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Variants search result for Homo sapiens
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46 records found for search term Plekho1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15137135CV778735single nucleotide variantNM_016274.6(PLEKHO1):c.31-4G>Tnot provided [RCV000965565]benign1150150908150150908Humanname
329389437CV2445060single nucleotide variantNM_016274.6(PLEKHO1):c.19T>C (p.Ser7Pro)not specified [RCV004261667]uncertain significance1150150276150150276Humanname
401932754CV2809234single nucleotide variantNM_016274.6(PLEKHO1):c.849T>A (p.Ser283=)not provided [RCV003408850]likely benign1150159142150159142Humanname
401932755CV2809235single nucleotide variantNM_016274.6(PLEKHO1):c.873T>A (p.Ala291=)not provided [RCV003408851]likely benign1150159166150159166Humanname
407519168CV3467333single nucleotide variantNM_016274.6(PLEKHO1):c.65C>G (p.Pro22Arg)not specified [RCV004651347]uncertain significance1150150946150150946Humanname
597681397CV3572866single nucleotide variantNM_016274.6(PLEKHO1):c.62C>T (p.Pro21Leu)not specified [RCV004837488]uncertain significance1150150943150150943Humanname
15109350CV718189single nucleotide variantNM_016274.6(PLEKHO1):c.865C>T (p.Leu289=)not provided [RCV000893847]benign1150159158150159158Humanname
401741063CV2680539single nucleotide variantNM_016274.6(PLEKHO1):c.193A>T (p.Asn65Tyr)not specified [RCV004291173]uncertain significance1150156081150156081Humanname
401898615CV2782544single nucleotide variantNM_016274.6(PLEKHO1):c.289C>T (p.Leu97Phe)not specified [RCV004359580]uncertain significance1150156177150156177Humanname
405792869CV3369528single nucleotide variantNM_016274.6(PLEKHO1):c.103G>A (p.Gly35Arg)not specified [RCV004506520]uncertain significance1150150984150150984Humanname
405792871CV3369529single nucleotide variantNM_016274.6(PLEKHO1):c.296A>G (p.His99Arg)not specified [RCV004506521]uncertain significance1150156184150156184Humanname
598174468CV4006830single nucleotide variantNM_016274.6(PLEKHO1):c.233G>C (p.Cys78Ser)not specified [RCV005393344]uncertain significance1150156121150156121Humanname
156318539CV2260703single nucleotide variantNM_016274.6(PLEKHO1):c.779A>G (p.Lys260Arg)not specified [RCV004125635]uncertain significance1150159072150159072Humanname
155979502CV2266637single nucleotide variantNM_016274.6(PLEKHO1):c.908G>A (p.Gly303Glu)not specified [RCV004131179]uncertain significance1150159201150159201Humanname
156250138CV2273245single nucleotide variantNM_016274.6(PLEKHO1):c.409C>T (p.Arg137Cys)not specified [RCV004132040]uncertain significance1150157001150157001Humanname
156103145CV2291579single nucleotide variantNM_016274.6(PLEKHO1):c.802C>T (p.Arg268Cys)not specified [RCV004155879]uncertain significance1150159095150159095Humanname
156079576CV2292610single nucleotide variantNM_016274.6(PLEKHO1):c.740C>T (p.Thr247Ile)not specified [RCV004154301]uncertain significance1150159033150159033Humanname
156142811CV2296138single nucleotide variantNM_016274.6(PLEKHO1):c.327C>G (p.Asn109Lys)not specified [RCV004154067]uncertain significance1150156919150156919Humanname
155986086CV2345463single nucleotide variantNM_016274.6(PLEKHO1):c.905C>T (p.Pro302Leu)not specified [RCV004198235]uncertain significance1150159198150159198Humanname
156230102CV2348651single nucleotide variantNM_016274.6(PLEKHO1):c.685C>T (p.Arg229Cys)not specified [RCV004201070]uncertain significance1150158978150158978Humanname
156388559CV2380520single nucleotide variantNM_016274.6(PLEKHO1):c.707G>A (p.Arg236Gln)not specified [RCV004218112]uncertain significance1150159000150159000Humanname
156160739CV2398216single nucleotide variantNM_016274.6(PLEKHO1):c.667C>T (p.Arg223Trp)not specified [RCV004235132]uncertain significance1150158960150158960Humanname
329398900CV2443091single nucleotide variantNM_016274.6(PLEKHO1):c.410G>A (p.Arg137His)not specified [RCV004253677]uncertain significance1150157002150157002Humanname
401771175CV2700909single nucleotide variantNM_016274.6(PLEKHO1):c.791C>T (p.Thr264Ile)not specified [RCV004307174]uncertain significance1150159084150159084Humanname
401881582CV2759470single nucleotide variantNM_016274.6(PLEKHO1):c.310G>A (p.Gly104Ser)not specified [RCV004338465]uncertain significance1150156198150156198Humanname
401870661CV2769241single nucleotide variantNM_016274.6(PLEKHO1):c.922A>C (p.Ile308Leu)not specified [RCV004357258]uncertain significance1150159215150159215Humanname
405792875CV3369530single nucleotide variantNM_016274.6(PLEKHO1):c.812C>G (p.Ser271Cys)not specified [RCV004506522]uncertain significance1150159105150159105Humanname
597681389CV3572865single nucleotide variantNM_016274.6(PLEKHO1):c.638A>G (p.Lys213Arg)not specified [RCV004837487]uncertain significance1150158931150158931Humanname
597681406CV3572867single nucleotide variantNM_016274.6(PLEKHO1):c.903C>G (p.Asn301Lys)not specified [RCV004837489]uncertain significance1150159196150159196Humanname
597681414CV3572868single nucleotide variantNM_016274.6(PLEKHO1):c.686G>A (p.Arg229His)not specified [RCV004837490]uncertain significance1150158979150158979Humanname
597681420CV3572869single nucleotide variantNM_016274.6(PLEKHO1):c.836G>T (p.Arg279Leu)not specified [RCV004837491]uncertain significance1150159129150159129Humanname
597681356CV3576756single nucleotide variantNM_016274.6(PLEKHO1):c.857C>G (p.Thr286Ser)not specified [RCV004837483]uncertain significance1150159150150159150Humanname
597681366CV3576757single nucleotide variantNM_016274.6(PLEKHO1):c.484C>T (p.His162Tyr)not specified [RCV004837484]uncertain significance1150157445150157445Humanname
597681373CV3576758single nucleotide variantNM_016274.6(PLEKHO1):c.326A>C (p.Asn109Thr)not specified [RCV004837485]uncertain significance1150156918150156918Humanname
598174476CV4006831single nucleotide variantNM_016274.6(PLEKHO1):c.808G>C (p.Ala270Pro)not specified [RCV005393345]uncertain significance1150159101150159101Humanname
598174492CV4006833single nucleotide variantNM_016274.6(PLEKHO1):c.868C>T (p.Arg290Trp)not specified [RCV005393347]uncertain significance1150159161150159161Humanname
598174499CV4006834single nucleotide variantNM_016274.6(PLEKHO1):c.655G>T (p.Ala219Ser)not specified [RCV005393348]uncertain significance1150158948150158948Humanname
598174512CV4006836single nucleotide variantNM_016274.6(PLEKHO1):c.671G>A (p.Arg224Lys)not specified [RCV005393350]uncertain significance1150158964150158964Humanname
598174519CV4006837single nucleotide variantNM_016274.6(PLEKHO1):c.622C>G (p.Arg208Gly)not specified [RCV005393351]uncertain significance1150158915150158915Humanname
156013107CV2359024single nucleotide variantNM_016274.6(PLEKHO1):c.1142A>G (p.Asp381Gly)not specified [RCV004212348]uncertain significance1150159435150159435Humanname
156058289CV2383396single nucleotide variantNM_016274.6(PLEKHO1):c.1176C>G (p.Asp392Glu)not specified [RCV004222420]uncertain significance1150159469150159469Humanname
401892256CV2776031single nucleotide variantNM_016274.6(PLEKHO1):c.1037C>T (p.Ser346Phe)not specified [RCV004353140]uncertain significance1150159330150159330Humanname
597768350CV3576755single nucleotide variantNM_016274.6(PLEKHO1):c.1172C>T (p.Pro391Leu)not specified [RCV004850671]uncertain significance1150159465150159465Humanname
597681381CV3576759single nucleotide variantNM_016274.6(PLEKHO1):c.1031C>T (p.Pro344Leu)not specified [RCV004837486]uncertain significance1150159324150159324Humanname
598174485CV4006832single nucleotide variantNM_016274.6(PLEKHO1):c.1001G>A (p.Arg334Gln)not specified [RCV005393346]uncertain significance1150159294150159294Humanname
598174505CV4006835single nucleotide variantNM_016274.6(PLEKHO1):c.1183C>T (p.Leu395Phe)not specified [RCV005393349]uncertain significance1150159476150159476Humanname