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 Eif2s2
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15180892CV742354single nucleotide variantNM_003908.5(EIF2S2):c.132G>C (p.Val44=)not provided [RCV000907461]likely benign203410542934105429Humanname
598179057CV3961342single nucleotide variantNM_003908.5(EIF2S2):c.36G>A (p.Met12Ile)not specified [RCV005332444]uncertain significance203410552534105525Humanname
15111286CV757463single nucleotide variantNM_003908.5(EIF2S2):c.987T>C (p.Arg329=)not provided [RCV000916702]likely benign203408974534089745Humanname
15150776CV757464single nucleotide variantNM_003908.5(EIF2S2):c.528C>T (p.Tyr176=)not provided [RCV000923540]benign203409742234097422Humanname
598179044CV3961340single nucleotide variantNM_003908.5(EIF2S2):c.158A>G (p.Asp53Gly)not specified [RCV005332442]uncertain significance203410540334105403Humanname
156255664CV2229318single nucleotide variantNM_003908.5(EIF2S2):c.582G>C (p.Met194Ile)not specified [RCV004101112]uncertain significance203409675834096758Humanname
156249126CV2264067single nucleotide variantNM_003908.5(EIF2S2):c.985C>T (p.Arg329Cys)not specified [RCV004138078]uncertain significance203408974734089747Humanname
407498851CV3438108single nucleotide variantNM_003908.5(EIF2S2):c.481A>C (p.Asn161His)not specified [RCV004622595]uncertain significance203409746934097469Humanname
597746571CV3674416single nucleotide variantNM_003908.5(EIF2S2):c.336A>C (p.Glu112Asp)not specified [RCV004922721]uncertain significance203409859534098595Humanname
597746577CV3674417single nucleotide variantNM_003908.5(EIF2S2):c.414A>C (p.Glu138Asp)not specified [RCV004922722]uncertain significance203409851734098517Humanname
597746583CV3674418single nucleotide variantNM_003908.5(EIF2S2):c.545G>A (p.Arg182Gln)not specified [RCV004922723]uncertain significance203409679534096795Humanname
598179051CV3961341single nucleotide variantNM_003908.5(EIF2S2):c.554A>G (p.Asn185Ser)not specified [RCV005332443]uncertain significance203409678634096786Humanname