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)

11 records found for search term Ing4
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597775741CV3686792single nucleotide variantNM_016162.4(ING4):c.15G>T (p.Met5Ile)not specified [RCV004929457]uncertain significance1266630876663087Humanname
405783366CV3267631single nucleotide variantNM_016162.4(ING4):c.651C>T (p.Ser217=)not specified [RCV004398005]likely benign1266513806651380Humanname
405783352CV3267629single nucleotide variantNM_016162.4(ING4):c.201G>C (p.Gln67His)not specified [RCV004398003]uncertain significance1266533056653305Humanname
9686837CV171530single nucleotide variantNM_016162.4(ING4):c.326C>A (p.Ala109Asp)Prostate cancer [RCV000149055]uncertain significance1266530016653001Human2name
156088932CV2259087single nucleotide variantNM_016162.4(ING4):c.478A>C (p.Lys160Gln)not specified [RCV004120343]uncertain significance1266526816652681Humanname
155926160CV2348637single nucleotide variantNM_016162.4(ING4):c.428G>A (p.Arg143His)not specified [RCV004195861]uncertain significance1266527316652731Humanname
155958203CV2395126single nucleotide variantNM_016162.4(ING4):c.493C>T (p.Arg165Cys)not specified [RCV004236803]uncertain significance1266526666652666Humanname
405783360CV3267630single nucleotide variantNM_016162.4(ING4):c.502C>G (p.Pro168Ala)not specified [RCV004398004]uncertain significance1266524146652414Humanname
597775732CV3686790single nucleotide variantNM_016162.4(ING4):c.469G>C (p.Ala157Pro)not specified [RCV004929455]uncertain significance1266526906652690Humanname
597775737CV3686791single nucleotide variantNM_016162.4(ING4):c.427C>T (p.Arg143Cys)not specified [RCV004929456]uncertain significance1266527326652732Humanname
598181151CV3972492single nucleotide variantNM_016162.4(ING4):c.505G>A (p.Glu169Lys)not specified [RCV005352449]uncertain significance1266524116652411Humanname