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)

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

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405689382CV3246429single nucleotide variantNM_001079862.4(DBI):c.70G>C (p.Glu24Gln)not specified [RCV004372999]uncertain significance2119368248119368248Humanname
155921912CV2350743single nucleotide variantNM_001079862.4(DBI):c.152C>T (p.Thr51Met)not specified [RCV004207084]uncertain significance2119370764119370764Humanname
156245650CV2396704single nucleotide variantNM_001079862.4(DBI):c.130C>T (p.Arg44Trp)not specified [RCV004233860]uncertain significance2119370742119370742Humanname
405689377CV3246428single nucleotide variantNM_001079862.4(DBI):c.104C>T (p.Ala35Val)not specified [RCV004372998]uncertain significance2119368282119368282Humanname
597800520CV3651810single nucleotide variantNM_001079862.4(DBI):c.119T>G (p.Ile40Arg)not specified [RCV004905725]uncertain significance2119368297119368297Humanname
597800522CV3651811single nucleotide variantNM_001079862.4(DBI):c.200A>G (p.Lys67Arg)not specified [RCV004905726]uncertain significance2119372254119372254Humanname
15182330CV732737single nucleotide variantNM_001079862.4(DBI):c.256G>A (p.Gly86Arg)not provided [RCV000907796]benign2119372310119372310Humanname