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Variants search result for Homo sapiens
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26 records found for search term Mageb3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407468768CV3449587single nucleotide variantNM_002365.5(MAGEB3):c.23C>T (p.Thr8Met)not specified [RCV004636400]uncertain significanceX3023594730235947Humanname
597623673CV3694089single nucleotide variantNM_002365.5(MAGEB3):c.22A>G (p.Thr8Ala)not specified [RCV004936690]uncertain significanceX3023594630235946Humanname
405651236CV3277541single nucleotide variantNM_002365.5(MAGEB3):c.98C>A (p.Thr33Asn)not specified [RCV004413519]uncertain significanceX3023602230236022Humanname
156385883CV2228061single nucleotide variantNM_002365.5(MAGEB3):c.176G>A (p.Arg59His)not specified [RCV004096296]uncertain significanceX3023610030236100Humanname
156143639CV2268810single nucleotide variantNM_002365.5(MAGEB3):c.248A>C (p.Tyr83Ser)not specified [RCV004124192]uncertain significanceX3023617230236172Humanname
156162444CV2272686single nucleotide variantNM_002365.5(MAGEB3):c.289T>C (p.Ser97Pro)not specified [RCV004135346]uncertain significanceX3023621330236213Humanname
405651229CV3277537single nucleotide variantNM_002365.5(MAGEB3):c.269T>C (p.Ile90Thr)not specified [RCV004413515]uncertain significanceX3023619330236193Humanname
156027876CV2195622single nucleotide variantNM_002365.5(MAGEB3):c.777G>C (p.Glu259Asp)not specified [RCV004082830]uncertain significanceX3023670130236701Humanname
156242373CV2210660single nucleotide variantNM_002365.5(MAGEB3):c.437A>G (p.Lys146Arg)not specified [RCV004083803]uncertain significanceX3023636130236361Humanname
155971108CV2237360single nucleotide variantNM_002365.5(MAGEB3):c.530C>T (p.Ser177Phe)not specified [RCV004104550]uncertain significanceX3023645430236454Humanname
156119327CV2275800single nucleotide variantNM_002365.5(MAGEB3):c.653C>T (p.Ala218Val)not specified [RCV004139472]uncertain significanceX3023657730236577Humanname
156139048CV2280718single nucleotide variantNM_002365.5(MAGEB3):c.302C>A (p.Ser101Tyr)not specified [RCV004143175]uncertain significanceX3023622630236226Humanname
156205577CV2311414single nucleotide variantNM_002365.5(MAGEB3):c.949A>G (p.Arg317Gly)not specified [RCV004168262]uncertain significanceX3023687330236873Humanname
155989812CV2371978single nucleotide variantNM_002365.5(MAGEB3):c.391C>T (p.Pro131Ser)not specified [RCV004221654]uncertain significanceX3023631530236315Humanname
155998074CV2373248single nucleotide variantNM_002365.5(MAGEB3):c.808C>A (p.Arg270Ser)not specified [RCV004217917]uncertain significanceX3023673230236732Humanname
401883436CV2761132single nucleotide variantNM_002365.5(MAGEB3):c.943G>A (p.Glu315Lys)not specified [RCV004338787]uncertain significanceX3023686730236867Humanname
405651230CV3277538single nucleotide variantNM_002365.5(MAGEB3):c.652G>A (p.Ala218Thr)not specified [RCV004413516]uncertain significanceX3023657630236576Humanname
405651234CV3277540single nucleotide variantNM_002365.5(MAGEB3):c.809G>A (p.Arg270His)not specified [RCV004413518]uncertain significanceX3023673330236733Humanname
407468771CV3449588single nucleotide variantNM_002365.5(MAGEB3):c.439A>G (p.Asn147Asp)not specified [RCV004636401]uncertain significanceX3023636330236363Humanname
407484327CV3449589single nucleotide variantNM_002365.5(MAGEB3):c.351G>A (p.Met117Ile)not specified [RCV004640508]uncertain significanceX3023627530236275Humanname
407484334CV3449590single nucleotide variantNM_002365.5(MAGEB3):c.956A>G (p.Gln319Arg)not specified [RCV004640509]uncertain significanceX3023688030236880Humanname
597623672CV3694088single nucleotide variantNM_002365.5(MAGEB3):c.628G>A (p.Val210Met)not specified [RCV004936689]uncertain significanceX3023655230236552Humanname
598183916CV3992320single nucleotide variantNM_002365.5(MAGEB3):c.433C>T (p.His145Tyr)not specified [RCV005373004]likely benignX3023635730236357Humanname
15201923CV706203single nucleotide variantNM_002365.5(MAGEB3):c.918G>T (p.Trp306Cys)not provided [RCV000957770]benignX3023684230236842Humanname
156111903CV2387865single nucleotide variantNM_002365.5(MAGEB3):c.1004G>A (p.Cys335Tyr)not specified [RCV004236419]uncertain significanceX3023692830236928Humanname
156146003CV2397384single nucleotide variantNM_002365.5(MAGEB3):c.1018G>A (p.Ala340Thr)not specified [RCV004238905]uncertain significanceX3023694230236942Humanname