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18 records found for search term Dusp14
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155932365CV2400008single nucleotide variantNM_007026.4(DUSP14):c.12A>T (p.Arg4Ser)not specified [RCV004246932]uncertain significance173751228437512284Humanname
401773502CV2709343single nucleotide variantNM_007026.4(DUSP14):c.46C>T (p.Pro16Ser)not specified [RCV004316488]uncertain significance173751231837512318Humanname
597802415CV3674030single nucleotide variantNM_007026.4(DUSP14):c.88A>G (p.Ile30Val)not specified [RCV004906672]uncertain significance173751236037512360Humanname
156242753CV2231456single nucleotide variantNM_007026.4(DUSP14):c.198C>A (p.Phe66Leu)not specified [RCV004096530]uncertain significance173751247037512470Humanname
155989648CV2244282single nucleotide variantNM_007026.4(DUSP14):c.154G>C (p.Gly52Arg)not specified [RCV004100275]uncertain significance173751242637512426Humanname
155926989CV2345314single nucleotide variantNM_007026.4(DUSP14):c.166A>G (p.Ile56Val)not specified [RCV004198094]uncertain significance173751243837512438Humanname
405734728CV3241227single nucleotide variantNM_007026.4(DUSP14):c.131A>G (p.Asn44Ser)not specified [RCV004379661]uncertain significance173751240337512403Humanname
405734740CV3241228single nucleotide variantNM_007026.4(DUSP14):c.182T>C (p.Ile61Thr)not specified [RCV004379662]uncertain significance173751245437512454Humanname
405734748CV3241229single nucleotide variantNM_007026.4(DUSP14):c.200A>G (p.Asn67Ser)not specified [RCV004379663]uncertain significance173751247237512472Humanname
598267082CV3957509single nucleotide variantNM_007026.4(DUSP14):c.134G>A (p.Arg45Gln)not specified [RCV005326807]uncertain significance173751240637512406Humanname
156185723CV2195593single nucleotide variantNM_007026.4(DUSP14):c.538A>G (p.Ile180Val)not specified [RCV004082803]uncertain significance173751281037512810Humanname
155921048CV2210959single nucleotide variantNM_007026.4(DUSP14):c.349C>G (p.Arg117Gly)not specified [RCV004086032]uncertain significance173751262137512621Humanname
156045011CV2305984single nucleotide variantNM_007026.4(DUSP14):c.493C>G (p.Leu165Val)not specified [RCV004169542]uncertain significance173751276537512765Humanname
156189654CV2356636single nucleotide variantNM_007026.4(DUSP14):c.394G>A (p.Val132Met)not specified [RCV004201998]uncertain significance173751266637512666Humanname
597802410CV3674028single nucleotide variantNM_007026.4(DUSP14):c.562G>A (p.Glu188Lys)not specified [RCV004906670]uncertain significance173751283437512834Humanname
597802412CV3674029single nucleotide variantNM_007026.4(DUSP14):c.488G>A (p.Arg163His)not specified [RCV004906671]uncertain significance173751276037512760Humanname
597802419CV3674032single nucleotide variantNM_007026.4(DUSP14):c.506C>T (p.Ser169Leu)not specified [RCV004906674]uncertain significance173751277837512778Humanname
598267079CV3957508single nucleotide variantNM_007026.4(DUSP14):c.569G>A (p.Arg190Gln)not specified [RCV005326806]uncertain significance173751284137512841Humanname