Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Behavioral & Substance Use Disorder Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

65 records found for search term Phc3
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

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