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 Homo sapiens
(View Results for all Objects and Ontologies)

20 records found for search term Nrsn1
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156220831CV2345085single nucleotide variantNM_080723.5(NRSN1):c.68G>A (p.Arg23His)not specified [RCV004193360]uncertain significance62413439524134395Humanname
156250815CV2359178single nucleotide variantNM_080723.5(NRSN1):c.37G>A (p.Ala13Thr)not specified [RCV004214532]uncertain significance62413436424134364Humanname
401734671CV2688588single nucleotide variantNM_080723.5(NRSN1):c.82T>G (p.Ser28Ala)not specified [RCV004301544]uncertain significance62413440924134409Humanname
598220503CV3998157single nucleotide variantNM_080723.5(NRSN1):c.67C>T (p.Arg23Cys)not specified [RCV005379520]uncertain significance62413439424134394Humanname
156284241CV2317525single nucleotide variantNM_080723.5(NRSN1):c.104A>G (p.Glu35Gly)not specified [RCV004172482]uncertain significance62413443124134431Humanname
156051120CV2328933single nucleotide variantNM_080723.5(NRSN1):c.110G>A (p.Cys37Tyr)not specified [RCV004180235]uncertain significance62413443724134437Humanname
156348420CV2383107single nucleotide variantNM_080723.5(NRSN1):c.295G>T (p.Val99Leu)not specified [RCV004217678]uncertain significance62414565324145653Humanname
401782511CV2719853single nucleotide variantNM_080723.5(NRSN1):c.110G>C (p.Cys37Ser)not specified [RCV004329267]uncertain significance62413443724134437Humanname
405709451CV3359278single nucleotide variantNM_080723.5(NRSN1):c.179T>C (p.Val60Ala)not specified [RCV004493625]uncertain significance62413450624134506Humanname
407477216CV3465933single nucleotide variantNM_080723.5(NRSN1):c.232A>G (p.Thr78Ala)not specified [RCV004638717]uncertain significance62414559024145590Humanname
597706959CV3576917single nucleotide variantNM_080723.5(NRSN1):c.220A>G (p.Ile74Val)not specified [RCV004840396]uncertain significance62414557824145578Humanname
598264801CV3998158single nucleotide variantNM_080723.5(NRSN1):c.171G>C (p.Trp57Cys)not specified [RCV005387830]uncertain significance62413449824134498Humanname
156118618CV2219188single nucleotide variantNM_080723.5(NRSN1):c.571C>G (p.Pro191Ala)not specified [RCV004093459]uncertain significance62414592924145929Humanname
156284172CV2288957single nucleotide variantNM_080723.5(NRSN1):c.488C>A (p.Ala163Asp)not specified [RCV004149919]uncertain significance62414584624145846Humanname
156270692CV2315591single nucleotide variantNM_080723.5(NRSN1):c.463A>C (p.Lys155Gln)not specified [RCV004169631]uncertain significance62414582124145821Humanname
155996122CV2393147single nucleotide variantNM_080723.5(NRSN1):c.500C>T (p.Pro167Leu)not specified [RCV004226624]uncertain significance62414585824145858Humanname
405709461CV3359279single nucleotide variantNM_080723.5(NRSN1):c.431C>T (p.Ser144Phe)not specified [RCV004493626]uncertain significance62414578924145789Humanname
407516966CV3465932single nucleotide variantNM_080723.5(NRSN1):c.304G>A (p.Asp102Asn)not specified [RCV004650470]uncertain significance62414566224145662Humanname
598220510CV3998159single nucleotide variantNM_080723.5(NRSN1):c.412G>A (p.Val138Met)not specified [RCV005379521]uncertain significance62414577024145770Humanname
598220517CV3998160single nucleotide variantNM_080723.5(NRSN1):c.374T>C (p.Ile125Thr)not specified [RCV005379522]uncertain significance62414573224145732Humanname