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18 records found for search term Dusp7
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156396008CV2326048single nucleotide variantNM_001947.4(DUSP7):c.25C>T (p.Pro9Ser)not specified [RCV004176252]uncertain significance35205634252056342Humanname
156292415CV2340138single nucleotide variantNM_001947.4(DUSP7):c.26C>A (p.Pro9Gln)not specified [RCV004192375]uncertain significance35205634152056341Humanname
401770367CV2711111single nucleotide variantNM_001947.4(DUSP7):c.32G>C (p.Arg11Pro)not specified [RCV004310794]uncertain significance35205633552056335Humanname
405735402CV3241308single nucleotide variantNM_001947.4(DUSP7):c.125G>C (p.Gly42Ala)not specified [RCV004379742]uncertain significance35205624252056242Humanname
156291898CV2306140single nucleotide variantNM_001947.4(DUSP7):c.940A>G (p.Ile314Val)not specified [RCV004162892]uncertain significance35205395252053952Humanname
401728112CV2685858single nucleotide variantNM_001947.4(DUSP7):c.562A>G (p.Thr188Ala)not specified [RCV004294842]uncertain significance35205433052054330Humanname
405735410CV3241309single nucleotide variantNM_001947.4(DUSP7):c.700G>A (p.Gly234Ser)not specified [RCV004379743]uncertain significance35205419252054192Humanname
407476832CV3431142single nucleotide variantNM_001947.4(DUSP7):c.440C>T (p.Pro147Leu)not specified [RCV004617213]uncertain significance35205592752055927Humanname
597735305CV3670232single nucleotide variantNM_001947.4(DUSP7):c.514C>G (p.Gln172Glu)not specified [RCV004920447]uncertain significance35205585352055853Humanname
597802549CV3670233single nucleotide variantNM_001947.4(DUSP7):c.527A>G (p.Asn176Ser)not specified [RCV004906741]uncertain significance35205436552054365Humanname
597802551CV3670234single nucleotide variantNM_001947.4(DUSP7):c.539C>T (p.Thr180Ile)not specified [RCV004906742]uncertain significance35205435352054353Humanname
597802553CV3670235single nucleotide variantNM_001947.4(DUSP7):c.539C>G (p.Thr180Arg)not specified [RCV004906743]uncertain significance35205435352054353Humanname
597735311CV3670236single nucleotide variantNM_001947.4(DUSP7):c.631C>T (p.Arg211Cys)not specified [RCV004920448]uncertain significance35205426152054261Humanname
598267310CV3957566single nucleotide variantNM_001947.4(DUSP7):c.438G>T (p.Glu146Asp)not specified [RCV005326864]uncertain significance35205592952055929Humanname
598267315CV3957567single nucleotide variantNM_001947.4(DUSP7):c.728C>A (p.Ala243Asp)not specified [RCV005326865]uncertain significance35205416452054164Humanname
156228621CV2393030single nucleotide variantNM_001947.4(DUSP7):c.1256C>T (p.Thr419Met)not specified [RCV004242881]uncertain significance35205081952050819Humanname
156262273CV2395692single nucleotide variantNM_001947.4(DUSP7):c.1187C>T (p.Ser396Leu)not specified [RCV004234877]uncertain significance35205088852050888Humanname
407476837CV3431143single nucleotide variantNM_001947.4(DUSP7):c.1078T>C (p.Phe360Leu)not specified [RCV004617214]uncertain significance35205099752050997Humanname