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Variants search result for Homo sapiens
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66 records found for search term Nol9
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329399704CV2467610single nucleotide variantNM_024654.5(NOL9):c.11C>T (p.Ser4Leu)not specified [RCV004287471]uncertain significance165544926554492Humanname
405677547CV3355513single nucleotide variantNM_024654.5(NOL9):c.22C>A (p.Leu8Ile)not specified [RCV004487963]uncertain significance165544816554481Humanname
156334300CV2333366single nucleotide variantNM_024654.5(NOL9):c.29G>A (p.Arg10Gln)not specified [RCV004190076]uncertain significance165544746554474Humanname
156339606CV2351606single nucleotide variantNM_024654.5(NOL9):c.61C>A (p.Arg21Ser)not specified [RCV004195323]uncertain significance165544426554442Humanname
598206880CV4004557single nucleotide variantNM_024654.5(NOL9):c.40C>T (p.Arg14Cys)not specified [RCV005377008]uncertain significance165544636554463Humanname
155964285CV2194287single nucleotide variantNM_024654.5(NOL9):c.218C>T (p.Ala73Val)not specified [RCV004079404]uncertain significance165542856554285Humanname
156270917CV2237074single nucleotide variantNM_024654.5(NOL9):c.241G>T (p.Ala81Ser)not specified [RCV004114835]uncertain significance165542626554262Humanname
156231617CV2264473single nucleotide variantNM_024654.5(NOL9):c.233C>G (p.Pro78Arg)not specified [RCV004138367]uncertain significance165542706554270Humanname
156337915CV2271200single nucleotide variantNM_024654.5(NOL9):c.188G>A (p.Arg63Lys)not specified [RCV004134561]uncertain significance165543156554315Humanname
329386926CV2428427single nucleotide variantNM_024654.5(NOL9):c.199C>A (p.Arg67Ser)not specified [RCV004253225]uncertain significance165543046554304Humanname
407509698CV3469079single nucleotide variantNM_024654.5(NOL9):c.245C>A (p.Thr82Asn)not specified [RCV004647488]uncertain significance165542586554258Humanname
597672368CV3563073single nucleotide variantNM_024654.5(NOL9):c.200G>A (p.Arg67His)not specified [RCV004829923]uncertain significance165543036554303Humanname
597672395CV3563077single nucleotide variantNM_024654.5(NOL9):c.175G>A (p.Gly59Ser)not specified [RCV004829927]uncertain significance165543286554328Humanname
598240125CV4004549single nucleotide variantNM_024654.5(NOL9):c.167A>G (p.Gln56Arg)not specified [RCV005383046]uncertain significance165543366554336Humanname
598206861CV4004552single nucleotide variantNM_024654.5(NOL9):c.104G>A (p.Arg35His)not specified [RCV005377004]uncertain significance165543996554399Humanname
598240129CV4004555single nucleotide variantNM_024654.5(NOL9):c.173C>T (p.Ser58Phe)not specified [RCV005383047]uncertain significance165543306554330Humanname
156253991CV2193182single nucleotide variantNM_024654.5(NOL9):c.329C>T (p.Pro110Leu)not specified [RCV004071173]uncertain significance165541746554174Humanname
156369203CV2193918single nucleotide variantNM_024654.5(NOL9):c.356T>G (p.Val119Gly)not specified [RCV004074650]uncertain significance165541476554147Humanname
156321206CV2197530single nucleotide variantNM_024654.5(NOL9):c.437A>G (p.Tyr146Cys)not specified [RCV004081254]uncertain significance165505756550575Humanname
156191452CV2206158single nucleotide variantNM_024654.5(NOL9):c.607C>G (p.Leu203Val)not specified [RCV004078558]uncertain significance165504056550405Humanname
156340614CV2229542single nucleotide variantNM_024654.5(NOL9):c.451G>C (p.Val151Leu)not specified [RCV004103080]uncertain significance165505616550561Humanname
156347625CV2315362single nucleotide variantNM_024654.5(NOL9):c.676C>T (p.His226Tyr)not specified [RCV004167335]uncertain significance165496396549639Humanname
156158743CV2322679single nucleotide variantNM_024654.5(NOL9):c.901G>A (p.Val301Ile)not specified [RCV004182807]likely benign165449026544902Humanname
155979423CV2340047single nucleotide variantNM_024654.5(NOL9):c.586C>T (p.Arg196Trp)not specified [RCV004192293]uncertain significance165504266550426Humanname
156122350CV2354324single nucleotide variantNM_024654.5(NOL9):c.716C>T (p.Pro239Leu)not specified [RCV004206741]uncertain significance165495996549599Humanname
329382206CV2424367single nucleotide variantNM_024654.5(NOL9):c.513C>G (p.His171Gln)not specified [RCV004252270]uncertain significance165504996550499Humanname
329382442CV2424470single nucleotide variantNM_024654.5(NOL9):c.594G>C (p.Leu198Phe)not specified [RCV004252360]uncertain significance165504186550418Humanname
329356845CV2431168single nucleotide variantNM_024654.5(NOL9):c.632C>T (p.Ser211Leu)not specified [RCV004250517]likely benign165496836549683Humanname
401730621CV2689757single nucleotide variantNM_024654.5(NOL9):c.424G>A (p.Val142Met)not specified [RCV004297668]uncertain significance165505886550588Humanname
401742687CV2715293single nucleotide variantNM_024654.5(NOL9):c.542A>G (p.Tyr181Cys)not specified [RCV004324631]uncertain significance165504706550470Humanname
401877832CV2757626single nucleotide variantNM_024654.5(NOL9):c.869A>G (p.Asn290Ser)not specified [RCV004334745]likely benign165450566545056Humanname
401870240CV2772658single nucleotide variantNM_024654.5(NOL9):c.395A>G (p.Gln132Arg)not specified [RCV004355402]uncertain significance165541086554108Humanname
401897713CV2772855single nucleotide variantNM_024654.5(NOL9):c.995A>C (p.Tyr332Ser)not specified [RCV004357637]uncertain significance165419106541910Humanname
405677551CV3355514single nucleotide variantNM_024654.5(NOL9):c.647C>T (p.Ser216Phe)not specified [RCV004487964]uncertain significance165496686549668Humanname
597672356CV3563071single nucleotide variantNM_024654.5(NOL9):c.737T>C (p.Val246Ala)not specified [RCV004829921]uncertain significance165495786549578Humanname
597672361CV3563072single nucleotide variantNM_024654.5(NOL9):c.947A>G (p.Asn316Ser)not specified [RCV004829922]uncertain significance165448566544856Humanname
597672375CV3563074single nucleotide variantNM_024654.5(NOL9):c.417C>G (p.Ile139Met)not specified [RCV004829924]uncertain significance165505956550595Humanname
597672387CV3563076single nucleotide variantNM_024654.5(NOL9):c.833C>T (p.Thr278Ile)not specified [RCV004829926]uncertain significance165450926545092Humanname
156238323CV2193629single nucleotide variantNM_024654.5(NOL9):c.1960C>A (p.Arg654Ser)not specified [RCV004074234]uncertain significance165260036526003Humanname
156138290CV2253657single nucleotide variantNM_024654.5(NOL9):c.1601C>T (p.Pro534Leu)not specified [RCV004125332]uncertain significance165320146532014Humanname
156176403CV2258092single nucleotide variantNM_024654.5(NOL9):c.1693G>A (p.Ala565Thr)not specified [RCV004121486]uncertain significance165291266529126Humanname
156029102CV2278590single nucleotide variantNM_024654.5(NOL9):c.1259T>A (p.Ile420Asn)not specified [RCV004133015]uncertain significance165327396532739Humanname
155931756CV2293684single nucleotide variantNM_024654.5(NOL9):c.1600C>T (p.Pro534Ser)not specified [RCV004153185]uncertain significance165320156532015Humanname
155939528CV2293926single nucleotide variantNM_024654.5(NOL9):c.1106A>T (p.Gln369Leu)not specified [RCV004155470]uncertain significance165334116533411Humanname
156181471CV2327821single nucleotide variantNM_024654.5(NOL9):c.1298A>G (p.Gln433Arg)not specified [RCV004179160]uncertain significance165327006532700Humanname
155902169CV2356403single nucleotide variantNM_024654.5(NOL9):c.1960C>T (p.Arg654Cys)not specified [RCV004206204]uncertain significance165260036526003Humanname
401762275CV2699581single nucleotide variantNM_024654.5(NOL9):c.1693G>T (p.Ala565Ser)not specified [RCV004299775]uncertain significance165291266529126Humanname
401887654CV2773574single nucleotide variantNM_024654.5(NOL9):c.1241A>G (p.Gln414Arg)not specified [RCV004355982]uncertain significance165327576532757Humanname
401893864CV2774088single nucleotide variantNM_024654.5(NOL9):c.1393A>G (p.Arg465Gly)not specified [RCV004345685]uncertain significance165326056532605Humanname
401860610CV2776114single nucleotide variantNM_024654.5(NOL9):c.2014C>G (p.Pro672Ala)not specified [RCV004353214]uncertain significance165259496525949Humanname
405677535CV3355510single nucleotide variantNM_024654.5(NOL9):c.1340C>T (p.Pro447Leu)not specified [RCV004487960]uncertain significance165326586532658Humanname
405677540CV3355511single nucleotide variantNM_024654.5(NOL9):c.1355A>G (p.Asp452Gly)not specified [RCV004487961]uncertain significance165326436532643Humanname
405677544CV3355512single nucleotide variantNM_024654.5(NOL9):c.1666G>T (p.Ala556Ser)not specified [RCV004487962]uncertain significance165291536529153Humanname
407509694CV3469077single nucleotide variantNM_024654.5(NOL9):c.1715C>T (p.Ala572Val)not specified [RCV004647487]uncertain significance165291046529104Humanname
407498073CV3469078single nucleotide variantNM_024654.5(NOL9):c.1933A>C (p.Ile645Leu)not specified [RCV004643909]uncertain significance165267226526722Humanname
597672379CV3563075single nucleotide variantNM_024654.5(NOL9):c.1538A>G (p.Glu513Gly)not specified [RCV004829925]uncertain significance165320776532077Humanname
597672403CV3563078single nucleotide variantNM_024654.5(NOL9):c.1271G>C (p.Arg424Pro)not specified [RCV004829928]uncertain significance165327276532727Humanname
597672411CV3563079single nucleotide variantNM_024654.5(NOL9):c.1375A>G (p.Lys459Glu)not specified [RCV004829929]uncertain significance165326236532623Humanname
597672418CV3563080single nucleotide variantNM_024654.5(NOL9):c.1970A>G (p.Glu657Gly)not specified [RCV004829930]uncertain significance165259936525993Humanname
597672425CV3563081single nucleotide variantNM_024654.5(NOL9):c.1570A>G (p.Ile524Val)not specified [RCV004829931]likely benign165320456532045Humanname
598206851CV4004550single nucleotide variantNM_024654.5(NOL9):c.1993A>G (p.Thr665Ala)not specified [RCV005377002]uncertain significance165259706525970Humanname
598206856CV4004551single nucleotide variantNM_024654.5(NOL9):c.1088C>T (p.Thr363Ile)not specified [RCV005377003]uncertain significance165334296533429Humanname
598206866CV4004553single nucleotide variantNM_024654.5(NOL9):c.1100C>T (p.Thr367Ile)not specified [RCV005377005]uncertain significance165334176533417Humanname
598206871CV4004554single nucleotide variantNM_024654.5(NOL9):c.1076G>T (p.Gly359Val)not specified [RCV005377006]uncertain significance165334416533441Humanname
598206876CV4004556single nucleotide variantNM_024654.5(NOL9):c.1264C>G (p.Leu422Val)not specified [RCV005377007]uncertain significance165327346532734Humanname
8625039CV80158single nucleotide variantNM_024654.4(NOL9):c.1651C>T (p.Pro551Ser)Malignant melanoma [RCV000060234]not provided165291686529168Humanname