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Variants search result for Homo sapiens
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43 records found for search term Fgfbp3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156272958CV2277628single nucleotide variantNM_152429.5(FGFBP3):c.64C>G (p.Leu22Val)not specified [RCV004147093]uncertain significance109190890691908906Humanname
155999434CV2396416single nucleotide variantNM_152429.5(FGFBP3):c.73G>A (p.Ala25Thr)not specified [RCV004242133]uncertain significance109190889791908897Humanname
405760260CV3253697single nucleotide variantNM_152429.5(FGFBP3):c.76G>A (p.Ala26Thr)not specified [RCV004394131]uncertain significance109190889491908894Humanname
405760266CV3253698single nucleotide variantNM_152429.5(FGFBP3):c.77C>T (p.Ala26Val)not specified [RCV004394132]uncertain significance109190889391908893Humanname
405760272CV3253699single nucleotide variantNM_152429.5(FGFBP3):c.85G>A (p.Glu29Lys)not specified [RCV004394133]uncertain significance109190888591908885Humanname
407501610CV3439155single nucleotide variantNM_152429.5(FGFBP3):c.97G>A (p.Ala33Thr)not specified [RCV004623297]uncertain significance109190887391908873Humanname
155923820CV2248617single nucleotide variantNM_152429.5(FGFBP3):c.148C>G (p.Arg50Gly)not specified [RCV004121803]uncertain significance109190882291908822Humanname
405760183CV3253684single nucleotide variantNM_152429.5(FGFBP3):c.124G>C (p.Gly42Arg)not specified [RCV004394118]uncertain significance109190884691908846Humanname
405760187CV3253685single nucleotide variantNM_152429.5(FGFBP3):c.179G>A (p.Ser60Asn)not specified [RCV004394119]uncertain significance109190879191908791Humanname
405760193CV3253686single nucleotide variantNM_152429.5(FGFBP3):c.253G>A (p.Gly85Arg)not specified [RCV004394120]uncertain significance109190871791908717Humanname
405760199CV3253687single nucleotide variantNM_152429.5(FGFBP3):c.266A>G (p.Gln89Arg)not specified [RCV004394121]uncertain significance109190870491908704Humanname
405760207CV3253688single nucleotide variantNM_152429.5(FGFBP3):c.293G>A (p.Arg98His)not specified [RCV004394122]uncertain significance109190867791908677Humanname
407501615CV3439156single nucleotide variantNM_152429.5(FGFBP3):c.230C>T (p.Ala77Val)not specified [RCV004623298]uncertain significance109190874091908740Humanname
597751948CV3672728single nucleotide variantNM_152429.5(FGFBP3):c.290A>G (p.Glu97Gly)not specified [RCV004923824]uncertain significance109190868091908680Humanname
598241792CV3955564single nucleotide variantNM_152429.5(FGFBP3):c.239G>A (p.Cys80Tyr)not specified [RCV005344409]uncertain significance109190873191908731Humanname
598241802CV3955566single nucleotide variantNM_152429.5(FGFBP3):c.225G>C (p.Glu75Asp)not specified [RCV005344411]uncertain significance109190874591908745Humanname
598241807CV3955567single nucleotide variantNM_152429.5(FGFBP3):c.295T>G (p.Cys99Gly)not specified [RCV005344412]uncertain significance109190867591908675Humanname
156225001CV2229947single nucleotide variantNM_152429.5(FGFBP3):c.353G>T (p.Arg118Leu)not specified [RCV004105484]uncertain significance109190861791908617Humanname
155920956CV2276222single nucleotide variantNM_152429.5(FGFBP3):c.635C>T (p.Ala212Val)not specified [RCV004142170]uncertain significance109190833591908335Humanname
156282086CV2317360single nucleotide variantNM_152429.5(FGFBP3):c.362G>T (p.Arg121Leu)not specified [RCV004172339]uncertain significance109190860891908608Humanname
156355218CV2324437single nucleotide variantNM_152429.5(FGFBP3):c.678C>A (p.Asp226Glu)not specified [RCV004178925]uncertain significance109190829291908292Humanname
156272979CV2344067single nucleotide variantNM_152429.5(FGFBP3):c.335A>G (p.Gln112Arg)not specified [RCV004195674]uncertain significance109190863591908635Humanname
156205305CV2385188single nucleotide variantNM_152429.5(FGFBP3):c.670G>C (p.Gly224Arg)not specified [RCV004228439]uncertain significance109190830091908300Humanname
329401093CV2446115single nucleotide variantNM_152429.5(FGFBP3):c.368C>T (p.Pro123Leu)not specified [RCV004270667]uncertain significance109190860291908602Humanname
329392886CV2469042single nucleotide variantNM_152429.5(FGFBP3):c.328T>G (p.Trp110Gly)not specified [RCV004274287]uncertain significance109190864291908642Humanname
401783695CV2723852single nucleotide variantNM_152429.5(FGFBP3):c.392A>G (p.Gln131Arg)not specified [RCV004325992]uncertain significance109190857891908578Humanname
401863830CV2770854single nucleotide variantNM_152429.5(FGFBP3):c.614A>G (p.Asn205Ser)not specified [RCV004343533]uncertain significance109190835691908356Humanname
401866073CV2786163single nucleotide variantNM_152429.5(FGFBP3):c.595C>G (p.Pro199Ala)not specified [RCV004359969]uncertain significance109190837591908375Humanname
405760218CV3253690single nucleotide variantNM_152429.5(FGFBP3):c.366G>T (p.Arg122Ser)not specified [RCV004394124]uncertain significance109190860491908604Humanname
405760224CV3253691single nucleotide variantNM_152429.5(FGFBP3):c.457C>T (p.Pro153Ser)not specified [RCV004394125]uncertain significance109190851391908513Humanname
405760230CV3253692single nucleotide variantNM_152429.5(FGFBP3):c.506G>C (p.Arg169Pro)not specified [RCV004394126]uncertain significance109190846491908464Humanname
405760237CV3253693single nucleotide variantNM_152429.5(FGFBP3):c.508G>T (p.Ala170Ser)not specified [RCV004394127]uncertain significance109190846291908462Humanname
405760240CV3253694single nucleotide variantNM_152429.5(FGFBP3):c.530G>C (p.Arg177Pro)not specified [RCV004394128]uncertain significance109190844091908440Humanname
405760246CV3253695single nucleotide variantNM_152429.5(FGFBP3):c.553G>C (p.Ala185Pro)not specified [RCV004394129]uncertain significance109190841791908417Humanname
405760253CV3253696single nucleotide variantNM_152429.5(FGFBP3):c.761A>G (p.Asn254Ser)not specified [RCV004394130]uncertain significance109190820991908209Humanname
407501603CV3439154single nucleotide variantNM_152429.5(FGFBP3):c.727G>A (p.Glu243Lys)not specified [RCV004623296]uncertain significance109190824391908243Humanname
407501620CV3439157single nucleotide variantNM_152429.5(FGFBP3):c.740C>T (p.Ser247Phe)not specified [RCV004623299]uncertain significance109190823091908230Humanname
597751942CV3672727single nucleotide variantNM_152429.5(FGFBP3):c.518G>C (p.Arg173Pro)not specified [RCV004923823]uncertain significance109190845291908452Humanname
597751957CV3672730single nucleotide variantNM_152429.5(FGFBP3):c.487G>A (p.Ala163Thr)not specified [RCV004923826]uncertain significance109190848391908483Humanname
597751962CV3672731single nucleotide variantNM_152429.5(FGFBP3):c.649G>A (p.Glu217Lys)not specified [RCV004923827]uncertain significance109190832191908321Humanname
597751967CV3672732single nucleotide variantNM_152429.5(FGFBP3):c.729G>C (p.Glu243Asp)not specified [RCV004923828]uncertain significance109190824191908241Humanname
597751975CV3672733single nucleotide variantNM_152429.5(FGFBP3):c.536G>C (p.Arg179Pro)not specified [RCV004923829]likely benign109190843491908434Humanname
598241797CV3955565single nucleotide variantNM_152429.5(FGFBP3):c.365G>T (p.Arg122Met)not specified [RCV005344410]uncertain significance109190860591908605Humanname