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Variants search result for Homo sapiens
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14 records found for search term Nudt18
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405729432CV3355892single nucleotide variantNM_024815.4(NUDT18):c.25G>A (p.Ala9Thr)not specified [RCV004496188]uncertain significance82210927622109276Humanname
156010556CV2291040single nucleotide variantNM_024815.4(NUDT18):c.94C>T (p.Pro32Ser)not specified [RCV004151576]uncertain significance82210920722109207Humanname
155939538CV2293929single nucleotide variantNM_024815.4(NUDT18):c.77C>T (p.Ser26Leu)not specified [RCV004155472]uncertain significance82210922422109224Humanname
156075792CV2331761single nucleotide variantNM_024815.4(NUDT18):c.58A>C (p.Ser20Arg)not specified [RCV004184385]likely benign82210924322109243Humanname
156090515CV2384488single nucleotide variantNM_024815.4(NUDT18):c.53G>C (p.Gly18Ala)not specified [RCV004230284]uncertain significance82210924822109248Humanname
156141601CV2288543single nucleotide variantNM_024815.4(NUDT18):c.230G>C (p.Arg77Thr)not specified [RCV004152070]uncertain significance82210827922108279Humanname
156301658CV2307091single nucleotide variantNM_024815.4(NUDT18):c.198G>C (p.Glu66Asp)not specified [RCV004159575]uncertain significance82210831122108311Humanname
156312218CV2196337single nucleotide variantNM_024815.4(NUDT18):c.815T>G (p.Val272Gly)not specified [RCV004072514]uncertain significance82210745722107457Humanname
156228180CV2199385single nucleotide variantNM_024815.4(NUDT18):c.414G>T (p.Glu138Asp)not specified [RCV004070956]uncertain significance82210785822107858Humanname
329387479CV2470744single nucleotide variantNM_024815.4(NUDT18):c.874G>A (p.Gly292Ser)not specified [RCV004275978]uncertain significance82210739822107398Humanname
405729450CV3355894single nucleotide variantNM_024815.4(NUDT18):c.880A>G (p.Asn294Asp)not specified [RCV004496190]uncertain significance82210739222107392Humanname
598265677CV3995101single nucleotide variantNM_024815.4(NUDT18):c.500C>T (p.Ala167Val)not specified [RCV005387986]uncertain significance82210777222107772Humanname
598265683CV3995102single nucleotide variantNM_024815.4(NUDT18):c.796G>A (p.Asp266Asn)not specified [RCV005387987]uncertain significance82210747622107476Humanname
598233865CV3995103single nucleotide variantNM_024815.4(NUDT18):c.685G>T (p.Gly229Cys)not specified [RCV005381781]uncertain significance82210758722107587Humanname