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)

7 records found for search term Rps5
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156046150CV2340229single nucleotide variantNM_001009.4(RPS5):c.32T>G (p.Val11Gly)not specified [RCV004192460]uncertain significance195838816958388169Humanname
401884888CV2786609single nucleotide variantNM_001009.4(RPS5):c.274A>G (p.Ile92Val)not specified [RCV004363748]uncertain significance195839314158393141Humanname
598220347CV3903019single nucleotide variantNM_001009.4(RPS5):c.148C>T (p.Pro50Ser)not specified [RCV005272458]uncertain significance195839301558393015Humanname
156071135CV2354347single nucleotide variantNM_001009.4(RPS5):c.476G>A (p.Arg159His)not specified [RCV004199885]uncertain significance195839452558394525Humanname
156263678CV2375229single nucleotide variantNM_001009.4(RPS5):c.475C>A (p.Arg159Ser)not specified [RCV004230262]uncertain significance195839452458394524Humanname
401734569CV2688561single nucleotide variantNM_001009.4(RPS5):c.506T>C (p.Ile169Thr)not specified [RCV004301521]uncertain significance195839455558394555Humanname
8637099CV92325single nucleotide variantNM_001009.3(RPS5):c.361C>T (p.Pro121Ser)Malignant melanoma [RCV000072423]not provided195839340158393401Humanname