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10 records found for search term Ndufb6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598230931CV4004099single nucleotide variantNM_002493.5(NDUFB6):c.13A>G (p.Thr5Ala)not specified [RCV005381276]uncertain significance93257304832573048Humanname
405801350CV3348513single nucleotide variantNM_002493.5(NDUFB6):c.62G>T (p.Arg21Leu)not specified [RCV004477776]uncertain significance93257299932572999Humanname
401724202CV2681347single nucleotide variantNM_002493.5(NDUFB6):c.266A>G (p.His89Arg)not specified [RCV004291895]uncertain significance93257096732570967Humanname
407525995CV3454709single nucleotide variantNM_002493.5(NDUFB6):c.194A>G (p.Tyr65Cys)not specified [RCV004654647]uncertain significance93257103932571039Humanname
597669451CV3555619single nucleotide variantNM_002493.5(NDUFB6):c.115A>G (p.Lys39Glu)not specified [RCV004829561]uncertain significance93257294632572946Humanname
597669460CV3555620single nucleotide variantNM_002493.5(NDUFB6):c.128T>C (p.Met43Thr)not specified [RCV004829562]uncertain significance93257293332572933Humanname
598230939CV4004100single nucleotide variantNM_002493.5(NDUFB6):c.205A>G (p.Ile69Val)not specified [RCV005381277]uncertain significance93257102832571028Humanname
156068538CV2341051single nucleotide variantNM_002493.5(NDUFB6):c.316C>T (p.Pro106Ser)not specified [RCV004181534]uncertain significance93255891232558912Humanname
405801326CV3348500single nucleotide variantNM_002493.5(NDUFB6):c.308G>T (p.Arg103Ile)not specified [RCV004477763]uncertain significance93255892032558920Humanname
405801338CV3348506single nucleotide variantNM_002493.5(NDUFB6):c.352C>G (p.Pro118Ala)not specified [RCV004477769]uncertain significance93255391132553911Humanname