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Variants search result for Homo sapiens
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22 records found for search term Rrad
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155963495CV2254564single nucleotide variantNM_004165.3(RRAD):c.22A>G (p.Ser8Gly)not specified [RCV004123914]uncertain significance166692515866925158Humanname
156291599CV2226345single nucleotide variantNM_004165.3(RRAD):c.35G>C (p.Gly12Ala)not specified [RCV004099577]uncertain significance166692514566925145Humanname
405740085CV3316532single nucleotide variantNM_004165.3(RRAD):c.40C>G (p.Arg14Gly)not specified [RCV004452243]uncertain significance166692514066925140Humanname
156115125CV2208974single nucleotide variantNM_004165.3(RRAD):c.295G>T (p.Ala99Ser)not specified [RCV004085310]uncertain significance166692488566924885Humanname
155993019CV2281272single nucleotide variantNM_004165.3(RRAD):c.155C>T (p.Thr52Ile)not specified [RCV004147513]uncertain significance166692502566925025Humanname
156187061CV2332692single nucleotide variantNM_004165.3(RRAD):c.164C>A (p.Ala55Asp)not specified [RCV004189369]uncertain significance166692501666925016Humanname
155919985CV2343267single nucleotide variantNM_004165.3(RRAD):c.120G>A (p.Met40Ile)not specified [RCV004194890]uncertain significance166692506066925060Humanname
401894330CV2780698single nucleotide variantNM_004165.3(RRAD):c.222G>C (p.Glu74Asp)not specified [RCV004352037]uncertain significance166692495866924958Humanname
597710422CV3604454single nucleotide variantNM_004165.3(RRAD):c.108C>A (p.His36Gln)not specified [RCV004860955]uncertain significance166692507266925072Humanname
598221783CV3903124single nucleotide variantNM_004165.3(RRAD):c.109C>A (p.Arg37Ser)not specified [RCV005272563]uncertain significance166692507166925071Humanname
156368856CV2193805single nucleotide variantNM_004165.3(RRAD):c.851G>A (p.Arg284His)not specified [RCV004074557]uncertain significance166692215266922152Humanname
329357554CV2427763single nucleotide variantNM_004165.3(RRAD):c.917C>T (p.Ser306Leu)not specified [RCV004252544]uncertain significance166692208666922086Humanname
401764991CV2701668single nucleotide variantNM_004165.3(RRAD):c.701C>T (p.Ala234Val)not specified [RCV004314080]uncertain significance166692230266922302Humanname
401728543CV2729643single nucleotide variantNM_004165.3(RRAD):c.912C>A (p.Asp304Glu)not specified [RCV004331905]uncertain significance166692209166922091Humanname
405740078CV3316531single nucleotide variantNM_004165.3(RRAD):c.386G>A (p.Arg129His)not specified [RCV004452242]uncertain significance166692390466923904Humanname
405740092CV3316533single nucleotide variantNM_004165.3(RRAD):c.455G>A (p.Arg152His)not specified [RCV004452244]uncertain significance166692371066923710Humanname
405740102CV3316534single nucleotide variantNM_004165.3(RRAD):c.869G>A (p.Ser290Asn)not specified [RCV004452245]uncertain significance166692213466922134Humanname
407488406CV3476294single nucleotide variantNM_004165.3(RRAD):c.325C>G (p.Arg109Gly)not specified [RCV004665861]uncertain significance166692485566924855Humanname
597786471CV3604452single nucleotide variantNM_004165.3(RRAD):c.818G>A (p.Ser273Asn)not specified [RCV004854988]uncertain significance166692218566922185Humanname
597710411CV3604453single nucleotide variantNM_004165.3(RRAD):c.641C>T (p.Ser214Leu)not specified [RCV004860954]uncertain significance166692352466923524Humanname
598221798CV3903121single nucleotide variantNM_004165.3(RRAD):c.616G>A (p.Asp206Asn)not specified [RCV005272560]uncertain significance166692354966923549Humanname
598221789CV3903123single nucleotide variantNM_004165.3(RRAD):c.677A>G (p.Asp226Gly)not specified [RCV005272562]uncertain significance166692232666922326Humanname