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Variants search result for Homo sapiens
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30 records found for search term Pgam1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405746596CV3368586single nucleotide variantNM_002629.4(PGAM1):c.11A>G (p.Tyr4Cys)not specified [RCV004498484]uncertain significance109742631897426318Humanname
15101256CV701503single nucleotide variantNM_002629.4(PGAM1):c.14A>G (p.Lys5Arg)not provided [RCV000959051]benign109742632197426321Humanname
15134568CV712543single nucleotide variantNM_002629.4(PGAM1):c.297T>C (p.Asn99=)not provided [RCV000965148]benign109743053697430536Humanname
156020646CV2226536single nucleotide variantNM_002629.4(PGAM1):c.77A>G (p.Tyr26Cys)not specified [RCV004101797]uncertain significance109742638497426384Humanname
156293308CV2336451single nucleotide variantNM_002629.4(PGAM1):c.67A>C (p.Ser23Arg)not specified [RCV004194665]uncertain significance109742637497426374Humanname
401858618CV2770559single nucleotide variantNM_002629.4(PGAM1):c.34G>A (p.Gly12Ser)not specified [RCV004349626]uncertain significance109742634197426341Humanname
15127605CV712544single nucleotide variantNM_002629.4(PGAM1):c.456C>T (p.Ser152=)not provided [RCV000963934]benign109743099697430996Humanname
156179362CV2229544single nucleotide variantNM_002629.4(PGAM1):c.239C>T (p.Pro80Leu)not specified [RCV004103082]uncertain significance109743047897430478Humanname
156109429CV2254557single nucleotide variantNM_002629.4(PGAM1):c.155T>C (p.Phe52Ser)not specified [RCV004123909]uncertain significance109743039497430394Humanname
156113389CV2261362single nucleotide variantNM_002629.4(PGAM1):c.193C>T (p.Arg65Trp)not specified [RCV004130004]uncertain significance109743043297430432Humanname
405746602CV3368587single nucleotide variantNM_002629.4(PGAM1):c.143C>T (p.Ala48Val)not specified [RCV004498485]uncertain significance109743038297430382Humanname
405746612CV3368588single nucleotide variantNM_002629.4(PGAM1):c.164G>C (p.Cys55Ser)not specified [RCV004498486]uncertain significance109743040397430403Humanname
405746616CV3368589single nucleotide variantNM_002629.4(PGAM1):c.280G>T (p.Gly94Cys)not specified [RCV004498487]uncertain significance109743051997430519Humanname
407464243CV3466856single nucleotide variantNM_002629.4(PGAM1):c.289G>A (p.Gly97Ser)not specified [RCV004659900]uncertain significance109743052897430528Humanname
156245762CV2219011single nucleotide variantNM_002629.4(PGAM1):c.682A>C (p.Lys228Gln)not specified [RCV004087185]uncertain significance109743244197432441Humanname
156102584CV2363174single nucleotide variantNM_002629.4(PGAM1):c.598C>G (p.Leu200Val)not specified [RCV004213743]uncertain significance109743235797432357Humanname
401740381CV2684344single nucleotide variantNM_002629.4(PGAM1):c.646A>C (p.Ile216Leu)not specified [RCV004288993]uncertain significance109743240597432405Humanname
401728204CV2685945single nucleotide variantNM_002629.4(PGAM1):c.511A>G (p.Ile171Val)not specified [RCV004294916]uncertain significance109743105197431051Humanname
401877909CV2757686single nucleotide variantNM_002629.4(PGAM1):c.679A>G (p.Ile227Val)not specified [RCV004334795]uncertain significance109743243897432438Humanname
401891430CV2780463single nucleotide variantNM_002629.4(PGAM1):c.742G>A (p.Ala248Thr)not specified [RCV004358162]uncertain significance109743250197432501Humanname
401891599CV2780565single nucleotide variantNM_002629.4(PGAM1):c.578T>C (p.Ile193Thr)not specified [RCV004351939]uncertain significance109743111897431118Humanname
405746634CV3368591single nucleotide variantNM_002629.4(PGAM1):c.598C>T (p.Leu200Phe)not specified [RCV004498489]uncertain significance109743235797432357Humanname
405746642CV3368592single nucleotide variantNM_002629.4(PGAM1):c.632C>T (p.Pro211Leu)not specified [RCV004498490]uncertain significance109743239197432391Humanname
407528931CV3466857single nucleotide variantNM_002629.4(PGAM1):c.398A>G (p.Tyr133Cys)not specified [RCV004655780]uncertain significance109743063797430637Humanname
597725081CV3575867single nucleotide variantNM_002629.4(PGAM1):c.583A>G (p.Lys195Glu)not specified [RCV004842259]uncertain significance109743112397431123Humanname
597725089CV3575868single nucleotide variantNM_002629.4(PGAM1):c.299A>T (p.Lys100Ile)not specified [RCV004842260]uncertain significance109743053897430538Humanname
597725098CV3575869single nucleotide variantNM_002629.4(PGAM1):c.356A>G (p.Tyr119Cys)not specified [RCV004842261]uncertain significance109743059597430595Humanname
598262250CV3999768single nucleotide variantNM_002629.4(PGAM1):c.314C>G (p.Ala105Gly)not specified [RCV005387051]uncertain significance109743055397430553Humanname
598196865CV3999769single nucleotide variantNM_002629.4(PGAM1):c.719G>A (p.Arg240His)not specified [RCV005397785]uncertain significance109743247897432478Humanname
598262257CV3999770single nucleotide variantNM_002629.4(PGAM1):c.709G>A (p.Glu237Lys)not specified [RCV005387052]uncertain significance109743246897432468Humanname