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13 records found for search term Mxd1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156165867CV2243532single nucleotide variantNM_002357.4(MXD1):c.122G>A (p.Arg41Lys)not specified [RCV004112485]uncertain significance26991616969916169Humanname
329375804CV2441135single nucleotide variantNM_002357.4(MXD1):c.241G>C (p.Gly81Arg)not specified [RCV004263535]uncertain significance26993538869935388Humanname
597644694CV3557990single nucleotide variantNM_002357.4(MXD1):c.146A>G (p.Lys49Arg)not specified [RCV004826000]uncertain significance26991619369916193Humanname
155978032CV2321331single nucleotide variantNM_002357.4(MXD1):c.630G>T (p.Lys210Asn)not specified [RCV004177336]uncertain significance26993824869938248Humanname
156243369CV2347072single nucleotide variantNM_002357.4(MXD1):c.544A>G (p.Ser182Gly)not specified [RCV004204555]uncertain significance26993816269938162Humanname
156075415CV2350877single nucleotide variantNM_002357.4(MXD1):c.448G>A (p.Val150Ile)not specified [RCV004211714]uncertain significance26993736469937364Humanname
401781004CV2681856single nucleotide variantNM_002357.4(MXD1):c.611C>T (p.Thr204Ile)not specified [RCV004296850]uncertain significance26993822969938229Humanname
401734915CV2688651single nucleotide variantNM_002357.4(MXD1):c.380G>A (p.Arg127Gln)not specified [RCV004301594]uncertain significance26993729669937296Humanname
401886138CV2774863single nucleotide variantNM_002357.4(MXD1):c.586G>A (p.Gly196Ser)not specified [RCV004343947]uncertain significance26993820469938204Humanname
405669742CV3308731single nucleotide variantNM_002357.4(MXD1):c.461G>A (p.Arg154His)not specified [RCV004441012]uncertain significance26993737769937377Humanname
407508165CV3458031single nucleotide variantNM_002357.4(MXD1):c.639C>G (p.Asp213Glu)not specified [RCV004647037]uncertain significance26993825769938257Humanname
407508170CV3458032single nucleotide variantNM_002357.4(MXD1):c.397C>A (p.Leu133Met)not specified [RCV004647038]uncertain significance26993731369937313Humanname
597644701CV3557991single nucleotide variantNM_002357.4(MXD1):c.487G>A (p.Asp163Asn)not specified [RCV004826001]uncertain significance26993810569938105Humanname