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33 records found for search term Cpeb4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8580624CV115056single nucleotide variantNM_030627.2(CPEB4):c.*1910G>ALung cancer [RCV000095579]uncertain significance5173958047173958047Humanname
401771728CV2722925single nucleotide variantNM_030627.4(CPEB4):c.13G>A (p.Gly5Arg)not specified [RCV004327108]uncertain significance5173889746173889746Humanname
401867719CV2780865single nucleotide variantNM_030627.4(CPEB4):c.116C>A (p.Pro39His)not specified [RCV004352176]uncertain significance5173889849173889849Humanname
597651022CV3651054single nucleotide variantNM_030627.4(CPEB4):c.238G>A (p.Ala80Thr)not specified [RCV004910526]uncertain significance5173889971173889971Humanname
598246295CV3945244single nucleotide variantNM_030627.4(CPEB4):c.155A>G (p.Asn52Ser)not specified [RCV005322299]uncertain significance5173889888173889888Humanname
598246317CV3945247single nucleotide variantNM_030627.4(CPEB4):c.106A>C (p.Asn36His)not specified [RCV005322302]uncertain significance5173889839173889839Humanname
155912552CV2332380single nucleotide variantNM_030627.4(CPEB4):c.821T>G (p.Leu274Trp)not specified [RCV004182538]uncertain significance5173890554173890554Humanname
155916283CV2336121single nucleotide variantNM_030627.4(CPEB4):c.401G>A (p.Arg134Lys)not specified [RCV004189715]uncertain significance5173890134173890134Humanname
155970841CV2392367single nucleotide variantNM_030627.4(CPEB4):c.470C>A (p.Pro157His)not specified [RCV004243958]uncertain significance5173890203173890203Humanname
329361513CV2459787single nucleotide variantNM_030627.4(CPEB4):c.373G>C (p.Glu125Gln)not specified [RCV004277200]uncertain significance5173890106173890106Humanname
405696685CV3245505single nucleotide variantNM_030627.4(CPEB4):c.584T>C (p.Val195Ala)not specified [RCV004374429]uncertain significance5173890317173890317Humanname
405696678CV3245506single nucleotide variantNM_030627.4(CPEB4):c.644G>A (p.Ser215Asn)not specified [RCV004374430]uncertain significance5173890377173890377Humanname
405696672CV3245507single nucleotide variantNM_030627.4(CPEB4):c.917A>G (p.Tyr306Cys)not specified [RCV004374431]uncertain significance5173890650173890650Humanname
407457046CV3419610single nucleotide variantNM_030627.4(CPEB4):c.468A>T (p.Gln156His)not specified [RCV004611004]uncertain significance5173890201173890201Humanname
407457049CV3419611single nucleotide variantNM_030627.4(CPEB4):c.555A>T (p.Glu185Asp)not specified [RCV004611005]uncertain significance5173890288173890288Humanname
407457255CV3419612single nucleotide variantNM_030627.4(CPEB4):c.589G>C (p.Ala197Pro)not specified [RCV004611006]uncertain significance5173890322173890322Humanname
597651029CV3651055single nucleotide variantNM_030627.4(CPEB4):c.956G>A (p.Arg319Lys)not specified [RCV004910527]uncertain significance5173890689173890689Humanname
597651039CV3651056single nucleotide variantNM_030627.4(CPEB4):c.367T>C (p.Ser123Pro)not specified [RCV004910528]uncertain significance5173890100173890100Humanname
597651056CV3651058single nucleotide variantNM_030627.4(CPEB4):c.488C>G (p.Ser163Trp)not specified [RCV004910530]uncertain significance5173890221173890221Humanname
598246309CV3945246single nucleotide variantNM_030627.4(CPEB4):c.630C>A (p.Phe210Leu)not specified [RCV005322301]uncertain significance5173890363173890363Humanname
156017892CV2302657single nucleotide variantNM_030627.4(CPEB4):c.1478G>A (p.Arg493His)not specified [RCV004162601]uncertain significance5173949529173949529Humanname
156152556CV2318926single nucleotide variantNM_030627.4(CPEB4):c.1330C>T (p.Arg444Cys)not specified [RCV004175818]uncertain significance5173945014173945014Humanname
156343760CV2349238single nucleotide variantNM_030627.4(CPEB4):c.1045G>T (p.Ala349Ser)not specified [RCV004199189]uncertain significance5173890778173890778Humanname
329370151CV2461633single nucleotide variantNM_030627.4(CPEB4):c.1287G>T (p.Gln429His)not specified [RCV004269806]uncertain significance5173944971173944971Humanname
401759428CV2690897single nucleotide variantNM_030627.4(CPEB4):c.1375T>G (p.Phe459Val)not specified [RCV004298591]uncertain significance5173945059173945059Humanname
401870891CV2788936single nucleotide variantNM_030627.4(CPEB4):c.1124C>T (p.Pro375Leu)not specified [RCV004363258]uncertain significance5173890857173890857Humanname
401942664CV2839745single nucleotide variantNM_030627.4(CPEB4):c.2021G>A (p.Arg674His)not provided [RCV003456616]uncertain significance5173955968173955968Humanname
405696690CV3245504single nucleotide variantNM_030627.4(CPEB4):c.1022A>G (p.Asn341Ser)not specified [RCV004374428]uncertain significance5173890755173890755Humanname
597651047CV3651057single nucleotide variantNM_030627.4(CPEB4):c.1028T>C (p.Ile343Thr)not specified [RCV004910529]uncertain significance5173890761173890761Humanname
597651064CV3651059single nucleotide variantNM_030627.4(CPEB4):c.1744A>G (p.Ile582Val)not specified [RCV004910531]uncertain significance5173951902173951902Humanname
598246302CV3945245single nucleotide variantNM_030627.4(CPEB4):c.1300C>G (p.Pro434Ala)not specified [RCV005322300]uncertain significance5173944984173944984Humanname
598246326CV3945248single nucleotide variantNM_030627.4(CPEB4):c.1237G>A (p.Asp413Asn)not specified [RCV005322303]uncertain significance5173932479173932479Humanname
598264946CV3945249single nucleotide variantNM_030627.4(CPEB4):c.1355G>T (p.Gly452Val)not specified [RCV005326233]uncertain significance5173945039173945039Humanname