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Variants search result for Homo sapiens
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61 records found for search term Mybl2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8586477CV121080single nucleotide variantNM_001278610.1(MYBL2):c.207+282G>TLung cancer [RCV000101600]uncertain significance204368316843683168Humanname
156397674CV2197408single nucleotide variantNM_002466.4(MYBL2):c.10C>T (p.Arg4Trp)not specified [RCV004081146]uncertain significance204366729343667293Humanname
401762101CV2714013single nucleotide variantNM_002466.4(MYBL2):c.22G>A (p.Glu8Lys)not specified [RCV004315420]uncertain significance204367380743673807Humanname
597640353CV3558133single nucleotide variantNM_002466.4(MYBL2):c.14C>A (p.Thr5Lys)not specified [RCV004825275]uncertain significance204366729743667297Humanname
15104143CV705496single nucleotide variantNM_002466.4(MYBL2):c.117C>T (p.Asp39=)not provided [RCV000959625]benign204368178643681786Humanname
155927705CV2391489single nucleotide variantNM_002466.4(MYBL2):c.32A>G (p.Asp11Gly)not specified [RCV004239876]uncertain significance204367381743673817Humanname
156326337CV2335447single nucleotide variantNM_002466.4(MYBL2):c.191G>A (p.Arg64His)not specified [RCV004186994]uncertain significance204368279843682798Humanname
401861568CV2779870single nucleotide variantNM_002466.4(MYBL2):c.286G>A (p.Glu96Lys)not specified [RCV004353488]uncertain significance204368685843686858Humanname
597645229CV3558134single nucleotide variantNM_002466.4(MYBL2):c.176G>A (p.Ser59Asn)not specified [RCV004826101]uncertain significance204368184543681845Humanname
155922548CV2251716single nucleotide variantNM_002466.4(MYBL2):c.619G>A (p.Glu207Lys)not specified [RCV004119723]uncertain significance204369227543692275Humanname
156293196CV2306301single nucleotide variantNM_002466.4(MYBL2):c.752C>T (p.Ser251Leu)not specified [RCV004163017]uncertain significance204369984543699845Humanname
156283517CV2360582single nucleotide variantNM_002466.4(MYBL2):c.950C>T (p.Ser317Leu)not specified [RCV004211339]uncertain significance204370004343700043Humanname
401730772CV2686710single nucleotide variantNM_002466.4(MYBL2):c.553G>C (p.Asp185His)not specified [RCV004300117]uncertain significance204369220943692209Humanname
401768585CV2716663single nucleotide variantNM_002466.4(MYBL2):c.428A>C (p.Asp143Ala)not specified [RCV004327720]uncertain significance204368700043687000Humanname
401725500CV2721801single nucleotide variantNM_002466.4(MYBL2):c.857C>T (p.Thr286Met)not specified [RCV004326319]likely benign204369995043699950Humanname
405714161CV3312886single nucleotide variantNM_002466.4(MYBL2):c.445G>T (p.Ala149Ser)not specified [RCV004448931]uncertain significance204368701743687017Humanname
405714200CV3312892single nucleotide variantNM_002466.4(MYBL2):c.652A>G (p.Thr218Ala)not specified [RCV004448937]likely benign204369230843692308Humanname
405714221CV3312895single nucleotide variantNM_002466.4(MYBL2):c.703A>G (p.Ile235Val)not specified [RCV004448940]uncertain significance204369979643699796Humanname
405714262CV3312901single nucleotide variantNM_002466.4(MYBL2):c.787G>A (p.Ala263Thr)not specified [RCV004448946]uncertain significance204369988043699880Humanname
405714281CV3312904single nucleotide variantNM_002466.4(MYBL2):c.800C>T (p.Pro267Leu)not specified [RCV004448949]uncertain significance204369989343699893Humanname
407504033CV3454156single nucleotide variantNM_002466.4(MYBL2):c.392C>G (p.Pro131Arg)not specified [RCV004645664]uncertain significance204368696443686964Humanname
407514591CV3454157single nucleotide variantNM_002466.4(MYBL2):c.420G>T (p.Glu140Asp)not specified [RCV004649565]uncertain significance204368699243686992Humanname
597645215CV3558130single nucleotide variantNM_002466.4(MYBL2):c.746C>T (p.Thr249Ile)not specified [RCV004826099]uncertain significance204369983943699839Humanname
597645238CV3558135single nucleotide variantNM_002466.4(MYBL2):c.730G>A (p.Glu244Lys)not specified [RCV004826102]uncertain significance204369982343699823Humanname
597645252CV3558137single nucleotide variantNM_002466.4(MYBL2):c.826C>A (p.Arg276Ser)not specified [RCV004826104]uncertain significance204369991943699919Humanname
598230117CV3983075single nucleotide variantNM_002466.4(MYBL2):c.827G>A (p.Arg276His)not specified [RCV005381135]uncertain significance204369992043699920Humanname
598263975CV3983078single nucleotide variantNM_002466.4(MYBL2):c.758A>G (p.Glu253Gly)not specified [RCV005387633]uncertain significance204369985143699851Humanname
598263978CV3983079single nucleotide variantNM_002466.4(MYBL2):c.346C>T (p.Arg116Trp)not specified [RCV005387634]uncertain significance204368691843686918Humanname
598230129CV3983082single nucleotide variantNM_002466.4(MYBL2):c.842G>T (p.Gly281Val)not specified [RCV005381137]uncertain significance204369993543699935Humanname
15123255CV716994single nucleotide variantNM_002466.4(MYBL2):c.691G>T (p.Val231Phe)not provided [RCV000963207]benign204369978443699784Humanname
15198636CV728668single nucleotide variantNM_002466.4(MYBL2):c.572G>A (p.Ser191Asn)not provided [RCV000890415]benign204369222843692228Humanname
156030276CV2202381single nucleotide variantNM_002466.4(MYBL2):c.1865C>T (p.Ser622Leu)not specified [RCV004080696]uncertain significance204371517443715174Humanname
156031434CV2202711single nucleotide variantNM_002466.4(MYBL2):c.1727G>A (p.Arg576Gln)not specified [RCV004082956]uncertain significance204371300943713009Humanname
156082476CV2244408single nucleotide variantNM_002466.4(MYBL2):c.1937C>G (p.Ala646Gly)not specified [RCV004100380]uncertain significance204371524643715246Humanname
156140938CV2280872single nucleotide variantNM_002466.4(MYBL2):c.1649G>A (p.Arg550His)not specified [RCV004145125]uncertain significance204371153143711531Humanname
156208216CV2298105single nucleotide variantNM_002466.4(MYBL2):c.1855C>A (p.Leu619Ile)not specified [RCV004157987]uncertain significance204371516443715164Humanname
155972679CV2334362single nucleotide variantNM_002466.4(MYBL2):c.1154G>A (p.Ser385Asn)not specified [RCV004188340]uncertain significance204370269243702692Humanname
155976039CV2338549single nucleotide variantNM_002466.4(MYBL2):c.1243A>G (p.Lys415Glu)not specified [RCV004189004]uncertain significance204370278143702781Humanname
155963077CV2388340single nucleotide variantNM_002466.4(MYBL2):c.1030C>G (p.Leu344Val)not specified [RCV004234791]uncertain significance204370256843702568Humanname
329355961CV2445637single nucleotide variantNM_002466.4(MYBL2):c.1234C>T (p.Arg412Trp)not specified [RCV004259719]uncertain significance204370277243702772Humanname
329356765CV2460535single nucleotide variantNM_002466.4(MYBL2):c.2060G>A (p.Arg687His)not specified [RCV004268817]uncertain significance204371604443716044Humanname
401758304CV2678338single nucleotide variantNM_002466.4(MYBL2):c.1970C>T (p.Ala657Val)not specified [RCV004290325]uncertain significance204371527943715279Humanname
401735153CV2699181single nucleotide variantNM_002466.4(MYBL2):c.1306T>C (p.Cys436Arg)not specified [RCV004303679]uncertain significance204370284443702844Humanname
401775158CV2713801single nucleotide variantNM_002466.4(MYBL2):c.1723C>T (p.Arg575Trp)not specified [RCV004321142]uncertain significance204371300543713005Humanname
401897712CV2772854single nucleotide variantNM_002466.4(MYBL2):c.1826C>T (p.Pro609Leu)not specified [RCV004357636]uncertain significance204371513543715135Humanname
405713828CV3312837single nucleotide variantNM_002466.4(MYBL2):c.1621C>A (p.Leu541Met)not specified [RCV004448882]uncertain significance204371150343711503Humanname
405713863CV3312842single nucleotide variantNM_002466.4(MYBL2):c.1648C>T (p.Arg550Cys)not specified [RCV004448887]uncertain significance204371153043711530Humanname
405713948CV3312854single nucleotide variantNM_002466.4(MYBL2):c.1780G>C (p.Asp594His)not specified [RCV004448899]uncertain significance204371306243713062Humanname
405714032CV3312866single nucleotide variantNM_002466.4(MYBL2):c.2092A>T (p.Ile698Phe)not specified [RCV004448911]uncertain significance204371607643716076Humanname
407514594CV3454159single nucleotide variantNM_002466.4(MYBL2):c.1217C>T (p.Pro406Leu)not specified [RCV004649567]uncertain significance204370275543702755Humanname
408367549CV3508368single nucleotide variantNM_002466.4(MYBL2):c.1765G>A (p.Asp589Asn)MYBL2-related condition [RCV004758986]uncertain significance204371304743713047Humanname , trait
597640347CV3558131single nucleotide variantNM_002466.4(MYBL2):c.1409G>C (p.Ser470Thr)not specified [RCV004825274]uncertain significance204370526243705262Humanname
597645222CV3558132single nucleotide variantNM_002466.4(MYBL2):c.1817T>A (p.Leu606Gln)not specified [RCV004826100]uncertain significance204371309943713099Humanname
597645245CV3558136single nucleotide variantNM_002466.4(MYBL2):c.1927G>T (p.Ala643Ser)not specified [RCV004826103]uncertain significance204371523643715236Humanname
598230112CV3983074single nucleotide variantNM_002466.4(MYBL2):c.1636A>G (p.Lys546Glu)not specified [RCV005381134]uncertain significance204371151843711518Humanname
598263972CV3983076single nucleotide variantNM_002466.4(MYBL2):c.1792A>T (p.Met598Leu)not specified [RCV005387632]uncertain significance204371307443713074Humanname
598230123CV3983077single nucleotide variantNM_002466.4(MYBL2):c.1961C>T (p.Thr654Met)not specified [RCV005381136]uncertain significance204371527043715270Humanname
598263981CV3983080single nucleotide variantNM_002466.4(MYBL2):c.1006G>T (p.Ala336Ser)not specified [RCV005387635]uncertain significance204370254443702544Humanname
598263984CV3983081single nucleotide variantNM_002466.4(MYBL2):c.1931C>T (p.Ala644Val)not specified [RCV005387636]likely benign204371524043715240Humanname
15202849CV705497single nucleotide variantNM_002466.4(MYBL2):c.1783G>A (p.Val595Met)not provided [RCV000958069]benign204371306543713065Humanname
15182157CV728669single nucleotide variantNM_002466.4(MYBL2):c.1022A>G (p.Asn341Ser)not provided [RCV000885927]benign204370256043702560Humanname