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Variants search result for Homo sapiens
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27 records found for search term Tnfaip6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597673402CV3620700single nucleotide variantNM_007115.4(TNFAIP6):c.4A>T (p.Ile2Phe)not specified [RCV004882750]uncertain significance2151357670151357670Humanname
597673427CV3620703single nucleotide variantNM_007115.4(TNFAIP6):c.6C>G (p.Ile2Met)not specified [RCV004882753]uncertain significance2151357672151357672Humanname
156399159CV2204952single nucleotide variantNM_007115.4(TNFAIP6):c.31C>G (p.Leu11Val)not specified [RCV004077576]uncertain significance2151357697151357697Humanname
401748108CV2700004single nucleotide variantNM_007115.4(TNFAIP6):c.98G>T (p.Arg33Leu)not specified [RCV004310433]uncertain significance2151363946151363946Humanname
598229113CV3935087single nucleotide variantNM_007115.4(TNFAIP6):c.77A>G (p.His26Arg)not specified [RCV005294835]uncertain significance2151357743151357743Humanname
329401162CV2446206single nucleotide variantNM_007115.4(TNFAIP6):c.128G>T (p.Arg43Leu)not specified [RCV004264607]uncertain significance2151363976151363976Humanname
401897395CV2786975single nucleotide variantNM_007115.4(TNFAIP6):c.269G>A (p.Gly90Asp)not specified [RCV004366104]uncertain significance2151366092151366092Humanname
405787159CV3339842single nucleotide variantNM_007115.4(TNFAIP6):c.124G>C (p.Ala42Pro)not specified [RCV004473078]uncertain significance2151363972151363972Humanname
405787164CV3339843single nucleotide variantNM_007115.4(TNFAIP6):c.144G>T (p.Lys48Asn)not specified [RCV004473079]uncertain significance2151363992151363992Humanname
405787169CV3339844single nucleotide variantNM_007115.4(TNFAIP6):c.193C>G (p.Leu65Val)not specified [RCV004473080]uncertain significance2151364041151364041Humanname
598229106CV3935086single nucleotide variantNM_007115.4(TNFAIP6):c.208C>A (p.Gln70Lys)not specified [RCV005294834]uncertain significance2151364056151364056Humanname
156139563CV2280757single nucleotide variantNM_007115.4(TNFAIP6):c.778A>T (p.Ser260Cys)not specified [RCV004145023]uncertain significance2151379477151379477Humanname
156281214CV2288728single nucleotide variantNM_007115.4(TNFAIP6):c.505T>C (p.Tyr169His)not specified [RCV004147953]uncertain significance2151370130151370130Humanname
401753181CV2674805single nucleotide variantNM_007115.4(TNFAIP6):c.739A>G (p.Met247Val)not specified [RCV004294084]likely benign2151379438151379438Humanname
405787179CV3339846single nucleotide variantNM_007115.4(TNFAIP6):c.402G>C (p.Glu134Asp)not specified [RCV004473082]uncertain significance2151370027151370027Humanname
405787183CV3339847single nucleotide variantNM_007115.4(TNFAIP6):c.412G>A (p.Val138Ile)not specified [RCV004473083]uncertain significance2151370037151370037Humanname
405787187CV3339848single nucleotide variantNM_007115.4(TNFAIP6):c.515G>A (p.Arg172His)not specified [RCV004473084]likely benign2151370140151370140Humanname
405787191CV3339849single nucleotide variantNM_007115.4(TNFAIP6):c.634G>A (p.Asp212Asn)not specified [RCV004473085]uncertain significance2151373559151373559Humanname
407527547CV3479166single nucleotide variantNM_007115.4(TNFAIP6):c.559G>A (p.Gly187Ser)not specified [RCV004680049]uncertain significance2151370184151370184Humanname
407459006CV3479167single nucleotide variantNM_007115.4(TNFAIP6):c.818G>T (p.Arg273Ile)not specified [RCV004687003]uncertain significance2151379517151379517Humanname
597673382CV3620698single nucleotide variantNM_007115.4(TNFAIP6):c.767G>A (p.Gly256Glu)not specified [RCV004882748]uncertain significance2151379466151379466Humanname
597673393CV3620699single nucleotide variantNM_007115.4(TNFAIP6):c.346C>T (p.Arg116Cys)not specified [RCV004882749]uncertain significance2151366169151366169Humanname
597673411CV3620701single nucleotide variantNM_007115.4(TNFAIP6):c.391C>T (p.His131Tyr)not specified [RCV004882751]uncertain significance2151366214151366214Humanname
597673419CV3620702single nucleotide variantNM_007115.4(TNFAIP6):c.550G>T (p.Asp184Tyr)not specified [RCV004882752]uncertain significance2151370175151370175Humanname
597673435CV3620704single nucleotide variantNM_007115.4(TNFAIP6):c.551A>G (p.Asp184Gly)not specified [RCV004882754]uncertain significance2151370176151370176Humanname
598253188CV3935088single nucleotide variantNM_007115.4(TNFAIP6):c.421G>A (p.Asp141Asn)not specified [RCV005278207]uncertain significance2151370046151370046Humanname
598229119CV3935089single nucleotide variantNM_007115.4(TNFAIP6):c.688C>A (p.Leu230Ile)not specified [RCV005294836]uncertain significance2151379387151379387Humanname