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16 records found for search term Zcchc17
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156106684CV2387090single nucleotide variantNM_016505.4(ZCCHC17):c.27G>A (p.Met9Ile)not specified [RCV004226828]uncertain significance13131012531310125Humanname
329377363CV2435895single nucleotide variantNM_016505.4(ZCCHC17):c.13A>G (p.Arg5Gly)not specified [RCV004255125]uncertain significance13131011131310111Humanname
401868526CV2767262single nucleotide variantNM_016505.4(ZCCHC17):c.10G>A (p.Gly4Arg)not specified [RCV004349434]uncertain significance13131010831310108Humanname
405812683CV3353419single nucleotide variantNM_016505.4(ZCCHC17):c.167A>G (p.Lys56Arg)not specified [RCV004483427]uncertain significance13133721731337217Humanname
405812685CV3353420single nucleotide variantNM_016505.4(ZCCHC17):c.265G>T (p.Val89Phe)not specified [RCV004483428]uncertain significance13133899631338996Humanname
597792957CV3630861single nucleotide variantNM_016505.4(ZCCHC17):c.172T>G (p.Ser58Ala)not specified [RCV004877163]uncertain significance13133722231337222Humanname
597753458CV3630862single nucleotide variantNM_016505.4(ZCCHC17):c.265G>A (p.Val89Ile)not specified [RCV004893163]uncertain significance13133899631338996Humanname
156051678CV2363237single nucleotide variantNM_016505.4(ZCCHC17):c.332G>A (p.Arg111Gln)not specified [RCV004213800]uncertain significance13134665431346654Humanname
401758991CV2705309single nucleotide variantNM_016505.4(ZCCHC17):c.544C>T (p.Pro182Ser)not specified [RCV004311996]likely benign13134895431348954Humanname
407457002CV3491978single nucleotide variantNM_016505.4(ZCCHC17):c.700A>C (p.Lys234Gln)not specified [RCV004686163]uncertain significance13136416731364167Humanname
407457005CV3491979single nucleotide variantNM_016505.4(ZCCHC17):c.305A>G (p.Asn102Ser)not specified [RCV004686164]uncertain significance13133903631339036Humanname
597792953CV3630858single nucleotide variantNM_016505.4(ZCCHC17):c.500A>G (p.Glu167Gly)not specified [RCV004877162]uncertain significance13134891031348910Humanname
597753454CV3630860single nucleotide variantNM_016505.4(ZCCHC17):c.502G>T (p.Ala168Ser)not specified [RCV004893162]uncertain significance13134891231348912Humanname
597753462CV3630863single nucleotide variantNM_016505.4(ZCCHC17):c.531C>A (p.Asp177Glu)not specified [RCV004893164]uncertain significance13134894131348941Humanname
598258093CV3926855single nucleotide variantNM_016505.4(ZCCHC17):c.303C>A (p.Asn101Lys)not specified [RCV005299949]uncertain significance13133903431339034Humanname
598258099CV3926856single nucleotide variantNM_016505.4(ZCCHC17):c.445C>G (p.Gln149Glu)not specified [RCV005299950]uncertain significance13134885531348855Humanname