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Variants search result for Homo sapiens
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24 records found for search term Aamp
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329373288CV2439387single nucleotide variantNM_001087.5(AAMP):c.44C>A (p.Pro15Gln)not specified [RCV004249681]uncertain significance2218270043218270043Humanname
405707970CV3297935single nucleotide variantNM_001087.5(AAMP):c.58A>G (p.Ser20Gly)not specified [RCV004426363]uncertain significance2218270029218270029Humanname
405707136CV3301817single nucleotide variantNM_001087.5(AAMP):c.43C>A (p.Pro15Thr)not specified [RCV004426244]uncertain significance2218270044218270044Humanname
598201634CV3938643single nucleotide variantNM_001087.5(AAMP):c.43C>G (p.Pro15Ala)not specified [RCV005314271]uncertain significance2218270044218270044Humanname
156111275CV2261726single nucleotide variantNM_001087.5(AAMP):c.158A>G (p.Glu53Gly)not specified [RCV004126027]uncertain significance2218269498218269498Humanname
155928548CV2363315single nucleotide variantNM_001087.5(AAMP):c.211G>A (p.Glu71Lys)not specified [RCV004213867]uncertain significance2218269445218269445Humanname
405705882CV3301641single nucleotide variantNM_001087.5(AAMP):c.141G>A (p.Met47Ile)not specified [RCV004426068]uncertain significance2218269515218269515Humanname
598276669CV3938743single nucleotide variantNM_001087.5(AAMP):c.113C>T (p.Pro38Leu)not specified [RCV005305803]uncertain significance2218269974218269974Humanname
598276429CV3942269single nucleotide variantNM_001087.5(AAMP):c.241G>A (p.Asp81Asn)not specified [RCV005305563]uncertain significance2218269415218269415Humanname
156375659CV2210260single nucleotide variantNM_001087.5(AAMP):c.367G>A (p.Asp123Asn)not specified [RCV004089425]uncertain significance2218267521218267521Humanname
156382980CV2223729single nucleotide variantNM_001087.5(AAMP):c.481T>A (p.Trp161Arg)not specified [RCV004093815]uncertain significance2218266900218266900Humanname
156292073CV2339993single nucleotide variantNM_001087.5(AAMP):c.575G>C (p.Gly192Ala)not specified [RCV004192244]uncertain significance2218266547218266547Humanname
156122720CV2354353single nucleotide variantNM_001087.5(AAMP):c.866C>T (p.Ala289Val)not specified [RCV004199891]uncertain significance2218265844218265844Humanname
405707624CV3297885single nucleotide variantNM_001087.5(AAMP):c.543G>C (p.Glu181Asp)not specified [RCV004426313]uncertain significance2218266579218266579Humanname
405667808CV3297972single nucleotide variantNM_001087.5(AAMP):c.632T>G (p.Phe211Cys)not specified [RCV004418879]uncertain significance2218266490218266490Humanname
405667954CV3298001single nucleotide variantNM_001087.5(AAMP):c.635A>C (p.Gln212Pro)not specified [RCV004418908]uncertain significance2218266487218266487Humanname
405727080CV3298056single nucleotide variantNM_001087.5(AAMP):c.911C>T (p.Ala304Val)not specified [RCV004428877]uncertain significance2218265651218265651Humanname
405706654CV3301747single nucleotide variantNM_001087.5(AAMP):c.347C>G (p.Ala116Gly)not specified [RCV004426174]uncertain significance2218267541218267541Humanname
407472505CV3427472single nucleotide variantNM_001087.5(AAMP):c.752A>G (p.His251Arg)not specified [RCV004600132]uncertain significance2218266075218266075Humanname
598247592CV3931260single nucleotide variantNM_001087.5(AAMP):c.898C>A (p.Pro300Thr)not specified [RCV005297904]uncertain significance2218265664218265664Humanname
597759336CV3642755single nucleotide variantNM_001087.5(AAMP):c.1300C>T (p.Arg434Cys)not specified [RCV004894502]uncertain significance2218264538218264538Humanname
598242975CV3930289single nucleotide variantNM_001087.5(AAMP):c.1043C>T (p.Thr348Met)not specified [RCV005297206]uncertain significance2218265402218265402Humanname
598171181CV3938182single nucleotide variantNM_001087.5(AAMP):c.1138G>A (p.Gly380Ser)not specified [RCV005309129]uncertain significance2218265111218265111Humanname
598271911CV3949183single nucleotide variantNM_001087.5(AAMP):c.1190G>A (p.Arg397Gln)not specified [RCV005303011]uncertain significance2218265059218265059Humanname