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Variants search result for Homo sapiens
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42 records found for search term Ddx49
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401908652CV2811869single nucleotide variantNM_019070.5(DDX49):c.171C>T (p.Val57=)not provided [RCV003423464]likely benign191892063518920635Humanname
598222681CV3956362single nucleotide variantNM_019070.5(DDX49):c.14C>G (p.Ala5Gly)not specified [RCV005317955]uncertain significance191891975518919755Humanname
401908608CV2811870single nucleotide variantNM_019070.5(DDX49):c.1260G>C (p.Gly420=)not provided [RCV003423465]likely benign191892803318928033Humanname
405705560CV3239915single nucleotide variantNM_019070.5(DDX49):c.106A>G (p.Ile36Val)not specified [RCV004375862]uncertain significance191891984718919847Humanname
407458773CV3426631single nucleotide variantNM_019070.5(DDX49):c.169G>C (p.Val57Leu)not specified [RCV004611677]uncertain significance191892063318920633Humanname
407458776CV3426632single nucleotide variantNM_019070.5(DDX49):c.271C>T (p.Arg91Trp)not specified [RCV004611678]uncertain significance191892169418921694Humanname
598222688CV3956363single nucleotide variantNM_019070.5(DDX49):c.182T>C (p.Leu61Ser)not specified [RCV005317956]uncertain significance191892064618920646Humanname
156019540CV2272638single nucleotide variantNM_019070.5(DDX49):c.530C>G (p.Pro177Arg)not specified [RCV004133518]uncertain significance191892240818922408Humanname
155984127CV2344693single nucleotide variantNM_019070.5(DDX49):c.815G>C (p.Ser272Thr)not specified [RCV004190853]uncertain significance191892427118924271Humanname
156118737CV2353973single nucleotide variantNM_019070.5(DDX49):c.440G>C (p.Arg147Pro)not specified [RCV004204409]uncertain significance191892195718921957Humanname
156195549CV2367144single nucleotide variantNM_019070.5(DDX49):c.979G>A (p.Gly327Arg)not specified [RCV004215580]uncertain significance191892493118924931Humanname
329396432CV2462668single nucleotide variantNM_019070.5(DDX49):c.634C>T (p.Pro212Ser)not specified [RCV004278603]uncertain significance191892251218922512Humanname
405705581CV3239917single nucleotide variantNM_019070.5(DDX49):c.305G>T (p.Cys102Phe)not specified [RCV004375864]uncertain significance191892172818921728Humanname
405705589CV3239918single nucleotide variantNM_019070.5(DDX49):c.348G>T (p.Glu116Asp)not specified [RCV004375865]uncertain significance191892186518921865Humanname
405705597CV3239919single nucleotide variantNM_019070.5(DDX49):c.499G>A (p.Val167Met)not specified [RCV004375866]uncertain significance191892237718922377Humanname
405705606CV3239920single nucleotide variantNM_019070.5(DDX49):c.521C>A (p.Ala174Glu)not specified [RCV004375867]uncertain significance191892239918922399Humanname
405705615CV3239921single nucleotide variantNM_019070.5(DDX49):c.521C>T (p.Ala174Val)not specified [RCV004375868]uncertain significance191892239918922399Humanname
405705621CV3239922single nucleotide variantNM_019070.5(DDX49):c.826G>A (p.Val276Met)not specified [RCV004375869]uncertain significance191892428218924282Humanname
405705628CV3239923single nucleotide variantNM_019070.5(DDX49):c.841A>G (p.Met281Val)not specified [RCV004375870]uncertain significance191892429718924297Humanname
407458779CV3426633single nucleotide variantNM_019070.5(DDX49):c.806G>A (p.Arg269His)not specified [RCV004611679]uncertain significance191892426218924262Humanname
407458783CV3426634single nucleotide variantNM_019070.5(DDX49):c.739G>A (p.Glu247Lys)not specified [RCV004611680]uncertain significance191892270718922707Humanname
407458789CV3426636single nucleotide variantNM_019070.5(DDX49):c.330G>A (p.Met110Ile)not specified [RCV004611682]uncertain significance191892184718921847Humanname
407458792CV3426637single nucleotide variantNM_019070.5(DDX49):c.697G>C (p.Ala233Pro)not specified [RCV004611683]uncertain significance191892266518922665Humanname
407458795CV3426638single nucleotide variantNM_019070.5(DDX49):c.653A>T (p.Gln218Leu)not specified [RCV004611684]uncertain significance191892262118922621Humanname
407458798CV3426639single nucleotide variantNM_019070.5(DDX49):c.422T>G (p.Phe141Cys)not specified [RCV004611685]uncertain significance191892193918921939Humanname
407458800CV3426640single nucleotide variantNM_019070.5(DDX49):c.899G>A (p.Arg300Gln)not specified [RCV004611686]uncertain significance191892466918924669Humanname
597805721CV3662212single nucleotide variantNM_019070.5(DDX49):c.397G>A (p.Asp133Asn)not specified [RCV004908801]uncertain significance191892191418921914Humanname
597805723CV3662214single nucleotide variantNM_019070.5(DDX49):c.898C>T (p.Arg300Trp)not specified [RCV004908803]uncertain significance191892466818924668Humanname
597805725CV3662216single nucleotide variantNM_019070.5(DDX49):c.646G>A (p.Val216Met)not specified [RCV004908805]uncertain significance191892261418922614Humanname
597805727CV3662218single nucleotide variantNM_019070.5(DDX49):c.868G>A (p.Ala290Thr)not specified [RCV004908807]uncertain significance191892463818924638Humanname
597805728CV3662219single nucleotide variantNM_019070.5(DDX49):c.940A>G (p.Ile314Val)not specified [RCV004908808]uncertain significance191892489218924892Humanname
598222657CV3956358single nucleotide variantNM_019070.5(DDX49):c.859C>T (p.Arg287Cys)not specified [RCV005317951]uncertain significance191892462918924629Humanname
598222693CV3956364single nucleotide variantNM_019070.5(DDX49):c.514A>G (p.Ile172Val)not specified [RCV005317957]uncertain significance191892239218922392Humanname
401873149CV2761378single nucleotide variantNM_019070.5(DDX49):c.1391G>A (p.Arg464His)not specified [RCV004334559]likely benign191892825518928255Humanname
401893054CV2762783single nucleotide variantNM_019070.5(DDX49):c.1031G>A (p.Arg344Gln)not specified [RCV004340335]uncertain significance191892630618926306Humanname
405705571CV3239916single nucleotide variantNM_019070.5(DDX49):c.1286G>A (p.Arg429His)not specified [RCV004375863]uncertain significance191892815018928150Humanname
407458770CV3426630single nucleotide variantNM_019070.5(DDX49):c.1238G>A (p.Arg413Gln)not specified [RCV004611676]uncertain significance191892801118928011Humanname
597805722CV3662213single nucleotide variantNM_019070.5(DDX49):c.1406C>T (p.Pro469Leu)not specified [RCV004908802]uncertain significance191892827018928270Humanname
597805724CV3662215single nucleotide variantNM_019070.5(DDX49):c.1108A>C (p.Lys370Gln)not specified [RCV004908804]uncertain significance191892777118927771Humanname
597805726CV3662217single nucleotide variantNM_019070.5(DDX49):c.1358G>A (p.Arg453Gln)not specified [RCV004908806]uncertain significance191892822218928222Humanname
598222668CV3956360single nucleotide variantNM_019070.5(DDX49):c.1274T>C (p.Leu425Pro)not specified [RCV005317953]uncertain significance191892813818928138Humanname
598222676CV3956361single nucleotide variantNM_019070.5(DDX49):c.1202C>T (p.Ala401Val)not specified [RCV005317954]uncertain significance191892797518927975Humanname