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7 records found for search term Chic2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405280708CV3195648single nucleotide variantNM_012110.4(CHIC2):c.175-5T>CCHIC2-related disorder [RCV003906884]likely benign45404911554049115Humanname , trait , alternate_id
156177485CV2298219single nucleotide variantNM_012110.4(CHIC2):c.59A>C (p.Glu20Ala)not specified [RCV004160146]uncertain significance45406424254064242Humanname
401757499CV2735052single nucleotide variantNM_012110.4(CHIC2):c.388C>T (p.Leu130=)not specified [RCV004333751]likely benign45401389654013896Humanname
405661618CV3297033single nucleotide variantNM_012110.4(CHIC2):c.47G>A (p.Arg16Gln)not specified [RCV004439230]uncertain significance45406425454064254Humanname
401743292CV2684667single nucleotide variantNM_012110.4(CHIC2):c.326A>G (p.Lys109Arg)not specified [RCV004293763]uncertain significance45404895954048959Humanname
405661614CV3297032single nucleotide variantNM_012110.4(CHIC2):c.453C>G (p.Ile151Met)not specified [RCV004439229]uncertain significance45401014054010140Humanname
598214426CV3951579single nucleotide variantNM_012110.4(CHIC2):c.411C>G (p.Ser137Arg)not specified [RCV005316567]uncertain significance45401387354013873Humanname