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Variants search result for Homo sapiens
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35 records found for search term Traf6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
150332381CV1164388duplicationNM_004620.4(TRAF6):c.448-15dupnot specified [RCV001528255]benign113649727436497275Humanname
401753167CV2725215single nucleotide variantNM_004620.4(TRAF6):c.59G>A (p.Cys20Tyr)not specified [RCV004321734]uncertain significance113650145736501457Humanname
407461293CV3492520single nucleotide variantNM_004620.4(TRAF6):c.88G>A (p.Val30Ile)not specified [RCV004687617]uncertain significance113650142836501428Humanname
15135671CV737959single nucleotide variantNM_004620.4(TRAF6):c.549A>G (p.Pro183=)not provided [RCV000898499]likely benign113649716536497165Humanname
15140184CV752660single nucleotide variantNM_004620.4(TRAF6):c.528T>A (p.Ile176=)not provided [RCV000921636]likely benign113649718636497186Humanname
156078495CV2230363single nucleotide variantNM_004620.4(TRAF6):c.131A>G (p.Asn44Ser)not specified [RCV004099960]uncertain significance113650138536501385Humanname
405776130CV3344101single nucleotide variantNM_004620.4(TRAF6):c.233G>A (p.Arg78Gln)not specified [RCV004471137]uncertain significance113650128336501283Humanname
597796337CV3621048single nucleotide variantNM_004620.4(TRAF6):c.158T>C (p.Ile53Thr)not specified [RCV004878396]uncertain significance113650135836501358Humanname
598265933CV3924625single nucleotide variantNM_004620.4(TRAF6):c.149T>C (p.Met50Thr)not specified [RCV005281060]uncertain significance113650136736501367Humanname
156367257CV2203491single nucleotide variantNM_004620.4(TRAF6):c.844G>A (p.Val282Ile)not specified [RCV004072701]uncertain significance113649056336490563Humanname
156055704CV2269665single nucleotide variantNM_004620.4(TRAF6):c.580G>A (p.Ala194Thr)not specified [RCV004126660]uncertain significance113649713436497134Humanname
155995686CV2286554single nucleotide variantNM_004620.4(TRAF6):c.430G>A (p.Glu144Lys)not specified [RCV004140049]uncertain significance113649850736498507Humanname
155933098CV2372217single nucleotide variantNM_004620.4(TRAF6):c.856T>C (p.Ser286Pro)not specified [RCV004216996]uncertain significance113649055136490551Humanname
401737147CV2699741single nucleotide variantNM_004620.4(TRAF6):c.586A>G (p.Met196Val)not specified [RCV004308402]likely benign113649712836497128Humanname
405270322CV3215492single nucleotide variantNM_004620.4(TRAF6):c.479T>C (p.Met160Thr)TRAF6-related disorder [RCV003949230]likely benign113649723536497235Humanname , trait , alternate_id
405776136CV3344102single nucleotide variantNM_004620.4(TRAF6):c.342A>C (p.Glu114Asp)not specified [RCV004471138]uncertain significance113649859536498595Humanname
405776142CV3344103single nucleotide variantNM_004620.4(TRAF6):c.481G>A (p.Asp161Asn)not specified [RCV004471139]likely benign113649723336497233Humanname
405776149CV3344104single nucleotide variantNM_004620.4(TRAF6):c.520A>G (p.Ile174Val)not specified [RCV004471140]uncertain significance113649719436497194Humanname
405776162CV3344106single nucleotide variantNM_004620.4(TRAF6):c.608T>C (p.Ile203Thr)not specified [RCV004471142]uncertain significance113649504636495046Humanname
405776167CV3344107single nucleotide variantNM_004620.4(TRAF6):c.809T>G (p.Met270Arg)not specified [RCV004471143]uncertain significance113649059836490598Humanname
407521796CV3492522single nucleotide variantNM_004620.4(TRAF6):c.759G>A (p.Met253Ile)not specified [RCV004677431]uncertain significance113649064836490648Humanname
407521802CV3492524single nucleotide variantNM_004620.4(TRAF6):c.848T>C (p.Ile283Thr)not specified [RCV004677433]likely benign113649055936490559Humanname
408367608CV3510177single nucleotide variantNM_004620.4(TRAF6):c.609C>G (p.Ile203Met)TRAF6-related disorder [RCV004759033]|not specified [RCV005291103]uncertain significance113649504536495045Humanname , trait , alternate_id
597796355CV3621042single nucleotide variantNM_004620.4(TRAF6):c.500G>A (p.Arg167His)not specified [RCV004878390]uncertain significance113649721436497214Humanname
597796352CV3621043single nucleotide variantNM_004620.4(TRAF6):c.975G>T (p.Met325Ile)not specified [RCV004878391]uncertain significance113649043236490432Humanname
597796350CV3621044single nucleotide variantNM_004620.4(TRAF6):c.583T>C (p.Ser195Pro)not specified [RCV004878392]uncertain significance113649713136497131Humanname
597796343CV3621046single nucleotide variantNM_004620.4(TRAF6):c.673G>C (p.Glu225Gln)not specified [RCV004878394]uncertain significance113649498136494981Humanname
155919548CV2202659single nucleotide variantNM_004620.4(TRAF6):c.1033G>A (p.Glu345Lys)not specified [RCV004082910]uncertain significance113649037436490374Humanname
156043327CV2307915single nucleotide variantNM_004620.4(TRAF6):c.1072G>A (p.Gly358Ser)not specified [RCV004170368]uncertain significance113649033536490335Humanname
156348197CV2375656single nucleotide variantNM_004620.4(TRAF6):c.1205G>A (p.Arg402His)not specified [RCV004226132]uncertain significance113649020236490202Humanname
401740144CV2683271single nucleotide variantNM_004620.4(TRAF6):c.1258A>C (p.Ser420Arg)not specified [RCV004288054]uncertain significance113649014936490149Humanname
407521799CV3492523single nucleotide variantNM_004620.4(TRAF6):c.1086G>A (p.Met362Ile)not specified [RCV004677432]uncertain significance113649032136490321Humanname
407521805CV3492525single nucleotide variantNM_004620.4(TRAF6):c.1084A>G (p.Met362Val)not specified [RCV004677434]uncertain significance113649032336490323Humanname
597796346CV3621045single nucleotide variantNM_004620.4(TRAF6):c.1561G>A (p.Gly521Arg)not specified [RCV004878393]uncertain significance113648984636489846Humanname
597796334CV3621049single nucleotide variantNM_004620.4(TRAF6):c.1436T>C (p.Leu479Pro)not specified [RCV004878397]uncertain significance113648997136489971Humanname