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Variants search result for All species
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23 records found for search term Ubxn7
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401942576CV2839664single nucleotide variantNM_015562.2(UBXN7):c.74-1G>Anot provided [RCV003456597]uncertain significance3196407394196407394Humanname
8578542CV112926single nucleotide variantNM_015562.1(UBXN7):c.73+6162G>TLung cancer [RCV000093449]uncertain significance3196426165196426165Humanname
329375748CV2468797single nucleotide variantNM_015562.2(UBXN7):c.80G>C (p.Ser27Thr)not specified [RCV004280113]uncertain significance3196407387196407387Humanname
407523167CV3491229single nucleotide variantNM_015562.2(UBXN7):c.35C>T (p.Ala12Val)not specified [RCV004677950]uncertain significance3196432365196432365Humanname
155971577CV2309314single nucleotide variantNM_015562.2(UBXN7):c.220G>C (p.Glu74Gln)not specified [RCV004165474]uncertain significance3196407247196407247Humanname
156211907CV2311658single nucleotide variantNM_015562.2(UBXN7):c.136G>A (p.Val46Ile)not specified [RCV004168753]uncertain significance3196407331196407331Humanname
401892079CV2777214single nucleotide variantNM_015562.2(UBXN7):c.158G>A (p.Gly53Glu)not specified [RCV004354247]uncertain significance3196407309196407309Humanname
405800422CV3337874single nucleotide variantNM_015562.2(UBXN7):c.223G>A (p.Glu75Lys)not specified [RCV004477261]uncertain significance3196403018196403018Humanname
597685215CV3622777single nucleotide variantNM_015562.2(UBXN7):c.167C>G (p.Ala56Gly)not specified [RCV004884023]uncertain significance3196407300196407300Humanname
156119275CV2219248single nucleotide variantNM_015562.2(UBXN7):c.994G>A (p.Val332Ile)not specified [RCV004095129]uncertain significance3196362528196362528Humanname
156070133CV2325054single nucleotide variantNM_015562.2(UBXN7):c.584A>G (p.Asn195Ser)not specified [RCV004175595]uncertain significance3196371927196371927Humanname
329396289CV2459487single nucleotide variantNM_015562.2(UBXN7):c.358C>T (p.Arg120Trp)not specified [RCV004276953]uncertain significance3196391923196391923Humanname
401721335CV2673681single nucleotide variantNM_015562.2(UBXN7):c.952T>A (p.Ser318Thr)not specified [RCV004282412]uncertain significance3196362570196362570Humanname
407523170CV3491230single nucleotide variantNM_015562.2(UBXN7):c.391A>G (p.Ile131Val)not specified [RCV004677951]uncertain significance3196391890196391890Humanname
597685233CV3622779single nucleotide variantNM_015562.2(UBXN7):c.305G>A (p.Arg102Gln)not specified [RCV004884025]uncertain significance3196393604196393604Humanname
597685243CV3622780single nucleotide variantNM_015562.2(UBXN7):c.479G>A (p.Cys160Tyr)not specified [RCV004884026]uncertain significance3196372032196372032Humanname
8630756CV85911single nucleotide variantNM_015562.1(UBXN7):c.795T>G (p.Asp265Glu)Malignant melanoma [RCV000065995]not provided3196368067196368067Humanname
156363529CV2265756single nucleotide variantNM_015562.2(UBXN7):c.1207G>C (p.Val403Leu)not specified [RCV004124464]uncertain significance3196362315196362315Humanname
405800420CV3337873single nucleotide variantNM_015562.2(UBXN7):c.1214G>A (p.Gly405Glu)not specified [RCV004477260]uncertain significance3196362308196362308Humanname
407523475CV3491231single nucleotide variantNM_015562.2(UBXN7):c.1216A>G (p.Ile406Val)not specified [RCV004677952]uncertain significance3196362306196362306Humanname
597685225CV3622778single nucleotide variantNM_015562.2(UBXN7):c.1379G>A (p.Arg460Gln)not specified [RCV004884024]uncertain significance3196356776196356776Humanname
598265893CV3929135single nucleotide variantNM_015562.2(UBXN7):c.1073G>A (p.Arg358Lys)not specified [RCV005301817]uncertain significance3196362449196362449Humanname
598265899CV3929136single nucleotide variantNM_015562.2(UBXN7):c.1034C>T (p.Ala345Val)not specified [RCV005301818]uncertain significance3196362488196362488Humanname