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Variants search result for Homo sapiens
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30 records found for search term Ppard
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8581868CV116316single nucleotide variantNM_006238.4(PPARD):c.285+600C>TLung cancer [RCV000096839]uncertain significance63542088135420881Humanname
156005605CV2401109single nucleotide variantNM_006238.5(PPARD):c.34C>T (p.Arg12Trp)not specified [RCV004245679]uncertain significance63541112135411121Humanname
329349815CV2457412single nucleotide variantNM_006238.5(PPARD):c.61G>C (p.Ala21Pro)not specified [RCV004267240]uncertain significance63541114835411148Humanname
156303771CV2359432single nucleotide variantNM_006238.5(PPARD):c.202G>A (p.Gly68Ser)not specified [RCV004214754]uncertain significance63542019835420198Humanname
156058535CV2396481single nucleotide variantNM_006238.5(PPARD):c.232G>A (p.Gly78Arg)not specified [RCV004242191]uncertain significance63542022835420228Humanname
401747095CV2707408single nucleotide variantNM_006238.5(PPARD):c.119G>A (p.Ser40Asn)not specified [RCV004312796]uncertain significance63541120635411206Humanname
405669590CV3370038single nucleotide variantNM_006238.5(PPARD):c.196T>G (p.Ser66Ala)not specified [RCV004514874]uncertain significance63542019235420192Humanname
597779196CV3581055single nucleotide variantNM_006238.5(PPARD):c.224G>A (p.Arg75Gln)not specified [RCV004853199]uncertain significance63542022035420220Humanname
156076191CV2251265single nucleotide variantNM_006238.5(PPARD):c.889A>G (p.Ile297Val)not specified [RCV004115483]uncertain significance63542459035424590Humanname
156035801CV2253202single nucleotide variantNM_006238.5(PPARD):c.953G>A (p.Arg318His)not specified [RCV004122754]uncertain significance63542465435424654Humanname
155919220CV2254828single nucleotide variantNM_006238.5(PPARD):c.574A>G (p.Met192Val)not specified [RCV004115290]uncertain significance63542409535424095Humanname
155940242CV2294048single nucleotide variantNM_006238.5(PPARD):c.623C>G (p.Thr208Arg)not specified [RCV004149432]uncertain significance63542414435424144Humanname
156290470CV2309831single nucleotide variantNM_006238.5(PPARD):c.507C>A (p.Asn169Lys)not specified [RCV004160944]uncertain significance63542402835424028Humanname
156390776CV2383408single nucleotide variantNM_006238.5(PPARD):c.892G>A (p.Val298Ile)not specified [RCV004222431]uncertain significance63542459335424593Humanname
155996409CV2398535single nucleotide variantNM_006238.5(PPARD):c.473C>T (p.Ala158Val)not specified [RCV004237854]uncertain significance63542399435423994Humanname
405669478CV3370039single nucleotide variantNM_006238.5(PPARD):c.308G>A (p.Arg103His)not specified [RCV004514875]uncertain significance63542184235421842Humanname
405669483CV3370040single nucleotide variantNM_006238.5(PPARD):c.643G>A (p.Asp215Asn)not specified [RCV004514876]uncertain significance63542434435424344Humanname
407529458CV3471304single nucleotide variantNM_006238.5(PPARD):c.874G>A (p.Ala292Thr)not specified [RCV004656056]uncertain significance63542457535424575Humanname
407529460CV3471305single nucleotide variantNM_006238.5(PPARD):c.626C>T (p.Ala209Val)not specified [RCV004656057]uncertain significance63542414735424147Humanname
407529462CV3471306single nucleotide variantNM_006238.5(PPARD):c.836T>C (p.Val279Ala)not specified [RCV004656058]uncertain significance63542453735424537Humanname
597779200CV3581056single nucleotide variantNM_006238.5(PPARD):c.338G>A (p.Arg113His)not specified [RCV004853200]uncertain significance63542187235421872Humanname
597779204CV3581057single nucleotide variantNM_006238.5(PPARD):c.723C>G (p.Ile241Met)not specified [RCV004853201]uncertain significance63542442435424424Humanname
597779208CV3581058single nucleotide variantNM_006238.5(PPARD):c.342C>A (p.Ser114Arg)not specified [RCV004853202]uncertain significance63542187635421876Humanname
598159679CV3901113single nucleotide variantNM_006238.5(PPARD):c.493G>A (p.Gly165Arg)not specified [RCV005260795]uncertain significance63542401435424014Humanname
155961081CV2285483single nucleotide variantNM_006238.5(PPARD):c.1234G>A (p.Glu412Lys)not specified [RCV004139332]uncertain significance63542598735425987Humanname
156079838CV2292636single nucleotide variantNM_006238.5(PPARD):c.1099G>A (p.Val367Ile)not specified [RCV004154325]uncertain significance63542585235425852Humanname
155915231CV2339086single nucleotide variantNM_006238.5(PPARD):c.1283C>T (p.Ser428Leu)not specified [RCV004187132]likely benign63542603635426036Humanname
155932228CV2364357single nucleotide variantNM_006238.5(PPARD):c.1126A>T (p.Thr376Ser)not specified [RCV004223575]uncertain significance63542587935425879Humanname
597779192CV3581054single nucleotide variantNM_006238.5(PPARD):c.1276G>C (p.Glu426Gln)not specified [RCV004853198]uncertain significance63542602935426029Humanname
597779212CV3581059single nucleotide variantNM_006238.5(PPARD):c.1193A>T (p.Lys398Met)not specified [RCV004853203]uncertain significance63542594635425946Humanname