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23 records found for search term Mgst1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156185487CV1686037single nucleotide variantNM_020300.5(MGST1):c.*57T>GPulmonary disease, chronic obstructive, susceptibility to [RCV002508837]protective121636409816364098Human1name
156185476CV1686036single nucleotide variantNM_020300.5(MGST1):c.-22-1869G>APulmonary disease, chronic obstructive, susceptibility to [RCV002508836]association121635236216352362Human1name
156185516CV1686040single nucleotide variantNM_020300.5(MGST1):c.221+2528G>CPulmonary disease, chronic obstructive, susceptibility to [RCV002508840]association121636022716360227Human1name
155933778CV1686039single nucleotide variantNM_001267598.2(MGST1):c.221+8635G>TPulmonary disease, chronic obstructive, susceptibility to [RCV002508839]protective121636633416366334Human1name
15105441CV753282single nucleotide variantNM_020300.5(MGST1):c.105A>C (p.Ala35=)not provided [RCV000915547]likely benign121635435716354357Humanname
597644981CV3563411single nucleotide variantNM_020300.5(MGST1):c.94A>T (p.Thr32Ser)not specified [RCV004832868]uncertain significance121635434616354346Humanname
156319740CV2260884single nucleotide variantNM_020300.5(MGST1):c.178A>G (p.Lys60Glu)not specified [RCV004125778]uncertain significance121635765616357656Humanname
155963143CV2330297single nucleotide variantNM_020300.5(MGST1):c.203G>A (p.Arg68Lys)not specified [RCV004180883]uncertain significance121635768116357681Humanname
156054489CV2385801single nucleotide variantNM_020300.5(MGST1):c.263G>A (p.Gly88Glu)not specified [RCV004226546]uncertain significance121636383616363836Humanname
401742954CV2677725single nucleotide variantNM_020300.5(MGST1):c.217C>T (p.Arg73Cys)not specified [RCV004291804]uncertain significance121635769516357695Humanname
405661021CV3289188single nucleotide variantNM_020300.5(MGST1):c.187C>G (p.Leu63Val)not specified [RCV004417309]uncertain significance121635766516357665Humanname
405661024CV3289189single nucleotide variantNM_020300.5(MGST1):c.218G>A (p.Arg73His)not specified [RCV004417310]uncertain significance121635769616357696Humanname
597645013CV3563415single nucleotide variantNM_020300.5(MGST1):c.235G>T (p.Asp79Tyr)not specified [RCV004832872]uncertain significance121636380816363808Humanname
598185525CV3982409single nucleotide variantNM_020300.5(MGST1):c.118A>G (p.Thr40Ala)not specified [RCV005373267]uncertain significance121635437016354370Humanname
155968834CV2244364single nucleotide variantNM_020300.5(MGST1):c.332T>C (p.Val111Ala)not specified [RCV004100344]uncertain significance121636390516363905Humanname
156100499CV2392950single nucleotide variantNM_020300.5(MGST1):c.430A>G (p.Met144Val)not specified [RCV004242805]uncertain significance121636400316364003Humanname
156171128CV2400647single nucleotide variantNM_020300.5(MGST1):c.370C>T (p.Pro124Ser)not specified [RCV004242330]uncertain significance121636394316363943Humanname
405661027CV3289190single nucleotide variantNM_020300.5(MGST1):c.406G>A (p.Val136Ile)not specified [RCV004417311]likely benign121636397916363979Humanname
405661032CV3289191single nucleotide variantNM_020300.5(MGST1):c.413A>G (p.Tyr138Cys)not specified [RCV004417312]uncertain significance121636398616363986Humanname
407503768CV3446794single nucleotide variantNM_020300.5(MGST1):c.409G>A (p.Gly137Arg)not specified [RCV004645581]uncertain significance121636398216363982Humanname
597644990CV3563412single nucleotide variantNM_020300.5(MGST1):c.317A>G (p.His106Arg)not specified [RCV004832869]uncertain significance121636389016363890Humanname
597644998CV3563413single nucleotide variantNM_020300.5(MGST1):c.299C>T (p.Pro100Leu)not specified [RCV004832870]likely benign121636387216363872Humanname
597645006CV3563414single nucleotide variantNM_020300.5(MGST1):c.359C>T (p.Ala120Val)not specified [RCV004832871]uncertain significance121636393216363932Humanname