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Variants search result for Homo sapiens
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27 records found for search term Fbxw2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329401310CV2442333single nucleotide variantNM_012164.4(FBXW2):c.283A>G (p.Thr95Ala)not specified [RCV004264806]uncertain significance9120787976120787976Humanname
597723545CV3666183single nucleotide variantNM_012164.4(FBXW2):c.173A>G (p.Lys58Arg)not specified [RCV004919017]uncertain significance9120788086120788086Humanname
156335051CV2228338single nucleotide variantNM_012164.4(FBXW2):c.850C>G (p.Leu284Val)not specified [RCV004098329]uncertain significance9120772810120772810Humanname
156297704CV2297707single nucleotide variantNM_012164.4(FBXW2):c.470A>G (p.Lys157Arg)not specified [RCV004155387]uncertain significance9120787789120787789Humanname
156243983CV2347116single nucleotide variantNM_012164.4(FBXW2):c.314T>G (p.Leu105Trp)not specified [RCV004204596]uncertain significance9120787945120787945Humanname
401763480CV2714567single nucleotide variantNM_012164.4(FBXW2):c.829C>G (p.Gln277Glu)not specified [RCV004318079]uncertain significance9120772831120772831Humanname
401896542CV2780920single nucleotide variantNM_012164.4(FBXW2):c.346G>A (p.Ala116Thr)not specified [RCV004354461]uncertain significance9120787913120787913Humanname
405723780CV3260526single nucleotide variantNM_012164.4(FBXW2):c.544T>C (p.Tyr182His)not specified [RCV004389128]uncertain significance9120778492120778492Humanname
405723785CV3260527single nucleotide variantNM_012164.4(FBXW2):c.683C>G (p.Ala228Gly)not specified [RCV004389129]uncertain significance9120778353120778353Humanname
405723793CV3260528single nucleotide variantNM_012164.4(FBXW2):c.973A>C (p.Ser325Arg)not specified [RCV004389130]uncertain significance9120771451120771451Humanname
597723555CV3666184single nucleotide variantNM_012164.4(FBXW2):c.355T>A (p.Trp119Arg)not specified [RCV004919018]uncertain significance9120787904120787904Humanname
598228377CV3962886single nucleotide variantNM_012164.4(FBXW2):c.862C>T (p.Pro288Ser)not specified [RCV005341920]uncertain significance9120772798120772798Humanname
598228385CV3962887single nucleotide variantNM_012164.4(FBXW2):c.334T>G (p.Ser112Ala)not specified [RCV005341921]uncertain significance9120787925120787925Humanname
598228404CV3962890single nucleotide variantNM_012164.4(FBXW2):c.518G>C (p.Trp173Ser)not specified [RCV005341923]uncertain significance9120778518120778518Humanname
598228411CV3962891single nucleotide variantNM_012164.4(FBXW2):c.667C>T (p.Arg223Trp)not specified [RCV005341924]uncertain significance9120778369120778369Humanname
329369490CV2461131single nucleotide variantNM_012164.4(FBXW2):c.1085A>G (p.Lys362Arg)not specified [RCV004265550]uncertain significance9120764839120764839Humanname
401881563CV2759460single nucleotide variantNM_012164.4(FBXW2):c.1151A>G (p.Asn384Ser)not specified [RCV004338455]uncertain significance9120764773120764773Humanname
405723561CV3260522single nucleotide variantNM_012164.4(FBXW2):c.1061G>C (p.Ser354Thr)not specified [RCV004389124]uncertain significance9120771363120771363Humanname
405723568CV3260523single nucleotide variantNM_012164.4(FBXW2):c.1153C>T (p.Arg385Cys)not specified [RCV004389125]uncertain significance9120764771120764771Humanname
405723574CV3260524single nucleotide variantNM_012164.4(FBXW2):c.1168A>T (p.Met390Leu)not specified [RCV004389126]uncertain significance9120764756120764756Humanname
405723770CV3260525single nucleotide variantNM_012164.4(FBXW2):c.1345T>G (p.Leu449Val)not specified [RCV004389127]uncertain significance9120764579120764579Humanname
407482337CV3442661single nucleotide variantNM_012164.4(FBXW2):c.1154G>A (p.Arg385His)not specified [RCV004618361]uncertain significance9120764770120764770Humanname
597723499CV3666179single nucleotide variantNM_012164.4(FBXW2):c.1198C>T (p.Arg400Cys)not specified [RCV004919013]uncertain significance9120764726120764726Humanname
597723521CV3666181single nucleotide variantNM_012164.4(FBXW2):c.1295C>T (p.Thr432Met)not specified [RCV004919015]uncertain significance9120764629120764629Humanname
597723533CV3666182single nucleotide variantNM_012164.4(FBXW2):c.1129A>G (p.Ile377Val)not specified [RCV004919016]likely benign9120764795120764795Humanname
597723564CV3666185single nucleotide variantNM_012164.4(FBXW2):c.1096A>G (p.Ile366Val)not specified [RCV004919019]uncertain significance9120764828120764828Humanname
598228395CV3962889single nucleotide variantNM_012164.4(FBXW2):c.1099G>C (p.Ala367Pro)not specified [RCV005341922]uncertain significance9120764825120764825Humanname