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Variants search result for All species
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46 records found for search term Pabpc4l
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597694486CV3578268single nucleotide variantNM_001114734.2(PABPC4L):c.-9G>Cnot specified [RCV004838968]uncertain significance4134201028134201028Humanname
156071979CV2233335single nucleotide variantNM_001114734.2(PABPC4L):c.-89A>Cnot specified [RCV004105708]uncertain significance4134201108134201108Humanname
329356862CV2431173single nucleotide variantNM_001114734.2(PABPC4L):c.-51G>Anot specified [RCV004250521]likely benign4134201070134201070Humanname
405740593CV3371430single nucleotide variantNM_001114734.2(PABPC4L):c.-19C>Gnot specified [RCV004497679]uncertain significance4134201038134201038Humanname
407517461CV3470027single nucleotide variantNM_001114734.2(PABPC4L):c.-29G>Anot specified [RCV004650662]uncertain significance4134201048134201048Humanname
597694540CV3578263single nucleotide variantNM_001114734.2(PABPC4L):c.-66G>Cnot specified [RCV004838963]likely benign4134201085134201085Humanname
156191852CV2335943single nucleotide variantNM_001114734.2(PABPC4L):c.-168G>Anot specified [RCV004189553]uncertain significance4134201187134201187Humanname
407478768CV3470030single nucleotide variantNM_001114734.2(PABPC4L):c.-170G>Anot specified [RCV004663980]uncertain significance4134201189134201189Humanname
597694495CV3578267single nucleotide variantNM_001114734.2(PABPC4L):c.-150G>Anot specified [RCV004838967]uncertain significance4134201169134201169Humanname
597694465CV3578270single nucleotide variantNM_001114734.2(PABPC4L):c.-152G>Tnot specified [RCV004838970]uncertain significance4134201171134201171Humanname
405740599CV3371431single nucleotide variantNM_001114734.2(PABPC4L):c.1A>G (p.Met1Val)not specified [RCV004497680]uncertain significance4134201019134201019Humanname
401724386CV2677863single nucleotide variantNM_001114734.2(PABPC4L):c.17A>G (p.Lys6Arg)not specified [RCV004294358]uncertain significance4134201003134201003Humanname
401883755CV2764556single nucleotide variantNM_001114734.2(PABPC4L):c.56C>T (p.Ala19Val)not specified [RCV004339111]uncertain significance4134200964134200964Humanname
401738090CV2714320single nucleotide variantNM_001114734.2(PABPC4L):c.151C>A (p.Leu51Met)not specified [RCV004316000]uncertain significance4134200869134200869Humanname
401887724CV2772114single nucleotide variantNM_001114734.2(PABPC4L):c.106G>A (p.Val36Met)not specified [RCV004344767]uncertain significance4134200914134200914Humanname
405740608CV3371432single nucleotide variantNM_001114734.2(PABPC4L):c.130G>A (p.Asp44Asn)not specified [RCV004497681]uncertain significance4134200890134200890Humanname
405740615CV3371433single nucleotide variantNM_001114734.2(PABPC4L):c.214A>G (p.Asn72Asp)not specified [RCV004497682]uncertain significance4134200806134200806Humanname
405740619CV3371434single nucleotide variantNM_001114734.2(PABPC4L):c.251T>C (p.Met84Thr)not specified [RCV004497683]uncertain significance4134200769134200769Humanname
405740627CV3371435single nucleotide variantNM_001114734.2(PABPC4L):c.289A>C (p.Ile97Leu)not specified [RCV004497684]uncertain significance4134200731134200731Humanname
407478773CV3470031single nucleotide variantNM_001114734.2(PABPC4L):c.158A>T (p.Tyr53Phe)not specified [RCV004663981]uncertain significance4134200862134200862Humanname
597694507CV3578266single nucleotide variantNM_001114734.2(PABPC4L):c.184G>A (p.Ala62Thr)not specified [RCV004838966]likely benign4134200836134200836Humanname
597694475CV3578269single nucleotide variantNM_001114734.2(PABPC4L):c.286G>A (p.Gly96Arg)not specified [RCV004838969]uncertain significance4134200734134200734Humanname
597694455CV3578271single nucleotide variantNM_001114734.2(PABPC4L):c.208A>C (p.Thr70Pro)not specified [RCV004838971]uncertain significance4134200812134200812Humanname
156333836CV2266929single nucleotide variantNM_001114734.2(PABPC4L):c.472A>G (p.Asn158Asp)not specified [RCV004131589]uncertain significance4134200548134200548Humanname
156100681CV2294728single nucleotide variantNM_001114734.2(PABPC4L):c.605A>T (p.Asp202Val)not specified [RCV004161967]uncertain significance4134200415134200415Humanname
156191034CV2301773single nucleotide variantNM_001114734.2(PABPC4L):c.412G>A (p.Gly138Ser)not specified [RCV004156581]uncertain significance4134200608134200608Humanname
156173117CV2326825single nucleotide variantNM_001114734.2(PABPC4L):c.691G>T (p.Gly231Cys)not specified [RCV004176658]uncertain significance4134200329134200329Humanname
329364758CV2443834single nucleotide variantNM_001114734.2(PABPC4L):c.649C>G (p.Leu217Val)not specified [RCV004258175]uncertain significance4134200371134200371Humanname
329351991CV2455582single nucleotide variantNM_001114734.2(PABPC4L):c.320A>G (p.Lys107Arg)not specified [RCV004276833]uncertain significance4134200700134200700Humanname
401734273CV2688454single nucleotide variantNM_001114734.2(PABPC4L):c.928C>G (p.Arg310Gly)not specified [RCV004301436]uncertain significance4134200092134200092Humanname
401735075CV2690768single nucleotide variantNM_001114734.2(PABPC4L):c.766A>G (p.Asn256Asp)not specified [RCV004298487]uncertain significance4134200254134200254Humanname
405740582CV3371428single nucleotide variantNM_001114734.2(PABPC4L):c.975G>T (p.Met325Ile)not specified [RCV004497677]uncertain significance4134200045134200045Humanname
405740631CV3371436single nucleotide variantNM_001114734.2(PABPC4L):c.409A>G (p.Lys137Glu)not specified [RCV004497685]uncertain significance4134200611134200611Humanname
405740638CV3371437single nucleotide variantNM_001114734.2(PABPC4L):c.529G>T (p.Asp177Tyr)not specified [RCV004497686]uncertain significance4134200491134200491Humanname
405740645CV3371438single nucleotide variantNM_001114734.2(PABPC4L):c.606T>A (p.Asp202Glu)not specified [RCV004497687]uncertain significance4134200414134200414Humanname
405740654CV3371439single nucleotide variantNM_001114734.2(PABPC4L):c.707G>C (p.Ser236Thr)not specified [RCV004497688]uncertain significance4134200313134200313Humanname
405740661CV3371440single nucleotide variantNM_001114734.2(PABPC4L):c.716G>A (p.Ser239Asn)not specified [RCV004497689]uncertain significance4134200304134200304Humanname
407517464CV3470028single nucleotide variantNM_001114734.2(PABPC4L):c.872A>G (p.Gln291Arg)not specified [RCV004650663]uncertain significance4134200148134200148Humanname
407478761CV3470029single nucleotide variantNM_001114734.2(PABPC4L):c.552C>G (p.Ser184Arg)not specified [RCV004663979]uncertain significance4134200468134200468Humanname
407517467CV3470032single nucleotide variantNM_001114734.2(PABPC4L):c.802A>C (p.Lys268Gln)not specified [RCV004650664]uncertain significance4134200218134200218Humanname
597694528CV3578264single nucleotide variantNM_001114734.2(PABPC4L):c.460A>G (p.Ile154Val)not specified [RCV004838964]uncertain significance4134200560134200560Humanname
597694518CV3578265single nucleotide variantNM_001114734.2(PABPC4L):c.750G>C (p.Met250Ile)not specified [RCV004838965]uncertain significance4134200270134200270Humanname
8631030CV86186single nucleotide variantNM_001114734.1(PABPC4L):c.715G>A (p.Glu239Lys)Malignant melanoma [RCV000066275]not provided4134200479134200479Humanname
401744131CV2688102single nucleotide variantNM_001114734.2(PABPC4L):c.1108C>T (p.His370Tyr)not specified [RCV004305159]likely benign4134199912134199912Humanname
405740588CV3371429single nucleotide variantNM_001114734.2(PABPC4L):c.1036A>G (p.Thr346Ala)not specified [RCV004497678]uncertain significance4134199984134199984Humanname
598163800CV3995943single nucleotide variantNM_001114734.2(PABPC4L):c.1037C>G (p.Thr346Ser)not specified [RCV005391052]uncertain significance4134199983134199983Humanname