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Variants search result for Homo sapiens
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78 records found for search term Nsmaf
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155968292CV2261977single nucleotide variantNM_003580.4(NSMAF):c.59+293C>Gnot specified [RCV004126470]uncertain significance85865928058659280Humanname
155953641CV2303097single nucleotide variantNM_003580.4(NSMAF):c.59+327C>Gnot specified [RCV004156878]uncertain significance85865924658659246Humanname
329382349CV2424440single nucleotide variantNM_003580.4(NSMAF):c.59+350C>Gnot specified [RCV004252335]uncertain significance85865922358659223Humanname
401772893CV2720402single nucleotide variantNM_003580.4(NSMAF):c.59+348G>Anot specified [RCV004325706]uncertain significance85865922558659225Humanname
405710500CV3359431single nucleotide variantNM_003580.4(NSMAF):c.59+341G>Anot specified [RCV004493779]uncertain significance85865923258659232Humanname
405710507CV3359432single nucleotide variantNM_003580.4(NSMAF):c.59+344T>Cnot specified [RCV004493780]uncertain significance85865922958659229Humanname
405710540CV3359436single nucleotide variantNM_003580.4(NSMAF):c.59+371A>Gnot specified [RCV004493784]uncertain significance85865920258659202Humanname
597707601CV3577055single nucleotide variantNM_003580.4(NSMAF):c.59+314C>Tnot specified [RCV004840469]uncertain significance85865925958659259Humanname
598220954CV3994753single nucleotide variantNM_003580.4(NSMAF):c.59+329G>Cnot specified [RCV005379585]uncertain significance85865924458659244Humanname
12895960CV390571duplicationNM_003580.4(NSMAF):c.1126-25_1126-23dupnot specified [RCV000454691]benign85860154658601547Humanname
598220942CV3994751single nucleotide variantNM_003580.4(NSMAF):c.85G>A (p.Glu29Lys)not specified [RCV005379583]uncertain significance85864304858643048Humanname
401725591CV2721844single nucleotide variantNM_003580.4(NSMAF):c.128A>C (p.His43Pro)not specified [RCV004326357]uncertain significance85864300558643005Humanname
597707521CV3577044single nucleotide variantNM_003580.4(NSMAF):c.126G>T (p.Leu42Phe)not specified [RCV004840460]uncertain significance85864300758643007Humanname
597707560CV3577048single nucleotide variantNM_003580.4(NSMAF):c.116A>G (p.Asn39Ser)not specified [RCV004840464]uncertain significance85864301758643017Humanname
156378870CV2207829single nucleotide variantNM_003580.4(NSMAF):c.329G>C (p.Ser110Thr)not specified [RCV004084262]uncertain significance85863519358635193Humanname
155926482CV2230631single nucleotide variantNM_003580.4(NSMAF):c.412G>A (p.Asp138Asn)not specified [RCV004097585]uncertain significance85862375358623753Humanname
156140455CV2280832single nucleotide variantNM_003580.4(NSMAF):c.526C>T (p.Arg176Cys)not specified [RCV004145091]uncertain significance85862325158623251Humanname
155963424CV2330326single nucleotide variantNM_003580.4(NSMAF):c.741G>T (p.Arg247Ser)not specified [RCV004180907]uncertain significance85860778758607787Humanname
156293181CV2336403single nucleotide variantNM_003580.4(NSMAF):c.611C>T (p.Thr204Met)not specified [RCV004194621]uncertain significance85860968058609680Humanname
156054731CV2344656single nucleotide variantNM_003580.4(NSMAF):c.370T>C (p.Tyr124His)not specified [RCV004197423]uncertain significance85863151058631510Humanname
155991929CV2355558single nucleotide variantNM_003580.4(NSMAF):c.527G>A (p.Arg176His)not specified [RCV004205405]uncertain significance85862325058623250Humanname
329359033CV2425477single nucleotide variantNM_003580.4(NSMAF):c.820G>A (p.Glu274Lys)not specified [RCV004251130]uncertain significance85860597558605975Humanname
329353597CV2469334single nucleotide variantNM_003580.4(NSMAF):c.673C>G (p.Leu225Val)not specified [RCV004280665]uncertain significance85860961858609618Humanname
401863974CV2767448single nucleotide variantNM_003580.4(NSMAF):c.538A>G (p.Thr180Ala)not specified [RCV004343616]uncertain significance85862323958623239Humanname
401895889CV2779530single nucleotide variantNM_003580.4(NSMAF):c.658C>A (p.Leu220Met)not specified [RCV004351150]uncertain significance85860963358609633Humanname
405710596CV3359444single nucleotide variantNM_003580.4(NSMAF):c.686C>T (p.Pro229Leu)not specified [RCV004493792]uncertain significance85860960558609605Humanname
407476997CV3462064single nucleotide variantNM_003580.4(NSMAF):c.631G>C (p.Gly211Arg)not specified [RCV004638743]uncertain significance85860966058609660Humanname
407477019CV3462070single nucleotide variantNM_003580.4(NSMAF):c.499G>T (p.Ala167Ser)not specified [RCV004638747]uncertain significance85862338258623382Humanname
597707509CV3577043single nucleotide variantNM_003580.4(NSMAF):c.724C>T (p.Arg242Cys)not specified [RCV004840459]uncertain significance85860780458607804Humanname
597707532CV3577045single nucleotide variantNM_003580.4(NSMAF):c.637G>T (p.Val213Leu)not specified [RCV004840461]uncertain significance85860965458609654Humanname
597643215CV3577052single nucleotide variantNM_003580.4(NSMAF):c.329G>A (p.Ser110Asn)not specified [RCV004832572]uncertain significance85863519358635193Humanname
597707592CV3577053single nucleotide variantNM_003580.4(NSMAF):c.962A>C (p.Asn321Thr)not specified [RCV004840468]uncertain significance85860329358603293Humanname
156070610CV2232463single nucleotide variantNM_003580.4(NSMAF):c.1063A>G (p.Thr355Ala)not specified [RCV004099077]uncertain significance85860212058602120Humanname
156186816CV2232700single nucleotide variantNM_003580.4(NSMAF):c.2384C>T (p.Ala795Val)not specified [RCV004101359]uncertain significance85858652058586520Humanname
156299900CV2244818single nucleotide variantNM_003580.4(NSMAF):c.1271T>G (p.Met424Arg)not specified [RCV004104581]uncertain significance85860129458601294Humanname
156199631CV2256009single nucleotide variantNM_003580.4(NSMAF):c.2053G>A (p.Ala685Thr)not specified [RCV004122448]uncertain significance85859004158590041Humanname
155993965CV2281381single nucleotide variantNM_003580.4(NSMAF):c.1047T>A (p.Asp349Glu)not specified [RCV004141178]uncertain significance85860213658602136Humanname
156077723CV2291672single nucleotide variantNM_003580.4(NSMAF):c.1679T>G (p.Phe560Cys)not specified [RCV004155955]uncertain significance85859750058597500Humanname
156007375CV2299711single nucleotide variantNM_003580.4(NSMAF):c.2144A>G (p.Asp715Gly)not specified [RCV004148878]uncertain significance85858951958589519Humanname
156158690CV2314552single nucleotide variantNM_003580.4(NSMAF):c.2320G>A (p.Ala774Thr)not specified [RCV004168641]uncertain significance85858658458586584Humanname
156235444CV2346358single nucleotide variantNM_003580.4(NSMAF):c.1184C>T (p.Pro395Leu)not specified [RCV004203840]uncertain significance85860147758601477Humanname
329353984CV2436725single nucleotide variantNM_003580.4(NSMAF):c.1416G>T (p.Gln472His)not specified [RCV004258093]uncertain significance85859978758599787Humanname
401726799CV2691848single nucleotide variantNM_003580.4(NSMAF):c.2357C>G (p.Thr786Arg)not specified [RCV004299595]uncertain significance85858654758586547Humanname
401883675CV2754929single nucleotide variantNM_003580.4(NSMAF):c.1705G>A (p.Val569Met)not specified [RCV004341398]uncertain significance85859747458597474Humanname
405710493CV3359430single nucleotide variantNM_003580.4(NSMAF):c.1061G>A (p.Gly354Glu)not specified [RCV004493778]uncertain significance85860212258602122Humanname
405710515CV3359433single nucleotide variantNM_003580.4(NSMAF):c.1163A>G (p.Tyr388Cys)not specified [RCV004493781]uncertain significance85860149858601498Humanname
405710525CV3359434single nucleotide variantNM_003580.4(NSMAF):c.1349A>G (p.Tyr450Cys)not specified [RCV004493782]uncertain significance85859985458599854Humanname
405710532CV3359435single nucleotide variantNM_003580.4(NSMAF):c.1351G>T (p.Gly451Cys)not specified [RCV004493783]uncertain significance85859985258599852Humanname
405710547CV3359437single nucleotide variantNM_003580.4(NSMAF):c.1403G>A (p.Arg468Lys)not specified [RCV004493785]uncertain significance85859980058599800Humanname
405710555CV3359438single nucleotide variantNM_003580.4(NSMAF):c.1849A>G (p.Ile617Val)not specified [RCV004493786]uncertain significance85859560358595603Humanname
405710561CV3359439single nucleotide variantNM_003580.4(NSMAF):c.1870G>C (p.Glu624Gln)not specified [RCV004493787]uncertain significance85859558258595582Humanname
405710567CV3359440single nucleotide variantNM_003580.4(NSMAF):c.2221G>A (p.Gly741Ser)not specified [RCV004493788]uncertain significance85858769258587692Humanname
405710578CV3359441single nucleotide variantNM_003580.4(NSMAF):c.2222G>A (p.Gly741Asp)not specified [RCV004493789]uncertain significance85858769158587691Humanname
405710584CV3359442single nucleotide variantNM_003580.4(NSMAF):c.2257C>A (p.His753Asn)not specified [RCV004493790]uncertain significance85858765658587656Humanname
405710589CV3359443single nucleotide variantNM_003580.4(NSMAF):c.2737T>C (p.Trp913Arg)not specified [RCV004493791]uncertain significance85858412358584123Humanname
407476991CV3462061single nucleotide variantNM_003580.4(NSMAF):c.2086G>T (p.Val696Phe)not specified [RCV004638742]uncertain significance85859000858590008Humanname
407477004CV3462065single nucleotide variantNM_003580.4(NSMAF):c.2345C>T (p.Thr782Ile)not specified [RCV004638744]uncertain significance85858655958586559Humanname
407517084CV3462066single nucleotide variantNM_003580.4(NSMAF):c.1066T>C (p.Phe356Leu)not specified [RCV004650515]uncertain significance85860211758602117Humanname
407517087CV3462067single nucleotide variantNM_003580.4(NSMAF):c.1140A>C (p.Glu380Asp)not specified [RCV004650516]uncertain significance85860152158601521Humanname
407477009CV3462068single nucleotide variantNM_003580.4(NSMAF):c.2084A>G (p.Asn695Ser)not specified [RCV004638745]uncertain significance85859001058590010Humanname
407477013CV3462069single nucleotide variantNM_003580.4(NSMAF):c.1523A>G (p.Glu508Gly)not specified [RCV004638746]uncertain significance85859929458599294Humanname
407517089CV3462071single nucleotide variantNM_003580.4(NSMAF):c.1925G>C (p.Gly642Ala)not specified [RCV004650517]uncertain significance85859425858594258Humanname
597707500CV3577042single nucleotide variantNM_003580.4(NSMAF):c.1091G>C (p.Gly364Ala)not specified [RCV004840458]uncertain significance85860209258602092Humanname
597707540CV3577046single nucleotide variantNM_003580.4(NSMAF):c.2381C>T (p.Thr794Met)not specified [RCV004840462]uncertain significance85858652358586523Humanname
597707549CV3577047single nucleotide variantNM_003580.4(NSMAF):c.1456C>T (p.Pro486Ser)not specified [RCV004840463]uncertain significance85859936158599361Humanname
597707566CV3577049single nucleotide variantNM_003580.4(NSMAF):c.2272G>A (p.Ala758Thr)not specified [RCV004840465]uncertain significance85858764158587641Humanname
597707575CV3577050single nucleotide variantNM_003580.4(NSMAF):c.1037C>T (p.Ser346Leu)not specified [RCV004840466]uncertain significance85860321858603218Humanname
597707582CV3577051single nucleotide variantNM_003580.4(NSMAF):c.1379G>A (p.Ser460Asn)not specified [RCV004840467]uncertain significance85859982458599824Humanname
597643223CV3577054single nucleotide variantNM_003580.4(NSMAF):c.1199T>C (p.Phe400Ser)not specified [RCV004832573]uncertain significance85860146258601462Humanname
597707609CV3577056single nucleotide variantNM_003580.4(NSMAF):c.1736A>G (p.Lys579Arg)not specified [RCV004840470]uncertain significance85859744358597443Humanname
597707617CV3577057single nucleotide variantNM_003580.4(NSMAF):c.2452C>T (p.Arg818Cys)not specified [RCV004840471]uncertain significance85858599558585995Humanname
597643230CV3577058single nucleotide variantNM_003580.4(NSMAF):c.2483G>A (p.Cys828Tyr)not specified [RCV004832574]uncertain significance85858596458585964Humanname
597707623CV3577059single nucleotide variantNM_003580.4(NSMAF):c.1318A>G (p.Thr440Ala)not specified [RCV004840472]uncertain significance85859998458599984Humanname
598264934CV3994748single nucleotide variantNM_003580.4(NSMAF):c.2608G>A (p.Val870Ile)not specified [RCV005387856]uncertain significance85858570358585703Humanname
598220935CV3994749single nucleotide variantNM_003580.4(NSMAF):c.1109G>A (p.Arg370Gln)not specified [RCV005379582]uncertain significance85860207458602074Humanname
598264939CV3994750single nucleotide variantNM_003580.4(NSMAF):c.1829A>C (p.Lys610Thr)not specified [RCV005387857]uncertain significance85859562358595623Humanname
598220946CV3994752single nucleotide variantNM_003580.4(NSMAF):c.1039G>A (p.Glu347Lys)not specified [RCV005379584]uncertain significance85860321658603216Humanname
598220963CV3994754single nucleotide variantNM_003580.4(NSMAF):c.2644A>G (p.Ile882Val)not specified [RCV005379586]uncertain significance85858566758585667Humanname