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Variants search result for Homo sapiens
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86 records found for search term Hjurp
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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