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)

28 records found for search term E2f5
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405752144CV3238252single nucleotide variantNM_001951.4(E2F5):c.92A>G (p.Gln31Arg)not specified [RCV004382128]uncertain significance88517751285177512Humanname
597735629CV3670595single nucleotide variantNM_001951.4(E2F5):c.67C>T (p.Pro23Ser)not specified [RCV004920507]uncertain significance88517748785177487Humanname
597802915CV3670598single nucleotide variantNM_001951.4(E2F5):c.32A>C (p.Gln11Pro)not specified [RCV004906925]uncertain significance88517745285177452Humanname
155915669CV2274335single nucleotide variantNM_001951.4(E2F5):c.233C>A (p.Ala78Glu)not specified [RCV004136724]uncertain significance88517765385177653Humanname
156197181CV2306785single nucleotide variantNM_001951.4(E2F5):c.124G>A (p.Gly42Arg)not specified [RCV004159360]uncertain significance88517754485177544Humanname
401726985CV2691925single nucleotide variantNM_001951.4(E2F5):c.211G>A (p.Asp71Asn)not specified [RCV004301661]uncertain significance88517763185177631Humanname
401773922CV2702496single nucleotide variantNM_001951.4(E2F5):c.243T>A (p.Asp81Glu)not specified [RCV004316999]uncertain significance88520215585202155Humanname
405752116CV3238248single nucleotide variantNM_001951.4(E2F5):c.139G>A (p.Gly47Ser)not specified [RCV004382124]uncertain significance88517755985177559Humanname
597802905CV3670592single nucleotide variantNM_001951.4(E2F5):c.143G>T (p.Ser48Ile)not specified [RCV004906920]uncertain significance88517756385177563Humanname
598268439CV3953858single nucleotide variantNM_001951.4(E2F5):c.116C>G (p.Pro39Arg)not specified [RCV005327099]uncertain significance88517753685177536Humanname
598268445CV3953859single nucleotide variantNM_001951.4(E2F5):c.245C>T (p.Thr82Ile)not specified [RCV005327100]uncertain significance88520215785202157Humanname
155971935CV2227995single nucleotide variantNM_001951.4(E2F5):c.903T>A (p.Asp301Glu)not specified [RCV004096239]uncertain significance88521217685212176Humanname
155914873CV2242859single nucleotide variantNM_001951.4(E2F5):c.381A>G (p.Ile127Met)not specified [RCV004107451]uncertain significance88520313085203130Humanname
156218189CV2253932single nucleotide variantNM_001951.4(E2F5):c.621G>C (p.Gln207His)not specified [RCV004127608]uncertain significance88520914785209147Humanname
156156852CV2266246single nucleotide variantNM_001951.4(E2F5):c.974A>T (p.Tyr325Phe)not specified [RCV004128809]uncertain significance88521379585213795Humanname
155977099CV2266373single nucleotide variantNM_001951.4(E2F5):c.531C>A (p.Asp177Glu)not specified [RCV004129184]uncertain significance88520620185206201Humanname
156035581CV2282990single nucleotide variantNM_001951.4(E2F5):c.574G>T (p.Ala192Ser)not specified [RCV004143619]uncertain significance88520744885207448Humanname
156174976CV2345981single nucleotide variantNM_001951.4(E2F5):c.549T>A (p.Asn183Lys)not specified [RCV004199013]uncertain significance88520621985206219Humanname
401888133CV2768950single nucleotide variantNM_001951.4(E2F5):c.470G>A (p.Ser157Asn)not specified [RCV004347046]uncertain significance88520321985203219Humanname
405752122CV3238249single nucleotide variantNM_001951.4(E2F5):c.694G>C (p.Glu232Gln)not specified [RCV004382125]uncertain significance88520922085209220Humanname
405752133CV3238250single nucleotide variantNM_001951.4(E2F5):c.827A>C (p.His276Pro)not specified [RCV004382126]uncertain significance88520935385209353Humanname
405752140CV3238251single nucleotide variantNM_001951.4(E2F5):c.853C>A (p.Gln285Lys)not specified [RCV004382127]uncertain significance88520937985209379Humanname
597802909CV3670594single nucleotide variantNM_001951.4(E2F5):c.962C>T (p.Pro321Leu)not specified [RCV004906922]uncertain significance88521378385213783Humanname
597802911CV3670596single nucleotide variantNM_001951.4(E2F5):c.685A>G (p.Ile229Val)not specified [RCV004906923]uncertain significance88520921185209211Humanname
597802913CV3670597single nucleotide variantNM_001951.4(E2F5):c.857A>G (p.Gln286Arg)not specified [RCV004906924]uncertain significance88520938385209383Humanname
597802918CV3670599single nucleotide variantNM_001951.4(E2F5):c.488A>G (p.Asp163Gly)not specified [RCV004906926]uncertain significance88520323785203237Humanname
598268432CV3953857single nucleotide variantNM_001951.4(E2F5):c.970G>A (p.Asp324Asn)not specified [RCV005327098]uncertain significance88521379185213791Humanname
598268450CV3953860single nucleotide variantNM_001951.4(E2F5):c.833C>T (p.Ser278Phe)not specified [RCV005327101]uncertain significance88520935985209359Humanname