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16 records found for search term Commd9
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405657032CV3305479single nucleotide variantNM_014186.4(COMMD9):c.23A>T (p.His8Leu)not specified [RCV004437760]uncertain significance113628939036289390Humanname
597648422CV3654101single nucleotide variantNM_014186.4(COMMD9):c.13A>G (p.Thr5Ala)not specified [RCV004910246]uncertain significance113628940036289400Humanname
15152650CV724420single nucleotide variantNM_014186.4(COMMD9):c.237C>T (p.Ala79=)not provided [RCV000879850]benign113627855736278557Humanname
597648430CV3654102single nucleotide variantNM_014186.4(COMMD9):c.70G>C (p.Val24Leu)not specified [RCV004910247]uncertain significance113628081936280819Humanname
156189098CV2342344single nucleotide variantNM_014186.4(COMMD9):c.136A>T (p.Thr46Ser)not specified [RCV004191910]uncertain significance113628075336280753Humanname
405657021CV3305476single nucleotide variantNM_014186.4(COMMD9):c.172G>C (p.Glu58Gln)not specified [RCV004437757]uncertain significance113628071736280717Humanname
405657024CV3305477single nucleotide variantNM_014186.4(COMMD9):c.202A>G (p.Thr68Ala)not specified [RCV004437758]uncertain significance113627859236278592Humanname
405657028CV3305478single nucleotide variantNM_014186.4(COMMD9):c.220C>T (p.Arg74Cys)not specified [RCV004437759]uncertain significance113627857436278574Humanname
598233672CV3948826single nucleotide variantNM_014186.4(COMMD9):c.238G>A (p.Glu80Lys)not specified [RCV005319964]uncertain significance113627855636278556Humanname
156222440CV2232728single nucleotide variantNM_014186.4(COMMD9):c.370G>A (p.Val124Ile)not specified [RCV004101384]uncertain significance113627622336276223Humanname
156277119CV2300108single nucleotide variantNM_014186.4(COMMD9):c.322A>G (p.Thr108Ala)not specified [RCV004151306]likely benign113627711936277119Humanname
155915878CV2339225single nucleotide variantNM_014186.4(COMMD9):c.425T>C (p.Met142Thr)not specified [RCV004191466]uncertain significance113627616836276168Humanname
156257840CV2383626single nucleotide variantNM_014186.4(COMMD9):c.524A>G (p.Lys175Arg)not specified [RCV004229517]uncertain significance113627470536274705Humanname
401744246CV2730635single nucleotide variantNM_014186.4(COMMD9):c.422G>A (p.Arg141His)not specified [RCV004331578]uncertain significance113627617136276171Humanname
401769268CV2734832single nucleotide variantNM_014186.4(COMMD9):c.364C>T (p.Arg122Cys)not specified [RCV004333638]uncertain significance113627622936276229Humanname
597648414CV3654100single nucleotide variantNM_014186.4(COMMD9):c.329G>A (p.Arg110Lys)not specified [RCV004910245]uncertain significance113627711236277112Humanname