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Variants search result for Homo sapiens
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23 records found for search term Tmem71
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407526932CV3482826single nucleotide variantNM_001382403.1(TMEM71):c.88T>C (p.Cys30Arg)not specified [RCV004679817]uncertain significance8132757247132757247Humanname
155904809CV2298867single nucleotide variantNM_001382403.1(TMEM71):c.296A>G (p.Tyr99Cys)not specified [RCV004156411]uncertain significance8132751803132751803Humanname
155902949CV2356558single nucleotide variantNM_001382403.1(TMEM71):c.274C>A (p.Pro92Thr)not specified [RCV004199466]uncertain significance8132751825132751825Humanname
156007419CV2401310single nucleotide variantNM_001382403.1(TMEM71):c.174C>G (p.His58Gln)not specified [RCV004245850]uncertain significance8132751925132751925Humanname
329387553CV2436546single nucleotide variantNM_001382403.1(TMEM71):c.110G>T (p.Cys37Phe)not specified [RCV004253704]uncertain significance8132751989132751989Humanname
405772070CV3346692single nucleotide variantNM_001382403.1(TMEM71):c.214T>C (p.Tyr72His)not specified [RCV004470463]uncertain significance8132751885132751885Humanname
405772076CV3346693single nucleotide variantNM_001382403.1(TMEM71):c.236G>A (p.Ser79Asn)not specified [RCV004470464]uncertain significance8132751863132751863Humanname
597800645CV3610669single nucleotide variantNM_001382403.1(TMEM71):c.131A>C (p.His44Pro)not specified [RCV004880316]uncertain significance8132751968132751968Humanname
597800647CV3610670single nucleotide variantNM_001382403.1(TMEM71):c.200T>C (p.Leu67Pro)not specified [RCV004880317]uncertain significance8132751899132751899Humanname
597800649CV3610671single nucleotide variantNM_001382403.1(TMEM71):c.218A>T (p.Tyr73Phe)not specified [RCV004880318]uncertain significance8132751881132751881Humanname
155980985CV2233027single nucleotide variantNM_001382403.1(TMEM71):c.537G>T (p.Lys179Asn)not specified [RCV004103665]uncertain significance8132727937132727937Humanname
156358814CV2260822single nucleotide variantNM_001382403.1(TMEM71):c.762G>A (p.Met254Ile)not specified [RCV004125732]uncertain significance8132714206132714206Humanname
156018855CV2370355single nucleotide variantNM_001382403.1(TMEM71):c.519T>A (p.Asp173Glu)not specified [RCV004213259]uncertain significance8132727955132727955Humanname
401783100CV2703786single nucleotide variantNM_001382403.1(TMEM71):c.742G>T (p.Ala248Ser)not specified [RCV004306659]uncertain significance8132722050132722050Humanname
401899131CV2783683single nucleotide variantNM_001382403.1(TMEM71):c.794C>T (p.Ser265Leu)not specified [RCV004360614]uncertain significance8132714174132714174Humanname
405772082CV3346694single nucleotide variantNM_001382403.1(TMEM71):c.683G>T (p.Arg228Met)not specified [RCV004470465]uncertain significance8132722109132722109Humanname
407526928CV3482825single nucleotide variantNM_001382403.1(TMEM71):c.560C>T (p.Thr187Ile)not specified [RCV004679816]uncertain significance8132727914132727914Humanname
597800643CV3610668single nucleotide variantNM_001382403.1(TMEM71):c.612C>G (p.Ser204Arg)not specified [RCV004880315]uncertain significance8132727862132727862Humanname
597800651CV3610672single nucleotide variantNM_001382403.1(TMEM71):c.475T>G (p.Cys159Gly)not specified [RCV004880319]uncertain significance8132746954132746954Humanname
597800653CV3610673single nucleotide variantNM_001382403.1(TMEM71):c.656A>G (p.Glu219Gly)not specified [RCV004880320]likely benign8132727818132727818Humanname
597800655CV3610674single nucleotide variantNM_001382403.1(TMEM71):c.619C>A (p.Leu207Ile)not specified [RCV004880321]uncertain significance8132727855132727855Humanname
598227467CV3914031single nucleotide variantNM_001382403.1(TMEM71):c.643G>A (p.Glu215Lys)not specified [RCV005294593]uncertain significance8132727831132727831Humanname
598227473CV3914032single nucleotide variantNM_001382403.1(TMEM71):c.684G>C (p.Arg228Ser)not specified [RCV005294594]likely benign8132722108132722108Humanname