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)

33 records found for search term Nop58
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405678260CV3355675single nucleotide variantNM_015934.5(NOP58):c.25G>C (p.Val9Leu)not specified [RCV004488125]uncertain significance2202265966202265966Humanname
155925743CV2277351single nucleotide variantNM_015934.5(NOP58):c.257C>A (p.Pro86Gln)not specified [RCV004144774]uncertain significance2202282432202282432Humanname
401865746CV2755622single nucleotide variantNM_015934.5(NOP58):c.154G>C (p.Asp52His)not specified [RCV004342009]uncertain significance2202277981202277981Humanname
405678253CV3355673single nucleotide variantNM_015934.5(NOP58):c.131T>G (p.Leu44Arg)not specified [RCV004488123]uncertain significance2202277958202277958Humanname
598207282CV4000721single nucleotide variantNM_015934.5(NOP58):c.182C>T (p.Thr61Ile)not specified [RCV005377080]uncertain significance2202282357202282357Humanname
598207289CV4000722single nucleotide variantNM_015934.5(NOP58):c.245A>C (p.Glu82Ala)not specified [RCV005377081]uncertain significance2202282420202282420Humanname
598240528CV4000724single nucleotide variantNM_015934.5(NOP58):c.277A>G (p.Lys93Glu)not specified [RCV005383082]uncertain significance2202282452202282452Humanname
156019165CV2370407single nucleotide variantNM_015934.5(NOP58):c.946G>A (p.Val316Ile)not specified [RCV004213304]uncertain significance2202295712202295712Humanname
155903405CV2386501single nucleotide variantNM_015934.5(NOP58):c.782T>C (p.Val261Ala)not specified [RCV004230861]uncertain significance2202292778202292778Humanname
329362442CV2466129single nucleotide variantNM_015934.5(NOP58):c.617A>G (p.Lys206Arg)not specified [RCV004279785]uncertain significance2202290440202290440Humanname
401777812CV2734205single nucleotide variantNM_015934.5(NOP58):c.511G>T (p.Asp171Tyr)not specified [RCV004332511]uncertain significance2202290334202290334Humanname
405678266CV3355676single nucleotide variantNM_015934.5(NOP58):c.398G>T (p.Arg133Leu)not specified [RCV004488126]uncertain significance2202284445202284445Humanname
597673114CV3563209single nucleotide variantNM_015934.5(NOP58):c.911C>G (p.Ser304Cys)not specified [RCV004830047]uncertain significance2202295677202295677Humanname
597673123CV3563210single nucleotide variantNM_015934.5(NOP58):c.386G>C (p.Gly129Ala)not specified [RCV004830048]uncertain significance2202284433202284433Humanname
597673130CV3563211single nucleotide variantNM_015934.5(NOP58):c.997C>G (p.Arg333Gly)not specified [RCV004830049]uncertain significance2202295763202295763Humanname
597673139CV3563212single nucleotide variantNM_015934.5(NOP58):c.841G>A (p.Ala281Thr)not specified [RCV004830050]uncertain significance2202292837202292837Humanname
598207270CV4000719single nucleotide variantNM_015934.5(NOP58):c.630A>T (p.Lys210Asn)not specified [RCV005377078]uncertain significance2202290453202290453Humanname
598207276CV4000720single nucleotide variantNM_015934.5(NOP58):c.637G>A (p.Asp213Asn)not specified [RCV005377079]uncertain significance2202291127202291127Humanname
598240534CV4000723single nucleotide variantNM_015934.5(NOP58):c.794C>G (p.Ser265Cys)not specified [RCV005383081]uncertain significance2202292790202292790Humanname
598207593CV4000725single nucleotide variantNM_015934.5(NOP58):c.854A>G (p.Asn285Ser)not specified [RCV005377082]uncertain significance2202292850202292850Humanname
155986170CV2233964single nucleotide variantNM_015934.5(NOP58):c.1036C>T (p.Leu346Phe)not specified [RCV004104306]uncertain significance2202295802202295802Humanname
156271280CV2286345single nucleotide variantNM_015934.5(NOP58):c.1166C>T (p.Ala389Val)not specified [RCV004146292]uncertain significance2202297473202297473Humanname
156013288CV2359052single nucleotide variantNM_015934.5(NOP58):c.1468A>G (p.Arg490Gly)not specified [RCV004212374]uncertain significance2202302986202302986Humanname
401719033CV2679393single nucleotide variantNM_015934.5(NOP58):c.1123T>C (p.Phe375Leu)not specified [RCV004285922]uncertain significance2202297430202297430Humanname
405678247CV3355672single nucleotide variantNM_015934.5(NOP58):c.1315T>C (p.Cys439Arg)not specified [RCV004488122]uncertain significance2202300280202300280Humanname
405678257CV3355674single nucleotide variantNM_015934.5(NOP58):c.1382A>G (p.Lys461Arg)not specified [RCV004488124]uncertain significance2202300347202300347Humanname
407498175CV3469165single nucleotide variantNM_015934.5(NOP58):c.1031C>T (p.Ala344Val)not specified [RCV004643935]uncertain significance2202295797202295797Humanname
407509934CV3469166single nucleotide variantNM_015934.5(NOP58):c.1255T>A (p.Tyr419Asn)not specified [RCV004647549]uncertain significance2202297893202297893Humanname
407498179CV3469167single nucleotide variantNM_015934.5(NOP58):c.1202G>A (p.Arg401Lys)not specified [RCV004643936]uncertain significance2202297509202297509Humanname
597673101CV3563207single nucleotide variantNM_015934.5(NOP58):c.1254A>T (p.Lys418Asn)not specified [RCV004830045]uncertain significance2202297892202297892Humanname
597673109CV3563208single nucleotide variantNM_015934.5(NOP58):c.1190C>G (p.Thr397Ser)not specified [RCV004830046]uncertain significance2202297497202297497Humanname
598207264CV4000718single nucleotide variantNM_015934.5(NOP58):c.1517C>G (p.Pro506Arg)not specified [RCV005377077]uncertain significance2202303035202303035Humanname
598207587CV4000726single nucleotide variantNM_015934.5(NOP58):c.1319C>G (p.Ser440Cys)not specified [RCV005377083]uncertain significance2202300284202300284Humanname