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Variants search result for All species
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16 records found for search term Nupr1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598235617CV4004890single nucleotide variantNM_012385.3(NUPR1):c.113-16C>Tnot specified [RCV005382035]uncertain significance162853817128538171Humanname
407478036CV3459035single nucleotide variantNM_012385.3(NUPR1):c.57C>G (p.Asp19Glu)not specified [RCV004638922]uncertain significance162853885128538851Humanname
597664851CV3570141single nucleotide variantNM_012385.3(NUPR1):c.50C>T (p.Pro17Leu)not specified [RCV004835520]uncertain significance162853885828538858Humanname
597664867CV3570143single nucleotide variantNM_012385.3(NUPR1):c.65C>G (p.Ser22Cys)not specified [RCV004835522]uncertain significance162853884328538843Humanname
155992329CV2255808single nucleotide variantNM_012385.3(NUPR1):c.225G>C (p.Arg75Ser)not specified [RCV004121972]uncertain significance162853804328538043Humanname
156148155CV2307321single nucleotide variantNM_012385.3(NUPR1):c.133C>T (p.Arg45Cys)not specified [RCV004166011]uncertain significance162853813528538135Humanname
156150796CV2318704single nucleotide variantNM_012385.3(NUPR1):c.236G>A (p.Gly79Glu)not specified [RCV004173596]uncertain significance162853803228538032Humanname
156237473CV2356186single nucleotide variantNM_012385.3(NUPR1):c.187G>A (p.Glu63Lys)not specified [RCV004206006]uncertain significance162853808128538081Humanname
329368421CV2428013single nucleotide variantNM_012385.3(NUPR1):c.220G>A (p.Glu74Lys)not specified [RCV004254392]uncertain significance162853804828538048Humanname
405681053CV3352561single nucleotide variantNM_012385.3(NUPR1):c.244C>T (p.Arg82Cys)not specified [RCV004488694]uncertain significance162853802428538024Humanname
407522138CV3459034single nucleotide variantNM_012385.3(NUPR1):c.124C>T (p.Arg42Trp)not specified [RCV004652781]uncertain significance162853814428538144Humanname
597664859CV3570142single nucleotide variantNM_012385.3(NUPR1):c.125G>A (p.Arg42Gln)not specified [RCV004835521]uncertain significance162853814328538143Humanname
597664874CV3570144single nucleotide variantNM_012385.3(NUPR1):c.166C>T (p.Arg56Cys)not specified [RCV004835523]uncertain significance162853810228538102Humanname
598266409CV4004889single nucleotide variantNM_012385.3(NUPR1):c.245G>A (p.Arg82His)not specified [RCV005388130]uncertain significance162853802328538023Humanname
598266413CV4004891single nucleotide variantNM_012385.3(NUPR1):c.134G>A (p.Arg45His)not specified [RCV005388131]uncertain significance162853813428538134Humanname
598235622CV4004892single nucleotide variantNM_012385.3(NUPR1):c.241C>T (p.Arg81Trp)not specified [RCV005382036]uncertain significance162853802728538027Humanname