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Variants search result for Homo sapiens
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16 records found for search term Chmp2a
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597769756CV3653188single nucleotide variantNM_014453.4(CHMP2A):c.16G>A (p.Gly6Arg)not specified [RCV004896796]uncertain significance195855419758554197Humanname
597769761CV3653189single nucleotide variantNM_014453.4(CHMP2A):c.80G>A (p.Arg27Gln)not specified [RCV004896797]uncertain significance195855413358554133Humanname
597769779CV3653192single nucleotide variantNM_014453.4(CHMP2A):c.54C>G (p.Asn18Lys)not specified [RCV004896800]uncertain significance195855415958554159Humanname
329393243CV2449590single nucleotide variantNM_014453.4(CHMP2A):c.156G>C (p.Lys52Asn)not specified [RCV004268515]uncertain significance195855405758554057Humanname
329377356CV2462566single nucleotide variantNM_014453.4(CHMP2A):c.257T>C (p.Val86Ala)not specified [RCV004278517]uncertain significance195855235058552350Humanname
401887523CV2773482single nucleotide variantNM_014453.4(CHMP2A):c.198G>C (p.Leu66Phe)not specified [RCV004354115]uncertain significance195855240958552409Humanname
407455734CV3422759single nucleotide variantNM_014453.4(CHMP2A):c.273G>C (p.Gln91His)not specified [RCV004610387]uncertain significance195855233458552334Humanname
155920963CV2240449single nucleotide variantNM_014453.4(CHMP2A):c.339G>A (p.Met113Ile)not specified [RCV004117335]uncertain significance195855226858552268Humanname
155978790CV2335191single nucleotide variantNM_014453.4(CHMP2A):c.426G>A (p.Met142Ile)not specified [RCV004186764]uncertain significance195855210858552108Humanname
156042951CV2387913single nucleotide variantNM_014453.4(CHMP2A):c.659G>A (p.Arg220Gln)not specified [RCV004236460]uncertain significance195855165958551659Humanname
405661859CV3297115single nucleotide variantNM_014453.4(CHMP2A):c.559G>C (p.Gly187Arg)not specified [RCV004439312]uncertain significance195855175958551759Humanname
597770355CV3653187single nucleotide variantNM_014453.4(CHMP2A):c.474G>C (p.Glu158Asp)not specified [RCV004896795]uncertain significance195855206058552060Humanname
597769766CV3653190single nucleotide variantNM_014453.4(CHMP2A):c.566T>A (p.Leu189His)not specified [RCV004896798]uncertain significance195855175258551752Humanname
598214700CV3951633single nucleotide variantNM_014453.4(CHMP2A):c.610G>A (p.Ala204Thr)not specified [RCV005316621]uncertain significance195855170858551708Humanname
598214707CV3951634single nucleotide variantNM_014453.4(CHMP2A):c.658C>T (p.Arg220Trp)not specified [RCV005316622]uncertain significance195855166058551660Humanname
598214712CV3951635single nucleotide variantNM_014453.4(CHMP2A):c.644G>A (p.Arg215Gln)not specified [RCV005316623]uncertain significance195855167458551674Humanname