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Variants search result for Homo sapiens
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27 records found for search term Meox2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8590682CV125390single nucleotide variantNM_005924.4(MEOX2):c.517+17174T>CLung cancer [RCV000105909]uncertain significance71566871215668712Humanname
405693711CV3282000single nucleotide variantNM_005924.5(MEOX2):c.35C>T (p.Pro12Leu)not specified [RCV004424152]uncertain significance71568636815686368Humanname
405693722CV3282002single nucleotide variantNM_005924.5(MEOX2):c.43A>G (p.Thr15Ala)not specified [RCV004424154]uncertain significance71568636015686360Humanname
407518118CV3449890single nucleotide variantNM_005924.5(MEOX2):c.98C>G (p.Ser33Cys)not specified [RCV004628759]uncertain significance71568630515686305Humanname
407518121CV3449893single nucleotide variantNM_005924.5(MEOX2):c.82G>T (p.Ala28Ser)not specified [RCV004628760]uncertain significance71568632115686321Humanname
155926873CV2208309single nucleotide variantNM_005924.5(MEOX2):c.272A>G (p.Asn91Ser)not specified [RCV004088747]uncertain significance71568613115686131Humanname
156295946CV2239814single nucleotide variantNM_005924.5(MEOX2):c.236A>C (p.His79Pro)not specified [RCV004108332]uncertain significance71568616715686167Humanname
155906598CV2279329single nucleotide variantNM_005924.5(MEOX2):c.149T>C (p.Ile50Thr)not specified [RCV004139845]uncertain significance71568625415686254Humanname
401770456CV2678683single nucleotide variantNM_005924.5(MEOX2):c.253C>G (p.His85Asp)not specified [RCV004294720]uncertain significance71568615015686150Humanname
401762035CV2722615single nucleotide variantNM_005924.5(MEOX2):c.273C>G (p.Asn91Lys)not specified [RCV004325072]uncertain significance71568613015686130Humanname
407502802CV3449891single nucleotide variantNM_005924.5(MEOX2):c.212A>G (p.His71Arg)not specified [RCV004645268]uncertain significance71568619115686191Humanname
597634806CV3556674single nucleotide variantNM_005924.5(MEOX2):c.218A>G (p.His73Arg)not specified [RCV004824226]uncertain significance71568618515686185Humanname
156398167CV2204349single nucleotide variantNM_005924.5(MEOX2):c.493G>T (p.Gly165Cys)not specified [RCV004079171]uncertain significance71568591015685910Humanname
156058398CV2262887single nucleotide variantNM_005924.5(MEOX2):c.844C>G (p.Gln282Glu)not specified [RCV004125032]uncertain significance71561245815612458Humanname
156348918CV2380954single nucleotide variantNM_005924.5(MEOX2):c.839T>A (p.Leu280His)not specified [RCV004220532]uncertain significance71561246315612463Humanname
401740917CV2679834single nucleotide variantNM_005924.5(MEOX2):c.813G>C (p.Glu271Asp)not specified [RCV004282290]uncertain significance71561248915612489Humanname
405693702CV3281998single nucleotide variantNM_005924.5(MEOX2):c.355G>A (p.Glu119Lys)not specified [RCV004424150]uncertain significance71568604815686048Humanname
405693717CV3282001single nucleotide variantNM_005924.5(MEOX2):c.433G>C (p.Ala145Pro)not specified [RCV004424153]uncertain significance71568597015685970Humanname
405693728CV3282003single nucleotide variantNM_005924.5(MEOX2):c.452G>T (p.Arg151Leu)not specified [RCV004424155]uncertain significance71568595115685951Humanname
407502794CV3449888single nucleotide variantNM_005924.5(MEOX2):c.451C>A (p.Arg151Ser)not specified [RCV004645266]uncertain significance71568595215685952Humanname
407502798CV3449889single nucleotide variantNM_005924.5(MEOX2):c.650G>A (p.Arg217Gln)not specified [RCV004645267]uncertain significance71562678615626786Humanname
407502805CV3449892single nucleotide variantNM_005924.5(MEOX2):c.547G>C (p.Val183Leu)not specified [RCV004645269]uncertain significance71562688915626889Humanname
407502808CV3449894single nucleotide variantNM_005924.5(MEOX2):c.472G>A (p.Glu158Lys)not specified [RCV004645270]uncertain significance71568593115685931Humanname
597677785CV3556671single nucleotide variantNM_005924.5(MEOX2):c.458C>T (p.Ala153Val)not specified [RCV004830517]uncertain significance71568594515685945Humanname
597634801CV3556672single nucleotide variantNM_005924.5(MEOX2):c.476C>A (p.Ala159Glu)not specified [RCV004824225]uncertain significance71568592715685927Humanname
597677793CV3556673single nucleotide variantNM_005924.5(MEOX2):c.347G>A (p.Gly116Glu)not specified [RCV004830518]uncertain significance71568605615686056Humanname
598241628CV3985841single nucleotide variantNM_005924.5(MEOX2):c.783T>G (p.Asn261Lys)not specified [RCV005364848]uncertain significance71561251915612519Humanname