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Variants search result for Homo sapiens
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10 records found for search term Dnajc24
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329396339CV2459536single nucleotide variantNM_181706.5(DNAJC24):c.203T>G (p.Ile68Ser)not specified [RCV004276995]uncertain significance113141490231414902Humanname
407505009CV3437574single nucleotide variantNM_181706.5(DNAJC24):c.239T>G (p.Leu80Arg)not specified [RCV004624218]uncertain significance113141493831414938Humanname
407505013CV3437575single nucleotide variantNM_181706.5(DNAJC24):c.233A>G (p.Tyr78Cys)not specified [RCV004624219]uncertain significance113141493231414932Humanname
597644139CV3663010single nucleotide variantNM_181706.5(DNAJC24):c.244C>T (p.Arg82Trp)not specified [RCV004909601]uncertain significance113141494331414943Humanname
598163826CV3953560single nucleotide variantNM_181706.5(DNAJC24):c.177C>G (p.Phe59Leu)not specified [RCV005329427]uncertain significance113141487631414876Humanname
598163832CV3953561single nucleotide variantNM_181706.5(DNAJC24):c.196T>C (p.Trp66Arg)not specified [RCV005329428]uncertain significance113141489531414895Humanname
598163840CV3953562single nucleotide variantNM_181706.5(DNAJC24):c.130A>G (p.Ser44Gly)not specified [RCV005329429]uncertain significance113141482931414829Humanname
405747205CV3240819single nucleotide variantNM_181706.5(DNAJC24):c.377A>G (p.Asp126Gly)not specified [RCV004381422]uncertain significance113143032831430328Humanname
405747214CV3240820single nucleotide variantNM_181706.5(DNAJC24):c.383C>T (p.Ala128Val)not specified [RCV004381423]uncertain significance113143033431430334Humanname
598163816CV3953558single nucleotide variantNM_181706.5(DNAJC24):c.394A>C (p.Ser132Arg)not specified [RCV005329425]uncertain significance113143034531430345Humanname