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22 records found for search term Ppa1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
12895750CV389893single nucleotide variantNM_021129.4(PPA1):c.-11A>Cnot provided [RCV004718687]|not specified [RCV000454401]benign107023333870233338Human1name
12895750CV389893single nucleotide variantNM_021129.4(PPA1):c.-11A>Cnot provided [RCV004718687]|not specified [RCV000454401]benign107023333870233339Human1name
156072879CV2233402single nucleotide variantNM_021129.4(PPA1):c.239A>G (p.Tyr80Cys)not specified [RCV004105760]uncertain significance107021787070217870Humanname
155927118CV2345340single nucleotide variantNM_021129.4(PPA1):c.749G>A (p.Ser250Asn)not specified [RCV004198120]uncertain significance107020631070206310Humanname
401855241CV2757202single nucleotide variantNM_021129.4(PPA1):c.704C>T (p.Thr235Met)not specified [RCV004338806]uncertain significance107020922670209226Humanname
401879215CV2764930single nucleotide variantNM_021129.4(PPA1):c.421C>A (p.Leu141Ile)not specified [RCV004335018]uncertain significance107021355370213553Humanname
401892260CV2776033single nucleotide variantNM_021129.4(PPA1):c.319A>G (p.Asn107Asp)not specified [RCV004353142]uncertain significance107021456570214565Humanname
405669817CV3370026single nucleotide variantNM_021129.4(PPA1):c.539C>G (p.Pro180Arg)not specified [RCV004514862]uncertain significance107020965870209658Humanname
405669812CV3370027single nucleotide variantNM_021129.4(PPA1):c.625G>A (p.Glu209Lys)not specified [RCV004514863]uncertain significance107020957270209572Humanname
407482485CV3471298single nucleotide variantNM_021129.4(PPA1):c.299C>T (p.Thr100Ile)not specified [RCV004664777]uncertain significance107021458570214585Humanname
597779144CV3581040single nucleotide variantNM_021129.4(PPA1):c.454A>T (p.Thr152Ser)not specified [RCV004853186]uncertain significance107021352070213520Humanname
597779148CV3581041single nucleotide variantNM_021129.4(PPA1):c.388T>A (p.Cys130Ser)not specified [RCV004853187]uncertain significance107021358670213586Humanname
597779152CV3581042single nucleotide variantNM_021129.4(PPA1):c.487G>C (p.Asp163His)not specified [RCV004853188]uncertain significance107021348770213487Humanname
597779156CV3581043single nucleotide variantNM_021129.4(PPA1):c.661A>G (p.Lys221Glu)not specified [RCV004853189]uncertain significance107020926970209269Humanname
598159629CV3901100single nucleotide variantNM_021129.4(PPA1):c.421C>G (p.Leu141Val)not specified [RCV005260782]uncertain significance107021355370213553Humanname
598159632CV3901101single nucleotide variantNM_021129.4(PPA1):c.478A>G (p.Asn160Asp)not specified [RCV005260783]uncertain significance107021349670213496Humanname
598159640CV3901103single nucleotide variantNM_021129.4(PPA1):c.809G>A (p.Cys270Tyr)not specified [RCV005260785]uncertain significance107020490270204902Humanname
598159644CV3901104single nucleotide variantNM_021129.4(PPA1):c.605A>C (p.Asn202Thr)not specified [RCV005260786]uncertain significance107020959270209592Humanname
598159648CV3901105single nucleotide variantNM_021129.4(PPA1):c.448G>C (p.Gly150Arg)not specified [RCV005260787]uncertain significance107021352670213526Humanname
598159651CV3901106single nucleotide variantNM_021129.4(PPA1):c.728T>C (p.Met243Thr)not specified [RCV005260788]uncertain significance107020633170206331Humanname
598159655CV3901107single nucleotide variantNM_021129.4(PPA1):c.379A>G (p.Ser127Gly)not specified [RCV005260789]uncertain significance107021450570214505Humanname
598159659CV3901108single nucleotide variantNM_021129.4(PPA1):c.512A>G (p.Asp171Gly)not specified [RCV005260790]uncertain significance107020968570209685Humanname