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Variants search result for Homo sapiens
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54 records found for search term Cpeb3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8652412CV128987single nucleotide variantNM_001178137.1(CPEB3):c.1005+13389G>TLung cancer [RCV000109474]uncertain significance109222595792225957Humanname
405696725CV3245498single nucleotide variantNM_014912.5(CPEB3):c.14T>C (p.Leu5Ser)not specified [RCV004374422]uncertain significance109224033792240337Humanname
598246230CV3945235single nucleotide variantNM_014912.5(CPEB3):c.35C>A (p.Thr12Asn)not specified [RCV005322290]uncertain significance109224031692240316Humanname
15146513CV712510single nucleotide variantNM_014912.5(CPEB3):c.840C>T (p.Val280=)not provided [RCV000967174]benign109223951192239511Humanname
156365495CV2272121single nucleotide variantNM_014912.5(CPEB3):c.101A>G (p.Glu34Gly)not specified [RCV004124904]uncertain significance109224025092240250Humanname
155915018CV2339046single nucleotide variantNM_014912.5(CPEB3):c.277C>T (p.Pro93Ser)not specified [RCV004187093]uncertain significance109224007492240074Humanname
329357250CV2431300single nucleotide variantNM_014912.5(CPEB3):c.187C>G (p.Pro63Ala)not specified [RCV004252423]uncertain significance109224016492240164Humanname
329356737CV2460513single nucleotide variantNM_014912.5(CPEB3):c.218T>C (p.Met73Thr)not specified [RCV004268799]uncertain significance109224013392240133Humanname
329377642CV2462776single nucleotide variantNM_014912.5(CPEB3):c.182C>T (p.Ala61Val)not specified [RCV004278695]uncertain significance109224016992240169Humanname
401888511CV2785039single nucleotide variantNM_014912.5(CPEB3):c.290C>T (p.Ala97Val)not specified [RCV004355057]uncertain significance109224006192240061Humanname
407457036CV3419606single nucleotide variantNM_014912.5(CPEB3):c.190G>A (p.Ala64Thr)not specified [RCV004611000]uncertain significance109224016192240161Humanname
407457041CV3419608single nucleotide variantNM_014912.5(CPEB3):c.203C>A (p.Pro68Gln)not specified [RCV004611002]uncertain significance109224014892240148Humanname
407457044CV3419609single nucleotide variantNM_014912.5(CPEB3):c.266A>C (p.Gln89Pro)not specified [RCV004611003]uncertain significance109224008592240085Humanname
597650964CV3651047single nucleotide variantNM_014912.5(CPEB3):c.269C>A (p.Pro90Gln)not specified [RCV004910519]uncertain significance109224008292240082Humanname
597650985CV3651050single nucleotide variantNM_014912.5(CPEB3):c.287C>G (p.Pro96Arg)not specified [RCV004910522]uncertain significance109224006492240064Humanname
597651002CV3651052single nucleotide variantNM_014912.5(CPEB3):c.116C>G (p.Pro39Arg)not specified [RCV004910524]uncertain significance109224023592240235Humanname
598246252CV3945238single nucleotide variantNM_014912.5(CPEB3):c.130A>T (p.Thr44Ser)not specified [RCV005322293]uncertain significance109224022192240221Humanname
156134390CV2196023single nucleotide variantNM_014912.5(CPEB3):c.646A>G (p.Met216Val)not specified [RCV004072266]uncertain significance109223970592239705Humanname
156122370CV2227124single nucleotide variantNM_014912.5(CPEB3):c.826G>A (p.Val276Met)not specified [RCV004091744]uncertain significance109223952592239525Humanname
156253757CV2232550single nucleotide variantNM_014912.5(CPEB3):c.759C>A (p.Ser253Arg)not specified [RCV004099147]uncertain significance109223959292239592Humanname
156182786CV2255271single nucleotide variantNM_014912.5(CPEB3):c.677T>C (p.Val226Ala)not specified [RCV004117657]likely benign109223967492239674Humanname
155952334CV2306072single nucleotide variantNM_014912.5(CPEB3):c.593A>G (p.Gln198Arg)not specified [RCV004162838]uncertain significance109223975892239758Humanname
156278271CV2328444single nucleotide variantNM_014912.5(CPEB3):c.615C>G (p.Ser205Arg)not specified [RCV004175542]uncertain significance109223973692239736Humanname
156035669CV2338947single nucleotide variantNM_014912.5(CPEB3):c.311C>T (p.Ser104Leu)not specified [RCV004184536]uncertain significance109224004092240040Humanname
156148482CV2394492single nucleotide variantNM_014912.5(CPEB3):c.541C>A (p.Pro181Thr)not specified [RCV004240851]uncertain significance109223981092239810Humanname
329355439CV2445433single nucleotide variantNM_014912.5(CPEB3):c.453C>G (p.Phe151Leu)not specified [RCV004257495]uncertain significance109223989892239898Humanname
329387627CV2446733single nucleotide variantNM_014912.5(CPEB3):c.412A>G (p.Asn138Asp)not specified [RCV004253773]uncertain significance109223993992239939Humanname
329359213CV2450925single nucleotide variantNM_014912.5(CPEB3):c.844G>T (p.Val282Leu)not specified [RCV004267822]uncertain significance109223950792239507Humanname
329360014CV2462403single nucleotide variantNM_014912.5(CPEB3):c.352G>A (p.Ala118Thr)not specified [RCV004268162]uncertain significance109223999992239999Humanname
329389368CV2467299single nucleotide variantNM_014912.5(CPEB3):c.760G>C (p.Ala254Pro)not specified [RCV004285101]uncertain significance109223959192239591Humanname
405696715CV3245500single nucleotide variantNM_014912.5(CPEB3):c.328A>G (p.Thr110Ala)not specified [RCV004374424]uncertain significance109224002392240023Humanname
405696707CV3245501single nucleotide variantNM_014912.5(CPEB3):c.547C>G (p.Gln183Glu)not specified [RCV004374425]uncertain significance109223980492239804Humanname
405696700CV3245502single nucleotide variantNM_014912.5(CPEB3):c.772C>A (p.Pro258Thr)not specified [RCV004374426]uncertain significance109223957992239579Humanname
405696695CV3245503single nucleotide variantNM_014912.5(CPEB3):c.793G>A (p.Gly265Ser)not specified [RCV004374427]uncertain significance109223955892239558Humanname
597650957CV3651046single nucleotide variantNM_014912.5(CPEB3):c.826G>T (p.Val276Leu)not specified [RCV004910518]uncertain significance109223952592239525Humanname
597651012CV3651053single nucleotide variantNM_014912.5(CPEB3):c.512C>T (p.Pro171Leu)not specified [RCV004910525]uncertain significance109223983992239839Humanname
598246237CV3945236single nucleotide variantNM_014912.5(CPEB3):c.944A>G (p.Lys315Arg)not specified [RCV005322291]uncertain significance109223940792239407Humanname
598246245CV3945237single nucleotide variantNM_014912.5(CPEB3):c.449C>G (p.Thr150Ser)not specified [RCV005322292]uncertain significance109223990292239902Humanname
598246260CV3945239single nucleotide variantNM_014912.5(CPEB3):c.497C>G (p.Pro166Arg)not specified [RCV005322294]uncertain significance109223985492239854Humanname
156027940CV2195641single nucleotide variantNM_014912.5(CPEB3):c.1105T>C (p.Tyr369His)not specified [RCV004076008]uncertain significance109219253792192537Humanname
156178331CV2201584single nucleotide variantNM_014912.5(CPEB3):c.1006G>A (p.Asp336Asn)not specified [RCV004080073]uncertain significance109219263692192636Humanname
155903618CV2282262single nucleotide variantNM_014912.5(CPEB3):c.2042C>T (p.Pro681Leu)not specified [RCV004133102]uncertain significance109205226792052267Humanname
329382947CV2424605single nucleotide variantNM_014912.5(CPEB3):c.1402G>A (p.Val468Ile)not specified [RCV004254102]uncertain significance109214308092143080Humanname
401895863CV2769083single nucleotide variantNM_014912.5(CPEB3):c.2075A>C (p.His692Pro)not specified [RCV004348943]uncertain significance109205223492052234Humanname
401866758CV2772735single nucleotide variantNM_014912.5(CPEB3):c.1250A>G (p.Asp417Gly)not specified [RCV004357542]uncertain significance109214505892145058Humanname
405696278CV3245496single nucleotide variantNM_014912.5(CPEB3):c.1162G>A (p.Ala388Thr)not specified [RCV004374420]uncertain significance109219248092192480Humanname
405696286CV3245497single nucleotide variantNM_014912.5(CPEB3):c.1373C>T (p.Thr458Ile)not specified [RCV004374421]uncertain significance109214310992143109Humanname
405696720CV3245499single nucleotide variantNM_014912.5(CPEB3):c.2002G>T (p.Ala668Ser)not specified [RCV004374423]uncertain significance109205230792052307Humanname
407457039CV3419607single nucleotide variantNM_014912.5(CPEB3):c.1478A>G (p.Glu493Gly)not specified [RCV004611001]uncertain significance109211117092111170Humanname
597650971CV3651048single nucleotide variantNM_014912.5(CPEB3):c.1966G>A (p.Val656Ile)not specified [RCV004910520]uncertain significance109205234392052343Humanname
597650979CV3651049single nucleotide variantNM_014912.5(CPEB3):c.2066G>A (p.Arg689His)not specified [RCV004910521]uncertain significance109205224392052243Humanname
597650994CV3651051single nucleotide variantNM_014912.5(CPEB3):c.1282A>G (p.Thr428Ala)not specified [RCV004910523]uncertain significance109214502692145026Humanname
598246278CV3945242single nucleotide variantNM_014912.5(CPEB3):c.1144A>G (p.Met382Val)not specified [RCV005322297]uncertain significance109219249892192498Humanname
598246286CV3945243single nucleotide variantNM_014912.5(CPEB3):c.1682G>A (p.Arg561Gln)not specified [RCV005322298]uncertain significance109209183592091835Humanname