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11 records found for search term Mafk
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405651084CV3281321single nucleotide variantNM_002360.4(MAFK):c.14C>G (p.Pro5Arg)not specified [RCV004413445]uncertain significance715392061539206Humanname
401753531CV2720792single nucleotide variantNM_002360.4(MAFK):c.50C>T (p.Ala17Val)not specified [RCV004329932]uncertain significance715399541539954Humanname
597623599CV3694009single nucleotide variantNM_002360.4(MAFK):c.52G>A (p.Gly18Ser)not specified [RCV004936616]uncertain significance715399561539956Humanname
401751075CV2700169single nucleotide variantNM_002360.4(MAFK):c.133A>T (p.Thr45Ser)not specified [RCV004310563]uncertain significance715400371540037Humanname
401751078CV2700170single nucleotide variantNM_002360.4(MAFK):c.148A>G (p.Thr50Ala)not specified [RCV004310564]uncertain significance715400521540052Humanname
401751082CV2700171single nucleotide variantNM_002360.4(MAFK):c.149C>T (p.Thr50Ile)not specified [RCV004310565]uncertain significance715400531540053Humanname
597646966CV3694008single nucleotide variantNM_002360.4(MAFK):c.206G>A (p.Arg69His)not specified [RCV004942567]uncertain significance715401101540110Humanname
598183763CV3992278single nucleotide variantNM_002360.4(MAFK):c.152G>A (p.Arg51His)not specified [RCV005372982]uncertain significance715400561540056Humanname
156006866CV2288952single nucleotide variantNM_002360.4(MAFK):c.389A>G (p.Lys130Arg)not specified [RCV004149917]uncertain significance715402931540293Humanname
407468732CV3449545single nucleotide variantNM_002360.4(MAFK):c.431A>G (p.Glu144Gly)not specified [RCV004636388]uncertain significance715403351540335Humanname
598164643CV3992279single nucleotide variantNM_002360.4(MAFK):c.406G>A (p.Val136Ile)not specified [RCV005369039]uncertain significance715403101540310Humanname