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)

27 records found for search term Coq10a
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598234199CV3944973single nucleotide variantNM_144576.4(COQ10A):c.8G>T (p.Trp3Leu)not specified [RCV005320045]uncertain significance125626712656267126Humanname
597649193CV3654202single nucleotide variantNM_144576.4(COQ10A):c.97C>G (p.Pro33Ala)not specified [RCV004910320]uncertain significance125626721556267215Humanname
598234191CV3944972single nucleotide variantNM_144576.4(COQ10A):c.38C>T (p.Thr13Met)not specified [RCV005320044]uncertain significance125626715656267156Humanname
598234205CV3944974single nucleotide variantNM_144576.4(COQ10A):c.82G>C (p.Gly28Arg)not specified [RCV005320046]uncertain significance125626720056267200Humanname
598234234CV3944978single nucleotide variantNM_144576.4(COQ10A):c.83G>A (p.Gly28Asp)not specified [RCV005320050]uncertain significance125626720156267201Humanname
156079616CV2248552single nucleotide variantNM_144576.4(COQ10A):c.184G>A (p.Ala62Thr)not specified [RCV004121462]uncertain significance125626784356267843Humanname
405684759CV3235583single nucleotide variantNM_144576.4(COQ10A):c.245A>G (p.Asn82Ser)not specified [RCV004372097]uncertain significance125626790456267904Humanname
597649186CV3654201single nucleotide variantNM_144576.4(COQ10A):c.103C>T (p.Pro35Ser)not specified [RCV004910319]uncertain significance125626722156267221Humanname
598234219CV3944976single nucleotide variantNM_144576.4(COQ10A):c.260A>G (p.Tyr87Cys)not specified [RCV005320048]uncertain significance125626791956267919Humanname
598234228CV3944977single nucleotide variantNM_144576.4(COQ10A):c.263C>T (p.Ser88Leu)not specified [RCV005320049]uncertain significance125626792256267922Humanname
156390031CV2222986single nucleotide variantNM_144576.4(COQ10A):c.671G>C (p.Arg224Pro)not specified [RCV004103578]uncertain significance125627024456270244Humanname
156069145CV2232154single nucleotide variantNM_144576.4(COQ10A):c.566T>C (p.Val189Ala)not specified [RCV004104961]uncertain significance125626955156269551Humanname
156148529CV2307349single nucleotide variantNM_144576.4(COQ10A):c.730G>T (p.Val244Leu)not specified [RCV004166036]uncertain significance125627030356270303Humanname
156348655CV2312891single nucleotide variantNM_144576.4(COQ10A):c.371C>A (p.Ser124Tyr)not specified [RCV004171380]uncertain significance125626914856269148Humanname
156363531CV2329920single nucleotide variantNM_144576.4(COQ10A):c.416C>G (p.Pro139Arg)not specified [RCV004183375]uncertain significance125626919356269193Humanname
155971147CV2334181single nucleotide variantNM_144576.4(COQ10A):c.740C>G (p.Thr247Ser)not specified [RCV004186168]uncertain significance125627031356270313Humanname
155998183CV2393394single nucleotide variantNM_144576.4(COQ10A):c.586G>A (p.Glu196Lys)not specified [RCV004228893]uncertain significance125627015956270159Humanname
401879225CV2787995single nucleotide variantNM_144576.4(COQ10A):c.501C>A (p.Phe167Leu)not specified [RCV004358648]uncertain significance125626948656269486Humanname
405684765CV3235584single nucleotide variantNM_144576.4(COQ10A):c.593G>A (p.Arg198His)not specified [RCV004372098]uncertain significance125627016656270166Humanname
405684767CV3235585single nucleotide variantNM_144576.4(COQ10A):c.664G>C (p.Glu222Gln)not specified [RCV004372099]uncertain significance125627023756270237Humanname
405684774CV3235586single nucleotide variantNM_144576.4(COQ10A):c.683A>G (p.Lys228Arg)not specified [RCV004372100]uncertain significance125627025656270256Humanname
405684780CV3235587single nucleotide variantNM_144576.4(COQ10A):c.710G>A (p.Arg237His)not specified [RCV004372101]uncertain significance125627028356270283Humanname
597649179CV3654200single nucleotide variantNM_144576.4(COQ10A):c.574T>C (p.Ser192Pro)not specified [RCV004910318]uncertain significance125626955956269559Humanname
597649202CV3654203single nucleotide variantNM_144576.4(COQ10A):c.680C>G (p.Thr227Ser)not specified [RCV004910321]uncertain significance125627025356270253Humanname
598234175CV3944970single nucleotide variantNM_144576.4(COQ10A):c.513G>C (p.Glu171Asp)not specified [RCV005320042]uncertain significance125626949856269498Humanname
598234184CV3944971single nucleotide variantNM_144576.4(COQ10A):c.317A>G (p.Asn106Ser)not specified [RCV005320043]uncertain significance125626909456269094Humanname
598234211CV3944975single nucleotide variantNM_144576.4(COQ10A):c.310G>A (p.Val104Met)not specified [RCV005320047]uncertain significance125626908756269087Humanname