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)

22 records found for search term Eif3k
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405719309CV3238610single nucleotide variantNM_013234.4(EIF3K):c.7A>G (p.Met3Val)not specified [RCV004377805]uncertain significance193861927538619275Humanname
405719258CV3238604single nucleotide variantNM_013234.4(EIF3K):c.32T>G (p.Val11Gly)not specified [RCV004377799]uncertain significance193861930038619300Humanname
329383739CV2434862single nucleotide variantNM_013234.4(EIF3K):c.199G>A (p.Ala67Thr)not specified [RCV004250738]uncertain significance193862411738624117Humanname
407498971CV3438147single nucleotide variantNM_013234.4(EIF3K):c.178T>C (p.Phe60Leu)not specified [RCV004622634]uncertain significance193862409638624096Humanname
407498974CV3438148single nucleotide variantNM_013234.4(EIF3K):c.232C>G (p.Pro78Ala)not specified [RCV004622635]uncertain significance193862415038624150Humanname
597832923CV3496654single nucleotide variantNM_013234.4(EIF3K):c.128A>G (p.Asp43Gly)EIF3K related disorder [RCV005054489]uncertain significance193862040538620405Humanname , trait
598179274CV3961379single nucleotide variantNM_013234.4(EIF3K):c.140A>G (p.Asn47Ser)not specified [RCV005332481]uncertain significance193862041738620417Humanname
598179281CV3961380single nucleotide variantNM_013234.4(EIF3K):c.295A>G (p.Ile99Val)not specified [RCV005332482]uncertain significance193862604338626043Humanname
598179299CV3961383single nucleotide variantNM_013234.4(EIF3K):c.280C>G (p.Gln94Glu)not specified [RCV005332485]uncertain significance193862602838626028Humanname
156084049CV2299031single nucleotide variantNM_013234.4(EIF3K):c.410C>G (p.Ser137Cys)not specified [RCV004158551]uncertain significance193863248538632485Humanname
156361344CV2326501single nucleotide variantNM_013234.4(EIF3K):c.316G>A (p.Gly106Arg)not specified [RCV004183058]uncertain significance193862606438626064Humanname
156038783CV2384205single nucleotide variantNM_013234.4(EIF3K):c.464G>A (p.Arg155His)not specified [RCV004227600]uncertain significance193863264338632643Humanname
329397383CV2466102single nucleotide variantNM_013234.4(EIF3K):c.484C>T (p.Leu162Phe)not specified [RCV004279768]uncertain significance193863266338632663Humanname
405719266CV3238605single nucleotide variantNM_013234.4(EIF3K):c.346G>T (p.Ala116Ser)not specified [RCV004377800]uncertain significance193862609438626094Humanname
405719275CV3238606single nucleotide variantNM_013234.4(EIF3K):c.403G>A (p.Glu135Lys)not specified [RCV004377801]uncertain significance193863247838632478Humanname
405719282CV3238607single nucleotide variantNM_013234.4(EIF3K):c.463C>T (p.Arg155Cys)not specified [RCV004377802]uncertain significance193863264238632642Humanname
405719297CV3238609single nucleotide variantNM_013234.4(EIF3K):c.584G>A (p.Ser195Asn)not specified [RCV004377804]uncertain significance193863507738635077Humanname
407498966CV3438146single nucleotide variantNM_013234.4(EIF3K):c.508C>G (p.Leu170Val)not specified [RCV004622633]uncertain significance193863500138635001Humanname
597664371CV3674481single nucleotide variantNM_013234.4(EIF3K):c.519G>C (p.Trp173Cys)not specified [RCV004912316]uncertain significance193863501238635012Humanname
597664378CV3674482single nucleotide variantNM_013234.4(EIF3K):c.491A>T (p.Asp164Val)not specified [RCV004912317]uncertain significance193863267038632670Humanname
598179293CV3961382single nucleotide variantNM_013234.4(EIF3K):c.503G>T (p.Ser168Ile)not specified [RCV005332484]uncertain significance193863499638634996Humanname
598179305CV3961384single nucleotide variantNM_013234.4(EIF3K):c.644C>T (p.Ala215Val)not specified [RCV005332486]uncertain significance193863690738636907Humanname