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6 records found for search term Gngt2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156081772CV2368833single nucleotide variantNM_001198754.2(GNGT2):c.83C>T (p.Pro28Leu)not specified [RCV004207795]uncertain significance174920734049207340Humanname
598264185CV3974387single nucleotide variantNM_001198754.2(GNGT2):c.98G>A (p.Gly33Glu)not specified [RCV005348797]uncertain significance174920686949206869Humanname
401781819CV2722289single nucleotide variantNM_001198754.2(GNGT2):c.134G>A (p.Gly45Glu)not specified [RCV004328841]uncertain significance174920683349206833Humanname
405768466CV3262111single nucleotide variantNM_001198754.2(GNGT2):c.158T>C (p.Ile53Thr)not specified [RCV004395501]uncertain significance174920680949206809Humanname
407520028CV3443591single nucleotide variantNM_001198754.2(GNGT2):c.107T>C (p.Ile36Thr)not specified [RCV004629900]uncertain significance174920686049206860Humanname
597788471CV3678252single nucleotide variantNM_001198754.2(GNGT2):c.204A>G (p.Ile68Met)not specified [RCV004932750]uncertain significance174920676349206763Humanname