Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Behavioral & Substance Use Disorder Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)
Variants search result for All species
(View Results for all Objects and Ontologies)

71 records found for search term Rrn3
Refine Term:
Sort By:
           Export CSV TAB Print

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