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27 records found for search term Eapp
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155905946CV2393834single nucleotide variantNM_018453.4(EAPP):c.56A>G (p.Glu19Gly)not specified [RCV004233662]uncertain significance143453957334539573Humanname
598268625CV3953895single nucleotide variantNM_018453.4(EAPP):c.51C>G (p.Ser17Arg)not specified [RCV005327136]uncertain significance143453957834539578Humanname
156262376CV2201088single nucleotide variantNM_018453.4(EAPP):c.140A>G (p.Glu47Gly)not specified [RCV004075211]uncertain significance143453621034536210Humanname
401751776CV2672573single nucleotide variantNM_018453.4(EAPP):c.218T>C (p.Met73Thr)not specified [RCV004287606]uncertain significance143453613234536132Humanname
41405788CV981857single nucleotide variantNM_018453.4(EAPP):c.130C>T (p.Leu44Phe)not provided [RCV001810566]uncertain significance143453622034536220Humanname
150472167CV1281152single nucleotide variantNM_018453.4(EAPP):c.716G>A (p.Arg239Gln)not provided [RCV001713323]benign143451645234516452Humanname
155925320CV2211810single nucleotide variantNM_018453.4(EAPP):c.334G>A (p.Glu112Lys)not specified [RCV004086638]uncertain significance143453346234533462Humanname
155916065CV2239650single nucleotide variantNM_018453.4(EAPP):c.788C>G (p.Ser263Cys)not specified [RCV004108202]uncertain significance143451638034516380Humanname
156265410CV2329528single nucleotide variantNM_018453.4(EAPP):c.679A>G (p.Lys227Glu)not specified [RCV004180659]uncertain significance143451648934516489Humanname
156036962CV2332495single nucleotide variantNM_018453.4(EAPP):c.708G>T (p.Arg236Ser)not specified [RCV004599577]uncertain significance143451646034516460Humanname
401759903CV2707184single nucleotide variantNM_018453.4(EAPP):c.707G>A (p.Arg236Lys)not specified [RCV004315545]uncertain significance143451646134516461Humanname
401751741CV2727125single nucleotide variantNM_018453.4(EAPP):c.703A>T (p.Met235Leu)not specified [RCV004325487]uncertain significance143451646534516465Humanname
405752554CV3238309single nucleotide variantNM_018453.4(EAPP):c.618T>G (p.Phe206Leu)not specified [RCV004382185]uncertain significance143451655034516550Humanname
405752561CV3238310single nucleotide variantNM_018453.4(EAPP):c.713A>C (p.Asn238Thr)not specified [RCV004382186]uncertain significance143451645534516455Humanname
405752569CV3238311single nucleotide variantNM_018453.4(EAPP):c.800C>T (p.Ala267Val)not specified [RCV004382187]uncertain significance143451636834516368Humanname
405752575CV3238312single nucleotide variantNM_018453.4(EAPP):c.836A>G (p.Asn279Ser)not specified [RCV004382188]uncertain significance143451633234516332Humanname
407478087CV3431379single nucleotide variantNM_018453.4(EAPP):c.614T>C (p.Met205Thr)not specified [RCV004617449]uncertain significance143451655434516554Humanname
407478092CV3431380single nucleotide variantNM_018453.4(EAPP):c.632C>G (p.Ser211Cys)not specified [RCV004617450]uncertain significance143451653634516536Humanname
407478098CV3431381single nucleotide variantNM_018453.4(EAPP):c.344A>C (p.Asp115Ala)not specified [RCV004617451]uncertain significance143453345234533452Humanname
597803144CV3667146single nucleotide variantNM_018453.4(EAPP):c.719A>G (p.Glu240Gly)not specified [RCV004906966]uncertain significance143451644934516449Humanname
597803142CV3667147single nucleotide variantNM_018453.4(EAPP):c.468G>C (p.Arg156Ser)not specified [RCV004906967]uncertain significance143452936034529360Humanname
597803141CV3667148single nucleotide variantNM_018453.4(EAPP):c.479G>A (p.Gly160Asp)not specified [RCV004906968]uncertain significance143452479934524799Humanname
598268610CV3953892single nucleotide variantNM_018453.4(EAPP):c.568C>G (p.Leu190Val)not specified [RCV005327133]uncertain significance143452471034524710Humanname
598268616CV3953893single nucleotide variantNM_018453.4(EAPP):c.389A>G (p.Lys130Arg)not specified [RCV005327134]likely benign143452943934529439Humanname
598268620CV3953894single nucleotide variantNM_018453.4(EAPP):c.773T>C (p.Met258Thr)not specified [RCV005327135]uncertain significance143451639534516395Humanname
598268628CV3953896single nucleotide variantNM_018453.4(EAPP):c.649G>A (p.Val217Ile)not specified [RCV005327137]likely benign143451651934516519Humanname
598268632CV3953897single nucleotide variantNM_018453.4(EAPP):c.509A>G (p.Gln170Arg)not specified [RCV005327138]uncertain significance143452476934524769Humanname