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9 records found for search term Hmgb2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405790860CV3266831single nucleotide variantNM_002129.4(HMGB2):c.168G>T (p.Glu56Asp)not specified [RCV004399654]uncertain significance4173333197173333197Humanname
597791260CV3682788single nucleotide variantNM_002129.4(HMGB2):c.216C>A (p.Asp72Glu)not specified [RCV004933447]uncertain significance4173333149173333149Humanname
156346927CV2300766single nucleotide variantNM_002129.4(HMGB2):c.601G>A (p.Glu201Lys)not specified [RCV004155697]uncertain significance4173332109173332109Humanname
156065635CV2376103single nucleotide variantNM_002129.4(HMGB2):c.493A>G (p.Lys165Glu)not specified [RCV004220337]uncertain significance4173332217173332217Humanname
329385907CV2428137single nucleotide variantNM_002129.4(HMGB2):c.556G>A (p.Glu186Lys)not specified [RCV004251179]uncertain significance4173332154173332154Humanname
329384241CV2435001single nucleotide variantNM_002129.4(HMGB2):c.567T>G (p.Asp189Glu)not specified [RCV004250866]uncertain significance4173332143173332143Humanname
407527647CV3433637single nucleotide variantNM_002129.4(HMGB2):c.591A>T (p.Glu197Asp)not specified [RCV004632863]uncertain significance4173332119173332119Humanname
407527651CV3433638single nucleotide variantNM_002129.4(HMGB2):c.373A>G (p.Thr125Ala)not specified [RCV004632864]uncertain significance4173332919173332919Humanname
597791257CV3682787single nucleotide variantNM_002129.4(HMGB2):c.344G>A (p.Ser115Asn)not specified [RCV004933446]uncertain significance4173332948173332948Humanname