly)not specified [RCV004380250]uncertain significance166719959067199590Humanname
405738903CV3248548single nucleotide variantNM_024712.5(ELMO3):c.241C>G (p.Pro81Ala)not specified [RCV004380251]uncertain significance166719999967199999Humanname
407506683CV3438310single nucleotide variantNM_024712.5(ELMO3):c.197G>A (p.Arg66His)not specified [RCV004624780]uncertain significance166719995567199955Humanname
597666436CV3670970single nucleotide variantNM_024712.5(ELMO3):c.113G>A (p.Cys38Tyr)not specified [RCV004912552]uncertain significance166719958767199587Humanname
597666466CV3670974single nucleotide variantNM_024712.5(ELMO3):c.151C>G (p.Leu51Val)not specified [RCV004912556]uncertain significance166719971567199715Humanname
156140485CV2212185single nucleotide variantNM_024712.5(ELMO3):c.866T>C (p.Met289Thr)not specified [RCV004089078]likely benign166720159067201590Humanname
155993890CV2252407single nucleotide variantNM_024712.5(ELMO3):c.940G>A (p.Val314Ile)not specified [RCV004116248]uncertain significance166720176367201763Humanname
156299825CV2326170single nucleotide variantNM_024712.5(ELMO3):c.469G>A (p.Gly157Ser)not specified [RCV004180439]uncertain significance166720050667200506Humanname
156002967CV2347740single nucleotide variantNM_024712.5(ELMO3):c.553G>A (p.Val185Met)not specified [RCV004202707]uncertain significance166720069667200696Humanname
156228189CV2392901single nucleotide variantNM_024712.5(ELMO3):c.886C>T (p.Arg296Cys)not specified [RCV004247250]uncertain significance166720161067201610Humanname
156448649CV2402058single nucleotide variantNM_024712.5(ELMO3):c.481T>G (p.Trp161Gly)not provided [RCV003120217]uncertain significance166720051867200518Humanname
329399183CV2436226single nucleotide variantNM_024712.5(ELMO3):c.791A>G (p.Tyr264Cys)not specified [RCV004249852]uncertain significance166720143167201431Humanname
401752861CV2682961single nucleotide variantNM_024712.5(ELMO3):c.896C>T (p.Thr299Met)not specified [RCV004283751]uncertain significance166720162067201620Humanname
401889945CV2765116single nucleotide variantNM_024712.5(ELMO3):c.694A>G (p.Met232Val)not specified [RCV004337610]uncertain significance166720091867200918Humanname
401899712CV2765117single nucleotide variantNM_024712.5(ELMO3):c.754G>A (p.Asp252Asn)not specified [RCV004337611]uncertain significance166720139467201394Humanname
405264227CV3185221single nucleotide variantNM_024712.5(ELMO3):c.850G>A (p.Val284Ile)not provided [RCV003885785]likely benign166720157467201574Humanname
405738909CV3248549single nucleotide variantNM_024712.5(ELMO3):c.479C>T (p.Ser160Phe)not specified [RCV004380252]uncertain significance166720051667200516Humanname
407506665CV3438303single nucleotide variantNM_024712.5(ELMO3):c.368G>A (p.Arg123His)not specified [RCV004624773]uncertain significance166720031667200316Humanname
407506668CV3438304single nucleotide variantNM_024712.5(ELMO3):c.674A>T (p.Gln225Leu)not specified [RCV004624774]uncertain significance166720089867200898Humanname
407506678CV3438308single nucleotide variantNM_024712.5(ELMO3):c.862C>T (p.Leu288Phe)not specified [RCV004624778]uncertain significance166720158667201586Humanname
597666443CV3670971single nucleotide variantNM_024712.5(ELMO3):c.854T>C (p.Leu285Pro)not specified [RCV004912553]uncertain significance166720157867201578Humanname
597666458CV3670973single nucleotide variantNM_024712.5(ELMO3):c.371A>T (p.Asn124Ile)not specified [RCV004912555]uncertain significance166720031967200319Humanname
597666472CV3670976single nucleotide variantNM_024712.5(ELMO3):c.424G>T (p.Val142Leu)not specified [RCV004912557]uncertain significance166720046167200461Humanname
597666479CV3670978single nucleotide variantNM_024712.5(ELMO3):c.652G>A (p.Val218Met)not specified [RCV004912558]uncertain significance166720079567200795Humanname
597666491CV3670980single nucleotide variantNM_024712.5(ELMO3):c.565G>A (p.Ala189Thr)not specified [RCV004912560]uncertain significance166720070867200708Humanname
597666499CV3670982single nucleotide variantNM_024712.5(ELMO3):c.773A>G (p.Asn258Ser)not specified [RCV004912561]uncertain significance166720141367201413Humanname
597666521CV3670987single nucleotide variantNM_024712.5(ELMO3):c.669G>A (p.Met223Ile)not specified [RCV004912564]uncertain significance166720089367200893Humanname
597666530CV3670988single nucleotide variantNM_024712.5(ELMO3):c.778C>T (p.Arg260Cys)not specified [RCV004912565]uncertain significance166720141867201418Humanname
597666537CV3670989single nucleotide variantNM_024712.5(ELMO3):c.402A>T (p.Glu134Asp)not specified [RCV004912566]uncertain significance166720035067200350Humanname
598191104CV3957772single nucleotide variantNM_024712.5(ELMO3):c.445G>A (p.Ala149Thr)not specified [RCV005334791]uncertain significance166720048267200482Humanname
598191136CV3957776single nucleotide variantNM_024712.5(ELMO3):c.748A>T (p.Met250Leu)not specified [RCV005334795]uncertain significance166720138867201388Humanname
598191170CV3957780single nucleotide variantNM_024712.5(ELMO3):c.721G>A (p.Gly241Arg)not specified [RCV005334799]uncertain significance166720094567200945Humanname
156317657CV2204027single nucleotide variantNM_024712.5(ELMO3):c.1901G>A (p.Arg634His)not specified [RCV004070065]likely benign166720353467203534Humanname
156110461CV2207633single nucleotide variantNM_024712.5(ELMO3):c.1834C>T (p.Arg612Trp)not specified [RCV004090411]uncertain significance166720338067203380Humanname
156378365CV2207701single nucleotide variantNM_024712.5(ELMO3):c.1085C>T (p.Pro362Leu)not specified [RCV004084150]uncertain significance166720201167202011Humanname
156312133CV2256821single nucleotide variantNM_024712.5(ELMO3):c.1319A>G (p.His440Arg)not specified [RCV004121041]uncertain significance166720245467202454Humanname
155921574CV2276330single nucleotide variantNM_024712.5(ELMO3):c.1183A>G (p.Lys395Glu)not specified [RCV004144075]uncertain significance166720220667202206Humanname
156243856CV2312968single nucleotide variantNM_024712.5(ELMO3):c.1252G>A (p.Gly418Arg)not specified [RCV004159473]uncertain significance166720227567202275Humanname
156179872CV2327698single nucleotide variantNM_024712.5(ELMO3):c.1508G>A (p.Arg503Gln)not specified [RCV004177269]uncertain significance166720273667202736Humanname
156208252CV2369972single nucleotide variantNM_024712.5(ELMO3):c.1835G>A (p.Arg612Gln)not specified [RCV004210878]uncertain significance166720338167203381Humanname
156200455CV2392393single nucleotide variantNM_024712.5(ELMO3):c.2123A>G (p.Asn708Ser)not specified [RCV004243978]uncertain significance166720383767203837Humanname
156171471CV2400682single nucleotide variantNM_024712.5(ELMO3):c.2005G>A (p.Glu669Lys)not specified [RCV004242358]uncertain significance166720371967203719Humanname
401757636CV2675426single nucleotide variantNM_024712.5(ELMO3):c.2144G>T (p.Cys715Phe)not specified [RCV004292226]uncertain significance166720385867203858Humanname
401744765CV2681120single nucleotide variantNM_024712.5(ELMO3):c.1150C>T (p.Arg384Trp)not specified [RCV004296176]uncertain significance166720207667202076Humanname
401729681CV2690439single nucleotide variantNM_024712.5(ELMO3):c.1663C>T (p.Arg555Trp)not specified [RCV004302421]uncertain significance166720299267202992Humanname
401763939CV2717171single nucleotide variantNM_024712.5(ELMO3):c.1132G>A (p.Ala378Thr)not specified [RCV004324041]uncertain significance166720205867202058Humanname
401871073CV2766773single nucleotide variantNM_024712.5(ELMO3):c.1063G>A (p.Ala355Thr)not specified [RCV004349162]uncertain significance166720198967201989Humanname
401869789CV2772521single nucleotide variantNM_024712.5(ELMO3):c.2152G>C (p.Ala718Pro)not specified [RCV004355289]uncertain significance166720386667203866Humanname
401872221CV2779595single nucleotide variantNM_024712.5(ELMO3):c.1571G>A (p.Arg524Gln)not specified [RCV004351305]uncertain significance166720290067202900Humanname
405738869CV3248543single nucleotide variantNM_024712.5(ELMO3):c.1006C>T (p.Arg336Cys)not specified [RCV004380246]uncertain significance166720182967201829Humanname
405738877CV3248544single nucleotide variantNM_024712.5(ELMO3):c.1186C>T (p.His396Tyr)not specified [RCV004380247]uncertain significance166720220967202209Humanname
405738883CV3248545single nucleotide variantNM_024712.5(ELMO3):c.1624C>T (p.Arg542Cys)not specified [RCV004380248]uncertain significance166720295367202953Humanname
407506670CV3438305single nucleotide variantNM_024712.5(ELMO3):c.1223C>T (p.Thr408Met)not specified [RCV004624775]uncertain significance166720224667202246Humanname
407506672CV3438306single nucleotide variantNM_024712.5(ELMO3):c.1834C>G (p.Arg612Gly)not specified [RCV004624776]uncertain significance166720338067203380Humanname
407506685CV3438311single nucleotide variantNM_024712.5(ELMO3):c.1804C>T (p.Leu602Phe)not specified [RCV004624781]uncertain significance166720335067203350Humanname
597666428CV3670969single nucleotide variantNM_024712.5(ELMO3):c.1141G>A (p.Ala381Thr)not specified [RCV004912551]uncertain significance166720206767202067Humanname
597666451CV3670972single nucleotide variantNM_024712.5(ELMO3):c.1247G>A (p.Arg416His)not specified [RCV004912554]likely benign166720227067202270Humanname
597746974CV3670977single nucleotide variantNM_024712.5(ELMO3):c.1116G>T (p.Leu372Phe)not specified [RCV004922808]uncertain significance166720204267202042Humanname
597666484CV3670979single nucleotide variantNM_024712.5(ELMO3):c.1331G>A (p.Cys444Tyr)not specified [RCV004912559]uncertain significance166720246667202466Humanname
597666515CV3670984single nucleotide variantNM_024712.5(ELMO3):c.1330T>C (p.Cys444Arg)not specified [RCV004912563]uncertain significance166720246567202465Humanname
597746984CV3670985single nucleotide variantNM_024712.5(ELMO3):c.1246C>T (p.Arg416Cys)not specified [RCV004922810]uncertain significance166720226967202269Humanname
598191121CV3957774single nucleotide variantNM_024712.5(ELMO3):c.1448C>G (p.Pro483Arg)not specified [RCV005334793]uncertain significance166720267667202676Humanname
598191127CV3957775single nucleotide variantNM_024712.5(ELMO3):c.2089G>A (p.Glu697Lys)not specified [RCV005334794]uncertain significance166720380367203803Humanname
598191144CV3957777single nucleotide variantNM_024712.5(ELMO3):c.1156G>A (p.Val386Met)not specified [RCV005334796]uncertain significance166720217967202179Humanname
598191175CV3957781single nucleotide variantNM_024712.5(ELMO3):c.1341C>G (p.Ile447Met)not specified [RCV005334800]uncertain significance166720247667202476Humanname