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24 records found for search term Tmem205
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407526334CV3482584single nucleotide variantNM_198536.3(TMEM205):c.7G>A (p.Glu3Lys)not specified [RCV004679608]uncertain significance191134561311345613Humanname
401874885CV2781341single nucleotide variantNM_198536.3(TMEM205):c.26G>C (p.Gly9Ala)not specified [RCV004352353]uncertain significance191134559411345594Humanname
405753680CV3336263single nucleotide variantNM_198536.3(TMEM205):c.81G>A (p.Met27Ile)not specified [RCV004467490]uncertain significance191134553911345539Humanname
407526340CV3482587single nucleotide variantNM_198536.3(TMEM205):c.39G>A (p.Met13Ile)not specified [RCV004679610]uncertain significance191134558111345581Humanname
155924609CV2277152single nucleotide variantNM_198536.3(TMEM205):c.257C>A (p.Ala86Asp)not specified [RCV004142796]uncertain significance191134525911345259Humanname
401732979CV2702316single nucleotide variantNM_198536.3(TMEM205):c.160T>C (p.Phe54Leu)not specified [RCV004314642]uncertain significance191134535611345356Humanname
401881408CV2759405single nucleotide variantNM_198536.3(TMEM205):c.191G>C (p.Cys64Ser)not specified [RCV004338406]uncertain significance191134532511345325Humanname
401865975CV2786217single nucleotide variantNM_198536.3(TMEM205):c.128G>A (p.Arg43Gln)not specified [RCV004360012]uncertain significance191134538811345388Humanname
405753650CV3336259single nucleotide variantNM_198536.3(TMEM205):c.203A>G (p.Asn68Ser)not specified [RCV004467486]uncertain significance191134531311345313Humanname
597753926CV3613681single nucleotide variantNM_198536.3(TMEM205):c.250T>C (p.Trp84Arg)not specified [RCV004867484]uncertain significance191134526611345266Humanname
156146864CV2289291single nucleotide variantNM_198536.3(TMEM205):c.382G>T (p.Gly128Trp)not specified [RCV004152271]uncertain significance191134300311343003Humanname
156270236CV2312141single nucleotide variantNM_198536.3(TMEM205):c.382G>A (p.Gly128Arg)not specified [RCV004165048]uncertain significance191134300311343003Humanname
156087862CV2366428single nucleotide variantNM_198536.3(TMEM205):c.493T>C (p.Ser165Pro)not specified [RCV004212472]uncertain significance191134289211342892Humanname
329382874CV2424582single nucleotide variantNM_198536.3(TMEM205):c.514G>A (p.Val172Ile)not specified [RCV004254081]uncertain significance191134287111342871Humanname
405753657CV3336260single nucleotide variantNM_198536.3(TMEM205):c.371G>A (p.Arg124Gln)not specified [RCV004467487]uncertain significance191134301411343014Humanname
405753664CV3336261single nucleotide variantNM_198536.3(TMEM205):c.460C>T (p.Arg154Cys)not specified [RCV004467488]uncertain significance191134292511342925Humanname
405753672CV3336262single nucleotide variantNM_198536.3(TMEM205):c.514G>T (p.Val172Phe)not specified [RCV004467489]uncertain significance191134287111342871Humanname
407458730CV3482585single nucleotide variantNM_198536.3(TMEM205):c.421C>T (p.Arg141Cys)not specified [RCV004686919]uncertain significance191134296411342964Humanname
407526337CV3482586single nucleotide variantNM_198536.3(TMEM205):c.310C>T (p.Arg104Cys)not specified [RCV004679609]uncertain significance191134307511343075Humanname
407458733CV3482588single nucleotide variantNM_198536.3(TMEM205):c.521G>A (p.Ser174Asn)not specified [RCV004686920]uncertain significance191134286411342864Humanname
597753913CV3613678single nucleotide variantNM_198536.3(TMEM205):c.412G>A (p.Asp138Asn)not specified [RCV004867481]uncertain significance191134297311342973Humanname
597753918CV3613679single nucleotide variantNM_198536.3(TMEM205):c.524A>G (p.Asn175Ser)not specified [RCV004867482]uncertain significance191134286111342861Humanname
597753922CV3613680single nucleotide variantNM_198536.3(TMEM205):c.443C>G (p.Pro148Arg)not specified [RCV004867483]uncertain significance191134294211342942Humanname
597795238CV3613682single nucleotide variantNM_198536.3(TMEM205):c.515T>A (p.Val172Asp)not specified [RCV004878148]uncertain significance191134287011342870Humanname