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)

9 records found for search term Hmgb2
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405790860CV3266831single nucleotide variantNM_002129.4(HMGB2):c.168G>T (p.Glu56Asp)not specified [RCV004399654]uncertain significance4173333197173333197Humanname
597791260CV3682788single nucleotide variantNM_002129.4(HMGB2):c.216C>A (p.Asp72Glu)not specified [RCV004933447]uncertain significance4173333149173333149Humanname
156346927CV2300766single nucleotide variantNM_002129.4(HMGB2):c.601G>A (p.Glu201Lys)not specified [RCV004155697]uncertain significance4173332109173332109Humanname
156065635CV2376103single nucleotide variantNM_002129.4(HMGB2):c.493A>G (p.Lys165Glu)not specified [RCV004220337]uncertain significance4173332217173332217Humanname
329385907CV2428137single nucleotide variantNM_002129.4(HMGB2):c.556G>A (p.Glu186Lys)not specified [RCV004251179]uncertain significance4173332154173332154Humanname
329384241CV2435001single nucleotide variantNM_002129.4(HMGB2):c.567T>G (p.Asp189Glu)not specified [RCV004250866]uncertain significance4173332143173332143Humanname
407527647CV3433637single nucleotide variantNM_002129.4(HMGB2):c.591A>T (p.Glu197Asp)not specified [RCV004632863]uncertain significance4173332119173332119Humanname
407527651CV3433638single nucleotide variantNM_002129.4(HMGB2):c.373A>G (p.Thr125Ala)not specified [RCV004632864]uncertain significance4173332919173332919Humanname
597791257CV3682787single nucleotide variantNM_002129.4(HMGB2):c.344G>A (p.Ser115Asn)not specified [RCV004933446]uncertain significance4173332948173332948Humanname