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Variants search result for Homo sapiens
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12 records found for search term Tmem60
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597800568CV3610596single nucleotide variantNM_032936.4(TMEM60):c.17C>T (p.Ala6Val)not specified [RCV004880278]uncertain significance77779435777794357Humanname
155934293CV2225246single nucleotide variantNM_032936.4(TMEM60):c.266C>T (p.Ala89Val)not specified [RCV004098897]uncertain significance77779410877794108Humanname
156079249CV2226527single nucleotide variantNM_032936.4(TMEM60):c.277G>A (p.Ala93Thr)not specified [RCV004101790]uncertain significance77779409777794097Humanname
156312621CV2256895single nucleotide variantNM_032936.4(TMEM60):c.241C>T (p.Leu81Phe)not specified [RCV004121099]uncertain significance77779413377794133Humanname
329362096CV2448289single nucleotide variantNM_032936.4(TMEM60):c.250A>G (p.Met84Val)not specified [RCV004263488]uncertain significance77779412477794124Humanname
405771603CV3346615single nucleotide variantNM_032936.4(TMEM60):c.135T>G (p.Phe45Leu)not specified [RCV004470386]uncertain significance77779423977794239Humanname
407526833CV3482785single nucleotide variantNM_032936.4(TMEM60):c.280C>G (p.Leu94Val)not specified [RCV004679780]uncertain significance77779409477794094Humanname
598252599CV3913972single nucleotide variantNM_032936.4(TMEM60):c.232G>T (p.Ala78Ser)not specified [RCV005278112]uncertain significance77779414277794142Humanname
598227220CV3913973single nucleotide variantNM_032936.4(TMEM60):c.233C>A (p.Ala78Asp)not specified [RCV005294552]uncertain significance77779414177794141Humanname
156018553CV2370294single nucleotide variantNM_032936.4(TMEM60):c.299A>G (p.Gln100Arg)not specified [RCV004213209]uncertain significance77779407577794075Humanname
401727813CV2678477single nucleotide variantNM_032936.4(TMEM60):c.394A>G (p.Arg132Gly)not specified [RCV004292494]uncertain significance77779398077793980Humanname
405771608CV3346616single nucleotide variantNM_032936.4(TMEM60):c.313A>T (p.Asn105Tyr)not specified [RCV004470387]uncertain significance77779406177794061Humanname