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Variants search result for Homo sapiens
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6 records found for search term Cetn2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155923763CV2351857single nucleotide variantNM_004344.3(CETN2):c.55A>G (p.Met19Val)not specified [RCV004198001]uncertain significanceX152829709152829709Humanname
405725021CV3293376single nucleotide variantNM_004344.3(CETN2):c.28A>G (p.Met10Val)not specified [RCV004428647]uncertain significanceX152829736152829736Humanname
156263681CV2315020single nucleotide variantNM_004344.3(CETN2):c.148G>A (p.Val50Ile)not specified [RCV004164937]uncertain significanceX152829616152829616Humanname
401730700CV2677265single nucleotide variantNM_004344.3(CETN2):c.147T>G (p.Asp49Glu)not specified [RCV004295885]uncertain significanceX152829617152829617Humanname
597790128CV3649754single nucleotide variantNM_004344.3(CETN2):c.209A>G (p.Lys70Arg)not specified [RCV004901924]uncertain significanceX152829231152829231Humanname
156007370CV2289093single nucleotide variantNM_004344.3(CETN2):c.473G>A (p.Ser158Asn)not provided [RCV004585007]|not specified [RCV004150032]likely benignX152827887152827887Humanname