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 Commd8
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405657014CV3305474single nucleotide variantNM_017845.5(COMMD8):c.7C>G (p.Pro3Ala)not specified [RCV004437755]uncertain significance44746364547463645Humanname
405657017CV3305475single nucleotide variantNM_017845.5(COMMD8):c.7C>T (p.Pro3Ser)not specified [RCV004437756]uncertain significance44746364547463645Humanname
405657007CV3305472single nucleotide variantNM_017845.5(COMMD8):c.23C>T (p.Pro8Leu)not specified [RCV004437753]likely benign44746362947463629Humanname
407452162CV3423297single nucleotide variantNM_017845.5(COMMD8):c.16G>A (p.Gly6Arg)not specified [RCV004608328]uncertain significance44746363647463636Humanname
597631022CV3552554single nucleotide variantNM_017845.5(COMMD8):c.26T>A (p.Leu9Ter)not provided [RCV004823295]uncertain significance44746362647463626Humanname
597773717CV3654098single nucleotide variantNM_017845.5(COMMD8):c.20C>G (p.Thr7Arg)not specified [RCV004897619]uncertain significance44746363247463632Humanname
597648407CV3654099single nucleotide variantNM_017845.5(COMMD8):c.19A>T (p.Thr7Ser)not specified [RCV004910244]uncertain significance44746363347463633Humanname
598233663CV3948825single nucleotide variantNM_017845.5(COMMD8):c.22C>T (p.Pro8Ser)not specified [RCV005319963]uncertain significance44746363047463630Humanname
405657011CV3305473single nucleotide variantNM_017845.5(COMMD8):c.47C>A (p.Pro16Gln)not specified [RCV004437754]uncertain significance44746360547463605Humanname
598233653CV3948824single nucleotide variantNM_017845.5(COMMD8):c.89G>A (p.Gly30Asp)not specified [RCV005319962]uncertain significance44746027747460277Humanname
156398433CV2200787single nucleotide variantNM_017845.5(COMMD8):c.178A>G (p.Lys60Glu)not specified [RCV004081426]uncertain significance44746018847460188Humanname
156177976CV2355894single nucleotide variantNM_017845.5(COMMD8):c.287G>T (p.Ser96Ile)not specified [RCV004201282]uncertain significance44745666547456665Humanname
407452160CV3423296single nucleotide variantNM_017845.5(COMMD8):c.103G>A (p.Ala35Thr)not specified [RCV004608327]likely benign44746026347460263Humanname
597648982CV3654096single nucleotide variantNM_017845.5(COMMD8):c.180A>C (p.Lys60Asn)not specified [RCV004910242]uncertain significance44746018647460186Humanname
598233645CV3948823single nucleotide variantNM_017845.5(COMMD8):c.140A>T (p.Glu47Val)not specified [RCV005319961]uncertain significance44746022647460226Humanname
156343235CV2364082single nucleotide variantNM_017845.5(COMMD8):c.410G>A (p.Arg137Gln)not specified [RCV004221464]likely benign44745318047453180Humanname
156143509CV2393582single nucleotide variantNM_017845.5(COMMD8):c.431A>G (p.His144Arg)not specified [RCV004231398]uncertain significance44745315947453159Humanname
401780814CV2723681single nucleotide variantNM_017845.5(COMMD8):c.364T>G (p.Trp122Gly)not provided [RCV004823141]|not specified [RCV004325853]uncertain significance44745658847456588Humanname
401871345CV2763642single nucleotide variantNM_017845.5(COMMD8):c.472A>G (p.Ile158Val)not specified [RCV004343148]likely benign44745311847453118Humanname
597648972CV3654095single nucleotide variantNM_017845.5(COMMD8):c.324A>C (p.Glu108Asp)not specified [RCV004910241]uncertain significance44745662847456628Humanname