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)

12 records found for search term Glrx2
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401744414CV2690655single nucleotide variantNM_016066.4(GLRX2):c.10C>G (p.Arg4Gly)not specified [RCV004298389]likely benign1193105629193105629Humanname
155960914CV2390783single nucleotide variantNM_016066.4(GLRX2):c.77T>C (p.Ile26Thr)not specified [RCV004241069]uncertain significance1193105562193105562Humanname
598263742CV3977965single nucleotide variantNM_016066.4(GLRX2):c.50T>G (p.Val17Gly)not specified [RCV005348644]uncertain significance1193105589193105589Humanname
156297487CV2246851single nucleotide variantNM_197962.3(GLRX2):c.161C>A (p.Thr54Lys)not specified [RCV004112662]uncertain significance1193101163193101163Humanname
329385997CV2458690single nucleotide variantNM_197962.3(GLRX2):c.157G>A (p.Ala53Thr)not specified [RCV004268351]uncertain significance1193101167193101167Humanname
401762128CV2699529single nucleotide variantNM_197962.3(GLRX2):c.139T>C (p.Ser47Pro)not specified [RCV004299736]uncertain significance1193101185193101185Humanname
598263739CV3977964single nucleotide variantNM_197962.3(GLRX2):c.180C>G (p.Ile60Met)not specified [RCV005348643]uncertain significance1193101144193101144Humanname
156060003CV2343745single nucleotide variantNM_197962.3(GLRX2):c.451C>T (p.His151Tyr)not specified [RCV004190767]uncertain significance1193096669193096669Humanname
156176779CV2374470single nucleotide variantNM_197962.3(GLRX2):c.485A>G (p.Glu162Gly)not specified [RCV004231977]uncertain significance1193096635193096635Humanname
401724206CV2714754single nucleotide variantNM_197962.3(GLRX2):c.299A>G (p.Asp100Gly)not specified [RCV004320323]uncertain significance1193097645193097645Humanname
597760026CV3681459single nucleotide variantNM_197962.3(GLRX2):c.313G>A (p.Gly105Arg)not specified [RCV004925625]uncertain significance1193097631193097631Humanname
598263736CV3977963single nucleotide variantNM_197962.3(GLRX2):c.419T>C (p.Leu140Pro)not specified [RCV005348642]uncertain significance1193096701193096701Humanname