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Variants search result for Homo sapiens
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13 records found for search term Dusp21
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597802468CV3670179single nucleotide variantNM_022076.4(DUSP21):c.13G>A (p.Ala5Thr)not specified [RCV004906700]uncertain significanceX4484414544844145Humanname
407490318CV3431107single nucleotide variantNM_022076.4(DUSP21):c.37G>A (p.Gly13Ser)not specified [RCV004620151]uncertain significanceX4484416944844169Humanname
407490321CV3431108single nucleotide variantNM_022076.4(DUSP21):c.74T>C (p.Ile25Thr)not specified [RCV004620152]uncertain significanceX4484420644844206Humanname
401751058CV2712367single nucleotide variantNM_022076.4(DUSP21):c.124C>T (p.Leu42Phe)not specified [RCV004313850]uncertain significanceX4484425644844256Humanname
156229948CV2235016single nucleotide variantNM_022076.4(DUSP21):c.521G>T (p.Gly174Val)not specified [RCV004113203]uncertain significanceX4484465344844653Humanname
156263995CV2312043single nucleotide variantNM_022076.4(DUSP21):c.311T>C (p.Leu104Pro)not specified [RCV004164974]uncertain significanceX4484444344844443Humanname
156391773CV2382566single nucleotide variantNM_022076.4(DUSP21):c.319A>G (p.Met107Val)not specified [RCV004232894]likely benignX4484445144844451Humanname
401752936CV2703523single nucleotide variantNM_022076.4(DUSP21):c.550C>G (p.Leu184Val)not specified [RCV004317701]likely benignX4484468244844682Humanname
405735158CV3241258single nucleotide variantNM_022076.4(DUSP21):c.569T>C (p.Met190Thr)not specified [RCV004379692]uncertain significanceX4484470144844701Humanname
597802470CV3670180single nucleotide variantNM_022076.4(DUSP21):c.533A>G (p.Asp178Gly)not specified [RCV004906701]uncertain significanceX4484466544844665Humanname
598267160CV3957531single nucleotide variantNM_022076.4(DUSP21):c.419G>A (p.Arg140His)not specified [RCV005326829]uncertain significanceX4484455144844551Humanname
598267164CV3957532single nucleotide variantNM_022076.4(DUSP21):c.380T>A (p.Met127Lys)not specified [RCV005326830]uncertain significanceX4484451244844512Humanname
598267167CV3957533single nucleotide variantNM_022076.4(DUSP21):c.455A>G (p.Gln152Arg)not specified [RCV005326831]uncertain significanceX4484458744844587Humanname