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Variants search result for Homo sapiens
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95 records found for search term Ndor1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155926891CV2365838single nucleotide variantNM_014434.4(NDOR1):c.11C>T (p.Pro4Leu)not specified [RCV004214373]uncertain significance9137205788137205788Humanname
329361364CV2436938single nucleotide variantNM_014434.4(NDOR1):c.23T>C (p.Val8Ala)not specified [RCV004260318]uncertain significance9137205800137205800Humanname
407488904CV3454620single nucleotide variantNM_014434.4(NDOR1):c.17T>C (p.Leu6Pro)not specified [RCV004641384]uncertain significance9137205794137205794Humanname
597668638CV3558926single nucleotide variantNM_014434.4(NDOR1):c.23T>A (p.Val8Glu)not specified [RCV004829454]uncertain significance9137205800137205800Humanname
156182804CV2201916single nucleotide variantNM_014434.4(NDOR1):c.73G>A (p.Gly25Ser)not specified [RCV004075497]uncertain significance9137205850137205850Humanname
155991730CV2379230single nucleotide variantNM_014434.4(NDOR1):c.46A>G (p.Thr16Ala)not specified [RCV004223709]uncertain significance9137205823137205823Humanname
405804988CV3338052single nucleotide variantNM_014434.4(NDOR1):c.65A>G (p.Glu22Gly)not specified [RCV004479509]uncertain significance9137205842137205842Humanname
407488909CV3454622single nucleotide variantNM_014434.4(NDOR1):c.54G>C (p.Gln18His)not specified [RCV004641385]uncertain significance9137205831137205831Humanname
598230568CV4003993single nucleotide variantNM_014434.4(NDOR1):c.77G>T (p.Arg26Leu)not specified [RCV005381211]uncertain significance9137205854137205854Humanname
156195655CV2223447single nucleotide variantNM_014434.4(NDOR1):c.247C>T (p.Pro83Ser)not specified [RCV004106024]uncertain significance9137212535137212535Humanname
329373008CV2451765single nucleotide variantNM_014434.4(NDOR1):c.130C>T (p.Pro44Ser)not specified [RCV004276454]uncertain significance9137205907137205907Humanname
401753073CV2674770single nucleotide variantNM_014434.4(NDOR1):c.235C>T (p.Arg79Trp)not specified [RCV004294050]uncertain significance9137212523137212523Humanname
405804928CV3338025single nucleotide variantNM_014434.4(NDOR1):c.257C>T (p.Ala86Val)not specified [RCV004479481]uncertain significance9137212545137212545Humanname
407488931CV3454628single nucleotide variantNM_014434.4(NDOR1):c.155C>T (p.Pro52Leu)not specified [RCV004641389]uncertain significance9137206251137206251Humanname
156385471CV2227933single nucleotide variantNM_014434.4(NDOR1):c.651G>T (p.Gln217His)not specified [RCV004096189]uncertain significance9137214342137214342Humanname
156089093CV2259100single nucleotide variantNM_014434.4(NDOR1):c.929G>A (p.Arg310His)not specified [RCV004120355]uncertain significance9137214882137214882Humanname
156020749CV2264389single nucleotide variantNM_014434.4(NDOR1):c.648C>G (p.Asn216Lys)not specified [RCV004138291]uncertain significance9137214339137214339Humanname
156364707CV2271975single nucleotide variantNM_014434.4(NDOR1):c.833C>T (p.Pro278Leu)not specified [RCV004124789]uncertain significance9137214680137214680Humanname
156259884CV2277870single nucleotide variantNM_014434.4(NDOR1):c.886C>T (p.Arg296Trp)not specified [RCV004147283]uncertain significance9137214839137214839Humanname
155982326CV2337147single nucleotide variantNM_014434.4(NDOR1):c.440G>C (p.Arg147Pro)not specified [RCV004192906]uncertain significance9137213996137213996Humanname
156006603CV2357790single nucleotide variantNM_014434.4(NDOR1):c.731C>T (p.Ala244Val)not specified [RCV004205079]uncertain significance9137214578137214578Humanname
156387367CV2372724single nucleotide variantNM_014434.4(NDOR1):c.682G>A (p.Val228Ile)not specified [RCV004221915]uncertain significance9137214373137214373Humanname
156061380CV2380233single nucleotide variantNM_014434.4(NDOR1):c.298T>G (p.Ser100Ala)not specified [RCV004224592]uncertain significance9137212586137212586Humanname
156061394CV2380234single nucleotide variantNM_014434.4(NDOR1):c.299C>A (p.Ser100Tyr)not specified [RCV004224593]uncertain significance9137212587137212587Humanname
329369194CV2450562single nucleotide variantNM_014434.4(NDOR1):c.377C>T (p.Pro126Leu)not specified [RCV004265466]uncertain significance9137213845137213845Humanname
329351987CV2455578single nucleotide variantNM_014434.4(NDOR1):c.515T>C (p.Leu172Pro)not specified [RCV004276829]uncertain significance9137214206137214206Humanname
329388206CV2468770single nucleotide variantNM_014434.4(NDOR1):c.848T>A (p.Val283Asp)not specified [RCV004280089]uncertain significance9137214801137214801Humanname
401730488CV2677192single nucleotide variantNM_014434.4(NDOR1):c.782G>A (p.Arg261Gln)not specified [RCV004295819]likely benign9137214629137214629Humanname
401767554CV2681701single nucleotide variantNM_014434.4(NDOR1):c.422C>T (p.Ala141Val)not specified [RCV004294250]uncertain significance9137213978137213978Humanname
401763294CV2714496single nucleotide variantNM_014434.4(NDOR1):c.814C>G (p.Gln272Glu)not specified [RCV004318018]uncertain significance9137214661137214661Humanname
401862651CV2762303single nucleotide variantNM_014434.4(NDOR1):c.931C>T (p.Arg311Cys)not specified [RCV004335419]uncertain significance9137214884137214884Humanname
401890815CV2778367single nucleotide variantNM_014434.4(NDOR1):c.675C>A (p.Phe225Leu)not specified [RCV004344055]uncertain significance9137214366137214366Humanname
405804945CV3338033single nucleotide variantNM_014434.4(NDOR1):c.322G>A (p.Val108Met)not specified [RCV004479489]uncertain significance9137213790137213790Humanname
405804970CV3338044single nucleotide variantNM_014434.4(NDOR1):c.571G>A (p.Gly191Arg)not specified [RCV004479500]uncertain significance9137214262137214262Humanname
405804995CV3338055single nucleotide variantNM_014434.4(NDOR1):c.661G>A (p.Gly221Ser)not specified [RCV004479512]uncertain significance9137214352137214352Humanname
405805061CV3338086single nucleotide variantNM_014434.4(NDOR1):c.835C>T (p.Arg279Trp)not specified [RCV004479543]uncertain significance9137214682137214682Humanname
405805081CV3348031single nucleotide variantNM_014434.4(NDOR1):c.901C>T (p.His301Tyr)not specified [RCV004479552]uncertain significance9137214854137214854Humanname
405805087CV3348034single nucleotide variantNM_014434.4(NDOR1):c.902A>G (p.His301Arg)not specified [RCV004479555]uncertain significance9137214855137214855Humanname
405805104CV3348042single nucleotide variantNM_014434.4(NDOR1):c.979C>T (p.Arg327Trp)not specified [RCV004479563]uncertain significance9137214932137214932Humanname
407525786CV3454621single nucleotide variantNM_014434.4(NDOR1):c.637A>G (p.Met213Val)not specified [RCV004654600]uncertain significance9137214328137214328Humanname
407488919CV3454624single nucleotide variantNM_014434.4(NDOR1):c.865C>G (p.Leu289Val)not specified [RCV004641387]uncertain significance9137214818137214818Humanname
407488926CV3454625single nucleotide variantNM_014434.4(NDOR1):c.866T>G (p.Leu289Arg)not specified [RCV004641388]uncertain significance9137214819137214819Humanname
407525793CV3454627single nucleotide variantNM_014434.4(NDOR1):c.716G>A (p.Gly239Asp)not specified [RCV004654602]uncertain significance9137214407137214407Humanname
597668590CV3558920single nucleotide variantNM_014434.4(NDOR1):c.682G>T (p.Val228Phe)not specified [RCV004829448]uncertain significance9137214373137214373Humanname
597668598CV3558921single nucleotide variantNM_014434.4(NDOR1):c.434G>C (p.Trp145Ser)not specified [RCV004829449]uncertain significance9137213990137213990Humanname
597668604CV3558922single nucleotide variantNM_014434.4(NDOR1):c.884T>C (p.Met295Thr)not specified [RCV004829450]uncertain significance9137214837137214837Humanname
597668613CV3558923single nucleotide variantNM_014434.4(NDOR1):c.943G>C (p.Glu315Gln)not specified [RCV004829451]uncertain significance9137214896137214896Humanname
597668629CV3558925single nucleotide variantNM_014434.4(NDOR1):c.917C>G (p.Ala306Gly)not specified [RCV004829453]uncertain significance9137214870137214870Humanname
597668655CV3558928single nucleotide variantNM_014434.4(NDOR1):c.928C>T (p.Arg310Cys)not specified [RCV004829456]uncertain significance9137214881137214881Humanname
598230470CV4003976single nucleotide variantNM_014434.4(NDOR1):c.881C>G (p.Ser294Cys)not specified [RCV005381196]uncertain significance9137214834137214834Humanname
598230476CV4003977single nucleotide variantNM_014434.4(NDOR1):c.807C>A (p.Asp269Glu)not specified [RCV005381197]uncertain significance9137214654137214654Humanname
598230483CV4003978single nucleotide variantNM_014434.4(NDOR1):c.505G>A (p.Gly169Arg)not specified [RCV005381198]uncertain significance9137214061137214061Humanname
598230498CV4003981single nucleotide variantNM_014434.4(NDOR1):c.877T>G (p.Cys293Gly)not specified [RCV005381200]uncertain significance9137214830137214830Humanname
598230514CV4003984single nucleotide variantNM_014434.4(NDOR1):c.577C>T (p.Arg193Trp)not specified [RCV005381202]uncertain significance9137214268137214268Humanname
598230521CV4003985single nucleotide variantNM_014434.4(NDOR1):c.476C>T (p.Pro159Leu)not specified [RCV005381203]uncertain significance9137214032137214032Humanname
598230528CV4003986single nucleotide variantNM_014434.4(NDOR1):c.605C>T (p.Pro202Leu)not specified [RCV005381204]uncertain significance9137214296137214296Humanname
598230535CV4003987single nucleotide variantNM_014434.4(NDOR1):c.650A>G (p.Gln217Arg)not specified [RCV005381205]uncertain significance9137214341137214341Humanname
598230539CV4003988single nucleotide variantNM_014434.4(NDOR1):c.742G>T (p.Val248Leu)not specified [RCV005381206]uncertain significance9137214589137214589Humanname
598230575CV4003994single nucleotide variantNM_014434.4(NDOR1):c.617C>G (p.Ser206Trp)not specified [RCV005381212]uncertain significance9137214308137214308Humanname
598253669CV4003995single nucleotide variantNM_014434.4(NDOR1):c.700G>C (p.Asp234His)not specified [RCV005385378]uncertain significance9137214391137214391Humanname
156184659CV2195505single nucleotide variantNM_014434.4(NDOR1):c.1513C>T (p.Arg505Trp)not specified [RCV004082726]uncertain significance9137215976137215976Humanname
156225379CV2203046single nucleotide variantNM_014434.4(NDOR1):c.1459C>T (p.Arg487Cys)not specified [RCV004069298]uncertain significance9137215922137215922Humanname
156138292CV2211877single nucleotide variantNM_014434.4(NDOR1):c.1622G>A (p.Arg541His)not specified [RCV004087011]likely benign9137216161137216161Humanname
156293823CV2233580single nucleotide variantNM_014434.4(NDOR1):c.1627G>C (p.Gly543Arg)not specified [RCV004100054]uncertain significance9137216166137216166Humanname
156284385CV2249838single nucleotide variantNM_014434.4(NDOR1):c.1138C>T (p.Arg380Trp)not specified [RCV004122585]uncertain significance9137215167137215167Humanname
155983565CV2273091single nucleotide variantNM_014434.4(NDOR1):c.1259C>T (p.Ser420Phe)not specified [RCV004137735]uncertain significance9137215492137215492Humanname
156081522CV2333322single nucleotide variantNM_014434.4(NDOR1):c.1516G>T (p.Asp506Tyr)not specified [RCV004197063]uncertain significance9137215979137215979Humanname
155985426CV2344516single nucleotide variantNM_014434.4(NDOR1):c.1514G>A (p.Arg505Gln)not specified [RCV004195254]uncertain significance9137215977137215977Humanname
156009867CV2362048single nucleotide variantNM_014434.4(NDOR1):c.1139G>A (p.Arg380Gln)not specified [RCV004209859]uncertain significance9137215168137215168Humanname
155935938CV2379735single nucleotide variantNM_014434.4(NDOR1):c.1675G>A (p.Val559Ile)not specified [RCV004219855]uncertain significance9137216297137216297Humanname
156133668CV2382997single nucleotide variantNM_014434.4(NDOR1):c.1108G>A (p.Asp370Asn)not specified [RCV004217582]uncertain significance9137215137137215137Humanname
156051450CV2386346single nucleotide variantNM_014434.4(NDOR1):c.1316G>A (p.Arg439Gln)not specified [RCV004228681]uncertain significance9137215686137215686Humanname
401731259CV2674314single nucleotide variantNM_014434.4(NDOR1):c.1226G>A (p.Arg409His)not specified [RCV004289192]uncertain significance9137215459137215459Humanname
401762872CV2720111single nucleotide variantNM_014434.4(NDOR1):c.1457G>C (p.Cys486Ser)not specified [RCV004323675]uncertain significance9137215920137215920Humanname
401864229CV2760857single nucleotide variantNM_014434.4(NDOR1):c.1727C>T (p.Pro576Leu)not specified [RCV004336493]uncertain significance9137216349137216349Humanname
401877446CV2764646single nucleotide variantNM_014434.4(NDOR1):c.1243C>T (p.Arg415Trp)not specified [RCV004341021]uncertain significance9137215476137215476Humanname
405800541CV3337961single nucleotide variantNM_014434.4(NDOR1):c.1225C>T (p.Arg409Cys)not specified [RCV004477348]uncertain significance9137215458137215458Humanname
405800560CV3337971single nucleotide variantNM_014434.4(NDOR1):c.1291C>T (p.Pro431Ser)not specified [RCV004477358]uncertain significance9137215661137215661Humanname
405804844CV3337986single nucleotide variantNM_014434.4(NDOR1):c.1489G>A (p.Ala497Thr)not specified [RCV004479442]uncertain significance9137215952137215952Humanname
405804885CV3338005single nucleotide variantNM_014434.4(NDOR1):c.1658A>C (p.Lys553Thr)not specified [RCV004479461]uncertain significance9137216280137216280Humanname
407488889CV3454617single nucleotide variantNM_014434.4(NDOR1):c.1472A>G (p.Gln491Arg)not specified [RCV004641381]uncertain significance9137215935137215935Humanname
407488894CV3454618single nucleotide variantNM_014434.4(NDOR1):c.1757A>G (p.Gln586Arg)not specified [RCV004641382]uncertain significance9137216379137216379Humanname
407488899CV3454619single nucleotide variantNM_014434.4(NDOR1):c.1255T>C (p.Ser419Pro)not specified [RCV004641383]uncertain significance9137215488137215488Humanname
407488913CV3454623single nucleotide variantNM_014434.4(NDOR1):c.1552C>G (p.Gln518Glu)not specified [RCV004641386]uncertain significance9137216015137216015Humanname
407525790CV3454626single nucleotide variantNM_014434.4(NDOR1):c.1132G>C (p.Val378Leu)not specified [RCV004654601]uncertain significance9137215161137215161Humanname
597668620CV3558924single nucleotide variantNM_014434.4(NDOR1):c.1778C>G (p.Thr593Arg)not specified [RCV004829452]uncertain significance9137216400137216400Humanname
597668647CV3558927single nucleotide variantNM_014434.4(NDOR1):c.1446G>C (p.Leu482Phe)not specified [RCV004829455]uncertain significance9137215909137215909Humanname
597668673CV3558930single nucleotide variantNM_014434.4(NDOR1):c.1670C>T (p.Ala557Val)not specified [RCV004829458]uncertain significance9137216292137216292Humanname
598230491CV4003979single nucleotide variantNM_014434.4(NDOR1):c.1579C>T (p.Arg527Trp)not specified [RCV005381199]uncertain significance9137216118137216118Humanname
598253657CV4003980single nucleotide variantNM_014434.4(NDOR1):c.1159G>A (p.Ala387Thr)not specified [RCV005385376]uncertain significance9137215188137215188Humanname
598253663CV4003982single nucleotide variantNM_014434.4(NDOR1):c.1739C>T (p.Ala580Val)not specified [RCV005385377]uncertain significance9137216361137216361Humanname
598230547CV4003989single nucleotide variantNM_014434.4(NDOR1):c.1354C>A (p.Pro452Thr)not specified [RCV005381207]uncertain significance9137215724137215724Humanname
598230551CV4003990single nucleotide variantNM_014434.4(NDOR1):c.1546C>T (p.Arg516Trp)not specified [RCV005381208]uncertain significance9137216009137216009Humanname
598230557CV4003991single nucleotide variantNM_014434.4(NDOR1):c.1636T>C (p.Phe546Leu)not specified [RCV005381209]uncertain significance9137216175137216175Humanname
598230565CV4003992single nucleotide variantNM_014434.4(NDOR1):c.1366G>A (p.Val456Met)not specified [RCV005381210]uncertain significance9137215736137215736Humanname