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Variants search result for Homo sapiens
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47 records found for search term Wee1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329359410CV2451002single nucleotide variantNM_003390.4(WEE1):c.13A>G (p.Ser5Gly)not specified [RCV004269670]uncertain significance1195739469573946Humanname
405807768CV3356612single nucleotide variantNM_003390.4(WEE1):c.58A>G (p.Thr20Ala)not specified [RCV004480872]uncertain significance1195739919573991Humanname
407524443CV3490009single nucleotide variantNM_003390.4(WEE1):c.59C>T (p.Thr20Ile)not specified [RCV004678426]uncertain significance1195739929573992Humanname
407524450CV3490011single nucleotide variantNM_003390.4(WEE1):c.43G>T (p.Ala15Ser)not specified [RCV004678428]uncertain significance1195739769573976Humanname
156169874CV2197832single nucleotide variantNM_003390.4(WEE1):c.263A>C (p.Glu88Ala)not specified [RCV004077069]uncertain significance1195741969574196Humanname
156085178CV2205646single nucleotide variantNM_003390.4(WEE1):c.130G>A (p.Gly44Ser)not specified [RCV004082555]uncertain significance1195740639574063Humanname
155904694CV2349546single nucleotide variantNM_003390.4(WEE1):c.253A>C (p.Ser85Arg)not specified [RCV004203978]uncertain significance1195741869574186Humanname
156038057CV2374124single nucleotide variantNM_003390.4(WEE1):c.242C>T (p.Pro81Leu)not specified [RCV004229282]uncertain significance1195741759574175Humanname
401749107CV2708470single nucleotide variantNM_003390.4(WEE1):c.107A>T (p.Glu36Val)not specified [RCV004313565]uncertain significance1195740409574040Humanname
405807762CV3356609single nucleotide variantNM_003390.4(WEE1):c.232T>G (p.Ser78Ala)not specified [RCV004480869]uncertain significance1195741659574165Humanname
598267112CV3933555single nucleotide variantNM_003390.4(WEE1):c.205A>G (p.Thr69Ala)not specified [RCV005302102]uncertain significance1195741389574138Humanname
156399185CV2204965single nucleotide variantNM_003390.4(WEE1):c.667A>G (p.Arg223Gly)not specified [RCV004077587]uncertain significance1195759789575978Humanname
156387598CV2221556single nucleotide variantNM_003390.4(WEE1):c.434G>A (p.Gly145Asp)not specified [RCV004096820]uncertain significance1195743679574367Humanname
156276333CV2287720single nucleotide variantNM_003390.4(WEE1):c.616G>T (p.Val206Phe)not specified [RCV004141137]uncertain significance1195759279575927Humanname
156292011CV2296743single nucleotide variantNM_003390.4(WEE1):c.466G>A (p.Ala156Thr)not specified [RCV004148648]uncertain significance1195743999574399Humanname
156071855CV2376798single nucleotide variantNM_003390.4(WEE1):c.566A>T (p.His189Leu)not specified [RCV004227460]uncertain significance1195744999574499Humanname
156071875CV2376799single nucleotide variantNM_003390.4(WEE1):c.568A>T (p.Thr190Ser)not specified [RCV004227461]uncertain significance1195745019574501Humanname
156071886CV2376800single nucleotide variantNM_003390.4(WEE1):c.575A>G (p.Lys192Arg)not specified [RCV004227462]uncertain significance1195745089574508Humanname
329367397CV2456829single nucleotide variantNM_003390.4(WEE1):c.523C>T (p.Pro175Ser)not specified [RCV004270794]uncertain significance1195744569574456Humanname
401876480CV2767603single nucleotide variantNM_003390.4(WEE1):c.695A>T (p.Gln232Leu)not specified [RCV004343748]uncertain significance1195760069576006Humanname
405807767CV3356611single nucleotide variantNM_003390.4(WEE1):c.494C>G (p.Ser165Trp)not specified [RCV004480871]uncertain significance1195744279574427Humanname
405807773CV3356614single nucleotide variantNM_003390.4(WEE1):c.675T>G (p.Phe225Leu)not specified [RCV004480874]uncertain significance1195759869575986Humanname
405807774CV3356615single nucleotide variantNM_003390.4(WEE1):c.926A>C (p.Glu309Ala)not specified [RCV004480875]uncertain significance1195765669576566Humanname
407465414CV3490007single nucleotide variantNM_003390.4(WEE1):c.823G>A (p.Glu275Lys)not specified [RCV004688762]uncertain significance1195762709576270Humanname
597739705CV3630171single nucleotide variantNM_003390.4(WEE1):c.319G>A (p.Gly107Ser)not specified [RCV004890383]uncertain significance1195742529574252Humanname
597792199CV3630173single nucleotide variantNM_003390.4(WEE1):c.419C>T (p.Pro140Leu)not specified [RCV004876914]uncertain significance1195743529574352Humanname
598267117CV3933556single nucleotide variantNM_003390.4(WEE1):c.389C>T (p.Ala130Val)not specified [RCV005302103]uncertain significance1195743229574322Humanname
598233023CV3933557single nucleotide variantNM_003390.4(WEE1):c.362C>G (p.Ser121Cys)not specified [RCV005295503]uncertain significance1195742959574295Humanname
15170780CV713266single nucleotide variantNM_003390.4(WEE1):c.628G>T (p.Gly210Cys)not provided [RCV000972075]benign1195759399575939Humanname
156235055CV2224014single nucleotide variantNM_003390.4(WEE1):c.1844C>T (p.Thr615Ile)not specified [RCV004094261]uncertain significance1195885059588505Humanname
156069545CV2270991single nucleotide variantNM_003390.4(WEE1):c.1340G>C (p.Gly447Ala)not specified [RCV004133808]uncertain significance1195853099585309Humanname
156247252CV2276842single nucleotide variantNM_003390.4(WEE1):c.1307G>A (p.Arg436Gln)not specified [RCV004140189]uncertain significance1195852769585276Humanname
155918769CV2279285single nucleotide variantNM_003390.4(WEE1):c.1343A>G (p.Asp448Gly)not specified [RCV004139804]uncertain significance1195853129585312Humanname
155940946CV2294166single nucleotide variantNM_003390.4(WEE1):c.1302A>G (p.Ile434Met)not specified [RCV004149531]uncertain significance1195852719585271Humanname
156263128CV2314947single nucleotide variantNM_003390.4(WEE1):c.1549C>G (p.Pro517Ala)not specified [RCV004171050]uncertain significance1195865279586527Humanname
329358802CV2450715single nucleotide variantNM_003390.4(WEE1):c.1369G>A (p.Val457Ile)not specified [RCV004267659]uncertain significance1195853389585338Humanname
329386604CV2456122single nucleotide variantNM_003390.4(WEE1):c.1528G>A (p.Ala510Thr)not specified [RCV004273011]uncertain significance1195865069586506Humanname
329397362CV2460188single nucleotide variantNM_003390.4(WEE1):c.1133A>G (p.Tyr378Cys)not specified [RCV004273286]uncertain significance1195772559577255Humanname
401773465CV2709324single nucleotide variantNM_003390.4(WEE1):c.1877G>T (p.Ser626Ile)not specified [RCV004316473]uncertain significance1195885389588538Humanname
401738645CV2721937single nucleotide variantNM_003390.4(WEE1):c.1583A>G (p.Gln528Arg)not specified [RCV004326435]uncertain significance1195865619586561Humanname
401890097CV2763518single nucleotide variantNM_003390.4(WEE1):c.1621G>A (p.Glu541Lys)not specified [RCV004343042]uncertain significance1195865999586599Humanname
405807759CV3356607single nucleotide variantNM_003390.4(WEE1):c.1300A>G (p.Ile434Val)not specified [RCV004480867]uncertain significance1195852699585269Humanname
405807976CV3356608single nucleotide variantNM_003390.4(WEE1):c.1849C>T (p.Arg617Trp)not specified [RCV004480868]uncertain significance1195885109588510Humanname
407524442CV3490008single nucleotide variantNM_003390.4(WEE1):c.1351G>T (p.Asp451Tyr)not specified [RCV004678425]uncertain significance1195853209585320Humanname
407524448CV3490010single nucleotide variantNM_003390.4(WEE1):c.1163T>C (p.Ile388Thr)not specified [RCV004678427]uncertain significance1195815539581553Humanname
597739709CV3630172single nucleotide variantNM_003390.4(WEE1):c.1525T>C (p.Cys509Arg)not specified [RCV004890384]uncertain significance1195865039586503Humanname
13607460CV513782single nucleotide variantNM_014159.7(SETD2):c.5143-1G>AWee1 Inhibitor response [RCV000626444]drug response34708824847088248Humantrait