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8 records found for search term Cplx4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407457093CV3419628single nucleotide variantNM_181654.4(CPLX4):c.23T>A (p.Met8Lys)not specified [RCV004611022]uncertain significance185931844059318440Humanname
155924199CV2212646single nucleotide variantNM_181654.4(CPLX4):c.34C>A (p.Gln12Lys)not specified [RCV004085171]uncertain significance185931842959318429Humanname
156154058CV2374896single nucleotide variantNM_181654.4(CPLX4):c.157A>G (p.Ile53Val)not specified [RCV004227920]uncertain significance185931830659318306Humanname
597651286CV3651094single nucleotide variantNM_181654.4(CPLX4):c.229C>T (p.Leu77Phe)not specified [RCV004910562]uncertain significance185931271159312711Humanname
597651140CV3651095single nucleotide variantNM_181654.4(CPLX4):c.104C>T (p.Ala35Val)not specified [RCV004910563]uncertain significance185931835959318359Humanname
597651150CV3651096single nucleotide variantNM_181654.4(CPLX4):c.142T>C (p.Tyr48His)not specified [RCV004910564]uncertain significance185931832159318321Humanname
401891948CV2777158single nucleotide variantNM_181654.4(CPLX4):c.355G>A (p.Asp119Asn)not specified [RCV004354204]uncertain significance185929682659296826Humanname
597651490CV3651093single nucleotide variantNM_181654.4(CPLX4):c.319C>T (p.Arg107Trp)not specified [RCV004910561]uncertain significance185929686259296862Humanname