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Variants search result for Homo sapiens
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12 records found for search term Tspan13
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401925610CV2828326single nucleotide variantNM_014399.4(TSPAN13):c.42C>T (p.Cys14=)not provided [RCV003436662]likely benign71675400916754009Humanname
156167001CV2279725single nucleotide variantNM_014399.4(TSPAN13):c.274G>A (p.Val92Ile)not specified [RCV004144340]uncertain significance71677708416777084Humanname
156012443CV2358902single nucleotide variantNM_014399.4(TSPAN13):c.131G>C (p.Arg44Pro)not specified [RCV004212241]uncertain significance71677627816776278Humanname
407528584CV3487041single nucleotide variantNM_014399.4(TSPAN13):c.112G>C (p.Gly38Arg)not specified [RCV004680455]uncertain significance71677625916776259Humanname
597788225CV3618038single nucleotide variantNM_014399.4(TSPAN13):c.152C>T (p.Ala51Val)not specified [RCV004875809]uncertain significance71677629916776299Humanname
598238271CV3928775single nucleotide variantNM_014399.4(TSPAN13):c.259A>G (p.Ile87Val)not specified [RCV005296387]uncertain significance71677706916777069Humanname
155917966CV2236698single nucleotide variantNM_014399.4(TSPAN13):c.439A>G (p.Ser147Gly)not specified [RCV004110653]uncertain significance71677901516779015Humanname
156362915CV2265632single nucleotide variantNM_014399.4(TSPAN13):c.317A>G (p.Gln106Arg)not specified [RCV004124360]uncertain significance71677780216777802Humanname
329372510CV2455246single nucleotide variantNM_014399.4(TSPAN13):c.403A>C (p.Asn135His)not specified [RCV004274465]uncertain significance71677788816777888Humanname
405798700CV3340874single nucleotide variantNM_014399.4(TSPAN13):c.469A>C (p.Ile157Leu)not specified [RCV004476619]uncertain significance71677904516779045Humanname
598238257CV3928773single nucleotide variantNM_014399.4(TSPAN13):c.502T>A (p.Phe168Ile)not specified [RCV005296385]uncertain significance71677907816779078Humanname
598238263CV3928774single nucleotide variantNM_014399.4(TSPAN13):c.485C>A (p.Ala162Asp)not specified [RCV005296386]uncertain significance71677906116779061Humanname