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Variants search result for Homo sapiens
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47 records found for search term Fkbp9
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597699697CV3666267single nucleotide variantNM_007270.5(FKBP9):c.13G>C (p.Gly5Arg)not specified [RCV004916250]uncertain significance73295758632957586Humanname
597699779CV3666277single nucleotide variantNM_007270.5(FKBP9):c.22C>T (p.Pro8Ser)not specified [RCV004916260]uncertain significance73295759532957595Humanname
156291938CV2306147single nucleotide variantNM_007270.5(FKBP9):c.29C>A (p.Pro10Gln)not specified [RCV004162898]uncertain significance73295760232957602Humanname
156184501CV2335612single nucleotide variantNM_007270.5(FKBP9):c.212T>G (p.Phe71Cys)not specified [RCV004193817]uncertain significance73295778532957785Humanname
405780352CV3260730single nucleotide variantNM_007270.5(FKBP9):c.142C>A (p.Pro48Thr)not specified [RCV004386665]uncertain significance73295771532957715Humanname
407502867CV3435967single nucleotide variantNM_007270.5(FKBP9):c.296T>A (p.Val99Asp)not specified [RCV004623611]uncertain significance73297469132974691Humanname
597699716CV3666269single nucleotide variantNM_007270.5(FKBP9):c.296T>C (p.Val99Ala)not specified [RCV004916252]uncertain significance73297469132974691Humanname
156086283CV2205720single nucleotide variantNM_007270.5(FKBP9):c.718G>A (p.Gly240Ser)not specified [RCV004075778]uncertain significance73298037832980378Humanname
156111407CV2207924single nucleotide variantNM_007270.5(FKBP9):c.911C>T (p.Thr304Met)not specified [RCV004084344]uncertain significance73298852432988524Humanname
156148283CV2265267single nucleotide variantNM_007270.5(FKBP9):c.584C>T (p.Thr195Met)not specified [RCV004126373]uncertain significance73297638032976380Humanname
156091530CV2302663single nucleotide variantNM_007270.5(FKBP9):c.454A>G (p.Thr152Ala)not specified [RCV004162606]uncertain significance73297526832975268Humanname
329360938CV2463129single nucleotide variantNM_007270.5(FKBP9):c.659T>A (p.Ile220Asn)not specified [RCV004274925]uncertain significance73297645532976455Humanname
329392583CV2471338single nucleotide variantNM_007270.5(FKBP9):c.625G>A (p.Gly209Arg)not specified [RCV004280348]uncertain significance73297642132976421Humanname
401783186CV2703860single nucleotide variantNM_007270.5(FKBP9):c.718G>C (p.Gly240Arg)not specified [RCV004306724]uncertain significance73298037832980378Humanname
401863901CV2784744single nucleotide variantNM_007270.5(FKBP9):c.427A>G (p.Asn143Asp)not specified [RCV004352547]uncertain significance73297524132975241Humanname
405780366CV3260732single nucleotide variantNM_007270.5(FKBP9):c.447G>C (p.Gln149His)not specified [RCV004386667]uncertain significance73297526132975261Humanname
405780371CV3260733single nucleotide variantNM_007270.5(FKBP9):c.651G>C (p.Glu217Asp)not specified [RCV004386668]uncertain significance73297644732976447Humanname
405780377CV3260734single nucleotide variantNM_007270.5(FKBP9):c.797T>C (p.Val266Ala)not specified [RCV004386669]uncertain significance73298045732980457Humanname
405780383CV3260735single nucleotide variantNM_007270.5(FKBP9):c.848A>G (p.Tyr283Cys)not specified [RCV004386670]uncertain significance73298050832980508Humanname
405780389CV3260736single nucleotide variantNM_007270.5(FKBP9):c.946C>T (p.Pro316Ser)not specified [RCV004386671]uncertain significance73298855932988559Humanname
407502857CV3435964single nucleotide variantNM_007270.5(FKBP9):c.908G>A (p.Arg303His)not specified [RCV004623608]uncertain significance73298852132988521Humanname
407502860CV3435965single nucleotide variantNM_007270.5(FKBP9):c.325G>A (p.Val109Met)not specified [RCV004623609]uncertain significance73297472032974720Humanname
407502875CV3435969single nucleotide variantNM_007270.5(FKBP9):c.448A>G (p.Ile150Val)not specified [RCV004623613]uncertain significance73297526232975262Humanname
597699706CV3666268single nucleotide variantNM_007270.5(FKBP9):c.817C>T (p.Arg273Trp)not specified [RCV004916251]uncertain significance73298047732980477Humanname
597699722CV3666270single nucleotide variantNM_007270.5(FKBP9):c.863C>T (p.Thr288Met)not specified [RCV004916253]uncertain significance73298052332980523Humanname
597699731CV3666271single nucleotide variantNM_007270.5(FKBP9):c.533T>C (p.Leu178Pro)not specified [RCV004916254]uncertain significance73297534732975347Humanname
597699740CV3666272single nucleotide variantNM_007270.5(FKBP9):c.656G>A (p.Arg219His)not specified [RCV004916255]uncertain significance73297645232976452Humanname
597699747CV3666273single nucleotide variantNM_007270.5(FKBP9):c.307G>T (p.Val103Leu)not specified [RCV004916256]uncertain significance73297470232974702Humanname
598200930CV3976801single nucleotide variantNM_007270.5(FKBP9):c.953T>C (p.Met318Thr)not specified [RCV005336740]uncertain significance73298856632988566Humanname
598200940CV3976803single nucleotide variantNM_007270.5(FKBP9):c.655C>A (p.Arg219Ser)not specified [RCV005336742]uncertain significance73297645132976451Humanname
155932749CV2228729single nucleotide variantNM_007270.5(FKBP9):c.1355A>G (p.Tyr452Cys)not specified [RCV004093205]uncertain significance73300024333000243Humanname
156080911CV2249028single nucleotide variantNM_007270.5(FKBP9):c.1409A>T (p.Asp470Val)not specified [RCV004116314]uncertain significance73300271233002712Humanname
156068701CV2270935single nucleotide variantNM_007270.5(FKBP9):c.1139C>G (p.Pro380Arg)not specified [RCV004131972]uncertain significance73299626232996262Humanname
156163634CV2319647single nucleotide variantNM_007270.5(FKBP9):c.1196C>T (p.Ser399Leu)not specified [RCV004185192]uncertain significance73299631932996319Humanname
329354905CV2449166single nucleotide variantNM_007270.5(FKBP9):c.1080T>G (p.His360Gln)not specified [RCV004264224]uncertain significance73299620332996203Humanname
401763060CV2707472single nucleotide variantNM_007270.5(FKBP9):c.1624T>C (p.Phe542Leu)not specified [RCV004312850]uncertain significance73300526233005262Humanname
401724828CV2714989single nucleotide variantNM_007270.5(FKBP9):c.1124C>A (p.Ser375Tyr)not specified [RCV004322306]uncertain significance73299624732996247Humanname
401880422CV2783204single nucleotide variantNM_007270.5(FKBP9):c.1534G>A (p.Glu512Lys)not specified [RCV004363544]uncertain significance73300283733002837Humanname
405780343CV3260728single nucleotide variantNM_007270.5(FKBP9):c.1325G>A (p.Arg442Gln)not specified [RCV004386663]uncertain significance73300021333000213Humanname
405780347CV3260729single nucleotide variantNM_007270.5(FKBP9):c.1343C>T (p.Pro448Leu)not specified [RCV004386664]uncertain significance73300023133000231Humanname
405780360CV3260731single nucleotide variantNM_007270.5(FKBP9):c.1504A>G (p.Lys502Glu)not specified [RCV004386666]uncertain significance73300280733002807Humanname
407502864CV3435966single nucleotide variantNM_007270.5(FKBP9):c.1455G>A (p.Met485Ile)not specified [RCV004623610]uncertain significance73300275833002758Humanname
407502871CV3435968single nucleotide variantNM_007270.5(FKBP9):c.1561G>A (p.Val521Met)not specified [RCV004623612]uncertain significance73300519933005199Humanname
597699754CV3666274single nucleotide variantNM_007270.5(FKBP9):c.1029G>C (p.Glu343Asp)not specified [RCV004916257]uncertain significance73298864232988642Humanname
597699769CV3666276single nucleotide variantNM_007270.5(FKBP9):c.1461A>G (p.Ile487Met)not specified [RCV004916259]uncertain significance73300276433002764Humanname
598200935CV3976802single nucleotide variantNM_007270.5(FKBP9):c.1027G>A (p.Glu343Lys)not specified [RCV005336741]uncertain significance73298864032988640Humanname
598200947CV3976804single nucleotide variantNM_007270.5(FKBP9):c.1610T>C (p.Ile537Thr)not specified [RCV005336743]uncertain significance73300524833005248Humanname