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Variants search result for Homo sapiens
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21 records found for search term Stx17
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156103582CV2260517single nucleotide variantNM_017919.3(STX17):c.7G>A (p.Glu3Lys)not specified [RCV004123300]uncertain significance99991524699915246Humanname
156328957CV2332331single nucleotide variantNM_017919.3(STX17):c.31C>T (p.Arg11Cys)not specified [RCV004182498]uncertain significance99991527099915270Humanname
156206534CV2385330single nucleotide variantNM_017919.3(STX17):c.35G>A (p.Arg12His)not specified [RCV004230606]uncertain significance99991527499915274Humanname
407496787CV3481729single nucleotide variantNM_017919.3(STX17):c.77C>T (p.Pro26Leu)not specified [RCV004668233]uncertain significance99991531699915316Humanname
156086119CV2205707single nucleotide variantNM_017919.3(STX17):c.178C>T (p.Arg60Cys)not specified [RCV004075768]uncertain significance99992883299928832Humanname
156280284CV2295026single nucleotide variantNM_017919.3(STX17):c.122A>G (p.Lys41Arg)not specified [RCV004156152]uncertain significance99991536199915361Humanname
156284913CV2360717single nucleotide variantNM_017919.3(STX17):c.239G>A (p.Arg80Gln)not specified [RCV004213506]uncertain significance99995110999951109Humanname
401742496CV2715244single nucleotide variantNM_017919.3(STX17):c.104A>G (p.His35Arg)not specified [RCV004324593]uncertain significance99991534399915343Humanname
405780667CV3331029single nucleotide variantNM_017919.3(STX17):c.155A>G (p.His52Arg)not specified [RCV004458607]uncertain significance99992880999928809Humanname
597758446CV3615162single nucleotide variantNM_017919.3(STX17):c.260T>G (p.Leu87Arg)not specified [RCV004868824]uncertain significance99995113099951130Humanname
156282099CV2295171single nucleotide variantNM_017919.3(STX17):c.739A>T (p.Ile247Phe)not specified [RCV004158268]uncertain significance99996850399968503Humanname
156065164CV2316319single nucleotide variantNM_017919.3(STX17):c.453G>T (p.Gln151His)not specified [RCV004174335]uncertain significance99995995499959954Humanname
155978324CV2321447single nucleotide variantNM_017919.3(STX17):c.850G>A (p.Glu284Lys)not specified [RCV004177425]uncertain significance99996861499968614Humanname
156119493CV2354074single nucleotide variantNM_017919.3(STX17):c.571C>T (p.Leu191Phe)not specified [RCV004206515]uncertain significance99996014499960144Humanname
401773589CV2709395single nucleotide variantNM_017919.3(STX17):c.718G>T (p.Gly240Trp)not specified [RCV004316531]uncertain significance99996848299968482Humanname
401723419CV2724894single nucleotide variantNM_017919.3(STX17):c.656A>G (p.Lys219Arg)not specified [RCV004319669]uncertain significance99996772699967726Humanname
405780671CV3331030single nucleotide variantNM_017919.3(STX17):c.745C>A (p.Leu249Ile)not specified [RCV004458608]uncertain significance99996850999968509Humanname
407496791CV3481730single nucleotide variantNM_017919.3(STX17):c.793G>A (p.Gly265Arg)not specified [RCV004668234]uncertain significance99996855799968557Humanname
407530171CV3481731single nucleotide variantNM_017919.3(STX17):c.739A>G (p.Ile247Val)not specified [RCV004681714]uncertain significance99996850399968503Humanname
407496796CV3481732single nucleotide variantNM_017919.3(STX17):c.383A>G (p.Gln128Arg)not specified [RCV004668235]uncertain significance99995125399951253Humanname
597794504CV3615161single nucleotide variantNM_017919.3(STX17):c.337G>A (p.Val113Ile)not specified [RCV004877875]uncertain significance99995120799951207Humanname