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53 records found for search term Numbl
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598234348CV4004601single nucleotide variantNM_004756.5(NUMBL):c.4T>A (p.Ser2Thr)not specified [RCV005381853]uncertain significance194069048040690480Humanname
155980966CV2272792single nucleotide variantNM_004756.5(NUMBL):c.59C>T (p.Pro20Leu)not specified [RCV004135705]uncertain significance194068696140686961Humanname
401746739CV2678907single nucleotide variantNM_004756.5(NUMBL):c.46C>T (p.Arg16Trp)not specified [RCV004292878]uncertain significance194068697440686974Humanname
401869514CV2782392single nucleotide variantNM_004756.5(NUMBL):c.77C>T (p.Pro26Leu)not specified [RCV004365131]likely benign194068694340686943Humanname
405730513CV3356028single nucleotide variantNM_004756.5(NUMBL):c.41C>T (p.Pro14Leu)not specified [RCV004496324]uncertain significance194068697940686979Humanname
8636831CV92056single nucleotide variantNM_004756.4(NUMBL):c.672C>T (p.Ser224=)Malignant melanoma [RCV000072154]not provided194067729040677290Humanname
8636832CV92057single nucleotide variantNM_004756.4(NUMBL):c.471C>T (p.Phe157=)Malignant melanoma [RCV000072155]not provided194068098640680986Humanname
156076965CV2198201single nucleotide variantNM_004756.5(NUMBL):c.276G>C (p.Glu92Asp)not specified [RCV004079785]uncertain significance194068294240682942Humanname
401887449CV2771944single nucleotide variantNM_004756.5(NUMBL):c.163G>A (p.Ala55Thr)not specified [RCV004344639]uncertain significance194068450340684503Humanname
407521902CV3462356single nucleotide variantNM_004756.5(NUMBL):c.169G>A (p.Val57Met)not specified [RCV004652678]uncertain significance194068449740684497Humanname
597644336CV3573702single nucleotide variantNM_004756.5(NUMBL):c.103G>A (p.Glu35Lys)not specified [RCV004832682]uncertain significance194068691740686917Humanname
156387091CV2221398single nucleotide variantNM_004756.5(NUMBL):c.593G>A (p.Arg198Gln)not specified [RCV004096695]uncertain significance194067736940677369Humanname
156192163CV2255345single nucleotide variantNM_004756.5(NUMBL):c.502C>T (p.Arg168Cys)not specified [RCV004117715]uncertain significance194068095540680955Humanname
156347819CV2382985single nucleotide variantNM_004756.5(NUMBL):c.829G>T (p.Ala277Ser)not specified [RCV004217571]uncertain significance194067355140673551Humanname
329392207CV2470476single nucleotide variantNM_004756.5(NUMBL):c.874C>T (p.Arg292Trp)not specified [RCV004273499]uncertain significance194067350640673506Humanname
401753147CV2674794single nucleotide variantNM_004756.5(NUMBL):c.784G>A (p.Val262Met)not specified [RCV004294073]uncertain significance194067359640673596Humanname
401719043CV2704931single nucleotide variantNM_004756.5(NUMBL):c.358G>T (p.Val120Leu)not specified [RCV004307501]uncertain significance194068276940682769Humanname
405730504CV3356027single nucleotide variantNM_004756.5(NUMBL):c.419C>T (p.Thr140Ile)not specified [RCV004496323]uncertain significance194068103840681038Humanname
407521908CV3462358single nucleotide variantNM_004756.5(NUMBL):c.676C>T (p.Arg226Cys)not specified [RCV004652680]uncertain significance194067728640677286Humanname
597663174CV3573698single nucleotide variantNM_004756.5(NUMBL):c.485G>A (p.Arg162His)not specified [RCV004835293]uncertain significance194068097240680972Humanname
597644175CV3573703single nucleotide variantNM_004756.5(NUMBL):c.664G>A (p.Glu222Lys)not specified [RCV004832683]uncertain significance194067729840677298Humanname
597663204CV3573705single nucleotide variantNM_004756.5(NUMBL):c.998C>T (p.Thr333Met)not specified [RCV004835297]uncertain significance194067338240673382Humanname
598234366CV4004604single nucleotide variantNM_004756.5(NUMBL):c.385G>A (p.Asp129Asn)not specified [RCV005381856]uncertain significance194068274240682742Humanname
598234390CV4004607single nucleotide variantNM_004756.5(NUMBL):c.950C>T (p.Ser317Leu)not specified [RCV005381859]uncertain significance194067343040673430Humanname
598265918CV4004608single nucleotide variantNM_004756.5(NUMBL):c.778G>A (p.Gly260Arg)not specified [RCV005388024]uncertain significance194067360240673602Humanname
156327049CV2219755single nucleotide variantNM_004756.5(NUMBL):c.1058G>A (p.Gly353Asp)not specified [RCV004095449]uncertain significance194066999940669999Humanname
156159975CV2262627single nucleotide variantNM_004756.5(NUMBL):c.1186G>A (p.Val396Met)not specified [RCV004130825]uncertain significance194066811240668112Humanname
156244634CV2267389single nucleotide variantNM_004756.5(NUMBL):c.1463C>T (p.Pro488Leu)not specified [RCV004134044]uncertain significance194066783540667835Humanname
155906989CV2279600single nucleotide variantNM_004756.5(NUMBL):c.1193C>A (p.Pro398His)not specified [RCV004142100]uncertain significance194066810540668105Humanname
156194942CV2309482single nucleotide variantNM_004756.5(NUMBL):c.1612G>A (p.Gly538Arg)not specified [RCV004158885]uncertain significance194066768640667686Humanname
156038521CV2313649single nucleotide variantNM_004756.5(NUMBL):c.1477G>A (p.Ala493Thr)not specified [RCV004157580]likely benign194066782140667821Humanname
156175381CV2327017single nucleotide variantNM_004756.5(NUMBL):c.1174G>T (p.Gly392Cys)not specified [RCV004178607]uncertain significance194066812440668124Humanname
156155329CV2371250single nucleotide variantNM_004756.5(NUMBL):c.1621C>A (p.Pro541Thr)not specified [RCV004220987]uncertain significance194066767740667677Humanname
156036567CV2373996single nucleotide variantNM_004756.5(NUMBL):c.1519G>A (p.Val507Met)not specified [RCV004227126]uncertain significance194066777940667779Humanname
156002031CV2378881single nucleotide variantNM_004756.5(NUMBL):c.1484C>T (p.Pro495Leu)not specified [RCV004231315]uncertain significance194066781440667814Humanname
156005855CV2394065single nucleotide variantNM_004756.5(NUMBL):c.1613G>A (p.Gly538Glu)not specified [RCV004236281]uncertain significance194066768540667685Humanname
156156858CV2397911single nucleotide variantNM_004756.5(NUMBL):c.1619T>C (p.Phe540Ser)not specified [RCV004241524]uncertain significance194066767940667679Humanname
401782182CV2686577single nucleotide variantNM_004756.5(NUMBL):c.1681C>A (p.Pro561Thr)not specified [RCV004300007]uncertain significance194066761740667617Humanname
401894156CV2770362single nucleotide variantNM_004756.5(NUMBL):c.1009C>T (p.Arg337Cys)not specified [RCV004358013]uncertain significance194067337140673371Humanname
405730485CV3356024single nucleotide variantNM_004756.5(NUMBL):c.1385C>A (p.Pro462His)not specified [RCV004496320]uncertain significance194066791340667913Humanname
405730499CV3356026single nucleotide variantNM_004756.5(NUMBL):c.1777C>T (p.Pro593Ser)not specified [RCV004496322]uncertain significance194066752140667521Humanname
407521905CV3462357single nucleotide variantNM_004756.5(NUMBL):c.1622C>T (p.Pro541Leu)not specified [RCV004652679]uncertain significance194066767640667676Humanname
597644514CV3573694single nucleotide variantNM_004756.5(NUMBL):c.1798G>A (p.Asp600Asn)not specified [RCV004832681]uncertain significance194066750040667500Humanname
597663149CV3573695single nucleotide variantNM_004756.5(NUMBL):c.1393G>A (p.Ala465Thr)not specified [RCV004835290]uncertain significance194066790540667905Humanname
597663158CV3573696single nucleotide variantNM_004756.5(NUMBL):c.1667G>A (p.Arg556His)not specified [RCV004835291]uncertain significance194066763140667631Humanname
597663165CV3573697single nucleotide variantNM_004756.5(NUMBL):c.1819A>G (p.Ile607Val)not specified [RCV004835292]uncertain significance194066747940667479Humanname
597663181CV3573699single nucleotide variantNM_004756.5(NUMBL):c.1661G>T (p.Arg554Leu)not specified [RCV004835294]uncertain significance194066763740667637Humanname
597663190CV3573700single nucleotide variantNM_004756.5(NUMBL):c.1628C>G (p.Pro543Arg)not specified [RCV004835295]uncertain significance194066767040667670Humanname
597663197CV3573701single nucleotide variantNM_004756.5(NUMBL):c.1189C>T (p.Pro397Ser)not specified [RCV004835296]uncertain significance194066810940668109Humanname
598234340CV4004600single nucleotide variantNM_004756.5(NUMBL):c.1510C>T (p.Arg504Trp)not specified [RCV005381852]uncertain significance194066778840667788Humanname
598234359CV4004603single nucleotide variantNM_004756.5(NUMBL):c.1592C>T (p.Ala531Val)not specified [RCV005381855]uncertain significance194066770640667706Humanname
598234373CV4004605single nucleotide variantNM_004756.5(NUMBL):c.1126G>A (p.Ala376Thr)not specified [RCV005381857]uncertain significance194066993140669931Humanname
598234382CV4004606single nucleotide variantNM_004756.5(NUMBL):c.1417G>A (p.Ala473Thr)not specified [RCV005381858]uncertain significance194066788140667881Humanname