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Variants search result for Homo sapiens
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35 records found for search term Wdr31
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8650990CV127565single nucleotide variantNM_001012361.2(WDR31):c.325-198G>ALung cancer [RCV000108052]uncertain significance9113323353113323353Humanname
8650991CV127566single nucleotide variantNM_001012361.2(WDR31):c.325-2217C>GLung cancer [RCV000108053]uncertain significance9113325372113325372Humanname
156102387CV2367759single nucleotide variantNM_001012361.4(WDR31):c.67G>A (p.Val23Met)not specified [RCV004213714]uncertain significance9113331956113331956Humanname
401783305CV2716265single nucleotide variantNM_001012361.4(WDR31):c.50C>T (p.Ser17Leu)not specified [RCV004323483]likely benign9113331973113331973Humanname
405802431CV3349242single nucleotide variantNM_001012361.4(WDR31):c.61T>C (p.Cys21Arg)not specified [RCV004478317]uncertain significance9113331962113331962Humanname
156252010CV2273463single nucleotide variantNM_001012361.4(WDR31):c.184A>T (p.Met62Leu)not specified [RCV004132214]uncertain significance9113331049113331049Humanname
329387606CV2464204single nucleotide variantNM_001012361.4(WDR31):c.286G>T (p.Val96Leu)not specified [RCV004273881]uncertain significance9113328919113328919Humanname
401734118CV2713336single nucleotide variantNM_001012361.4(WDR31):c.170A>G (p.Tyr57Cys)not specified [RCV004318637]uncertain significance9113331063113331063Humanname
401862622CV2775242single nucleotide variantNM_001012361.4(WDR31):c.294G>T (p.Arg98Ser)not specified [RCV004348369]uncertain significance9113328911113328911Humanname
407523849CV3489755single nucleotide variantNM_001012361.4(WDR31):c.160T>C (p.Phe54Leu)not specified [RCV004678207]uncertain significance9113331073113331073Humanname
407523852CV3489756single nucleotide variantNM_001012361.4(WDR31):c.134T>C (p.Ile45Thr)not specified [RCV004678208]uncertain significance9113331099113331099Humanname
156025214CV2242214single nucleotide variantNM_001012361.4(WDR31):c.526G>C (p.Val176Leu)not specified [RCV004111247]uncertain significance9113322855113322855Humanname
156176803CV2258126single nucleotide variantNM_001012361.4(WDR31):c.906T>G (p.His302Gln)not specified [RCV004121516]uncertain significance9113318512113318512Humanname
156261219CV2287477single nucleotide variantNM_001012361.4(WDR31):c.736A>G (p.Ile246Val)not specified [RCV004140945]likely benign9113320401113320401Humanname
156200915CV2290518single nucleotide variantNM_001012361.4(WDR31):c.439A>G (p.Met147Val)not specified [RCV004155206]uncertain significance9113323041113323041Humanname
156081399CV2301079single nucleotide variantNM_001012361.4(WDR31):c.298A>G (p.Lys100Glu)not specified [RCV004158223]uncertain significance9113328907113328907Humanname
156096770CV2310211single nucleotide variantNM_001012361.4(WDR31):c.371A>G (p.Asp124Gly)not specified [RCV004163313]uncertain significance9113323109113323109Humanname
156084505CV2381991single nucleotide variantNM_001012361.4(WDR31):c.932A>G (p.Gln311Arg)not specified [RCV004225919]uncertain significance9113318486113318486Humanname
156391279CV2385229single nucleotide variantNM_001012361.4(WDR31):c.853G>C (p.Val285Leu)not specified [RCV004228475]uncertain significance9113318565113318565Humanname
156252914CV2390101single nucleotide variantNM_001012361.4(WDR31):c.853G>A (p.Val285Ile)not specified [RCV004238701]uncertain significance9113318565113318565Humanname
156095174CV2398920single nucleotide variantNM_001012361.4(WDR31):c.609A>G (p.Ile203Met)not specified [RCV004245235]uncertain significance9113321540113321540Humanname
401752972CV2703636single nucleotide variantNM_001012361.4(WDR31):c.653G>A (p.Arg218Gln)not specified [RCV004317798]uncertain significance9113320484113320484Humanname
401773061CV2716444single nucleotide variantNM_001012361.4(WDR31):c.829C>A (p.His277Asn)not specified [RCV004325752]uncertain significance9113318589113318589Humanname
401753672CV2722547single nucleotide variantNM_001012361.4(WDR31):c.814T>C (p.Cys272Arg)not specified [RCV004322926]uncertain significance9113318604113318604Humanname
401882787CV2778592single nucleotide variantNM_001012361.4(WDR31):c.803G>A (p.Arg268Gln)not specified [RCV004344243]uncertain significance9113318615113318615Humanname
401898641CV2782570single nucleotide variantNM_001012361.4(WDR31):c.519G>T (p.Trp173Cys)not specified [RCV004359604]uncertain significance9113322862113322862Humanname
405802426CV3349240single nucleotide variantNM_001012361.4(WDR31):c.416G>A (p.Arg139Lys)not specified [RCV004478315]uncertain significance9113323064113323064Humanname
405802428CV3349241single nucleotide variantNM_001012361.4(WDR31):c.533G>A (p.Gly178Glu)not specified [RCV004478316]uncertain significance9113322848113322848Humanname
407465277CV3489754single nucleotide variantNM_001012361.4(WDR31):c.743G>A (p.Cys248Tyr)not specified [RCV004688727]uncertain significance9113320394113320394Humanname
407523855CV3489757single nucleotide variantNM_001012361.4(WDR31):c.556G>A (p.Val186Ile)not specified [RCV004678209]likely benign9113322825113322825Humanname
597691273CV3633541single nucleotide variantNM_001012361.4(WDR31):c.779C>T (p.Thr260Met)not specified [RCV004884649]uncertain significance9113320358113320358Humanname
597691286CV3633542single nucleotide variantNM_001012361.4(WDR31):c.455T>C (p.Leu152Ser)not specified [RCV004884650]uncertain significance9113323025113323025Humanname
597691297CV3633543single nucleotide variantNM_001012361.4(WDR31):c.893C>T (p.Ala298Val)not specified [RCV004884651]uncertain significance9113318525113318525Humanname
597691308CV3633544single nucleotide variantNM_001012361.4(WDR31):c.599A>G (p.Glu200Gly)not specified [RCV004884652]uncertain significance9113321550113321550Humanname
8633193CV88406single nucleotide variantNM_001012361.2(WDR31):c.1013C>T (p.Ser338Phe)Malignant melanoma [RCV000068498]not provided9113316840113316840Humanname