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Variants search result for Homo sapiens
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71 records found for search term Rrn3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156069088CV2355754single nucleotide variantNM_018427.5(RRN3):c.5C>T (p.Ala2Val)not specified [RCV004201160]uncertain significance161509422915094229Humanname
15161931CV739976single nucleotide variantNM_018427.5(RRN3):c.63T>C (p.Val21=)not provided [RCV000903449]likely benign161509417115094171Humanname
405740804CV3316637single nucleotide variantNM_018427.5(RRN3):c.22A>G (p.Thr8Ala)not specified [RCV004452348]uncertain significance161509421215094212Humanname
329349732CV2443101single nucleotide variantNM_018427.5(RRN3):c.91A>G (p.Ile31Val)not specified [RCV004253687]uncertain significance161509261315092613Humanname
405740825CV3316640single nucleotide variantNM_018427.5(RRN3):c.40G>A (p.Ala14Thr)not specified [RCV004452351]uncertain significance161509419415094194Humanname
401859465CV2786612single nucleotide variantNM_018427.5(RRN3):c.203C>G (p.Thr68Arg)not specified [RCV004363751]uncertain significance161509136415091364Humanname
401904603CV2807663single nucleotide variantNM_018427.5(RRN3):c.1854C>T (p.Thr618=)not provided [RCV003426599]likely benign161506184615061846Humanname
405740757CV3316630single nucleotide variantNM_018427.5(RRN3):c.144A>C (p.Lys48Asn)not specified [RCV004452341]uncertain significance161509256015092560Humanname
405740769CV3316632single nucleotide variantNM_018427.5(RRN3):c.170C>G (p.Thr57Arg)not specified [RCV004452343]uncertain significance161509253415092534Humanname
405740779CV3316633single nucleotide variantNM_018427.5(RRN3):c.172G>C (p.Glu58Gln)not specified [RCV004452344]uncertain significance161509253215092532Humanname
597687161CV3604555single nucleotide variantNM_018427.5(RRN3):c.247A>G (p.Ile83Val)not specified [RCV004860989]uncertain significance161509132015091320Humanname
597687170CV3604557single nucleotide variantNM_018427.5(RRN3):c.269A>G (p.Asn90Ser)not specified [RCV004860990]uncertain significance161508643815086438Humanname
597686654CV3604565single nucleotide variantNM_018427.5(RRN3):c.182T>A (p.Leu61Gln)not specified [RCV004855042]uncertain significance161509252215092522Humanname
597686666CV3604566single nucleotide variantNM_018427.5(RRN3):c.266T>C (p.Ile89Thr)not specified [RCV004855043]uncertain significance161508644115086441Humanname
598192158CV3903192single nucleotide variantNM_018427.5(RRN3):c.287G>A (p.Arg96His)not specified [RCV005267097]uncertain significance161508642015086420Humanname
598192194CV3903196single nucleotide variantNM_018427.5(RRN3):c.297C>G (p.Ile99Met)not specified [RCV005267101]uncertain significance161508641015086410Humanname
598192224CV3903200single nucleotide variantNM_018427.5(RRN3):c.228C>A (p.Asn76Lys)not specified [RCV005267105]uncertain significance161509133915091339Humanname
15192631CV703499single nucleotide variantNM_018427.5(RRN3):c.238G>A (p.Asp80Asn)not provided [RCV000955129]benign161509132915091329Human7name
15192631CV703499single nucleotide variantNM_018427.5(RRN3):c.238G>A (p.Asp80Asn)not provided [RCV000955129]benign161509132915091330Human7name
156260868CV2204845single nucleotide variantNM_018427.5(RRN3):c.406C>G (p.Leu136Val)not specified [RCV004075095]uncertain significance161508619515086195Humanname
156234010CV2245311single nucleotide variantNM_018427.5(RRN3):c.559C>T (p.His187Tyr)not specified [RCV004107067]uncertain significance161508467915084679Humanname
155978240CV2266496single nucleotide variantNM_018427.5(RRN3):c.530A>G (p.Asp177Gly)not specified [RCV004131064]uncertain significance161508564115085641Humanname
156066614CV2270789single nucleotide variantNM_018427.5(RRN3):c.910G>T (p.Asp304Tyr)not specified [RCV004131842]uncertain significance161507481015074810Humanname
156293801CV2293108single nucleotide variantNM_018427.5(RRN3):c.535C>A (p.Leu179Ile)not specified [RCV004148846]uncertain significance161508470315084703Humanname
156200144CV2313049single nucleotide variantNM_018427.5(RRN3):c.676G>A (p.Val226Ile)not specified [RCV004161327]uncertain significance161508008715080087Humanname
156300892CV2322611single nucleotide variantNM_018427.5(RRN3):c.328A>G (p.Ile110Val)not specified [RCV004182751]uncertain significance161508637915086379Humanname
156383958CV2361763single nucleotide variantNM_018427.5(RRN3):c.622C>G (p.Leu208Val)not specified [RCV004223238]uncertain significance161508355715083557Humanname
401747011CV2694950single nucleotide variantNM_018427.5(RRN3):c.589G>A (p.Val197Ile)not specified [RCV004301335]uncertain significance161508464915084649Humanname
401748517CV2720034single nucleotide variantNM_018427.5(RRN3):c.698G>C (p.Ser233Thr)not specified [RCV004323610]uncertain significance161508006515080065Humanname
405740813CV3316638single nucleotide variantNM_018427.5(RRN3):c.311A>G (p.Lys104Arg)not specified [RCV004452349]uncertain significance161508639615086396Humanname
405740819CV3316639single nucleotide variantNM_018427.5(RRN3):c.400G>A (p.Gly134Ser)not specified [RCV004452350]uncertain significance161508620115086201Humanname
405740833CV3316641single nucleotide variantNM_018427.5(RRN3):c.805A>G (p.Thr269Ala)not specified [RCV004452352]likely benign161507661115076611Humanname
407450769CV3476346single nucleotide variantNM_018427.5(RRN3):c.736C>G (p.Leu246Val)not specified [RCV004665901]uncertain significance161508002715080027Humanname
407451258CV3476349single nucleotide variantNM_018427.5(RRN3):c.655G>A (p.Glu219Lys)not specified [RCV004674282]uncertain significance161508352415083524Humanname
407450777CV3476350single nucleotide variantNM_018427.5(RRN3):c.680A>T (p.His227Leu)not specified [RCV004665904]uncertain significance161508008315080083Humanname
597686625CV3604556single nucleotide variantNM_018427.5(RRN3):c.839C>G (p.Thr280Arg)not specified [RCV004855038]uncertain significance161507657715076577Humanname
597686635CV3604561single nucleotide variantNM_018427.5(RRN3):c.938G>A (p.Arg313His)not specified [RCV004855040]uncertain significance161507478215074782Humanname
597686644CV3604562single nucleotide variantNM_018427.5(RRN3):c.949C>G (p.Leu317Val)not specified [RCV004855041]uncertain significance161507477115074771Humanname
597687179CV3604563single nucleotide variantNM_018427.5(RRN3):c.778C>T (p.Arg260Trp)not specified [RCV004860991]uncertain significance161507663815076638Humanname
597686677CV3604567single nucleotide variantNM_018427.5(RRN3):c.809C>G (p.Ala270Gly)not specified [RCV004855044]uncertain significance161507660715076607Humanname
597686687CV3604568single nucleotide variantNM_018427.5(RRN3):c.880C>G (p.His294Asp)not specified [RCV004855045]uncertain significance161507484015074840Humanname
598192146CV3903191single nucleotide variantNM_018427.5(RRN3):c.437C>T (p.Pro146Leu)not specified [RCV005267096]uncertain significance161508616415086164Humanname
598192168CV3903193single nucleotide variantNM_018427.5(RRN3):c.334A>G (p.Ile112Val)not specified [RCV005267098]uncertain significance161508637315086373Humanname
598192234CV3903202single nucleotide variantNM_018427.5(RRN3):c.299T>C (p.Met100Thr)not specified [RCV005267107]uncertain significance161508640815086408Humanname
598192240CV3903203single nucleotide variantNM_018427.5(RRN3):c.922C>T (p.His308Tyr)not specified [RCV005267108]uncertain significance161507479815074798Humanname
598192253CV3903205single nucleotide variantNM_018427.5(RRN3):c.629A>G (p.Glu210Gly)not specified [RCV005267110]uncertain significance161508355015083550Humanname
156068887CV2237086single nucleotide variantNM_018427.5(RRN3):c.1517T>G (p.Leu506Arg)not specified [RCV004114846]uncertain significance161506820515068205Humanname
155924551CV2277142single nucleotide variantNM_018427.5(RRN3):c.1634G>T (p.Gly545Val)not specified [RCV004142788]uncertain significance161506529115065291Humanname
156003958CV2295803single nucleotide variantNM_018427.5(RRN3):c.1921C>T (p.Pro641Ser)not specified [RCV004151726]uncertain significance161506177915061779Humanname
155981796CV2337088single nucleotide variantNM_018427.5(RRN3):c.1405T>G (p.Phe469Val)not specified [RCV004192851]uncertain significance161507010915070109Humanname
329350454CV2469220single nucleotide variantNM_018427.5(RRN3):c.1642T>C (p.Ser548Pro)not specified [RCV004280567]uncertain significance161506528315065283Humanname
329350532CV2470056single nucleotide variantNM_018427.5(RRN3):c.1490G>A (p.Ser497Asn)not specified [RCV004287325]uncertain significance161506823215068232Humanname
401745822CV2704933single nucleotide variantNM_018427.5(RRN3):c.1608G>T (p.Met536Ile)not specified [RCV004307503]uncertain significance161506531715065317Humanname
401856900CV2759325single nucleotide variantNM_018427.5(RRN3):c.1429G>A (p.Gly477Arg)not specified [RCV004335908]uncertain significance161507008515070085Humanname
401859388CV2789447single nucleotide variantNM_018427.5(RRN3):c.1660A>G (p.Asn554Asp)not specified [RCV004360079]uncertain significance161506526515065265Humanname
405740762CV3316631single nucleotide variantNM_018427.5(RRN3):c.1490G>C (p.Ser497Thr)not specified [RCV004452342]uncertain significance161506823215068232Humanname
405740785CV3316634single nucleotide variantNM_018427.5(RRN3):c.1753A>C (p.Ser585Arg)not specified [RCV004452345]uncertain significance161506323715063237Humanname
405740800CV3316636single nucleotide variantNM_018427.5(RRN3):c.1855G>A (p.Val619Met)not specified [RCV004452347]uncertain significance161506184515061845Humanname
407450766CV3476345single nucleotide variantNM_018427.5(RRN3):c.1036G>T (p.Asp346Tyr)not specified [RCV004665900]uncertain significance161507304215073042Humanname
407450771CV3476347single nucleotide variantNM_018427.5(RRN3):c.1913T>A (p.Val638Glu)not specified [RCV004665902]uncertain significance161506178715061787Humanname
407450774CV3476348single nucleotide variantNM_018427.5(RRN3):c.1409G>A (p.Arg470Lys)not specified [RCV004665903]uncertain significance161507010515070105Humanname
407450779CV3476351single nucleotide variantNM_018427.5(RRN3):c.1174G>T (p.Asp392Tyr)not specified [RCV004665905]uncertain significance161507120615071206Humanname
407450783CV3476352single nucleotide variantNM_018427.5(RRN3):c.1449G>C (p.Leu483Phe)not specified [RCV004665906]uncertain significance161506827315068273Humanname
597687188CV3604564single nucleotide variantNM_018427.5(RRN3):c.1205C>T (p.Ala402Val)not specified [RCV004860992]uncertain significance161507117515071175Humanname
597686696CV3604569single nucleotide variantNM_018427.5(RRN3):c.1036G>A (p.Asp346Asn)not specified [RCV004855046]uncertain significance161507304215073042Humanname
598192176CV3903194single nucleotide variantNM_018427.5(RRN3):c.1478G>A (p.Arg493Gln)not specified [RCV005267099]uncertain significance161506824415068244Humanname
598192185CV3903195single nucleotide variantNM_018427.5(RRN3):c.1195A>G (p.Ile399Val)not specified [RCV005267100]uncertain significance161507118515071185Humanname
598192203CV3903197single nucleotide variantNM_018427.5(RRN3):c.1274G>A (p.Cys425Tyr)not specified [RCV005267102]uncertain significance161507024015070240Humanname
598192213CV3903198single nucleotide variantNM_018427.5(RRN3):c.1744G>A (p.Glu582Lys)not specified [RCV005267103]uncertain significance161506324615063246Humanname
598192229CV3903201single nucleotide variantNM_018427.5(RRN3):c.1951C>T (p.Leu651Phe)not specified [RCV005267106]uncertain significance161506174915061749Humanname
598192247CV3903204single nucleotide variantNM_018427.5(RRN3):c.1159T>C (p.Trp387Arg)not specified [RCV005267109]uncertain significance161507122115071221Humanname