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20 records found for search term Ube2z
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8585383CV119969single nucleotide variantNM_023079.4(UBE2Z):c.390+403G>ALung cancer [RCV000100489]uncertain significance174891128348911283Humanname
155901658CV2242070single nucleotide variantNM_023079.5(UBE2Z):c.94G>A (p.Gly32Ser)not specified [RCV004109004]uncertain significance174890859748908597Humanname
156137627CV2280601single nucleotide variantNM_023079.5(UBE2Z):c.80T>G (p.Val27Gly)not specified [RCV004143080]uncertain significance174890858348908583Humanname
405799630CV3341358single nucleotide variantNM_023079.5(UBE2Z):c.76G>T (p.Gly26Cys)not specified [RCV004476911]uncertain significance174890857948908579Humanname
8636221CV91445single nucleotide variantNM_023079.4(UBE2Z):c.799C>T (p.Leu267=)Malignant melanoma [RCV000071543]not provided174892126848921268Humanname
155975746CV2211307single nucleotide variantNM_023079.5(UBE2Z):c.143C>T (p.Ala48Val)not specified [RCV004090237]uncertain significance174890864648908646Humanname
401718754CV2704790single nucleotide variantNM_023079.5(UBE2Z):c.170G>C (p.Gly57Ala)not specified [RCV004307384]uncertain significance174890867348908673Humanname
401868086CV2787735single nucleotide variantNM_023079.5(UBE2Z):c.245A>G (p.His82Arg)not specified [RCV004356649]uncertain significance174890874848908748Humanname
405799624CV3341356single nucleotide variantNM_023079.5(UBE2Z):c.164C>T (p.Ala55Val)not specified [RCV004476909]uncertain significance174890866748908667Humanname
407522761CV3491064single nucleotide variantNM_023079.5(UBE2Z):c.167G>C (p.Gly56Ala)not specified [RCV004677806]uncertain significance174890867048908670Humanname
597682662CV3625869single nucleotide variantNM_023079.5(UBE2Z):c.106G>T (p.Gly36Trp)not specified [RCV004883714]uncertain significance174890860948908609Humanname
598265137CV3928849single nucleotide variantNM_023079.5(UBE2Z):c.230C>T (p.Ala77Val)not specified [RCV005301663]uncertain significance174890873348908733Humanname
156226804CV2216050single nucleotide variantNM_023079.5(UBE2Z):c.793G>A (p.Glu265Lys)not specified [RCV004097085]uncertain significance174892126248921262Humanname
156389981CV2222916single nucleotide variantNM_023079.5(UBE2Z):c.866G>A (p.Arg289His)not specified [RCV004101728]uncertain significance174892290948922909Humanname
156152766CV2265939single nucleotide variantNM_023079.5(UBE2Z):c.538A>G (p.Asn180Asp)not specified [RCV004126784]uncertain significance174891298148912981Humanname
156204062CV2314047single nucleotide variantNM_023079.5(UBE2Z):c.892C>A (p.Gln298Lys)not specified [RCV004164328]uncertain significance174892293548922935Humanname
401749236CV2708512single nucleotide variantNM_023079.5(UBE2Z):c.394C>G (p.His132Asp)not specified [RCV004313600]uncertain significance174891283748912837Humanname
405799627CV3341357single nucleotide variantNM_023079.5(UBE2Z):c.376G>A (p.Val126Ile)not specified [RCV004476910]uncertain significance174891086648910866Humanname
407522758CV3491063single nucleotide variantNM_023079.5(UBE2Z):c.451G>C (p.Val151Leu)not specified [RCV004677805]uncertain significance174891289448912894Humanname
597682653CV3625870single nucleotide variantNM_023079.5(UBE2Z):c.361G>A (p.Val121Ile)not specified [RCV004883715]uncertain significance174891085148910851Humanname