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)

24 records found for search term Map2k4
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
151662523CV1330413single nucleotide variantNM_003010.4(MAP2K4):c.1087-1G>Cnot provided [RCV001823950]not provided171214114612141146Humanname
156388285CV2231764single nucleotide variantNM_003010.4(MAP2K4):c.14G>T (p.Ser5Ile)not specified [RCV004098578]uncertain significance171202090012020900Humanname
156307385CV2331963single nucleotide variantNM_003010.4(MAP2K4):c.16C>G (p.Pro6Ala)not specified [RCV004189023]uncertain significance171202090212020902Humanname
155968533CV2337853single nucleotide variantNM_003010.4(MAP2K4):c.25G>A (p.Gly9Ser)not specified [RCV004183863]uncertain significance171202091112020911Humanname
156090337CV2344653single nucleotide variantNM_003010.4(MAP2K4):c.25G>C (p.Gly9Arg)not specified [RCV004197420]uncertain significance171202091112020911Humanname
597626690CV3699994single nucleotide variantNM_003010.4(MAP2K4):c.26G>A (p.Gly9Asp)not specified [RCV004938731]uncertain significance171202091212020912Humanname
156056008CV2326628single nucleotide variantNM_003010.4(MAP2K4):c.70G>A (p.Val24Ile)not specified [RCV004183166]uncertain significance171202095612020956Humanname
156049000CV2336488single nucleotide variantNM_003010.4(MAP2K4):c.59C>T (p.Thr20Ile)not specified [RCV004194699]uncertain significance171202094512020945Humanname
401731859CV2674501single nucleotide variantNM_003010.4(MAP2K4):c.43G>A (p.Gly15Ser)not specified [RCV004291384]uncertain significance171202092912020929Humanname
405657610CV3288574single nucleotide variantNM_003010.4(MAP2K4):c.67C>A (p.Pro23Thr)not specified [RCV004416170]uncertain significance171202095312020953Humanname
597626700CV3699997single nucleotide variantNM_003010.4(MAP2K4):c.80C>A (p.Pro27Gln)not specified [RCV004938734]uncertain significance171202096612020966Humanname
401894518CV2788308single nucleotide variantNM_003010.4(MAP2K4):c.265A>C (p.Ile89Leu)not specified [RCV004352893]uncertain significance171208140212081402Humanname
405657605CV3288573single nucleotide variantNM_003010.4(MAP2K4):c.188C>A (p.Pro63His)not specified [RCV004416169]uncertain significance171205496112054961Humanname
156115687CV2221529single nucleotide variantNM_003010.4(MAP2K4):c.357G>T (p.Met119Ile)not specified [RCV004096797]uncertain significance171208149412081494Humanname
156290718CV2226220single nucleotide variantNM_003010.4(MAP2K4):c.868G>A (p.Val290Ile)not specified [RCV004099478]uncertain significance171212534812125348Humanname
401732510CV2675105single nucleotide variantNM_003010.4(MAP2K4):c.572A>G (p.Tyr191Cys)not specified [RCV004289885]uncertain significance171210784812107848Humanname
407424921CV3410863single nucleotide variantNM_003010.4(MAP2K4):c.947A>T (p.Gln316Leu)Neurodevelopmental disorder [RCV004586507]uncertain significance171212919412129194Human1name
597626693CV3699995single nucleotide variantNM_003010.4(MAP2K4):c.598A>G (p.Ile200Val)not specified [RCV004938732]uncertain significance171210787412107874Humanname
598196854CV3988652single nucleotide variantNM_003010.4(MAP2K4):c.706C>A (p.Leu236Ile)not specified [RCV005375337]uncertain significance171211325312113253Humanname
598166184CV3988653single nucleotide variantNM_003010.4(MAP2K4):c.784A>G (p.Arg262Gly)not specified [RCV005369302]uncertain significance171211333112113331Humanname
13435619CV432406single nucleotide variantNM_003010.4(MAP2K4):c.538C>G (p.Leu180Val)Neuroblastoma [RCV000505661]other171210781412107814Human2name
155978698CV2266542single nucleotide variantNM_003010.4(MAP2K4):c.1141G>A (p.Val381Ile)not specified [RCV004131099]uncertain significance171214120112141201Humanname
598166189CV3988654single nucleotide variantNM_003010.4(MAP2K4):c.1132G>C (p.Ala378Pro)not specified [RCV005369303]uncertain significance171214119212141192Humanname
8636011CV91234single nucleotide variantNM_001281435.1(MAP2K4):c.1010C>T (p.Pro337Leu)Malignant melanoma [RCV000071332]not provided171212922412129224Humanname