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Variants search result for Homo sapiens
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79 records found for search term Map3k11
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597626925CV3700054single nucleotide variantNM_002419.4(MAP3K11):c.132G>A (p.Pro44=)not specified [RCV004938772]likely benign116561362565613625Humanname
155968360CV2339303single nucleotide variantNM_002419.4(MAP3K11):c.67G>A (p.Gly23Ser)not specified [RCV004191538]uncertain significance116561369065613690Humanname
155941242CV2232516single nucleotide variantNM_002419.4(MAP3K11):c.218G>A (p.Arg73Gln)not specified [RCV004099118]uncertain significance116561353965613539Humanname
156252957CV2311416single nucleotide variantNM_002419.4(MAP3K11):c.124G>T (p.Ala42Ser)not specified [RCV004168264]uncertain significance116561363365613633Humanname
401762841CV2720098single nucleotide variantNM_002419.4(MAP3K11):c.157G>A (p.Glu53Lys)not specified [RCV004323664]uncertain significance116561360065613600Humanname
405657747CV3288636single nucleotide variantNM_002419.4(MAP3K11):c.226G>A (p.Ala76Thr)not specified [RCV004416232]uncertain significance116561353165613531Humanname
405657752CV3288637single nucleotide variantNM_002419.4(MAP3K11):c.227C>T (p.Ala76Val)not specified [RCV004416233]uncertain significance116561353065613530Humanname
407493782CV3446468single nucleotide variantNM_002419.4(MAP3K11):c.116C>G (p.Ala39Gly)not specified [RCV004642827]uncertain significance116561364165613641Humanname
597626918CV3700052single nucleotide variantNM_002419.4(MAP3K11):c.167G>A (p.Gly56Glu)not specified [RCV004938770]uncertain significance116561359065613590Humanname
597626942CV3700059single nucleotide variantNM_002419.4(MAP3K11):c.290C>A (p.Ser97Tyr)not specified [RCV004938777]uncertain significance116561346765613467Humanname
598196982CV3988695single nucleotide variantNM_002419.4(MAP3K11):c.2520G>A (p.Pro840=)not specified [RCV005375361]likely benign116559831565598315Humanname
156398086CV2204188single nucleotide variantNM_002419.4(MAP3K11):c.670C>T (p.Arg224Cys)not specified [RCV004076984]uncertain significance116561308765613087Humanname
155901460CV2242017single nucleotide variantNM_002419.4(MAP3K11):c.329A>G (p.Glu110Gly)not specified [RCV004108960]uncertain significance116561342865613428Humanname
156166214CV2243576single nucleotide variantNM_002419.4(MAP3K11):c.550C>G (p.Leu184Val)not specified [RCV004114310]uncertain significance116561320765613207Humanname
329396563CV2462752single nucleotide variantNM_002419.4(MAP3K11):c.449C>T (p.Pro150Leu)not specified [RCV004278674]uncertain significance116561330865613308Humanname
329395995CV2463152single nucleotide variantNM_002419.4(MAP3K11):c.479G>A (p.Ser160Asn)not specified [RCV004274942]uncertain significance116561327865613278Humanname
401748779CV2709581single nucleotide variantNM_002419.4(MAP3K11):c.364G>A (p.Val122Met)not specified [RCV004318809]uncertain significance116561339365613393Humanname
401890596CV2778925single nucleotide variantNM_002419.4(MAP3K11):c.844G>C (p.Ala282Pro)not specified [RCV004346799]uncertain significance116560834465608344Humanname
405657922CV3288638single nucleotide variantNM_002419.4(MAP3K11):c.523A>C (p.Asn175His)not specified [RCV004416234]uncertain significance116561323465613234Humanname
405657758CV3288639single nucleotide variantNM_002419.4(MAP3K11):c.626G>C (p.Arg209Pro)not specified [RCV004416235]uncertain significance116561313165613131Humanname
405657761CV3288640single nucleotide variantNM_002419.4(MAP3K11):c.694G>A (p.Glu232Lys)not specified [RCV004416236]uncertain significance116561306365613063Humanname
405657764CV3288641single nucleotide variantNM_002419.4(MAP3K11):c.859G>A (p.Ala287Thr)not specified [RCV004416237]uncertain significance116560832965608329Humanname
407493786CV3446469single nucleotide variantNM_002419.4(MAP3K11):c.680A>G (p.His227Arg)not specified [RCV004642828]uncertain significance116561307765613077Humanname
407493806CV3446474single nucleotide variantNM_002419.4(MAP3K11):c.709G>A (p.Val237Ile)not specified [RCV004642833]uncertain significance116561304865613048Humanname
597626909CV3700050single nucleotide variantNM_002419.4(MAP3K11):c.893C>T (p.Thr298Ile)not specified [RCV004938768]uncertain significance116560829565608295Humanname
597626914CV3700051single nucleotide variantNM_002419.4(MAP3K11):c.751C>A (p.Gln251Lys)not specified [RCV004938769]uncertain significance116560843765608437Humanname
597626933CV3700056single nucleotide variantNM_002419.4(MAP3K11):c.415G>A (p.Glu139Lys)not specified [RCV004938774]uncertain significance116561334265613342Humanname
597626936CV3700057single nucleotide variantNM_002419.4(MAP3K11):c.626G>A (p.Arg209His)not specified [RCV004938775]uncertain significance116561313165613131Humanname
598166272CV3988694single nucleotide variantNM_002419.4(MAP3K11):c.971G>A (p.Gly324Asp)not specified [RCV005369320]uncertain significance116560802065608020Humanname
598196990CV3988697single nucleotide variantNM_002419.4(MAP3K11):c.566T>C (p.Leu189Pro)not specified [RCV005375362]uncertain significance116561319165613191Humanname
40815075CV970316single nucleotide variantNM_002419.4(MAP3K11):c.847G>A (p.Ala283Thr)Moyamoya angiopathy [RCV004704487]likely pathogenic116560834165608341Humanname
156342260CV2226051single nucleotide variantNM_002419.4(MAP3K11):c.1070A>C (p.Asp357Ala)not specified [RCV004105203]uncertain significance116560781665607816Humanname
156290731CV2226221single nucleotide variantNM_002419.4(MAP3K11):c.2239C>T (p.Arg747Cys)not specified [RCV004099479]uncertain significance116559859665598596Humanname
155947254CV2234792single nucleotide variantNM_002419.4(MAP3K11):c.2186G>A (p.Arg729Gln)not specified [RCV004111232]uncertain significance116559941465599414Humanname
156151375CV2245163single nucleotide variantNM_002419.4(MAP3K11):c.1454C>T (p.Ala485Val)not specified [RCV004106945]uncertain significance116560730565607305Humanname
156278891CV2252119single nucleotide variantNM_002419.4(MAP3K11):c.1840C>T (p.Pro614Ser)not specified [RCV004122143]uncertain significance116559976065599760Humanname
156016037CV2270132single nucleotide variantNM_002419.4(MAP3K11):c.2497A>C (p.Lys833Gln)not specified [RCV004129083]uncertain significance116559833865598338Humanname
156094126CV2309988single nucleotide variantNM_002419.4(MAP3K11):c.1779T>A (p.Asp593Glu)not specified [RCV004163130]uncertain significance116560581365605813Humanname
155958322CV2313773single nucleotide variantNM_002419.4(MAP3K11):c.1843C>T (p.Arg615Trp)not specified [RCV004170279]uncertain significance116559975765599757Humanname
156167277CV2330183single nucleotide variantNM_002419.4(MAP3K11):c.1988C>T (p.Pro663Leu)not specified [RCV004185668]uncertain significance116559961265599612Humanname
156346616CV2375265single nucleotide variantNM_002419.4(MAP3K11):c.2243C>T (p.Ser748Phe)not specified [RCV004232677]uncertain significance116559859265598592Humanname
155904964CV2385648single nucleotide variantNM_002419.4(MAP3K11):c.1109C>T (p.Ala370Val)not specified [RCV004233280]uncertain significance116560777765607777Humanname
155903896CV2386652single nucleotide variantNM_002419.4(MAP3K11):c.2083C>T (p.Leu695Phe)not specified [RCV004230993]uncertain significance116559951765599517Humanname
156007651CV2392637single nucleotide variantNM_002419.4(MAP3K11):c.1432T>C (p.Phe478Leu)not specified [RCV004245872]uncertain significance116560732765607327Humanname
329377662CV2435994single nucleotide variantNM_002419.4(MAP3K11):c.1131G>C (p.Glu377Asp)not specified [RCV004255215]uncertain significance116560775565607755Humanname
329376615CV2438150single nucleotide variantNM_002419.4(MAP3K11):c.1682G>A (p.Arg561Gln)not specified [RCV004256927]uncertain significance116560600365606003Humanname
329371130CV2461958single nucleotide variantNM_002419.4(MAP3K11):c.1446G>T (p.Lys482Asn)not specified [RCV004271857]uncertain significance116560731365607313Humanname
329393211CV2466784single nucleotide variantNM_002419.4(MAP3K11):c.1054G>T (p.Ala352Ser)not specified [RCV004280733]uncertain significance116560793765607937Humanname
329375806CV2468845single nucleotide variantNM_002419.4(MAP3K11):c.1709C>T (p.Ser570Phe)not specified [RCV004280153]uncertain significance116560597665605976Humanname
401771372CV2675574single nucleotide variantNM_002419.4(MAP3K11):c.1208T>C (p.Ile403Thr)not specified [RCV004295187]uncertain significance116560767865607678Humanname
401759869CV2698657single nucleotide variantNM_002419.4(MAP3K11):c.2423A>C (p.Asp808Ala)not specified [RCV004299126]uncertain significance116559841265598412Humanname
401865163CV2757580single nucleotide variantNM_002419.4(MAP3K11):c.2278C>T (p.Pro760Ser)not specified [RCV004340949]uncertain significance116559855765598557Humanname
401872805CV2764346single nucleotide variantNM_002419.4(MAP3K11):c.2086A>G (p.Ile696Val)not specified [RCV004338919]uncertain significance116559951465599514Humanname
401892422CV2781921single nucleotide variantNM_002419.4(MAP3K11):c.1453G>A (p.Ala485Thr)not specified [RCV004357163]uncertain significance116560730665607306Humanname
405657858CV3288627single nucleotide variantNM_002419.4(MAP3K11):c.1112C>G (p.Ser371Cys)not specified [RCV004416223]uncertain significance116560777465607774Humanname
405657855CV3288628single nucleotide variantNM_002419.4(MAP3K11):c.1121A>C (p.Gln374Pro)not specified [RCV004416224]uncertain significance116560776565607765Humanname
405657755CV3288630single nucleotide variantNM_002419.4(MAP3K11):c.1465G>C (p.Gly489Arg)not specified [RCV004416226]uncertain significance116560729465607294Humanname
405657733CV3288631single nucleotide variantNM_002419.4(MAP3K11):c.1538G>A (p.Arg513Lys)not specified [RCV004416227]uncertain significance116560675665606756Humanname
405657735CV3288632single nucleotide variantNM_002419.4(MAP3K11):c.1793C>T (p.Ser598Phe)not specified [RCV004416228]uncertain significance116560579965605799Humanname
405657738CV3288633single nucleotide variantNM_002419.4(MAP3K11):c.1957G>A (p.Ala653Thr)not specified [RCV004416229]uncertain significance116559964365599643Humanname
405657741CV3288634single nucleotide variantNM_002419.4(MAP3K11):c.1991C>T (p.Pro664Leu)not specified [RCV004416230]uncertain significance116559960965599609Humanname
405657744CV3288635single nucleotide variantNM_002419.4(MAP3K11):c.2053C>T (p.Pro685Ser)not specified [RCV004416231]uncertain significance116559954765599547Humanname
407493769CV3446463single nucleotide variantNM_002419.4(MAP3K11):c.2041C>T (p.Pro681Ser)not specified [RCV004642824]uncertain significance116559955965599559Humanname
407493775CV3446465single nucleotide variantNM_002419.4(MAP3K11):c.2012G>A (p.Arg671His)not specified [RCV004642825]uncertain significance116559958865599588Humanname
407493778CV3446466single nucleotide variantNM_002419.4(MAP3K11):c.1820C>T (p.Pro607Leu)not specified [RCV004642826]uncertain significance116560577265605772Humanname
407469001CV3446467single nucleotide variantNM_002419.4(MAP3K11):c.2255C>T (p.Thr752Ile)not specified [RCV004636478]uncertain significance116559858065598580Humanname
407493790CV3446470single nucleotide variantNM_002419.4(MAP3K11):c.2309C>T (p.Ser770Leu)not specified [RCV004642829]uncertain significance116559852665598526Humanname
407493794CV3446471single nucleotide variantNM_002419.4(MAP3K11):c.1895G>A (p.Gly632Asp)not specified [RCV004642830]uncertain significance116559970565599705Humanname
407493798CV3446472single nucleotide variantNM_002419.4(MAP3K11):c.2324G>T (p.Arg775Leu)not specified [RCV004642831]uncertain significance116559851165598511Humanname
407493803CV3446473single nucleotide variantNM_002419.4(MAP3K11):c.2111A>G (p.Asp704Gly)not specified [RCV004642832]uncertain significance116559948965599489Humanname
597626901CV3700048single nucleotide variantNM_002419.4(MAP3K11):c.1844G>A (p.Arg615Gln)not specified [RCV004938766]uncertain significance116559975665599756Humanname
597626905CV3700049single nucleotide variantNM_002419.4(MAP3K11):c.1132G>A (p.Ala378Thr)not specified [RCV004938767]uncertain significance116560775465607754Humanname
597626922CV3700053single nucleotide variantNM_002419.4(MAP3K11):c.1979A>T (p.Asp660Val)not specified [RCV004938771]uncertain significance116559962165599621Humanname
597626930CV3700055single nucleotide variantNM_002419.4(MAP3K11):c.1241A>G (p.Glu414Gly)not specified [RCV004938773]uncertain significance116560764565607645Humanname
597626944CV3700060single nucleotide variantNM_002419.4(MAP3K11):c.1775T>C (p.Leu592Pro)not specified [RCV004938778]uncertain significance116560581765605817Humanname
598196976CV3988693single nucleotide variantNM_002419.4(MAP3K11):c.2024C>T (p.Pro675Leu)not specified [RCV005375360]uncertain significance116559957665599576Humanname
598166278CV3988696single nucleotide variantNM_002419.4(MAP3K11):c.1793C>G (p.Ser598Cys)not specified [RCV005369321]uncertain significance116560579965605799Humanname
598175641CV3988698single nucleotide variantNM_002419.4(MAP3K11):c.2135T>C (p.Leu712Pro)not specified [RCV005371297]uncertain significance116559946565599465Humanname
8627104CV82248single nucleotide variantNM_002419.3(MAP3K11):c.2047C>T (p.Pro683Ser)Malignant melanoma [RCV000062327]not provided116559955365599553Humanname