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10 records found for search term Cox19
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156031177CV2202616single nucleotide variantNM_001031617.3(COX19):c.13A>G (p.Met5Val)not specified [RCV004082873]uncertain significance7975497975497Humanname
156234543CV2245356single nucleotide variantNM_001031617.3(COX19):c.17A>G (p.Asn6Ser)not specified [RCV004107106]uncertain significance7975493975493Humanname
401753243CV2722404single nucleotide variantNM_001031617.3(COX19):c.73G>C (p.Asp25His)not specified [RCV004322807]uncertain significance7975437975437Humanname
598234792CV3945065single nucleotide variantNM_001031617.3(COX19):c.40C>G (p.Pro14Ala)not specified [RCV005320134]uncertain significance7975470975470Humanname
401887321CV2771886single nucleotide variantNM_001031617.3(COX19):c.129C>G (p.Asn43Lys)not specified [RCV004344598]uncertain significance7973246973246Humanname
405685584CV3235744single nucleotide variantNM_001031617.3(COX19):c.146C>G (p.Ala49Gly)not specified [RCV004372258]uncertain significance7973229973229Humanname
405685589CV3235745single nucleotide variantNM_001031617.3(COX19):c.196A>C (p.Lys66Gln)not specified [RCV004372259]likely benign7969455969455Humanname
407456818CV3423414single nucleotide variantNM_001031617.3(COX19):c.177A>C (p.Leu59Phe)not specified [RCV004610878]uncertain significance7973198973198Humanname
597649815CV3654310single nucleotide variantNM_001031617.3(COX19):c.131A>G (p.Asn44Ser)not specified [RCV004910388]uncertain significance7973244973244Humanname
598234799CV3945066single nucleotide variantNM_001031617.3(COX19):c.118T>C (p.Cys40Arg)not specified [RCV005320135]uncertain significance7973257973257Humanname