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Pathways
Variants search result for All species
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4 records found for search term Commd6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156138625CV2211949single nucleotide variantNM_203495.4(COMMD6):c.97G>A (p.Asp33Asn)not specified [RCV004087076]uncertain significance137553022475530224Humanname
598233613CV3948819single nucleotide variantNM_203495.4(COMMD6):c.82A>G (p.Met28Val)not specified [RCV005319957]uncertain significance137553023975530239Humanname
155969498CV2335472single nucleotide variantNM_203495.4(COMMD6):c.171G>C (p.Lys57Asn)not specified [RCV004191643]uncertain significance137553015075530150Humanname
597648328CV3654088single nucleotide variantNM_203495.4(COMMD6):c.182T>C (p.Phe61Ser)not specified [RCV004910234]uncertain significance137553013975530139Humanname