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39 records found for search term Mboat2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8577648CV112024single nucleotide variantNM_138799.2(MBOAT2):c.395+4637A>TLung cancer [RCV000092547]uncertain significance289039848903984Humanname
156081150CV2244301single nucleotide variantNM_138799.4(MBOAT2):c.128G>A (p.Arg43Gln)not specified [RCV004100290]uncertain significance289585908958590Humanname
156400172CV2199017single nucleotide variantNM_138799.4(MBOAT2):c.343G>A (p.Val115Ile)not specified [RCV004080424]likely benign289086738908673Humanname
156096062CV2210363single nucleotide variantNM_138799.4(MBOAT2):c.811C>A (p.Pro271Thr)not specified [RCV004089514]uncertain significance288731808873180Humanname
155930513CV2224755single nucleotide variantNM_138799.4(MBOAT2):c.674C>A (p.Thr225Lys)not specified [RCV004092579]uncertain significance288770468877046Humanname
156292834CV2306272single nucleotide variantNM_138799.4(MBOAT2):c.323G>T (p.Gly108Val)not specified [RCV004162995]uncertain significance289086938908693Humanname
156062608CV2355643single nucleotide variantNM_138799.4(MBOAT2):c.947G>T (p.Arg316Leu)not specified [RCV004198603]uncertain significance288684868868486Humanname
156303434CV2359344single nucleotide variantNM_138799.4(MBOAT2):c.460C>T (p.Arg154Trp)not specified [RCV004212624]uncertain significance288825578882557Humanname
329389969CV2457380single nucleotide variantNM_138799.4(MBOAT2):c.814A>G (p.Thr272Ala)not specified [RCV004267211]uncertain significance288731778873177Humanname
329352721CV2470375single nucleotide variantNM_138799.4(MBOAT2):c.995C>T (p.Thr332Ile)not specified [RCV004279757]uncertain significance288642278864227Humanname
401892228CV2776014single nucleotide variantNM_138799.4(MBOAT2):c.673A>G (p.Thr225Ala)not specified [RCV004353125]likely benign288770478877047Humanname
405668295CV3278231single nucleotide variantNM_138799.4(MBOAT2):c.743T>G (p.Leu248Trp)not specified [RCV004418976]uncertain significance288732488873248Humanname
405668300CV3278232single nucleotide variantNM_138799.4(MBOAT2):c.820A>G (p.Ile274Val)not specified [RCV004418977]likely benign288731718873171Humanname
405668305CV3278233single nucleotide variantNM_138799.4(MBOAT2):c.946C>T (p.Arg316Cys)not specified [RCV004418978]uncertain significance288684878868487Humanname
597647095CV3694603single nucleotide variantNM_138799.4(MBOAT2):c.704A>G (p.Gln235Arg)not specified [RCV004942609]uncertain significance288732878873287Humanname
597647119CV3694606single nucleotide variantNM_138799.4(MBOAT2):c.847G>T (p.Ala283Ser)not specified [RCV004942612]uncertain significance288731448873144Humanname
597647126CV3694607single nucleotide variantNM_138799.4(MBOAT2):c.518G>A (p.Ser173Asn)not specified [RCV004942613]uncertain significance288772028877202Humanname
597647149CV3694610single nucleotide variantNM_138799.4(MBOAT2):c.998G>T (p.Ser333Ile)not specified [RCV004942616]uncertain significance288642248864224Humanname
597647157CV3694611single nucleotide variantNM_138799.4(MBOAT2):c.930C>A (p.Asp310Glu)not specified [RCV004942617]uncertain significance288685038868503Humanname
597647181CV3694614single nucleotide variantNM_138799.4(MBOAT2):c.596T>G (p.Ile199Ser)not specified [RCV004942620]uncertain significance288771248877124Humanname
597647203CV3694617single nucleotide variantNM_138799.4(MBOAT2):c.974T>C (p.Ile325Thr)not specified [RCV004942623]uncertain significance288684598868459Humanname
598209980CV3981943single nucleotide variantNM_138799.4(MBOAT2):c.298A>G (p.Asn100Asp)not specified [RCV005377790]uncertain significance289431888943188Humanname
598209987CV3981944single nucleotide variantNM_138799.4(MBOAT2):c.667G>A (p.Glu223Lys)not specified [RCV005377791]uncertain significance288770538877053Humanname
155960018CV2194111single nucleotide variantNM_138799.4(MBOAT2):c.1007T>A (p.Met336Lys)not specified [RCV004076867]uncertain significance288642158864215Humanname
156201488CV2363032single nucleotide variantNM_138799.4(MBOAT2):c.1402A>G (p.Thr468Ala)not specified [RCV004211166]uncertain significance288588408858840Humanname
156114846CV2397214single nucleotide variantNM_138799.4(MBOAT2):c.1276A>G (p.Ile426Val)not specified [RCV004238751]uncertain significance288606748860674Humanname
401749802CV2719404single nucleotide variantNM_138799.4(MBOAT2):c.1396A>G (p.Lys466Glu)not specified [RCV004326811]uncertain significance288588468858846Humanname
405668279CV3278228single nucleotide variantNM_138799.4(MBOAT2):c.1054G>C (p.Val352Leu)not specified [RCV004418973]uncertain significance288627218862721Humanname
405668285CV3278229single nucleotide variantNM_138799.4(MBOAT2):c.1517A>G (p.Asn506Ser)not specified [RCV004418974]likely benign288587258858725Humanname
407472993CV3457112single nucleotide variantNM_138799.4(MBOAT2):c.1382T>C (p.Leu461Ser)not specified [RCV004637768]uncertain significance288588608858860Humanname
407472997CV3457113single nucleotide variantNM_138799.4(MBOAT2):c.1538C>T (p.Ser513Leu)not specified [RCV004637769]uncertain significance288587048858704Humanname
597647111CV3694605single nucleotide variantNM_138799.4(MBOAT2):c.1547C>T (p.Ser516Leu)not specified [RCV004942611]uncertain significance288586958858695Humanname
597647134CV3694608single nucleotide variantNM_138799.4(MBOAT2):c.1102C>T (p.Leu368Phe)not specified [RCV004942614]uncertain significance288626738862673Humanname
597647141CV3694609single nucleotide variantNM_138799.4(MBOAT2):c.1084A>G (p.Thr362Ala)not specified [RCV004942615]uncertain significance288626918862691Humanname
597647164CV3694612single nucleotide variantNM_138799.4(MBOAT2):c.1451A>G (p.Lys484Arg)not specified [RCV004942618]uncertain significance288587918858791Humanname
597647173CV3694613single nucleotide variantNM_138799.4(MBOAT2):c.1065A>T (p.Glu355Asp)not specified [RCV004942619]uncertain significance288627108862710Humanname
597647196CV3694616single nucleotide variantNM_138799.4(MBOAT2):c.1328C>A (p.Thr443Lys)not specified [RCV004942622]uncertain significance288606228860622Humanname
597647208CV3694618single nucleotide variantNM_138799.4(MBOAT2):c.1318C>G (p.Pro440Ala)not specified [RCV004942624]uncertain significance288606328860632Humanname
598177979CV3981945single nucleotide variantNM_138799.4(MBOAT2):c.1411A>G (p.Arg471Gly)not specified [RCV005371703]likely benign288588318858831Humanname