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65 records found for search term Phc3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407529122CV3467025single nucleotide variantNM_024947.4(PHC3):c.83C>G (p.Thr28Ser)not specified [RCV004655882]uncertain significance3170178870170178870Humanname
156277849CV2330872single nucleotide variantNM_024947.4(PHC3):c.164A>G (p.Asp55Gly)not specified [RCV004185927]uncertain significance3170178789170178789Humanname
401922979CV2825055single nucleotide variantNM_024947.4(PHC3):c.2877T>C (p.Asp959=)not provided [RCV003434791]likely benign3170097341170097341Humanname
156363664CV2262676single nucleotide variantNM_024947.4(PHC3):c.799T>G (p.Ser267Ala)not specified [RCV004130870]uncertain significance3170136539170136539Humanname
156347462CV2315301single nucleotide variantNM_024947.4(PHC3):c.437C>T (p.Thr146Ile)not specified [RCV004167286]uncertain significance3170149222170149222Humanname
156392531CV2386443single nucleotide variantNM_024947.4(PHC3):c.691C>T (p.Arg231Cys)not specified [RCV004228767]uncertain significance3170136647170136647Humanname
401865939CV2762463single nucleotide variantNM_024947.4(PHC3):c.966G>C (p.Gln322His)not specified [RCV004338000]uncertain significance3170129506170129506Humanname
405763141CV3365114single nucleotide variantNM_024947.4(PHC3):c.677A>G (p.Gln226Arg)not specified [RCV004500960]uncertain significance3170136661170136661Humanname
405763148CV3365115single nucleotide variantNM_024947.4(PHC3):c.769A>G (p.Ile257Val)not specified [RCV004500961]uncertain significance3170136569170136569Humanname
597676743CV3572277single nucleotide variantNM_024947.4(PHC3):c.454A>G (p.Ser152Gly)not specified [RCV004836953]uncertain significance3170149205170149205Humanname
598248149CV3996502single nucleotide variantNM_024947.4(PHC3):c.321C>G (p.Ser107Arg)not specified [RCV005384276]uncertain significance3170172572170172572Humanname
155972408CV2214303single nucleotide variantNM_024947.4(PHC3):c.2521C>T (p.Pro841Ser)not specified [RCV004086293]uncertain significance3170102882170102882Humanname
155929118CV2224498single nucleotide variantNM_024947.4(PHC3):c.1339A>G (p.Asn447Asp)not specified [RCV004098087]uncertain significance3170129133170129133Humanname
156188252CV2226750single nucleotide variantNM_024947.4(PHC3):c.1337C>G (p.Pro446Arg)not specified [RCV004101969]uncertain significance3170129135170129135Humanname
155949633CV2242736single nucleotide variantNM_024947.4(PHC3):c.1042C>G (p.Pro348Ala)not specified [RCV004113769]uncertain significance3170129430170129430Humanname
155950566CV2242937single nucleotide variantNM_024947.4(PHC3):c.1492C>T (p.His498Tyr)not specified [RCV004107522]uncertain significance3170128980170128980Humanname
156356930CV2253750single nucleotide variantNM_024947.4(PHC3):c.1561C>T (p.Pro521Ser)not specified [RCV004127460]uncertain significance3170128911170128911Humanname
156036525CV2283072single nucleotide variantNM_024947.4(PHC3):c.1994C>G (p.Ser665Cys)not specified [RCV004143686]uncertain significance3170117425170117425Humanname
156278285CV2284921single nucleotide variantNM_024947.4(PHC3):c.1532T>C (p.Ile511Thr)not specified [RCV004143369]uncertain significance3170128940170128940Humanname
156185210CV2294930single nucleotide variantNM_024947.4(PHC3):c.1190C>G (p.Ser397Cys)not specified [RCV004156079]uncertain significance3170129282170129282Humanname
155977518CV2338781single nucleotide variantNM_024947.4(PHC3):c.2496T>G (p.Phe832Leu)not specified [RCV004182340]uncertain significance3170102907170102907Humanname
156337545CV2343066single nucleotide variantNM_024947.4(PHC3):c.1531A>G (p.Ile511Val)not specified [RCV004192663]uncertain significance3170128941170128941Humanname
156244296CV2347139single nucleotide variantNM_024947.4(PHC3):c.2122A>G (p.Ile708Val)not specified [RCV004204616]uncertain significance3170117297170117297Humanname
155928185CV2361876single nucleotide variantNM_024947.4(PHC3):c.2075C>A (p.Ser692Tyr)not specified [RCV004207651]uncertain significance3170117344170117344Humanname
156264351CV2388945single nucleotide variantNM_024947.4(PHC3):c.1045A>G (p.Ile349Val)not specified [RCV004241946]uncertain significance3170129427170129427Humanname
329386734CV2452475single nucleotide variantNM_024947.4(PHC3):c.2129A>C (p.Lys710Thr)not specified [RCV004273077]uncertain significance3170117290170117290Humanname
401743082CV2677761single nucleotide variantNM_024947.4(PHC3):c.2083A>T (p.Ser695Cys)not specified [RCV004291834]uncertain significance3170117336170117336Humanname
401724389CV2677864single nucleotide variantNM_024947.4(PHC3):c.1213C>G (p.Gln405Glu)not specified [RCV004294359]uncertain significance3170129259170129259Humanname
401747171CV2692086single nucleotide variantNM_024947.4(PHC3):c.2356A>G (p.Thr786Ala)not specified [RCV004301800]uncertain significance3170106944170106944Humanname
401771954CV2711999single nucleotide variantNM_024947.4(PHC3):c.2710C>T (p.Arg904Cys)not specified [RCV004311421]uncertain significance3170102602170102602Humanname
401780363CV2726019single nucleotide variantNM_024947.4(PHC3):c.1459G>A (p.Val487Ile)not specified [RCV004324380]uncertain significance3170129013170129013Humanname
401876938CV2764231single nucleotide variantNM_024947.4(PHC3):c.2546G>A (p.Arg849His)not specified [RCV004336770]uncertain significance3170102857170102857Humanname
401863562CV2770706single nucleotide variantNM_024947.4(PHC3):c.2644C>T (p.His882Tyr)not specified [RCV004349750]uncertain significance3170102668170102668Humanname
401880086CV2783089single nucleotide variantNM_024947.4(PHC3):c.1463C>G (p.Ser488Cys)not specified [RCV004363446]uncertain significance3170129009170129009Humanname
401885359CV2783246single nucleotide variantNM_024947.4(PHC3):c.1157C>T (p.Pro386Leu)not specified [RCV004363864]uncertain significance3170129315170129315Humanname
405762894CV3365097single nucleotide variantNM_024947.4(PHC3):c.1010T>G (p.Leu337Arg)not specified [RCV004500943]uncertain significance3170129462170129462Humanname
405762902CV3365098single nucleotide variantNM_024947.4(PHC3):c.1123G>T (p.Ala375Ser)not specified [RCV004500944]uncertain significance3170129349170129349Humanname
405762909CV3365099single nucleotide variantNM_024947.4(PHC3):c.1130G>A (p.Ser377Asn)not specified [RCV004500945]uncertain significance3170129342170129342Humanname
405762922CV3365101single nucleotide variantNM_024947.4(PHC3):c.1366G>A (p.Val456Met)not specified [RCV004500947]uncertain significance3170129106170129106Humanname
405762928CV3365102single nucleotide variantNM_024947.4(PHC3):c.1550T>C (p.Met517Thr)not specified [RCV004500948]uncertain significance3170128922170128922Humanname
405762934CV3365103single nucleotide variantNM_024947.4(PHC3):c.1568C>T (p.Ala523Val)not specified [RCV004500949]uncertain significance3170128904170128904Humanname
405762946CV3365105single nucleotide variantNM_024947.4(PHC3):c.1994C>T (p.Ser665Phe)not specified [RCV004500951]uncertain significance3170117425170117425Humanname
405762953CV3365106single nucleotide variantNM_024947.4(PHC3):c.2077A>G (p.Met693Val)not specified [RCV004500952]uncertain significance3170117342170117342Humanname
405762959CV3365107single nucleotide variantNM_024947.4(PHC3):c.2260A>G (p.Ile754Val)not specified [RCV004500953]uncertain significance3170113453170113453Humanname
405763109CV3365109single nucleotide variantNM_024947.4(PHC3):c.2579C>T (p.Ala860Val)not specified [RCV004500955]uncertain significance3170102824170102824Humanname
405763115CV3365110single nucleotide variantNM_024947.4(PHC3):c.2677C>T (p.Arg893Cys)not specified [RCV004500956]uncertain significance3170102635170102635Humanname
405763122CV3365111single nucleotide variantNM_024947.4(PHC3):c.2711G>A (p.Arg904His)not specified [RCV004500957]uncertain significance3170102601170102601Humanname
405763128CV3365112single nucleotide variantNM_024947.4(PHC3):c.2972C>T (p.Ser991Phe)not specified [RCV004500958]uncertain significance3170097246170097246Humanname
407529116CV3467021single nucleotide variantNM_024947.4(PHC3):c.1306C>T (p.Pro436Ser)not specified [RCV004655879]uncertain significance3170129166170129166Humanname
407529118CV3467022single nucleotide variantNM_024947.4(PHC3):c.2683C>T (p.Arg895Cys)not specified [RCV004655880]uncertain significance3170102629170102629Humanname
407529120CV3467023single nucleotide variantNM_024947.4(PHC3):c.2719C>T (p.Arg907Trp)not specified [RCV004655881]uncertain significance3170102593170102593Humanname
407530322CV3467024single nucleotide variantNM_024947.4(PHC3):c.2735G>A (p.Arg912Gln)not specified [RCV004656993]uncertain significance3170102577170102577Humanname
597676733CV3572275single nucleotide variantNM_024947.4(PHC3):c.1123G>A (p.Ala375Thr)not specified [RCV004836952]uncertain significance3170129349170129349Humanname
597766938CV3572276single nucleotide variantNM_024947.4(PHC3):c.2708A>G (p.Glu903Gly)not specified [RCV004850367]uncertain significance3170102604170102604Humanname
597676753CV3572278single nucleotide variantNM_024947.4(PHC3):c.2075C>G (p.Ser692Cys)not specified [RCV004836954]uncertain significance3170117344170117344Humanname
597676762CV3572279single nucleotide variantNM_024947.4(PHC3):c.1573A>G (p.Ile525Val)not specified [RCV004836955]uncertain significance3170128899170128899Humanname
597676771CV3572280single nucleotide variantNM_024947.4(PHC3):c.2552G>A (p.Arg851His)not specified [RCV004836956]uncertain significance3170102851170102851Humanname
597676783CV3572281single nucleotide variantNM_024947.4(PHC3):c.2332A>G (p.Met778Val)not specified [RCV004836957]uncertain significance3170113381170113381Humanname
598248128CV3996496single nucleotide variantNM_024947.4(PHC3):c.1849C>T (p.Arg617Trp)not specified [RCV005384273]uncertain significance3170122684170122684Humanname
598197078CV3996497single nucleotide variantNM_024947.4(PHC3):c.2620T>C (p.Ser874Pro)not specified [RCV005397819]uncertain significance3170102692170102692Humanname
598248136CV3996498single nucleotide variantNM_024947.4(PHC3):c.1376C>T (p.Thr459Ile)not specified [RCV005384274]uncertain significance3170129096170129096Humanname
598197085CV3996499single nucleotide variantNM_024947.4(PHC3):c.1733A>G (p.Gln578Arg)not specified [RCV005397820]uncertain significance3170128739170128739Humanname
598248142CV3996500single nucleotide variantNM_024947.4(PHC3):c.1321G>C (p.Ala441Pro)not specified [RCV005384275]uncertain significance3170129151170129151Humanname
598197089CV3996501single nucleotide variantNM_024947.4(PHC3):c.2270T>C (p.Val757Ala)not specified [RCV005397821]uncertain significance3170113443170113443Humanname
598248156CV3996503single nucleotide variantNM_024947.4(PHC3):c.1814A>T (p.Glu605Val)not specified [RCV005384277]uncertain significance3170122719170122719Humanname