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Variants search result for Homo sapiens
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35 records found for search term Art5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155990797CV2276509single nucleotide variantNM_053017.5(ART5):c.64G>C (p.Ala22Pro)not specified [RCV004144222]uncertain significance1136403653640365Humanname
156139052CV2374270single nucleotide variantNM_053017.5(ART5):c.40G>A (p.Gly14Ser)not specified [RCV004229407]uncertain significance1136418233641823Humanname
405664933CV3286571single nucleotide variantNM_053017.5(ART5):c.31G>T (p.Gly11Cys)not specified [RCV004418309]uncertain significance1136418323641832Humanname
597776276CV3586600single nucleotide variantNM_053017.5(ART5):c.64G>A (p.Ala22Thr)not specified [RCV004852473]uncertain significance1136403653640365Humanname
155946874CV2262483single nucleotide variantNM_053017.5(ART5):c.191T>C (p.Leu64Pro)not specified [RCV004128916]uncertain significance1136402383640238Humanname
155983666CV2273103single nucleotide variantNM_053017.5(ART5):c.205G>A (p.Glu69Lys)not specified [RCV004137745]uncertain significance1136402243640224Humanname
155964884CV2330506single nucleotide variantNM_053017.5(ART5):c.242G>A (p.Gly81Glu)not specified [RCV004181071]uncertain significance1136401873640187Humanname
401769810CV2693017single nucleotide variantNM_053017.5(ART5):c.275A>G (p.Asn92Ser)not specified [RCV004308567]uncertain significance1136401543640154Humanname
405664927CV3286570single nucleotide variantNM_053017.5(ART5):c.239G>A (p.Arg80Gln)not specified [RCV004418308]uncertain significance1136401903640190Humanname
598255783CV3909043single nucleotide variantNM_053017.5(ART5):c.109G>A (p.Asp37Asn)not specified [RCV005259971]uncertain significance1136403203640320Humanname
598255809CV3909048single nucleotide variantNM_053017.5(ART5):c.109G>C (p.Asp37His)not specified [RCV005259976]uncertain significance1136403203640320Humanname
156313626CV2196526single nucleotide variantNM_053017.5(ART5):c.677C>G (p.Pro226Arg)not specified [RCV004073816]uncertain significance1136397523639752Humanname
156111458CV2261752single nucleotide variantNM_053017.5(ART5):c.445G>A (p.Gly149Ser)not specified [RCV004126043]uncertain significance1136399843639984Humanname
156028530CV2278538single nucleotide variantNM_053017.5(ART5):c.736C>T (p.Leu246Phe)not specified [RCV004132973]uncertain significance1136396933639693Humanname
156104368CV2310957single nucleotide variantNM_053017.5(ART5):c.707C>G (p.Ser236Cys)not specified [RCV004163991]uncertain significance1136397223639722Humanname
155919063CV2333125single nucleotide variantNM_053017.5(ART5):c.671T>G (p.Ile224Ser)not specified [RCV004194418]uncertain significance1136397583639758Humanname
155914226CV2341951single nucleotide variantNM_053017.5(ART5):c.544G>A (p.Ala182Thr)not specified [RCV004184895]uncertain significance1136398853639885Humanname
156096897CV2399139single nucleotide variantNM_053017.5(ART5):c.677C>A (p.Pro226His)not specified [RCV004246572]uncertain significance1136397523639752Humanname
329398531CV2471154single nucleotide variantNM_053017.5(ART5):c.733A>C (p.Thr245Pro)not specified [RCV004278404]uncertain significance1136396963639696Humanname
401781005CV2681857single nucleotide variantNM_053017.5(ART5):c.595C>A (p.Leu199Ile)not specified [RCV004296851]uncertain significance1136398343639834Humanname
401757885CV2685616single nucleotide variantNM_053017.5(ART5):c.361C>T (p.Arg121Trp)not specified [RCV004294625]uncertain significance1136400683640068Humanname
401759643CV2698576single nucleotide variantNM_053017.5(ART5):c.724A>G (p.Ser242Gly)not specified [RCV004299061]uncertain significance1136397053639705Humanname
405664939CV3286572single nucleotide variantNM_053017.5(ART5):c.520G>A (p.Asp174Asn)not specified [RCV004418310]uncertain significance1136399093639909Humanname
407491669CV3480353single nucleotide variantNM_053017.5(ART5):c.506C>G (p.Pro169Arg)not specified [RCV004666947]uncertain significance1136399233639923Humanname
597776216CV3586563single nucleotide variantNM_053017.5(ART5):c.347C>A (p.Thr116Lys)not specified [RCV004852456]uncertain significance1136400823640082Humanname
597788391CV3586572single nucleotide variantNM_053017.5(ART5):c.352G>A (p.Gly118Arg)not specified [RCV004855488]uncertain significance1136400773640077Humanname
597776240CV3586581single nucleotide variantNM_053017.5(ART5):c.833C>G (p.Thr278Arg)not specified [RCV004852464]uncertain significance1136387813638781Humanname
597788424CV3586590single nucleotide variantNM_053017.5(ART5):c.524C>T (p.Ser175Phe)not specified [RCV004855497]uncertain significance1136399053639905Humanname
597788466CV3586610single nucleotide variantNM_053017.5(ART5):c.422T>C (p.Leu141Pro)not specified [RCV004855507]uncertain significance1136400073640007Humanname
598255751CV3909036single nucleotide variantNM_053017.5(ART5):c.622G>A (p.Ala208Thr)not specified [RCV005259964]uncertain significance1136398073639807Humanname
598255760CV3909038single nucleotide variantNM_053017.5(ART5):c.751C>A (p.Gln251Lys)not specified [RCV005259966]uncertain significance1136396783639678Humanname
598255770CV3909040single nucleotide variantNM_053017.5(ART5):c.428T>C (p.Leu143Pro)not specified [RCV005259968]uncertain significance1136400013640001Humanname
598255788CV3909044single nucleotide variantNM_053017.5(ART5):c.792G>C (p.Glu264Asp)not specified [RCV005259972]uncertain significance1136390313639031Humanname
15171834CV712812single nucleotide variantNM_053017.5(ART5):c.466G>A (p.Glu156Lys)not provided [RCV000972277]benign1136399633639963Humanname
15120551CV737958single nucleotide variantNM_053017.5(ART5):c.811T>A (p.Ser271Thr)not provided [RCV000895913]benign1136390123639012Humanname