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55 records found for search term Nedd1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329388436CV2437406single nucleotide variantNM_152905.4(NEDD1):c.-6G>Anot specified [RCV004256275]uncertain significance129690975496909754Humanname
407526106CV3454788single nucleotide variantNM_152905.4(NEDD1):c.80A>G (p.Lys27Arg)not specified [RCV004654691]uncertain significance129690983996909839Humanname
156066496CV2193345single nucleotide variantNM_152905.4(NEDD1):c.262A>T (p.Thr88Ser)not specified [RCV004072849]uncertain significance129691765196917651Humanname
405807807CV3356631single nucleotide variantNM_152905.4(NEDD1):c.266C>G (p.Ser89Cys)not specified [RCV004480891]uncertain significance129691765596917655Humanname
597670164CV3555790single nucleotide variantNM_152905.4(NEDD1):c.205G>C (p.Val69Leu)not specified [RCV004829648]uncertain significance129691279196912791Humanname
597670180CV3555792single nucleotide variantNM_152905.4(NEDD1):c.134A>G (p.Asn45Ser)not specified [RCV004829650]uncertain significance129690989396909893Humanname
598231452CV3990613single nucleotide variantNM_152905.4(NEDD1):c.137A>G (p.Asn46Ser)not specified [RCV005381360]uncertain significance129691272396912723Humanname
156200386CV2290461single nucleotide variantNM_152905.4(NEDD1):c.499C>A (p.His167Asn)not specified [RCV004155163]uncertain significance129693498596934985Humanname
156200399CV2290462single nucleotide variantNM_152905.4(NEDD1):c.500A>C (p.His167Pro)not specified [RCV004155164]uncertain significance129693498696934986Humanname
156076213CV2291492single nucleotide variantNM_152905.4(NEDD1):c.377C>T (p.Thr126Ile)not specified [RCV004155806]uncertain significance129692001396920013Humanname
156076864CV2291565single nucleotide variantNM_152905.4(NEDD1):c.577A>G (p.Asn193Asp)not specified [RCV004155867]uncertain significance129693506396935063Humanname
156283880CV2334714single nucleotide variantNM_152905.4(NEDD1):c.512C>G (p.Ser171Cys)not specified [RCV004188695]uncertain significance129693499896934998Humanname
156219400CV2344892single nucleotide variantNM_152905.4(NEDD1):c.607A>G (p.Ser203Gly)not specified [RCV004191030]uncertain significance129693509396935093Humanname
156154602CV2369522single nucleotide variantNM_152905.4(NEDD1):c.400A>G (p.Ile134Val)not specified [RCV004210456]likely benign129692003696920036Humanname
401740572CV2684389single nucleotide variantNM_152905.4(NEDD1):c.436C>T (p.His146Tyr)not specified [RCV004289030]uncertain significance129692007296920072Humanname
401734212CV2690513single nucleotide variantNM_152905.4(NEDD1):c.481A>G (p.Ser161Gly)not specified [RCV004304632]uncertain significance129692011796920117Humanname
401748907CV2708403single nucleotide variantNM_152905.4(NEDD1):c.805C>T (p.Arg269Trp)not specified [RCV004313511]uncertain significance129693669696936696Humanname
401739798CV2709666single nucleotide variantNM_152905.4(NEDD1):c.855G>C (p.Lys285Asn)not specified [RCV004318878]uncertain significance129693674696936746Humanname
405807828CV3342362single nucleotide variantNM_152905.4(NEDD1):c.491C>T (p.Ser164Phe)not specified [RCV004480902]uncertain significance129693497796934977Humanname
405807850CV3342373single nucleotide variantNM_152905.4(NEDD1):c.769A>G (p.Met257Val)not specified [RCV004480913]uncertain significance129693666096936660Humanname
405811716CV3342383single nucleotide variantNM_152905.4(NEDD1):c.831A>C (p.Leu277Phe)not specified [RCV004482905]uncertain significance129693672296936722Humanname
407526103CV3454787single nucleotide variantNM_152905.4(NEDD1):c.685A>C (p.Lys229Gln)not specified [RCV004654690]uncertain significance129693517196935171Humanname
597670195CV3555794single nucleotide variantNM_152905.4(NEDD1):c.626C>T (p.Ala209Val)not specified [RCV004829652]uncertain significance129693511296935112Humanname
598231445CV3990611single nucleotide variantNM_152905.4(NEDD1):c.740C>G (p.Ala247Gly)not specified [RCV005381359]uncertain significance129693663196936631Humanname
156373343CV2204947single nucleotide variantNM_152905.4(NEDD1):c.1384C>T (p.Leu462Phe)not specified [RCV004075185]uncertain significance129694364996943649Humanname
156399266CV2205018single nucleotide variantNM_152905.4(NEDD1):c.1501G>A (p.Ala501Thr)not specified [RCV004077635]uncertain significance129694464296944642Humanname
156243691CV2242961single nucleotide variantNM_152905.4(NEDD1):c.1633A>G (p.Ile545Val)not specified [RCV004107846]likely benign129694477496944774Humanname
156035060CV2282948single nucleotide variantNM_152905.4(NEDD1):c.1313A>G (p.Gln438Arg)not specified [RCV004143586]uncertain significance129694357896943578Humanname
156067767CV2289423single nucleotide variantNM_152905.4(NEDD1):c.1868A>T (p.His623Leu)not specified [RCV004152377]uncertain significance129695148896951488Humanname
156301016CV2307022single nucleotide variantNM_152905.4(NEDD1):c.1291G>C (p.Asp431His)not specified [RCV004159525]uncertain significance129694262196942621Humanname
156277045CV2316578single nucleotide variantNM_152905.4(NEDD1):c.1820G>A (p.Cys607Tyr)not specified [RCV004171827]uncertain significance129695144096951440Humanname
155938324CV2365010single nucleotide variantNM_152905.4(NEDD1):c.1034C>T (p.Pro345Leu)not specified [RCV004224171]uncertain significance129693731096937310Humanname
155902495CV2378544single nucleotide variantNM_152905.4(NEDD1):c.1549C>A (p.Pro517Thr)not specified [RCV004228593]uncertain significance129694469096944690Humanname
329357212CV2431281single nucleotide variantNM_152905.4(NEDD1):c.1768C>T (p.Arg590Cys)not specified [RCV004250614]uncertain significance129694580696945806Humanname
329397158CV2459973single nucleotide variantNM_152905.4(NEDD1):c.1562A>T (p.Gln521Leu)not specified [RCV004279451]uncertain significance129694470396944703Humanname
329397538CV2463832single nucleotide variantNM_152905.4(NEDD1):c.1037C>G (p.Ala346Gly)not specified [RCV004279916]uncertain significance129693731396937313Humanname
401732959CV2691161single nucleotide variantNM_152905.4(NEDD1):c.1433A>T (p.Asp478Val)not specified [RCV004302941]uncertain significance129694369896943698Humanname
401862705CV2758835single nucleotide variantNM_152905.4(NEDD1):c.1342A>G (p.Asn448Asp)not specified [RCV004339928]uncertain significance129694360796943607Humanname
401897126CV2789846single nucleotide variantNM_152905.4(NEDD1):c.1019T>C (p.Ile340Thr)not specified [RCV004362236]uncertain significance129693729596937295Humanname
405807949CV3356579single nucleotide variantNM_152905.4(NEDD1):c.1237A>G (p.Ile413Val)not specified [RCV004480839]likely benign129694052896940528Humanname
405807755CV3356605single nucleotide variantNM_152905.4(NEDD1):c.1609G>T (p.Ala537Ser)not specified [RCV004480865]uncertain significance129694475096944750Humanname
405807764CV3356610single nucleotide variantNM_152905.4(NEDD1):c.1721G>A (p.Ser574Asn)not specified [RCV004480870]uncertain significance129694575996945759Humanname
405807771CV3356613single nucleotide variantNM_152905.4(NEDD1):c.1735C>T (p.Arg579Trp)not specified [RCV004480873]uncertain significance129694577396945773Humanname
405807779CV3356617single nucleotide variantNM_152905.4(NEDD1):c.1736G>A (p.Arg579Gln)not specified [RCV004480877]uncertain significance129694577496945774Humanname
407526099CV3454786single nucleotide variantNM_152905.4(NEDD1):c.1333C>T (p.Pro445Ser)not specified [RCV004654689]uncertain significance129694359896943598Humanname
597670173CV3555791single nucleotide variantNM_152905.4(NEDD1):c.1535A>C (p.Asn512Thr)not specified [RCV004829649]uncertain significance129694467696944676Humanname
597670189CV3555793single nucleotide variantNM_152905.4(NEDD1):c.1282G>C (p.Gly428Arg)not specified [RCV004829651]uncertain significance129694261296942612Humanname
597670203CV3555795single nucleotide variantNM_152905.4(NEDD1):c.1040C>T (p.Thr347Met)not specified [RCV004829653]uncertain significance129693731696937316Humanname
598231426CV3990608single nucleotide variantNM_152905.4(NEDD1):c.1324G>A (p.Val442Met)not specified [RCV005381356]uncertain significance129694358996943589Humanname
598231432CV3990609single nucleotide variantNM_152905.4(NEDD1):c.1441G>C (p.Ala481Pro)not specified [RCV005381357]uncertain significance129694370696943706Humanname
598231438CV3990610single nucleotide variantNM_152905.4(NEDD1):c.1816G>A (p.Ala606Thr)not specified [RCV005381358]uncertain significance129695143696951436Humanname
598254129CV3990612single nucleotide variantNM_152905.4(NEDD1):c.1520G>A (p.Gly507Asp)not specified [RCV005385458]uncertain significance129694466196944661Humanname
598254140CV3990614single nucleotide variantNM_152905.4(NEDD1):c.1018A>T (p.Ile340Phe)not specified [RCV005385459]uncertain significance129693729496937294Humanname
598254149CV3990615single nucleotide variantNM_152905.4(NEDD1):c.1333C>G (p.Pro445Ala)not specified [RCV005385460]uncertain significance129694359896943598Humanname
598231456CV3990616single nucleotide variantNM_152905.4(NEDD1):c.1225A>G (p.Met409Val)not specified [RCV005381361]uncertain significance129694051696940516Humanname