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)

61 records found for search term Mybl2
Refine Term:
Sort By:
           Export CSV TAB Print

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