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)

16 records found for search term Rspo3
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401768081CV2735165single nucleotide variantNM_032784.5(RSPO3):c.25C>T (p.Leu9Phe)not specified [RCV004333861]likely benign6127119217127119217Humanname
405756750CV3313415single nucleotide variantNM_032784.5(RSPO3):c.46A>G (p.Met16Val)not specified [RCV004454620]uncertain significance6127119238127119238Humanname
401880073CV2769898single nucleotide variantNM_032784.5(RSPO3):c.245G>A (p.Ser82Asn)not specified [RCV004353744]uncertain significance6127148795127148795Humanname
405756745CV3313414single nucleotide variantNM_032784.5(RSPO3):c.103C>A (p.Pro35Thr)not specified [RCV004454619]uncertain significance6127148653127148653Humanname
407513965CV3472988single nucleotide variantNM_032784.5(RSPO3):c.229C>G (p.Leu77Val)not specified [RCV004674319]uncertain significance6127148779127148779Humanname
597711819CV3604839single nucleotide variantNM_032784.5(RSPO3):c.107A>G (p.Asn36Ser)not specified [RCV004861116]uncertain significance6127148657127148657Humanname
156384148CV2220293single nucleotide variantNM_032784.5(RSPO3):c.770G>A (p.Arg257Gln)not specified [RCV004095719]uncertain significance6127195958127195958Humanname
156159685CV2322760single nucleotide variantNM_032784.5(RSPO3):c.635G>C (p.Gly212Ala)not specified [RCV004182869]uncertain significance6127195823127195823Humanname
329378768CV2459934single nucleotide variantNM_032784.5(RSPO3):c.689A>C (p.Glu230Ala)not specified [RCV004279422]uncertain significance6127195877127195877Humanname
401740487CV2684369single nucleotide variantNM_032784.5(RSPO3):c.547C>T (p.Pro183Ser)not specified [RCV004289014]uncertain significance6127155351127155351Humanname
405756757CV3313416single nucleotide variantNM_032784.5(RSPO3):c.754C>G (p.Gln252Glu)not specified [RCV004454621]uncertain significance6127195942127195942Humanname
405756764CV3313417single nucleotide variantNM_032784.5(RSPO3):c.794C>T (p.Ser265Leu)not specified [RCV004454622]uncertain significance6127195982127195982Humanname
597711808CV3604838single nucleotide variantNM_032784.5(RSPO3):c.348T>A (p.Ser116Arg)not specified [RCV004861115]uncertain significance6127150484127150484Humanname
597711828CV3604840single nucleotide variantNM_032784.5(RSPO3):c.539T>C (p.Ile180Thr)not specified [RCV004861117]uncertain significance6127155343127155343Humanname
598193269CV3899512single nucleotide variantNM_032784.5(RSPO3):c.593A>G (p.Lys198Arg)not specified [RCV005267307]uncertain significance6127155397127155397Humanname
598193277CV3899513single nucleotide variantNM_032784.5(RSPO3):c.398T>G (p.Leu133Trp)not specified [RCV005267308]uncertain significance6127150534127150534Humanname