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)

10 records found for search term Mapre3
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407494637CV3456836single nucleotide variantNM_012326.4(MAPRE3):c.248A>G (p.Lys83Arg)not specified [RCV004643039]uncertain significance22702345827023458Humanname
155980413CV2263653single nucleotide variantNM_012326.4(MAPRE3):c.460G>A (p.Gly154Ser)not specified [RCV004135654]uncertain significance22702428827024288Humanname
156179103CV2298349single nucleotide variantNM_012326.4(MAPRE3):c.610G>A (p.Glu204Lys)not specified [RCV004160244]uncertain significance22702572327025723Humanname
156039268CV2332705single nucleotide variantNM_012326.4(MAPRE3):c.814G>C (p.Glu272Gln)not specified [RCV004189380]uncertain significance22702631627026316Humanname
329382458CV2449004single nucleotide variantNM_012326.4(MAPRE3):c.407C>T (p.Ala136Val)not specified [RCV004264083]uncertain significance22702423527024235Humanname
401760706CV2695133single nucleotide variantNM_012326.4(MAPRE3):c.632A>T (p.Asp211Val)not specified [RCV004303289]uncertain significance22702588727025887Humanname
401780023CV2725829single nucleotide variantNM_012326.4(MAPRE3):c.569C>T (p.Ser190Leu)not specified [RCV004316295]uncertain significance22702568227025682Humanname
597635870CV3697471single nucleotide variantNM_012326.4(MAPRE3):c.542C>A (p.Pro181His)not specified [RCV004940676]uncertain significance22702565527025655Humanname
597635874CV3697472single nucleotide variantNM_012326.4(MAPRE3):c.440A>G (p.Asn147Ser)not specified [RCV004940677]uncertain significance22702426827024268Humanname
597635880CV3697473single nucleotide variantNM_012326.4(MAPRE3):c.503A>T (p.Asn168Ile)not specified [RCV004940678]uncertain significance22702561627025616Humanname