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Variants search result for Homo sapiens
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24 records found for search term Ube2q1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8574908CV109247single nucleotide variantNM_017582.6(UBE2Q1):c.-2025G>ALung cancer [RCV000089772]uncertain significance1154560578154560578Humanname
156036262CV2249867single nucleotide variantNM_017582.7(UBE2Q1):c.95G>A (p.Gly32Glu)not specified [RCV004122847]uncertain significance1154558459154558459Humanname
156067927CV2341005single nucleotide variantNM_017582.7(UBE2Q1):c.95G>C (p.Gly32Ala)not specified [RCV004181496]uncertain significance1154558459154558459Humanname
401728318CV2672874single nucleotide variantNM_017582.7(UBE2Q1):c.97G>T (p.Gly33Trp)not specified [RCV004282045]uncertain significance1154558457154558457Humanname
401753205CV2674813single nucleotide variantNM_017582.7(UBE2Q1):c.35C>T (p.Pro12Leu)not specified [RCV004294092]uncertain significance1154558519154558519Humanname
597682058CV3625851single nucleotide variantNM_017582.7(UBE2Q1):c.77G>A (p.Gly26Glu)not specified [RCV004883696]uncertain significance1154558477154558477Humanname
597682080CV3625853single nucleotide variantNM_017582.7(UBE2Q1):c.65G>A (p.Gly22Glu)not specified [RCV004883698]uncertain significance1154558489154558489Humanname
598189076CV3932721single nucleotide variantNM_017582.7(UBE2Q1):c.97G>A (p.Gly33Arg)not specified [RCV005288024]uncertain significance1154558457154558457Humanname
156139587CV2280759single nucleotide variantNM_017582.7(UBE2Q1):c.253G>T (p.Ala85Ser)not specified [RCV004145024]uncertain significance1154558301154558301Humanname
155928768CV2363354single nucleotide variantNM_017582.7(UBE2Q1):c.284G>A (p.Gly95Glu)not specified [RCV004213897]uncertain significance1154558270154558270Humanname
329362413CV2444688single nucleotide variantNM_017582.7(UBE2Q1):c.278C>A (p.Pro93Gln)not specified [RCV004258946]uncertain significance1154558276154558276Humanname
401767925CV2678091single nucleotide variantNM_017582.7(UBE2Q1):c.278C>G (p.Pro93Arg)not specified [RCV004296606]uncertain significance1154558276154558276Humanname
401757786CV2731452single nucleotide variantNM_017582.7(UBE2Q1):c.266C>T (p.Pro89Leu)not specified [RCV004330809]uncertain significance1154558288154558288Humanname
405799714CV3341329single nucleotide variantNM_017582.7(UBE2Q1):c.280C>G (p.Arg94Gly)not specified [RCV004476882]uncertain significance1154558274154558274Humanname
407522726CV3491050single nucleotide variantNM_017582.7(UBE2Q1):c.1026G>A (p.Gly342=)not specified [RCV004677793]likely benign1154551819154551819Humanname
597682027CV3625848single nucleotide variantNM_017582.7(UBE2Q1):c.259C>T (p.Pro87Ser)not specified [RCV004883693]uncertain significance1154558295154558295Humanname
597682049CV3625850single nucleotide variantNM_017582.7(UBE2Q1):c.109C>T (p.Pro37Ser)not specified [RCV004883695]uncertain significance1154558445154558445Humanname
156069841CV2295767single nucleotide variantNM_017582.7(UBE2Q1):c.764G>A (p.Arg255Gln)not specified [RCV004151695]uncertain significance1154552786154552786Humanname
156166050CV2319911single nucleotide variantNM_017582.7(UBE2Q1):c.949C>T (p.Leu317Phe)not specified [RCV004167790]uncertain significance1154552110154552110Humanname
405799537CV3341330single nucleotide variantNM_017582.7(UBE2Q1):c.803G>T (p.Ser268Ile)not specified [RCV004476883]uncertain significance1154552747154552747Humanname
597682069CV3625852single nucleotide variantNM_017582.7(UBE2Q1):c.634G>A (p.Ala212Thr)not specified [RCV004883697]uncertain significance1154553127154553127Humanname
598265097CV3932722single nucleotide variantNM_017582.7(UBE2Q1):c.734C>T (p.Ala245Val)not specified [RCV005301656]uncertain significance1154552816154552816Humanname
405799531CV3341328single nucleotide variantNM_017582.7(UBE2Q1):c.1039G>A (p.Gly347Arg)not specified [RCV004476881]uncertain significance1154551806154551806Humanname
597682092CV3625854single nucleotide variantNM_017582.7(UBE2Q1):c.1166A>G (p.Asn389Ser)not specified [RCV004883699]uncertain significance1154551401154551401Humanname