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Variants search result for Homo sapiens
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31 records found for search term Znf524
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156219651CV2254073single nucleotide variantNM_153219.4(ZNF524):c.21C>A (p.Asp7Glu)not specified [RCV004129520]uncertain significance195560213355602133Humanname
156180080CV2201708single nucleotide variantNM_153219.4(ZNF524):c.77C>T (p.Pro26Leu)not specified [RCV004082156]uncertain significance195560218955602189Humanname
401742777CV2715316single nucleotide variantNM_153219.4(ZNF524):c.65C>T (p.Ala22Val)not specified [RCV004324652]uncertain significance195560217755602177Humanname
405700137CV3350928single nucleotide variantNM_153219.4(ZNF524):c.41C>T (p.Pro14Leu)not specified [RCV004492329]uncertain significance195560215355602153Humanname
405700155CV3350931single nucleotide variantNM_153219.4(ZNF524):c.70T>C (p.Ser24Pro)not specified [RCV004492332]likely benign195560218255602182Humanname
405700162CV3350932single nucleotide variantNM_153219.4(ZNF524):c.74C>T (p.Pro25Leu)not specified [RCV004492333]uncertain significance195560218655602186Humanname
597709612CV3638818single nucleotide variantNM_153219.4(ZNF524):c.76C>T (p.Pro26Ser)not specified [RCV004886589]uncertain significance195560218855602188Humanname
598172186CV3931005single nucleotide variantNM_153219.4(ZNF524):c.86G>T (p.Arg29Leu)not specified [RCV005309351]uncertain significance195560219855602198Humanname
156136366CV2245698single nucleotide variantNM_153219.4(ZNF524):c.182G>A (p.Gly61Glu)not specified [RCV004111576]uncertain significance195560229455602294Humanname
156357606CV2254076single nucleotide variantNM_153219.4(ZNF524):c.229G>A (p.Gly77Ser)not specified [RCV004129523]uncertain significance195560234155602341Humanname
156245285CV2310323single nucleotide variantNM_153219.4(ZNF524):c.115G>A (p.Ala39Thr)not specified [RCV004163374]uncertain significance195560222755602227Humanname
156347402CV2315268single nucleotide variantNM_153219.4(ZNF524):c.152C>T (p.Pro51Leu)not specified [RCV004167257]uncertain significance195560226455602264Humanname
156396605CV2322471single nucleotide variantNM_153219.4(ZNF524):c.176A>G (p.Lys59Arg)not specified [RCV004180592]uncertain significance195560228855602288Humanname
401768312CV2675244single nucleotide variantNM_153219.4(ZNF524):c.166C>T (p.Arg56Cys)not specified [RCV004290012]uncertain significance195560227855602278Humanname
401860862CV2758667single nucleotide variantNM_153219.4(ZNF524):c.167G>A (p.Arg56His)not specified [RCV004337735]uncertain significance195560227955602279Humanname
405700132CV3350927single nucleotide variantNM_153219.4(ZNF524):c.214G>T (p.Val72Leu)not specified [RCV004492328]uncertain significance195560232655602326Humanname
407470467CV3420810single nucleotide variantNM_153219.4(ZNF524):c.173C>T (p.Pro58Leu)not specified [RCV004599663]uncertain significance195560228555602285Humanname
407470471CV3420812single nucleotide variantNM_153219.4(ZNF524):c.154C>T (p.Arg52Cys)not specified [RCV004599664]uncertain significance195560226655602266Humanname
597709622CV3638819single nucleotide variantNM_153219.4(ZNF524):c.250C>T (p.Leu84Phe)not specified [RCV004886590]uncertain significance195560236255602362Humanname
598172181CV3934893single nucleotide variantNM_153219.4(ZNF524):c.163G>T (p.Gly55Cys)not specified [RCV005309350]uncertain significance195560227555602275Humanname
156236933CV2193525single nucleotide variantNM_153219.4(ZNF524):c.677G>A (p.Gly226Glu)not specified [RCV004073005]uncertain significance195560278955602789Humanname
156047607CV2212732single nucleotide variantNM_153219.4(ZNF524):c.335C>T (p.Ala112Val)not specified [RCV004097158]uncertain significance195560244755602447Humanname
156295378CV2233728single nucleotide variantNM_153219.4(ZNF524):c.427C>G (p.Gln143Glu)not specified [RCV004100173]likely benign195560253955602539Humanname
156290807CV2296555single nucleotide variantNM_153219.4(ZNF524):c.694C>G (p.Pro232Ala)not specified [RCV004154625]uncertain significance195560280655602806Humanname
156167482CV2373688single nucleotide variantNM_153219.4(ZNF524):c.736C>T (p.Pro246Ser)not specified [RCV004222769]uncertain significance195560284855602848Humanname
401749441CV2712354single nucleotide variantNM_153219.4(ZNF524):c.533G>T (p.Arg178Leu)not specified [RCV004313837]uncertain significance195560264555602645Humanname
405700142CV3350929single nucleotide variantNM_153219.4(ZNF524):c.683C>T (p.Pro228Leu)not specified [RCV004492330]uncertain significance195560279555602795Humanname
405700148CV3350930single nucleotide variantNM_153219.4(ZNF524):c.692C>T (p.Ala231Val)not specified [RCV004492331]uncertain significance195560280455602804Humanname
407468217CV3420811single nucleotide variantNM_153219.4(ZNF524):c.686T>G (p.Leu229Arg)not specified [RCV004614633]uncertain significance195560279855602798Humanname
598246482CV3934894single nucleotide variantNM_153219.4(ZNF524):c.775G>A (p.Gly259Arg)not specified [RCV005297749]uncertain significance195560288755602887Humanname
598246490CV3934895single nucleotide variantNM_153219.4(ZNF524):c.635C>T (p.Thr212Met)not specified [RCV005297750]uncertain significance195560274755602747Humanname