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Variants search result for Homo sapiens
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75 records found for search term Plcd3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329388056CV2437084single nucleotide variantNM_133373.5(PLCD3):c.56C>T (p.Ala19Val)not specified [RCV004262892]uncertain significance174513235545132355Humanname
329378433CV2463733single nucleotide variantNM_133373.5(PLCD3):c.31C>T (p.Arg11Cys)not specified [RCV004279297]uncertain significance174513238045132380Humanname
405657571CV3372788single nucleotide variantNM_133373.5(PLCD3):c.47C>T (p.Pro16Leu)not specified [RCV004511823]uncertain significance174513236445132364Humanname
405657575CV3372790single nucleotide variantNM_133373.5(PLCD3):c.94C>G (p.Leu32Val)not specified [RCV004511825]uncertain significance174513231745132317Humanname
597726909CV3579915single nucleotide variantNM_133373.5(PLCD3):c.43G>A (p.Glu15Lys)not specified [RCV004842482]uncertain significance174513236845132368Humanname
597726971CV3579922single nucleotide variantNM_133373.5(PLCD3):c.29G>A (p.Arg10His)not specified [RCV004842489]uncertain significance174513238245132382Humanname
598206607CV3996960single nucleotide variantNM_133373.5(PLCD3):c.28C>T (p.Arg10Cys)not specified [RCV005399665]uncertain significance174513238345132383Humanname
8636198CV91422single nucleotide variantNM_133373.4(PLCD3):c.993C>T (p.Thr331=)Malignant melanoma [RCV000071520]not provided174511841345118413Humanname
156062926CV2199808single nucleotide variantNM_133373.5(PLCD3):c.280G>C (p.Val94Leu)not specified [RCV004074009]uncertain significance174512125645121256Humanname
156129446CV2238536single nucleotide variantNM_133373.5(PLCD3):c.162G>A (p.Met54Ile)not specified [RCV004107152]uncertain significance174513224945132249Humanname
156345633CV2291134single nucleotide variantNM_133373.5(PLCD3):c.247C>G (p.Arg83Gly)not specified [RCV004151657]uncertain significance174512128945121289Humanname
156287597CV2327335single nucleotide variantNM_133373.5(PLCD3):c.113C>A (p.Pro38His)not specified [RCV004174772]uncertain significance174513229845132298Humanname
155966641CV2329823single nucleotide variantNM_133373.5(PLCD3):c.104C>T (p.Pro35Leu)not specified [RCV004183284]uncertain significance174513230745132307Humanname
329354744CV2448959single nucleotide variantNM_133373.5(PLCD3):c.184G>T (p.Val62Leu)not specified [RCV004264044]uncertain significance174512135245121352Humanname
405657547CV3372781single nucleotide variantNM_133373.5(PLCD3):c.184G>A (p.Val62Met)not specified [RCV004511816]uncertain significance174512135245121352Humanname
405657550CV3372782single nucleotide variantNM_133373.5(PLCD3):c.190G>A (p.Ala64Thr)not specified [RCV004511817]uncertain significance174512134645121346Humanname
405657561CV3372785single nucleotide variantNM_133373.5(PLCD3):c.248G>A (p.Arg83Gln)not specified [RCV004511820]uncertain significance174512128845121288Humanname
597726922CV3579916single nucleotide variantNM_133373.5(PLCD3):c.238C>T (p.His80Tyr)not specified [RCV004842483]uncertain significance174512129845121298Humanname
597726933CV3579917single nucleotide variantNM_133373.5(PLCD3):c.230G>A (p.Arg77His)not specified [RCV004842484]uncertain significance174512130645121306Humanname
156245754CV2310427single nucleotide variantNM_133373.5(PLCD3):c.352C>A (p.Arg118Ser)not specified [RCV004163466]uncertain significance174512110445121104Humanname
329384132CV2434970single nucleotide variantNM_133373.5(PLCD3):c.817C>T (p.Pro273Ser)not specified [RCV004250837]uncertain significance174511891145118911Humanname
329396743CV2458994single nucleotide variantNM_133373.5(PLCD3):c.638T>C (p.Met213Thr)not specified [RCV004272473]uncertain significance174512037145120371Humanname
401859497CV2771660single nucleotide variantNM_133373.5(PLCD3):c.754A>G (p.Lys252Glu)not specified [RCV004350458]uncertain significance174511897445118974Humanname
401894346CV2780756single nucleotide variantNM_133373.5(PLCD3):c.503C>G (p.Thr168Ser)not specified [RCV004352083]uncertain significance174512095345120953Humanname
405657564CV3372786single nucleotide variantNM_133373.5(PLCD3):c.395C>T (p.Ala132Val)not specified [RCV004511821]uncertain significance174512106145121061Humanname
405657568CV3372787single nucleotide variantNM_133373.5(PLCD3):c.455T>A (p.Leu152Gln)not specified [RCV004511822]uncertain significance174512100145121001Humanname
405657573CV3372789single nucleotide variantNM_133373.5(PLCD3):c.710G>A (p.Arg237His)not specified [RCV004511824]uncertain significance174511901845119018Humanname
405657578CV3372791single nucleotide variantNM_133373.5(PLCD3):c.963G>T (p.Leu321Phe)not specified [RCV004511826]uncertain significance174511844345118443Humanname
407470374CV3470872single nucleotide variantNM_133373.5(PLCD3):c.310C>G (p.Pro104Ala)not specified [RCV004662027]uncertain significance174512122645121226Humanname
407518790CV3470873single nucleotide variantNM_133373.5(PLCD3):c.706G>A (p.Asp236Asn)not specified [RCV004651127]uncertain significance174511902245119022Humanname
407470381CV3470877single nucleotide variantNM_133373.5(PLCD3):c.331G>C (p.Val111Leu)not specified [RCV004662029]uncertain significance174512112545121125Humanname
407470384CV3470879single nucleotide variantNM_133373.5(PLCD3):c.850G>A (p.Glu284Lys)not specified [RCV004662030]uncertain significance174511887845118878Humanname
597726843CV3579909single nucleotide variantNM_133373.5(PLCD3):c.425C>T (p.Ala142Val)not specified [RCV004842476]uncertain significance174512103145121031Humanname
597726851CV3579910single nucleotide variantNM_133373.5(PLCD3):c.758G>A (p.Arg253Gln)not specified [RCV004842477]uncertain significance174511897045118970Humanname
597726956CV3579920single nucleotide variantNM_133373.5(PLCD3):c.769G>A (p.Glu257Lys)not specified [RCV004842487]uncertain significance174511895945118959Humanname
597726965CV3579921single nucleotide variantNM_133373.5(PLCD3):c.526G>A (p.Ala176Thr)not specified [RCV004842488]uncertain significance174512093045120930Humanname
597726997CV3579925single nucleotide variantNM_133373.5(PLCD3):c.771G>C (p.Glu257Asp)not specified [RCV004842492]uncertain significance174511895745118957Humanname
598206617CV3996962single nucleotide variantNM_133373.5(PLCD3):c.746G>A (p.Arg249Gln)not specified [RCV005399667]uncertain significance174511898245118982Humanname
598206632CV3996965single nucleotide variantNM_133373.5(PLCD3):c.589A>C (p.Asn197His)not specified [RCV005399670]uncertain significance174512042045120420Humanname
598206643CV3996967single nucleotide variantNM_133373.5(PLCD3):c.627C>G (p.Ser209Arg)not specified [RCV005399672]uncertain significance174512038245120382Humanname
156066942CV2193457single nucleotide variantNM_133373.5(PLCD3):c.1463G>A (p.Arg488Gln)not specified [RCV004072947]uncertain significance174511544145115441Humanname
156076996CV2198203single nucleotide variantNM_133373.5(PLCD3):c.1012G>A (p.Asp338Asn)not specified [RCV004079787]uncertain significance174511839445118394Humanname
156222228CV2232678single nucleotide variantNM_133373.5(PLCD3):c.1492C>T (p.Arg498Trp)not specified [RCV004101344]uncertain significance174511541245115412Humanname
155981418CV2272850single nucleotide variantNM_133373.5(PLCD3):c.1330C>T (p.Arg444Cys)not specified [RCV004135754]uncertain significance174511671545116715Humanname
156071625CV2325229single nucleotide variantNM_133373.5(PLCD3):c.1215T>G (p.Ile405Met)not specified [RCV004177635]uncertain significance174511803945118039Humanname
156390373CV2373349single nucleotide variantNM_133373.5(PLCD3):c.1616G>A (p.Arg539His)not specified [RCV004220057]uncertain significance174511518945115189Humanname
329360115CV2446597single nucleotide variantNM_133373.5(PLCD3):c.2233A>G (p.Asn745Asp)not specified [RCV004251489]uncertain significance174511291145112911Humanname
401740846CV2679817single nucleotide variantNM_133373.5(PLCD3):c.2087C>T (p.Pro696Leu)not specified [RCV004282277]uncertain significance174511316645113166Humanname
401735376CV2687566single nucleotide variantNM_133373.5(PLCD3):c.2179C>T (p.Pro727Ser)not specified [RCV004300792]uncertain significance174511296545112965Humanname
401748360CV2698364single nucleotide variantNM_133373.5(PLCD3):c.1477C>T (p.Arg493Trp)not specified [RCV004304904]uncertain significance174511542745115427Humanname
401861524CV2756328single nucleotide variantNM_133373.5(PLCD3):c.1240G>A (p.Val414Met)not specified [RCV004342874]uncertain significance174511801445118014Humanname
401865878CV2786183single nucleotide variantNM_133373.5(PLCD3):c.1642A>G (p.Asn548Asp)not specified [RCV004359985]uncertain significance174511516345115163Humanname
401885131CV2786684single nucleotide variantNM_133373.5(PLCD3):c.1136G>A (p.Arg379His)not specified [RCV004363809]uncertain significance174511811845118118Humanname
405657529CV3372776single nucleotide variantNM_133373.5(PLCD3):c.1084G>A (p.Gly362Arg)not specified [RCV004511811]uncertain significance174511832245118322Humanname
405657533CV3372777single nucleotide variantNM_133373.5(PLCD3):c.1091C>G (p.Pro364Arg)not specified [RCV004511812]uncertain significance174511831545118315Humanname
405657536CV3372778single nucleotide variantNM_133373.5(PLCD3):c.1555C>T (p.Arg519Trp)not specified [RCV004511813]uncertain significance174511534945115349Humanname
405657541CV3372779single nucleotide variantNM_133373.5(PLCD3):c.1586C>T (p.Ser529Leu)not specified [RCV004511814]uncertain significance174511521945115219Humanname
405657544CV3372780single nucleotide variantNM_133373.5(PLCD3):c.1609G>A (p.Ala537Thr)not specified [RCV004511815]uncertain significance174511519645115196Humanname
405657553CV3372783single nucleotide variantNM_133373.5(PLCD3):c.2076C>G (p.Ile692Met)not specified [RCV004511818]uncertain significance174511317745113177Humanname
405657557CV3372784single nucleotide variantNM_133373.5(PLCD3):c.2318C>T (p.Ala773Val)not specified [RCV004511819]uncertain significance174511266845112668Humanname
407518792CV3470874single nucleotide variantNM_133373.5(PLCD3):c.2134T>C (p.Phe712Leu)not specified [RCV004651128]uncertain significance174511301045113010Humanname
407518795CV3470875single nucleotide variantNM_133373.5(PLCD3):c.1252G>T (p.Ala418Ser)not specified [RCV004651129]uncertain significance174511800245118002Humanname
407518797CV3470878single nucleotide variantNM_133373.5(PLCD3):c.1462C>T (p.Arg488Trp)not specified [RCV004651130]uncertain significance174511544245115442Humanname
597726862CV3579911single nucleotide variantNM_133373.5(PLCD3):c.1099A>G (p.Thr367Ala)not specified [RCV004842478]uncertain significance174511830745118307Humanname
597726883CV3579913single nucleotide variantNM_133373.5(PLCD3):c.1393G>A (p.Glu465Lys)not specified [RCV004842480]uncertain significance174511665245116652Humanname
597726896CV3579914single nucleotide variantNM_133373.5(PLCD3):c.1136G>T (p.Arg379Leu)not specified [RCV004842481]uncertain significance174511811845118118Humanname
597726939CV3579918single nucleotide variantNM_133373.5(PLCD3):c.1884C>G (p.Phe628Leu)not specified [RCV004842485]uncertain significance174511355045113550Humanname
597726948CV3579919single nucleotide variantNM_133373.5(PLCD3):c.1625C>G (p.Thr542Ser)not specified [RCV004842486]uncertain significance174511518045115180Humanname
597726989CV3579924single nucleotide variantNM_133373.5(PLCD3):c.1707G>T (p.Glu569Asp)not specified [RCV004842491]uncertain significance174511509845115098Humanname
598206598CV3996958single nucleotide variantNM_133373.5(PLCD3):c.1243C>T (p.Arg415Cys)not specified [RCV005399663]uncertain significance174511801145118011Humanname
598206603CV3996959single nucleotide variantNM_133373.5(PLCD3):c.1244G>A (p.Arg415His)not specified [RCV005399664]uncertain significance174511801045118010Humanname
598206612CV3996961single nucleotide variantNM_133373.5(PLCD3):c.1577C>T (p.Pro526Leu)not specified [RCV005399666]uncertain significance174511522845115228Humanname
598206622CV3996963single nucleotide variantNM_133373.5(PLCD3):c.1490A>G (p.Asp497Gly)not specified [RCV005399668]uncertain significance174511541445115414Humanname
598206627CV3996964single nucleotide variantNM_133373.5(PLCD3):c.1390C>A (p.Pro464Thr)not specified [RCV005399669]uncertain significance174511665545116655Humanname
598206638CV3996966single nucleotide variantNM_133373.5(PLCD3):c.1852G>T (p.Gly618Cys)not specified [RCV005399671]uncertain significance174511358245113582Humanname