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)

6 records found for search term Tmem203
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597753888CV3613671single nucleotide variantNM_053045.2(TMEM203):c.4C>T (p.Leu2Phe)not specified [RCV004867475]uncertain significance9137205411137205411Humanname
597753897CV3613673single nucleotide variantNM_053045.2(TMEM203):c.11C>T (p.Ser4Leu)not specified [RCV004867477]uncertain significance9137205404137205404Humanname
598213736CV3917595single nucleotide variantNM_053045.2(TMEM203):c.125C>G (p.Pro42Arg)not specified [RCV005292380]uncertain significance9137205290137205290Humanname
156283588CV2360589single nucleotide variantNM_053045.2(TMEM203):c.317C>A (p.Ala106Glu)not specified [RCV004211346]uncertain significance9137205098137205098Humanname
597753901CV3613674single nucleotide variantNM_053045.2(TMEM203):c.308A>G (p.Gln103Arg)not specified [RCV004867478]uncertain significance9137205107137205107Humanname
598252145CV3917593single nucleotide variantNM_053045.2(TMEM203):c.349A>C (p.Ile117Leu)not specified [RCV005278035]uncertain significance9137205066137205066Humanname