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30 records found for search term Tmem171
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329361800CV2468325single nucleotide variantNM_173490.8(TMEM171):c.96G>T (p.Leu32Phe)not specified [RCV004275874]uncertain significance57312346973123469Humanname
407453406CV3486440single nucleotide variantNM_173490.8(TMEM171):c.77T>G (p.Phe26Cys)not specified [RCV004684533]uncertain significance57312345073123450Humanname
15176432CV709993single nucleotide variantNM_173490.8(TMEM171):c.459A>G (p.Ser153=)not provided [RCV000973185]benign57312383273123832Humanname
156267730CV2198844single nucleotide variantNM_173490.8(TMEM171):c.257G>T (p.Arg86Leu)not specified [RCV004077881]uncertain significance57312363073123630Humanname
155979774CV2263577single nucleotide variantNM_173490.8(TMEM171):c.130T>C (p.Phe44Leu)not specified [RCV004133800]uncertain significance57312350373123503Humanname
156188203CV2302843single nucleotide variantNM_173490.8(TMEM171):c.296G>T (p.Arg99Leu)not specified [RCV004162743]uncertain significance57312366973123669Humanname
156289183CV2333078single nucleotide variantNM_173490.8(TMEM171):c.266T>C (p.Leu89Pro)not specified [RCV004194373]uncertain significance57312363973123639Humanname
156192554CV2356985single nucleotide variantNM_173490.8(TMEM171):c.179A>G (p.Lys60Arg)not specified [RCV004204350]uncertain significance57312355273123552Humanname
401779643CV2676640single nucleotide variantNM_173490.8(TMEM171):c.121A>T (p.Ile41Phe)not specified [RCV004282599]uncertain significance57312349473123494Humanname
405794789CV3336082single nucleotide variantNM_173490.8(TMEM171):c.119C>T (p.Ser40Phe)not specified [RCV004475327]uncertain significance57312349273123492Humanname
405794792CV3336083single nucleotide variantNM_173490.8(TMEM171):c.184G>T (p.Ala62Ser)not specified [RCV004475328]uncertain significance57312355773123557Humanname
405794795CV3336084single nucleotide variantNM_173490.8(TMEM171):c.269A>T (p.Gln90Leu)not specified [RCV004475329]likely benign57312364273123642Humanname
597753257CV3613515single nucleotide variantNM_173490.8(TMEM171):c.139T>A (p.Cys47Ser)not specified [RCV004867330]uncertain significance57312351273123512Humanname
156120054CV2233596single nucleotide variantNM_173490.8(TMEM171):c.466C>G (p.Arg156Gly)not specified [RCV004100066]uncertain significance57312383973123839Humanname
156034050CV2236455single nucleotide variantNM_173490.8(TMEM171):c.314A>C (p.Glu105Ala)not specified [RCV004108124]uncertain significance57312368773123687Humanname
156234118CV2245319single nucleotide variantNM_173490.8(TMEM171):c.647C>T (p.Ser216Leu)not specified [RCV004107073]uncertain significance57312839673128396Humanname
155964001CV2261558single nucleotide variantNM_173490.8(TMEM171):c.416A>T (p.Asn139Ile)not specified [RCV004125893]uncertain significance57312378973123789Humanname
156281292CV2295104single nucleotide variantNM_173490.8(TMEM171):c.449C>T (p.Thr150Ile)not specified [RCV004156208]uncertain significance57312382273123822Humanname
156288929CV2299265single nucleotide variantNM_173490.8(TMEM171):c.382G>A (p.Val128Ile)not specified [RCV004152593]likely benign57312375573123755Humanname
401779929CV2676738single nucleotide variantNM_173490.8(TMEM171):c.535G>C (p.Val179Leu)not specified [RCV004290912]uncertain significance57312390873123908Humanname
405794798CV3336085single nucleotide variantNM_173490.8(TMEM171):c.413C>G (p.Ser138Cys)not specified [RCV004475330]uncertain significance57312378673123786Humanname
405794801CV3336086single nucleotide variantNM_173490.8(TMEM171):c.786G>C (p.Arg262Ser)not specified [RCV004475331]uncertain significance57313154173131541Humanname
405794804CV3336087single nucleotide variantNM_173490.8(TMEM171):c.851C>T (p.Thr284Met)not specified [RCV004475332]uncertain significance57313160673131606Humanname
405794808CV3336088single nucleotide variantNM_173490.8(TMEM171):c.890C>T (p.Pro297Leu)not specified [RCV004475333]uncertain significance57313164573131645Humanname
407453402CV3486439single nucleotide variantNM_173490.8(TMEM171):c.834A>G (p.Ile278Met)not specified [RCV004684532]uncertain significance57313158973131589Humanname
597753262CV3613516single nucleotide variantNM_173490.8(TMEM171):c.340A>C (p.Ile114Leu)not specified [RCV004867331]uncertain significance57312371373123713Humanname
598213349CV3917474single nucleotide variantNM_173490.8(TMEM171):c.688G>A (p.Glu230Lys)not specified [RCV005292300]uncertain significance57312843773128437Humanname
598213354CV3917475single nucleotide variantNM_173490.8(TMEM171):c.749A>C (p.Asn250Thr)not specified [RCV005292301]uncertain significance57312849873128498Humanname
598213360CV3917476single nucleotide variantNM_173490.8(TMEM171):c.646T>C (p.Ser216Pro)not specified [RCV005292302]uncertain significance57312839573128395Humanname
598178413CV3917477single nucleotide variantNM_173490.8(TMEM171):c.847G>C (p.Gly283Arg)not specified [RCV005285973]likely benign57313160273131602Humanname