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11 records found for search term Edf1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155942981CV2244869single nucleotide variantNM_003792.4(EDF1):c.12C>A (p.Ser4Arg)not specified [RCV004104627]uncertain significance9136866247136866247Humanname
401894816CV2785341single nucleotide variantNM_003792.4(EDF1):c.23C>T (p.Thr8Met)not specified [RCV004357094]uncertain significance9136866236136866236Humanname
597644344CV3667484single nucleotide variantNM_003792.4(EDF1):c.14A>G (p.Asp5Gly)not specified [RCV004909655]uncertain significance9136866245136866245Humanname
155968871CV2312894single nucleotide variantNM_003792.4(EDF1):c.43A>C (p.Lys15Gln)not specified [RCV004171382]uncertain significance9136866216136866216Humanname
597644359CV3667486single nucleotide variantNM_003792.4(EDF1):c.275A>G (p.Gln92Arg)not specified [RCV004909657]uncertain significance9136863304136863304Humanname
597644369CV3667487single nucleotide variantNM_003792.4(EDF1):c.217G>A (p.Val73Met)not specified [RCV004909658]uncertain significance9136863362136863362Humanname
156024185CV2242100single nucleotide variantNM_003792.4(EDF1):c.398G>A (p.Arg133Gln)not specified [RCV004109324]uncertain significance9136862333136862333Humanname
401735303CV2687547single nucleotide variantNM_003792.4(EDF1):c.403A>G (p.Lys135Glu)not specified [RCV004300776]uncertain significance9136862328136862328Humanname
405767499CV3248255single nucleotide variantNM_003792.4(EDF1):c.440C>T (p.Ala147Val)not specified [RCV004384548]uncertain significance9136862291136862291Humanname
597644374CV3667488single nucleotide variantNM_003792.4(EDF1):c.376C>T (p.Arg126Trp)not specified [RCV004909659]uncertain significance9136862915136862915Humanname
598166004CV3954099single nucleotide variantNM_003792.4(EDF1):c.358G>C (p.Val120Leu)not specified [RCV005329798]uncertain significance9136862933136862933Humanname