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15 records found for search term Shisa5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156061049CV2236058single nucleotide variantNM_016479.6(SHISA5):c.247G>A (p.Val83Ile)not specified [RCV004114218]uncertain significance34847924448479244Humanname
155986163CV2345471single nucleotide variantNM_016479.6(SHISA5):c.274G>A (p.Ala92Thr)not specified [RCV004198240]uncertain significance34847921748479217Humanname
156149841CV2265377single nucleotide variantNM_016479.6(SHISA5):c.460G>A (p.Val154Met)not specified [RCV004128259]uncertain significance34846954448469544Humanname
156283315CV2288887single nucleotide variantNM_016479.6(SHISA5):c.572A>G (p.Tyr191Cys)not specified [RCV004148076]uncertain significance34846943248469432Humanname
156057568CV2322860single nucleotide variantNM_016479.6(SHISA5):c.419G>A (p.Arg140His)not specified [RCV004185319]uncertain significance34846973948469739Humanname
156325694CV2335345single nucleotide variantNM_016479.6(SHISA5):c.472C>T (p.Pro158Ser)not specified [RCV004186905]uncertain significance34846953248469532Humanname
156160798CV2371305single nucleotide variantNM_016479.6(SHISA5):c.620C>T (p.Pro207Leu)not specified [RCV004223317]uncertain significance34846938448469384Humanname
401720170CV2705739single nucleotide variantNM_016479.6(SHISA5):c.497C>T (p.Pro166Leu)not specified [RCV004318579]uncertain significance34846950748469507Humanname
405731376CV3314473single nucleotide variantNM_016479.6(SHISA5):c.403C>A (p.Leu135Ile)not specified [RCV004451058]uncertain significance34846975548469755Humanname
405731385CV3314474single nucleotide variantNM_016479.6(SHISA5):c.413C>T (p.Thr138Met)not specified [RCV004451059]likely benign34846974548469745Humanname
405731391CV3314475single nucleotide variantNM_016479.6(SHISA5):c.577A>G (p.Met193Val)not specified [RCV004451060]uncertain significance34846942748469427Humanname
405731402CV3314476single nucleotide variantNM_016479.6(SHISA5):c.692C>T (p.Ala231Val)not specified [RCV004451061]uncertain significance34846913848469138Humanname
597698779CV3602600single nucleotide variantNM_016479.6(SHISA5):c.655G>A (p.Ala219Thr)not specified [RCV004859674]uncertain significance34846917548469175Humanname
598241776CV3914191single nucleotide variantNM_016479.6(SHISA5):c.427C>T (p.Arg143Cys)not specified [RCV005276407]uncertain significance34846973148469731Humanname
598241783CV3914192single nucleotide variantNM_016479.6(SHISA5):c.631G>A (p.Glu211Lys)not specified [RCV005276408]uncertain significance34846937348469373Humanname