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40 records found for search term Trdmt1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401766655CV2673447single nucleotide variantNM_004412.7(TRDMT1):c.76C>G (p.Pro26Ala)not specified [RCV004288420]uncertain significance101717464917174649Humanname
401855994CV2754199single nucleotide variantNM_004412.7(TRDMT1):c.61A>G (p.Arg21Gly)not specified [RCV004334388]uncertain significance101720157417201574Humanname
598202095CV3924815single nucleotide variantNM_004412.7(TRDMT1):c.54C>G (p.His18Gln)not specified [RCV005290310]likely benign101720158117201581Humanname
15116202CV712293single nucleotide variantNM_004412.7(TRDMT1):c.547C>T (p.Leu183=)not provided [RCV000961992]benign101715778117157781Humanname
155922647CV2219053single nucleotide variantNM_004412.7(TRDMT1):c.260G>A (p.Arg87Gln)not specified [RCV004087222]uncertain significance101716222917162229Humanname
156177889CV2287884single nucleotide variantNM_004412.7(TRDMT1):c.278A>G (p.Asp93Gly)not specified [RCV004147671]uncertain significance101716221117162211Humanname
155909531CV2397849single nucleotide variantNM_004412.7(TRDMT1):c.187G>C (p.Glu63Gln)not specified [RCV004239319]uncertain significance101716890517168905Humanname
401721626CV2683593single nucleotide variantNM_004412.7(TRDMT1):c.287C>T (p.Thr96Met)not specified [RCV004282519]uncertain significance101716220217162202Humanname
401897263CV2789942single nucleotide variantNM_004412.7(TRDMT1):c.230C>T (p.Pro77Leu)not specified [RCV004362317]uncertain significance101716886217168862Humanname
405789032CV3340434single nucleotide variantNM_004412.7(TRDMT1):c.118A>G (p.Asn40Asp)not specified [RCV004473479]uncertain significance101717460717174607Humanname
405789036CV3340435single nucleotide variantNM_004412.7(TRDMT1):c.152A>C (p.Gln51Pro)not specified [RCV004473480]uncertain significance101717457317174573Humanname
405789040CV3340436single nucleotide variantNM_004412.7(TRDMT1):c.170T>C (p.Ile57Thr)not specified [RCV004473481]uncertain significance101717455517174555Humanname
156053513CV2269508single nucleotide variantNM_004412.7(TRDMT1):c.570A>T (p.Glu190Asp)not specified [RCV004124618]uncertain significance101715775817157758Humanname
156053529CV2269509single nucleotide variantNM_004412.7(TRDMT1):c.572C>T (p.Ser191Phe)not specified [RCV004124619]uncertain significance101715775617157756Humanname
155945175CV2269510single nucleotide variantNM_004412.7(TRDMT1):c.574G>C (p.Val192Leu)not specified [RCV004124620]uncertain significance101715775417157754Humanname
155971055CV2335646single nucleotide variantNM_004412.7(TRDMT1):c.554A>G (p.Glu185Gly)not specified [RCV004193848]uncertain significance101715777417157774Humanname
156082903CV2384902single nucleotide variantNM_004412.7(TRDMT1):c.460C>A (p.Leu154Ile)not specified [RCV004225776]uncertain significance101715922917159229Humanname
156269590CV2398591single nucleotide variantNM_004412.7(TRDMT1):c.409A>G (p.Ile137Val)not specified [RCV004237902]uncertain significance101716035517160355Humanname
329385811CV2462378single nucleotide variantNM_004412.7(TRDMT1):c.931G>A (p.Ala311Thr)not specified [RCV004268143]likely benign101715469117154691Humanname
401877120CV2769343single nucleotide variantNM_004412.7(TRDMT1):c.454A>G (p.Thr152Ala)not specified [RCV004357338]uncertain significance101716031017160310Humanname
405789047CV3340438single nucleotide variantNM_004412.7(TRDMT1):c.352T>G (p.Leu118Val)not specified [RCV004473483]uncertain significance101716152017161520Humanname
405789055CV3340440single nucleotide variantNM_004412.7(TRDMT1):c.826T>C (p.Tyr276His)not specified [RCV004473485]uncertain significance101715750217157502Humanname
407522074CV3492647single nucleotide variantNM_004412.7(TRDMT1):c.775G>A (p.Asp259Asn)not specified [RCV004677541]uncertain significance101715755317157553Humanname
407522077CV3492648single nucleotide variantNM_004412.7(TRDMT1):c.568G>C (p.Glu190Gln)not specified [RCV004677542]uncertain significance101715776017157760Humanname
597796662CV3617411single nucleotide variantNM_004412.7(TRDMT1):c.871G>A (p.Val291Met)not specified [RCV004878570]likely benign101715745717157457Humanname
597796664CV3617412single nucleotide variantNM_004412.7(TRDMT1):c.641T>C (p.Ile214Thr)not specified [RCV004878571]uncertain significance101715768717157687Humanname
597796671CV3617414single nucleotide variantNM_004412.7(TRDMT1):c.580C>A (p.Pro194Thr)not specified [RCV004878573]uncertain significance101715774817157748Humanname
597796674CV3617415single nucleotide variantNM_004412.7(TRDMT1):c.776A>T (p.Asp259Val)not specified [RCV004878574]uncertain significance101715755217157552Humanname
597796677CV3617416single nucleotide variantNM_004412.7(TRDMT1):c.485G>A (p.Arg162Gln)not specified [RCV004878575]uncertain significance101715920417159204Humanname
598273833CV3924814single nucleotide variantNM_004412.7(TRDMT1):c.536C>G (p.Pro179Arg)not specified [RCV005303624]uncertain significance101715915317159153Humanname
598273835CV3924816single nucleotide variantNM_004412.7(TRDMT1):c.796T>C (p.Tyr266His)not specified [RCV005303625]uncertain significance101715753217157532Humanname
598273836CV3924817single nucleotide variantNM_004412.7(TRDMT1):c.544G>T (p.Val182Leu)not specified [RCV005303626]uncertain significance101715778417157784Humanname
15166417CV701273single nucleotide variantNM_004412.7(TRDMT1):c.678T>G (p.Asp226Glu)not provided [RCV000948831]benign101715765017157650Humanname
156157309CV2314442single nucleotide variantNM_004412.7(TRDMT1):c.1012C>T (p.Leu338Phe)not specified [RCV004168551]uncertain significance101715357017153570Humanname
329375598CV2441008single nucleotide variantNM_004412.7(TRDMT1):c.1091T>C (p.Ile364Thr)not specified [RCV004261381]uncertain significance101714912517149125Humanname
401740171CV2705895single nucleotide variantNM_004412.7(TRDMT1):c.1105C>T (p.Arg369Cys)not specified [RCV004320826]uncertain significance101714911117149111Humanname
401894837CV2785372single nucleotide variantNM_004412.7(TRDMT1):c.1135G>C (p.Val379Leu)not specified [RCV004357118]uncertain significance101714908117149081Humanname
405789028CV3340433single nucleotide variantNM_004412.7(TRDMT1):c.1102C>G (p.Gln368Glu)not specified [RCV004473478]uncertain significance101714911417149114Humanname
597796658CV3617410single nucleotide variantNM_004412.7(TRDMT1):c.1106G>A (p.Arg369His)not specified [RCV004878569]uncertain significance101714911017149110Humanname
597796667CV3617413single nucleotide variantNM_004412.7(TRDMT1):c.1024T>C (p.Tyr342His)not specified [RCV004878572]uncertain significance101715355817153558Humanname