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)

20 records found for search term Mrpl34
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156378310CV2207686single nucleotide variantNM_023937.4(MRPL34):c.95T>C (p.Phe32Ser)not specified [RCV004084139]uncertain significance191730619517306195Humanname
156118880CV2279179single nucleotide variantNM_023937.4(MRPL34):c.77C>A (p.Pro26His)not specified [RCV004599526]uncertain significance191730617717306177Humanname
156383377CV2361529single nucleotide variantNM_023937.4(MRPL34):c.39T>G (p.Ser13Arg)not specified [RCV004221163]uncertain significance191730593117305931Humanname
405786258CV3371101single nucleotide variantNM_023937.4(MRPL34):c.71T>C (p.Leu24Pro)not specified [RCV004504872]uncertain significance191730617117306171Humanname
407474524CV3450343single nucleotide variantNM_023937.4(MRPL34):c.61G>A (p.Gly21Ser)not specified [RCV004638176]uncertain significance191730595317305953Humanname
156399957CV2202326single nucleotide variantNM_023937.4(MRPL34):c.113T>C (p.Leu38Pro)not specified [RCV004078253]uncertain significance191730621317306213Humanname
156378296CV2207682single nucleotide variantNM_023937.4(MRPL34):c.101A>G (p.Asp34Gly)not specified [RCV004084136]uncertain significance191730620117306201Humanname
156378302CV2207683single nucleotide variantNM_023937.4(MRPL34):c.104C>T (p.Ala35Val)not specified [RCV004084137]uncertain significance191730620417306204Humanname
155934584CV2225338single nucleotide variantNM_023937.4(MRPL34):c.179G>T (p.Arg60Leu)not specified [RCV004100761]uncertain significance191730627917306279Humanname
156053778CV2320407single nucleotide variantNM_023937.4(MRPL34):c.218C>T (p.Pro73Leu)not specified [RCV004178561]uncertain significance191730631817306318Humanname
156271390CV2333838single nucleotide variantNM_023937.4(MRPL34):c.202C>G (p.Arg68Gly)not specified [RCV004181337]uncertain significance191730630217306302Humanname
156096612CV2375427single nucleotide variantNM_023937.4(MRPL34):c.186C>G (p.Asn62Lys)not specified [RCV004232818]uncertain significance191730628617306286Humanname
401761167CV2689050single nucleotide variantNM_023937.4(MRPL34):c.161A>G (p.Gln54Arg)not specified [RCV004305823]uncertain significance191730626117306261Humanname
401889793CV2763399single nucleotide variantNM_023937.4(MRPL34):c.110G>T (p.Gly37Val)not specified [RCV004349288]uncertain significance191730621017306210Humanname
405786090CV3371067single nucleotide variantNM_023937.4(MRPL34):c.109G>A (p.Gly37Ser)not specified [RCV004504838]uncertain significance191730620917306209Humanname
407474530CV3450344single nucleotide variantNM_023937.4(MRPL34):c.103G>A (p.Ala35Thr)not specified [RCV004638177]uncertain significance191730620317306203Humanname
407474532CV3450345single nucleotide variantNM_023937.4(MRPL34):c.205C>T (p.Arg69Cys)not specified [RCV004638178]uncertain significance191730630517306305Humanname
597633796CV3561146single nucleotide variantNM_023937.4(MRPL34):c.167G>A (p.Ser56Asn)not specified [RCV004830861]uncertain significance191730626717306267Humanname
597633802CV3561147single nucleotide variantNM_023937.4(MRPL34):c.131C>A (p.Ala44Asp)not specified [RCV004830862]uncertain significance191730623117306231Humanname
597633808CV3561148single nucleotide variantNM_023937.4(MRPL34):c.102C>A (p.Asp34Glu)not specified [RCV004830863]uncertain significance191730620217306202Humanname