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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401753384CV2674874single nucleotide variantNM_001080837.4(SEBOX):c.-26C>Tnot specified [RCV004294143]uncertain significance172836517728365177Humanname
405703611CV3310563single nucleotide variantNM_001080837.4(SEBOX):c.-11T>Cnot specified [RCV004447451]likely benign172836516228365162Humanname
405703598CV3310561single nucleotide variantNM_001080837.2(SEBOX):c.4G>A (p.Gly2Arg)not specified [RCV004447449]uncertain significance172836522728365227Humanname
405703574CV3310558single nucleotide variantNM_001080837.4(SEBOX):c.34G>A (p.Gly12Ser)not specified [RCV004447446]uncertain significance172836495328364953Humanname
405703580CV3310559single nucleotide variantNM_001080837.4(SEBOX):c.58C>T (p.Arg20Trp)not specified [RCV004447447]uncertain significance172836492928364929Humanname
407476783CV3476599single nucleotide variantNM_001080837.4(SEBOX):c.59G>A (p.Arg20Gln)not specified [RCV004663564]likely benign172836492828364928Humanname
401747559CV2696732single nucleotide variantNM_001080837.4(SEBOX):c.186G>C (p.Lys62Asn)not specified [RCV004290706]uncertain significance172836480128364801Humanname
401777756CV2704318single nucleotide variantNM_001080837.4(SEBOX):c.153C>G (p.His51Gln)not specified [RCV004311301]uncertain significance172836483428364834Humanname
405703590CV3310560single nucleotide variantNM_001080837.4(SEBOX):c.292G>A (p.Asp98Asn)not specified [RCV004447448]uncertain significance172836454928364549Humanname
407491969CV3476601single nucleotide variantNM_001080837.4(SEBOX):c.134A>G (p.Asn45Ser)not specified [RCV004666991]uncertain significance172836485328364853Humanname
401894168CV2770377single nucleotide variantNM_001080837.4(SEBOX):c.482C>G (p.Ser161Cys)not specified [RCV004358026]uncertain significance172836435928364359Humanname
405703602CV3310562single nucleotide variantNM_001080837.4(SEBOX):c.448T>C (p.Trp150Arg)not specified [RCV004447450]likely benign172836439328364393Humanname
407491965CV3476600single nucleotide variantNM_001080837.4(SEBOX):c.413G>A (p.Arg138Gln)not specified [RCV004666990]uncertain significance172836442828364428Humanname
597714623CV3605338single nucleotide variantNM_001080837.4(SEBOX):c.412C>T (p.Arg138Trp)not specified [RCV004861383]uncertain significance172836442928364429Humanname
598209979CV3907050single nucleotide variantNM_001080837.4(SEBOX):c.362G>A (p.Arg121His)not specified [RCV005270601]uncertain significance172836447928364479Humanname
598209986CV3907051single nucleotide variantNM_001080837.4(SEBOX):c.430G>T (p.Ala144Ser)not specified [RCV005270602]uncertain significance172836441128364411Humanname
598209993CV3907052single nucleotide variantNM_001080837.4(SEBOX):c.554T>A (p.Val185Asp)not specified [RCV005270603]uncertain significance172836428728364287Humanname