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 All species
(View Results for all Objects and Ontologies)

86 records found for search term Hjurp
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155995041CV2374864single nucleotide variantNM_018410.5(HJURP):c.11C>T (p.Thr4Met)not specified [RCV004227892]uncertain significance2233854490233854490Humanname
156240031CV2350315single nucleotide variantNM_018410.5(HJURP):c.36C>A (p.Asp12Glu)not specified [RCV004202265]uncertain significance2233854465233854465Humanname
401736396CV2688778single nucleotide variantNM_018410.5(HJURP):c.93G>T (p.Arg31Ser)not specified [RCV004303802]uncertain significance2233854408233854408Humanname
401919517CV2819061single nucleotide variantNM_018410.5(HJURP):c.537G>A (p.Pro179=)not provided [RCV003431181]likely benign2233844242233844242Humanname
405790334CV3266645single nucleotide variantNM_018410.5(HJURP):c.34G>T (p.Asp12Tyr)not specified [RCV004399467]uncertain significance2233854467233854467Humanname
405790337CV3266646single nucleotide variantNM_018410.5(HJURP):c.35A>T (p.Asp12Val)not specified [RCV004399468]likely benign2233854466233854466Humanname
597790518CV3682594single nucleotide variantNM_018410.5(HJURP):c.47A>T (p.Asp16Val)not specified [RCV004933261]uncertain significance2233854454233854454Humanname
156401362CV2210985single nucleotide variantNM_018410.5(HJURP):c.121A>G (p.Asn41Asp)not specified [RCV004086052]uncertain significance2233853907233853907Humanname
155980320CV2263641single nucleotide variantNM_018410.5(HJURP):c.243C>A (p.Asp81Glu)not specified [RCV004135642]uncertain significance2233849857233849857Humanname
401872091CV2769597single nucleotide variantNM_018410.5(HJURP):c.280G>A (p.Val94Met)not specified [RCV004351242]uncertain significance2233849820233849820Humanname
405790309CV3266636single nucleotide variantNM_018410.5(HJURP):c.104G>A (p.Arg35Gln)not specified [RCV004399458]likely benign2233854397233854397Humanname
407510696CV3437429single nucleotide variantNM_018410.5(HJURP):c.256C>G (p.Pro86Ala)not specified [RCV004626207]uncertain significance2233849844233849844Humanname
597790565CV3682605single nucleotide variantNM_018410.5(HJURP):c.123C>A (p.Asn41Lys)not specified [RCV004933272]uncertain significance2233853905233853905Humanname
156223739CV2229620single nucleotide variantNM_018410.5(HJURP):c.659C>T (p.Pro220Leu)not specified [RCV004103435]uncertain significance2233842121233842121Humanname
155918389CV2332993single nucleotide variantNM_018410.5(HJURP):c.944G>A (p.Arg315His)not specified [RCV004194293]likely benign2233841836233841836Humanname
156391626CV2382451single nucleotide variantNM_018410.5(HJURP):c.772G>A (p.Val258Met)not specified [RCV004230786]uncertain significance2233842008233842008Humanname
329379867CV2448000single nucleotide variantNM_018410.5(HJURP):c.526C>T (p.Arg176Cys)not specified [RCV004260796]uncertain significance2233844253233844253Humanname
329369870CV2461255single nucleotide variantNM_018410.5(HJURP):c.306G>C (p.Glu102Asp)not specified [RCV004267436]uncertain significance2233849794233849794Humanname
401721065CV2673588single nucleotide variantNM_018410.5(HJURP):c.860C>T (p.Thr287Met)not provided [RCV004696409]|not specified [RCV004282326]uncertain significance2233841920233841920Humanname
401757254CV2675194single nucleotide variantNM_018410.5(HJURP):c.988C>T (p.Pro330Ser)not specified [RCV004289966]uncertain significance2233841792233841792Humanname
401771490CV2686196single nucleotide variantNM_018410.5(HJURP):c.587G>A (p.Arg196His)not specified [RCV004297292]uncertain significance2233842193233842193Humanname
401725472CV2697426single nucleotide variantNM_018410.5(HJURP):c.818G>A (p.Arg273Gln)not specified [RCV004304174]uncertain significance2233841962233841962Humanname
401882087CV2784064single nucleotide variantNM_018410.5(HJURP):c.811A>G (p.Met271Val)not specified [RCV004362467]uncertain significance2233841969233841969Humanname
405790331CV3266644single nucleotide variantNM_018410.5(HJURP):c.347G>C (p.Ser116Thr)not specified [RCV004399466]uncertain significance2233847452233847452Humanname
405790340CV3266647single nucleotide variantNM_018410.5(HJURP):c.502G>A (p.Gly168Ser)not specified [RCV004399469]uncertain significance2233844277233844277Humanname
405790343CV3266648single nucleotide variantNM_018410.5(HJURP):c.527G>A (p.Arg176His)not specified [RCV004399470]likely benign2233844252233844252Humanname
405790346CV3266649single nucleotide variantNM_018410.5(HJURP):c.943C>G (p.Arg315Gly)not specified [RCV004399471]uncertain significance2233841837233841837Humanname
407527385CV3437424single nucleotide variantNM_018410.5(HJURP):c.793G>A (p.Ala265Thr)not specified [RCV004632776]uncertain significance2233841987233841987Humanname
407510693CV3437428single nucleotide variantNM_018410.5(HJURP):c.892A>G (p.Arg298Gly)not specified [RCV004626206]uncertain significance2233841888233841888Humanname
597790552CV3682602single nucleotide variantNM_018410.5(HJURP):c.320G>A (p.Arg107His)not specified [RCV004933269]uncertain significance2233849780233849780Humanname
597790561CV3682604single nucleotide variantNM_018410.5(HJURP):c.379G>A (p.Glu127Lys)not specified [RCV004933271]uncertain significance2233847420233847420Humanname
597790569CV3682606single nucleotide variantNM_018410.5(HJURP):c.694G>A (p.Asp232Asn)not specified [RCV004933273]uncertain significance2233842086233842086Humanname
597790574CV3682607single nucleotide variantNM_018410.5(HJURP):c.632C>T (p.Ser211Phe)not specified [RCV004933274]uncertain significance2233842148233842148Humanname
597790586CV3682610single nucleotide variantNM_018410.5(HJURP):c.943C>T (p.Arg315Cys)not specified [RCV004933277]uncertain significance2233841837233841837Humanname
598178714CV3975225single nucleotide variantNM_018410.5(HJURP):c.832A>G (p.Lys278Glu)not specified [RCV005352031]uncertain significance2233841948233841948Humanname
598248381CV3975227single nucleotide variantNM_018410.5(HJURP):c.964G>A (p.Glu322Lys)not specified [RCV005345436]uncertain significance2233841816233841816Humanname
156321015CV2197469single nucleotide variantNM_018410.5(HJURP):c.1732G>A (p.Asp578Asn)not specified [RCV004081202]uncertain significance2233841048233841048Humanname
156191182CV2223076single nucleotide variantNM_018410.5(HJURP):c.1045C>T (p.Arg349Cys)not specified [RCV004103931]uncertain significance2233841735233841735Humanname
155981827CV2244122single nucleotide variantNM_018410.5(HJURP):c.2098G>A (p.Ala700Thr)not specified [RCV004108583]uncertain significance2233840682233840682Humanname
156091652CV2300077single nucleotide variantNM_018410.5(HJURP):c.1054G>C (p.Gly352Arg)not specified [RCV004151278]uncertain significance2233841726233841726Humanname
155907086CV2302148single nucleotide variantNM_018410.5(HJURP):c.1019G>C (p.Cys340Ser)not specified [RCV004159162]uncertain significance2233841761233841761Humanname
156290951CV2324958single nucleotide variantNM_018410.5(HJURP):c.1397T>C (p.Met466Thr)not specified [RCV004175213]uncertain significance2233841383233841383Humanname
156072180CV2325294single nucleotide variantNM_018410.5(HJURP):c.1597G>A (p.Ala533Thr)not specified [RCV004177687]uncertain significance2233841183233841183Humanname
156071185CV2337740single nucleotide variantNM_018410.5(HJURP):c.1810T>C (p.Cys604Arg)not specified [RCV004183761]uncertain significance2233840970233840970Humanname
156070444CV2354180single nucleotide variantNM_018410.5(HJURP):c.1604G>A (p.Arg535His)not specified [RCV004206612]likely benign2233841176233841176Humanname
156266869CV2372557single nucleotide variantNM_018410.5(HJURP):c.1630G>A (p.Val544Ile)not specified [RCV004219349]uncertain significance2233841150233841150Humanname
155998384CV2373284single nucleotide variantNM_018410.5(HJURP):c.2014G>A (p.Gly672Ser)not specified [RCV004219997]uncertain significance2233840766233840766Humanname
156347339CV2382880single nucleotide variantNM_018410.5(HJURP):c.1607C>T (p.Pro536Leu)not specified [RCV004217479]uncertain significance2233841173233841173Humanname
156062552CV2392134single nucleotide variantNM_018410.5(HJURP):c.1810T>G (p.Cys604Gly)not specified [RCV004238027]uncertain significance2233840970233840970Humanname
156165552CV2398831single nucleotide variantNM_018410.5(HJURP):c.1406G>C (p.Gly469Ala)not specified [RCV004245154]uncertain significance2233841374233841374Humanname
329356293CV2442573single nucleotide variantNM_018410.5(HJURP):c.1678A>G (p.Lys560Glu)not specified [RCV004266793]uncertain significance2233841102233841102Humanname
329362868CV2449451single nucleotide variantNM_018410.5(HJURP):c.1390A>G (p.Met464Val)not specified [RCV004268397]likely benign2233841390233841390Humanname
329395054CV2457786single nucleotide variantNM_018410.5(HJURP):c.1023G>T (p.Lys341Asn)not specified [RCV004269616]uncertain significance2233841757233841757Humanname
329356753CV2460526single nucleotide variantNM_018410.5(HJURP):c.2181C>G (p.Asn727Lys)not specified [RCV004268809]uncertain significance2233837643233837643Humanname
401727279CV2684546single nucleotide variantNM_018410.5(HJURP):c.1103A>G (p.His368Arg)not specified [RCV004293657]likely benign2233841677233841677Humanname
401759015CV2705326single nucleotide variantNM_018410.5(HJURP):c.1024A>C (p.Asn342His)not specified [RCV004312007]uncertain significance2233841756233841756Humanname
401761772CV2713888single nucleotide variantNM_018410.5(HJURP):c.1399T>C (p.Tyr467His)not specified [RCV004315321]uncertain significance2233841381233841381Humanname
401752911CV2720561single nucleotide variantNM_018410.5(HJURP):c.2183C>T (p.Thr728Met)not specified [RCV004327950]uncertain significance2233837641233837641Humanname
401753072CV2720620single nucleotide variantNM_018410.5(HJURP):c.1268G>A (p.Arg423Gln)not specified [RCV004327987]likely benign2233841512233841512Humanname
401774543CV2727873single nucleotide variantNM_018410.5(HJURP):c.1793A>C (p.Gln598Pro)not specified [RCV004323888]uncertain significance2233840987233840987Humanname
401898113CV2769989single nucleotide variantNM_018410.5(HJURP):c.1252T>G (p.Ser418Ala)not specified [RCV004353822]uncertain significance2233841528233841528Humanname
401896316CV2773981single nucleotide variantNM_018410.5(HJURP):c.2199A>C (p.Glu733Asp)not specified [RCV004358393]uncertain significance2233837625233837625Humanname
401881215CV2789495single nucleotide variantNM_018410.5(HJURP):c.1102C>G (p.His368Asp)not specified [RCV004360110]uncertain significance2233841678233841678Humanname
405790312CV3266637single nucleotide variantNM_018410.5(HJURP):c.1122G>T (p.Trp374Cys)not specified [RCV004399459]uncertain significance2233841658233841658Humanname
405790314CV3266638single nucleotide variantNM_018410.5(HJURP):c.1277A>G (p.His426Arg)not specified [RCV004399460]uncertain significance2233841503233841503Humanname
405790316CV3266639single nucleotide variantNM_018410.5(HJURP):c.1529A>G (p.Glu510Gly)not specified [RCV004399461]uncertain significance2233841251233841251Humanname
405790320CV3266640single nucleotide variantNM_018410.5(HJURP):c.1535G>T (p.Gly512Val)not specified [RCV004399462]uncertain significance2233841245233841245Humanname
405790323CV3266641single nucleotide variantNM_018410.5(HJURP):c.1603C>T (p.Arg535Cys)not specified [RCV004399463]uncertain significance2233841177233841177Humanname
405790325CV3266642single nucleotide variantNM_018410.5(HJURP):c.1666G>A (p.Val556Met)not specified [RCV004399464]uncertain significance2233841114233841114Humanname
405790328CV3266643single nucleotide variantNM_018410.5(HJURP):c.1775G>A (p.Cys592Tyr)not specified [RCV004399465]uncertain significance2233841005233841005Humanname
407527388CV3437425single nucleotide variantNM_018410.5(HJURP):c.1717G>A (p.Gly573Arg)not specified [RCV004632777]likely benign2233841063233841063Humanname
407527391CV3437426single nucleotide variantNM_018410.5(HJURP):c.1435G>A (p.Gly479Ser)not specified [RCV004632778]uncertain significance2233841345233841345Humanname
407527394CV3437427single nucleotide variantNM_018410.5(HJURP):c.1837A>G (p.Ser613Gly)not specified [RCV004632779]uncertain significance2233840943233840943Humanname
597790523CV3682595single nucleotide variantNM_018410.5(HJURP):c.1748A>T (p.Glu583Val)not specified [RCV004933262]uncertain significance2233841032233841032Humanname
597790527CV3682596single nucleotide variantNM_018410.5(HJURP):c.1145C>T (p.Ser382Leu)not specified [RCV004933263]uncertain significance2233841635233841635Humanname
597790532CV3682597single nucleotide variantNM_018410.5(HJURP):c.2122G>T (p.Val708Phe)not specified [RCV004933264]uncertain significance2233840658233840658Humanname
597790536CV3682598single nucleotide variantNM_018410.5(HJURP):c.1604G>T (p.Arg535Leu)not specified [RCV004933265]uncertain significance2233841176233841176Humanname
597790540CV3682599single nucleotide variantNM_018410.5(HJURP):c.2102C>T (p.Ser701Leu)not specified [RCV004933266]uncertain significance2233840678233840678Humanname
597790548CV3682601single nucleotide variantNM_018410.5(HJURP):c.2169G>T (p.Glu723Asp)not specified [RCV004933268]uncertain significance2233840611233840611Humanname
597790556CV3682603single nucleotide variantNM_018410.5(HJURP):c.2144G>A (p.Ser715Asn)not specified [RCV004933270]uncertain significance2233840636233840636Humanname
597790582CV3682609single nucleotide variantNM_018410.5(HJURP):c.2059G>A (p.Glu687Lys)not specified [RCV004933276]uncertain significance2233840721233840721Humanname
598248386CV3975228single nucleotide variantNM_018410.5(HJURP):c.1064T>C (p.Leu355Ser)not specified [RCV005345437]uncertain significance2233841716233841716Humanname
598178726CV3975229single nucleotide variantNM_018410.5(HJURP):c.1392G>A (p.Met464Ile)not specified [RCV005352033]uncertain significance2233841388233841388Humanname
598178732CV3975230single nucleotide variantNM_018410.5(HJURP):c.2212T>A (p.Phe738Ile)not specified [RCV005352034]uncertain significance2233837612233837612Humanname
598178738CV3975231single nucleotide variantNM_018410.5(HJURP):c.1396A>G (p.Met466Val)not specified [RCV005352035]likely benign2233841384233841384Humanname
598178742CV3975232single nucleotide variantNM_018410.5(HJURP):c.1460T>C (p.Leu487Ser)not specified [RCV005352036]likely benign2233841320233841320Humanname