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17 records found for search term Cops8
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155971771CV2334254single nucleotide variantNM_006710.5(COPS8):c.23A>G (p.Glu8Gly)not specified [RCV004186237]uncertain significance2237085987237085987Humanname
597649143CV3654196single nucleotide variantNM_006710.5(COPS8):c.22G>A (p.Glu8Lys)not specified [RCV004910314]uncertain significance2237085986237085986Humanname
155945358CV2269582single nucleotide variantNM_006710.5(COPS8):c.59G>A (p.Cys20Tyr)not specified [RCV004124682]uncertain significance2237086023237086023Humanname
598234146CV3944966single nucleotide variantNM_006710.5(COPS8):c.44A>T (p.Lys15Met)not specified [RCV005320038]uncertain significance2237086008237086008Humanname
156150087CV2265397single nucleotide variantNM_006710.5(COPS8):c.172A>G (p.Lys58Glu)not specified [RCV004128274]uncertain significance2237088627237088627Humanname
156135442CV2284737single nucleotide variantNM_006710.5(COPS8):c.240A>T (p.Arg80Ser)not specified [RCV004140882]uncertain significance2237089903237089903Humanname
401894000CV2770208single nucleotide variantNM_006710.5(COPS8):c.202A>C (p.Asn68His)not specified [RCV004356099]uncertain significance2237089865237089865Humanname
405684715CV3235574single nucleotide variantNM_006710.5(COPS8):c.122T>C (p.Leu41Pro)not specified [RCV004372088]uncertain significance2237087170237087170Humanname
405684719CV3235575single nucleotide variantNM_006710.5(COPS8):c.197C>G (p.Ser66Cys)not specified [RCV004372089]uncertain significance2237088652237088652Humanname
597774008CV3654194single nucleotide variantNM_006710.5(COPS8):c.283G>A (p.Ala95Thr)not specified [RCV004897622]uncertain significance2237089946237089946Humanname
598234153CV3944967single nucleotide variantNM_006710.5(COPS8):c.281A>G (p.Asn94Ser)not specified [RCV005320039]uncertain significance2237089944237089944Humanname
156399711CV2202167single nucleotide variantNM_006710.5(COPS8):c.356C>G (p.Ala119Gly)not specified [RCV004078116]uncertain significance2237094114237094114Humanname
156188750CV2292571single nucleotide variantNM_006710.5(COPS8):c.355G>A (p.Ala119Thr)not specified [RCV004150339]uncertain significance2237094113237094113Humanname
156037800CV2332570single nucleotide variantNM_006710.5(COPS8):c.367C>A (p.Gln123Lys)not specified [RCV004196284]uncertain significance2237094125237094125Humanname
401745194CV2693203single nucleotide variantNM_006710.5(COPS8):c.346C>T (p.Arg116Cys)not specified [RCV004293131]uncertain significance2237094104237094104Humanname
405684724CV3235576single nucleotide variantNM_006710.5(COPS8):c.421G>A (p.Val141Ile)not specified [RCV004372090]uncertain significance2237094179237094179Humanname
597649134CV3654195single nucleotide variantNM_006710.5(COPS8):c.413G>C (p.Gly138Ala)not specified [RCV004910313]uncertain significance2237094171237094171Humanname