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8 records found for search term Ube2g2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405814414CV3341294single nucleotide variantNM_003343.6(UBE2G2):c.58C>A (p.Pro20Thr)not specified [RCV004484369]uncertain significance214478808144788081Humanname
407462293CV3491029single nucleotide variantNM_003343.6(UBE2G2):c.284C>T (p.Ala95Val)not specified [RCV004687913]uncertain significance214477364844773648Humanname
597803313CV3625814single nucleotide variantNM_003343.6(UBE2G2):c.292G>A (p.Asp98Asn)not specified [RCV004881675]uncertain significance214477364044773640Humanname
598264971CV3932691single nucleotide variantNM_003343.6(UBE2G2):c.272C>A (p.Ser91Tyr)not specified [RCV005301638]uncertain significance214477366044773660Humanname
156176146CV2254709single nucleotide variantNM_003343.6(UBE2G2):c.446A>G (p.Glu149Gly)not specified [RCV004115186]uncertain significance214477142944771429Humanname
329381887CV2467405single nucleotide variantNM_003343.6(UBE2G2):c.460A>C (p.Ile154Leu)not specified [RCV004287023]uncertain significance214477141544771415Humanname
407522681CV3491028single nucleotide variantNM_003343.6(UBE2G2):c.392A>G (p.Asn131Ser)not specified [RCV004677775]uncertain significance214477148344771483Humanname
12740729CV360495single nucleotide variantNM_003343.6(UBE2G2):c.330G>A (p.Trp110Ter)not specified [RCV000412951]uncertain significance214477360244773602Humanname