Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.161544671C>TCA2648790062FCGR3Ac.577+30G>A (n.577+30G>A)
c.574+30G>A (n.574+30G>A)
c.607G>A (p.Gly203Arg)
c.526+30G>A (n.526+30G>A)
c.685+30G>A (n.685+30G>A)
c.627+30G>A
c.682+30G>A (n.682+30G>A)
c.428-1472G>A (n.428-1472G>A)
c.892+30G>A (n.892+30G>A)
c.889+30G>A (n.889+30G>A)
c.635-1472G>A (n.635-1472G>A)
 gnomAD v4
1g.161544672_161544683delinsTGGGCATTCCAGCA1202785196FCGR3Ac.577+18_577+29delinsCTGGAATGCCCA (n.577+18_577+29delinsCTGGAATGCCCA)
c.574+18_574+29delinsCTGGAATGCCCA (n.574+18_574+29delinsCTGGAATGCCCA)
c.595_606delinsCTGGAATGCCCA (p.Leu199=)
c.526+18_526+29delinsCTGGAATGCCCA (n.526+18_526+29delinsCTGGAATGCCCA)
c.685+18_685+29delinsCTGGAATGCCCA (n.685+18_685+29delinsCTGGAATGCCCA)
c.627+18_627+29delinsCTGGAATGCCCA
c.682+18_682+29delinsCTGGAATGCCCA (n.682+18_682+29delinsCTGGAATGCCCA)
c.428-1484_428-1473delinsCTGGAATGCCCA (n.428-1484_428-1473delinsCTGGAATGCCCA)
c.892+18_892+29delinsCTGGAATGCCCA (n.892+18_892+29delinsCTGGAATGCCCA)
c.889+18_889+29delinsCTGGAATGCCCA (n.889+18_889+29delinsCTGGAATGCCCA)
c.635-1484_635-1473delinsCTGGAATGCCCA (n.635-1484_635-1473delinsCTGGAATGCCCA)
1g.161544673G=CA1202785197FCGR3Ac.577+28C= (n.577+28C=)
c.574+28C= (n.574+28C=)
c.605C= (p.Pro202=)
c.526+28C= (n.526+28C=)
c.685+28C= (n.685+28C=)
c.627+28C=
c.682+28C= (n.682+28C=)
c.428-1474C= (n.428-1474C=)
c.892+28C= (n.892+28C=)
c.889+28C= (n.889+28C=)
c.635-1474C= (n.635-1474C=)
1g.161544673G>TCA890213966FCGR3Ac.577+28C>A (n.577+28C>A)
c.574+28C>A (n.574+28C>A)
c.605C>A (p.Pro202Gln)
c.526+28C>A (n.526+28C>A)
c.685+28C>A (n.685+28C>A)
c.627+28C>A
c.682+28C>A (n.682+28C>A)
c.428-1474C>A (n.428-1474C>A)
c.892+28C>A (n.892+28C>A)
c.889+28C>A (n.889+28C>A)
c.635-1474C>A (n.635-1474C>A)
 dbSNP gnomAD v3 gnomAD v4
1g.161544675_161544685delCA1211367FCGR3Ac.577+18_577+28del (n.577+18_577+28del)
c.574+18_574+28del (n.574+18_574+28del)
c.595_605del (p.Leu199ArgfsTer21)
c.526+18_526+28del (n.526+18_526+28del)
c.685+18_685+28del (n.685+18_685+28del)
c.627+18_627+28del
c.682+18_682+28del (n.682+18_682+28del)
c.428-1484_428-1474del (n.428-1484_428-1474del)
c.892+18_892+28del (n.892+18_892+28del)
c.889+18_889+28del (n.889+18_889+28del)
c.635-1484_635-1474del (n.635-1484_635-1474del)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.161544674G>ACA1202785199FCGR3Ac.577+27C>T (n.577+27C>T)
c.574+27C>T (n.574+27C>T)
c.604C>T (p.Pro202Ser)
c.526+27C>T (n.526+27C>T)
c.685+27C>T (n.685+27C>T)
c.627+27C>T
c.682+27C>T (n.682+27C>T)
c.428-1475C>T (n.428-1475C>T)
c.892+27C>T (n.892+27C>T)
c.889+27C>T (n.889+27C>T)
c.635-1475C>T (n.635-1475C>T)
 dbSNP gnomAD v4
1g.161544674G=CA1202785198FCGR3Ac.577+27C= (n.577+27C=)
c.574+27C= (n.574+27C=)
c.604C= (p.Pro202=)
c.526+27C= (n.526+27C=)
c.685+27C= (n.685+27C=)
c.627+27C=
c.682+27C= (n.682+27C=)
c.428-1475C= (n.428-1475C=)
c.892+27C= (n.892+27C=)
c.889+27C= (n.889+27C=)
c.635-1475C= (n.635-1475C=)
1g.161544675G>ACA2648790063FCGR3Ac.577+26C>T (n.577+26C>T)
c.574+26C>T (n.574+26C>T)
c.603C>T (p.Cys201=)
c.526+26C>T (n.526+26C>T)
c.685+26C>T (n.685+26C>T)
c.627+26C>T
c.682+26C>T (n.682+26C>T)
c.428-1476C>T (n.428-1476C>T)
c.892+26C>T (n.892+26C>T)
c.889+26C>T (n.889+26C>T)
c.635-1476C>T (n.635-1476C>T)
 gnomAD v4
1g.161544675G>CCA2648790064FCGR3Ac.577+26C>G (n.577+26C>G)
c.574+26C>G (n.574+26C>G)
c.603C>G (p.Cys201Trp)
c.526+26C>G (n.526+26C>G)
c.685+26C>G (n.685+26C>G)
c.627+26C>G
c.682+26C>G (n.682+26C>G)
c.428-1476C>G (n.428-1476C>G)
c.892+26C>G (n.892+26C>G)
c.889+26C>G (n.889+26C>G)
c.635-1476C>G (n.635-1476C>G)
 gnomAD v4
1g.161544676C>ACA646114577FCGR3Ac.577+25G>T (n.577+25G>T)
c.574+25G>T (n.574+25G>T)
c.602G>T (p.Cys201Phe)
c.526+25G>T (n.526+25G>T)
c.685+25G>T (n.685+25G>T)
c.627+25G>T
c.682+25G>T (n.682+25G>T)
c.428-1477G>T (n.428-1477G>T)
c.892+25G>T (n.892+25G>T)
c.889+25G>T (n.889+25G>T)
c.635-1477G>T (n.635-1477G>T)
 COSMIC
1g.161544678T>ACA2648790065FCGR3Ac.577+23A>T (n.577+23A>T)
c.574+23A>T (n.574+23A>T)
c.600A>T (p.Glu200Asp)
c.526+23A>T (n.526+23A>T)
c.685+23A>T (n.685+23A>T)
c.627+23A>T
c.682+23A>T (n.682+23A>T)
c.428-1479A>T (n.428-1479A>T)
c.892+23A>T (n.892+23A>T)
c.889+23A>T (n.889+23A>T)
c.635-1479A>T (n.635-1479A>T)
 gnomAD v4
1g.161544680C=CA1202785200FCGR3Ac.577+21G= (n.577+21G=)
c.574+21G= (n.574+21G=)
c.598G= (p.Glu200=)
c.526+21G= (n.526+21G=)
c.685+21G= (n.685+21G=)
c.627+21G=
c.682+21G= (n.682+21G=)
c.428-1481G= (n.428-1481G=)
c.892+21G= (n.892+21G=)
c.889+21G= (n.889+21G=)
c.635-1481G= (n.635-1481G=)
1g.161544680C>GCA526885029FCGR3Ac.577+21G>C (n.577+21G>C)
c.574+21G>C (n.574+21G>C)
c.598G>C (p.Glu200Gln)
c.526+21G>C (n.526+21G>C)
c.685+21G>C (n.685+21G>C)
c.627+21G>C
c.682+21G>C (n.682+21G>C)
c.428-1481G>C (n.428-1481G>C)
c.892+21G>C (n.892+21G>C)
c.889+21G>C (n.889+21G>C)
c.635-1481G>C (n.635-1481G>C)
 dbSNP gnomAD v2 gnomAD v4
1g.161544681C>GCA2648790066FCGR3Ac.577+20G>C (n.577+20G>C)
c.574+20G>C (n.574+20G>C)
c.597G>C (p.Leu199=)
c.526+20G>C (n.526+20G>C)
c.685+20G>C (n.685+20G>C)
c.627+20G>C
c.682+20G>C (n.682+20G>C)
c.428-1482G>C (n.428-1482G>C)
c.892+20G>C (n.892+20G>C)
c.889+20G>C (n.889+20G>C)
c.635-1482G>C (n.635-1482G>C)
 gnomAD v4
1g.161544682A>GCA2648790067FCGR3Ac.577+19T>C (n.577+19T>C)
c.574+19T>C (n.574+19T>C)
c.596T>C (p.Leu199Pro)
c.526+19T>C (n.526+19T>C)
c.685+19T>C (n.685+19T>C)
c.627+19T>C
c.682+19T>C (n.682+19T>C)
c.428-1483T>C (n.428-1483T>C)
c.892+19T>C (n.892+19T>C)
c.889+19T>C (n.889+19T>C)
c.635-1483T>C (n.635-1483T>C)
 gnomAD v4
1g.161544685G>TCA2573939349FCGR3Ac.577+16C>A (n.577+16C>A)
c.574+16C>A (n.574+16C>A)
c.593C>A (p.Thr198Asn)
c.526+16C>A (n.526+16C>A)
c.685+16C>A (n.685+16C>A)
c.627+16C>A
c.682+16C>A (n.682+16C>A)
c.428-1486C>A (n.428-1486C>A)
c.892+16C>A (n.892+16C>A)
c.889+16C>A (n.889+16C>A)
c.635-1486C>A (n.635-1486C>A)
1g.161544687G>TCA2648790068FCGR3Ac.577+14C>A (n.577+14C>A)
c.574+14C>A (n.574+14C>A)
c.591C>A (p.Ala197=)
c.526+14C>A (n.526+14C>A)
c.685+14C>A (n.685+14C>A)
c.627+14C>A
c.682+14C>A (n.682+14C>A)
c.428-1488C>A (n.428-1488C>A)
c.892+14C>A (n.892+14C>A)
c.889+14C>A (n.889+14C>A)
c.635-1488C>A (n.635-1488C>A)
 gnomAD v4
1g.161544688G>ACA1211369FCGR3Ac.577+13C>T (n.577+13C>T)
c.574+13C>T (n.574+13C>T)
c.590C>T (p.Ala197Val)
c.526+13C>T (n.526+13C>T)
c.685+13C>T (n.685+13C>T)
c.627+13C>T
c.682+13C>T (n.682+13C>T)
c.428-1489C>T (n.428-1489C>T)
c.892+13C>T (n.892+13C>T)
c.889+13C>T (n.889+13C>T)
c.635-1489C>T (n.635-1489C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.161544688G=CA1202785201FCGR3Ac.577+13C= (n.577+13C=)
c.574+13C= (n.574+13C=)
c.590C= (p.Ala197=)
c.526+13C= (n.526+13C=)
c.685+13C= (n.685+13C=)
c.627+13C=
c.682+13C= (n.682+13C=)
c.428-1489C= (n.428-1489C=)
c.892+13C= (n.892+13C=)
c.889+13C= (n.889+13C=)
c.635-1489C= (n.635-1489C=)
1g.161544688G>TCA1211368FCGR3Ac.577+13C>A (n.577+13C>A)
c.574+13C>A (n.574+13C>A)
c.590C>A (p.Ala197Asp)
c.526+13C>A (n.526+13C>A)
c.685+13C>A (n.685+13C>A)
c.627+13C>A
c.682+13C>A (n.682+13C>A)
c.428-1489C>A (n.428-1489C>A)
c.892+13C>A (n.892+13C>A)
c.889+13C>A (n.889+13C>A)
c.635-1489C>A (n.635-1489C>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.161544689C>TCA2648790069FCGR3Ac.577+12G>A (n.577+12G>A)
c.574+12G>A (n.574+12G>A)
c.589G>A (p.Ala197Thr)
c.526+12G>A (n.526+12G>A)
c.685+12G>A (n.685+12G>A)
c.627+12G>A
c.682+12G>A (n.682+12G>A)
c.428-1490G>A (n.428-1490G>A)
c.892+12G>A (n.892+12G>A)
c.889+12G>A (n.889+12G>A)
c.635-1490G>A (n.635-1490G>A)
 gnomAD v4
1g.161544690A=CA1148884114FCGR3Ac.577+11T= (n.577+11T=)
c.574+11T= (n.574+11T=)
c.588T= (p.Cys196=)
c.526+11T= (n.526+11T=)
c.685+11T= (n.685+11T=)
c.627+11T=
c.682+11T= (n.682+11T=)
c.428-1491T= (n.428-1491T=)
c.892+11T= (n.892+11T=)
c.889+11T= (n.889+11T=)
c.635-1491T= (n.635-1491T=)
1g.161544690A>CCA1211370FCGR3Ac.577+11T>G (n.577+11T>G)
c.574+11T>G (n.574+11T>G)
c.588T>G (p.Cys196Trp)
c.526+11T>G (n.526+11T>G)
c.685+11T>G (n.685+11T>G)
c.627+11T>G
c.682+11T>G (n.682+11T>G)
c.428-1491T>G (n.428-1491T>G)
c.892+11T>G (n.892+11T>G)
c.889+11T>G (n.889+11T>G)
c.635-1491T>G (n.635-1491T>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.161544690A>TCA2648790070FCGR3Ac.577+11T>A (n.577+11T>A)
c.574+11T>A (n.574+11T>A)
c.588T>A (p.Cys196Ter)
c.526+11T>A (n.526+11T>A)
c.685+11T>A (n.685+11T>A)
c.627+11T>A
c.682+11T>A (n.682+11T>A)
c.428-1491T>A (n.428-1491T>A)
c.892+11T>A (n.892+11T>A)
c.889+11T>A (n.889+11T>A)
c.635-1491T>A (n.635-1491T>A)
 gnomAD v4
1g.161544691C>ACA2746378702FCGR3Ac.577+10G>T (n.577+10G>T)
c.574+10G>T (n.574+10G>T)
c.587G>T (p.Cys196Phe)
c.526+10G>T (n.526+10G>T)
c.685+10G>T (n.685+10G>T)
c.627+10G>T
c.682+10G>T (n.682+10G>T)
c.428-1492G>T (n.428-1492G>T)
c.892+10G>T (n.892+10G>T)
c.889+10G>T (n.889+10G>T)
c.635-1492G>T (n.635-1492G>T)
1g.161544691C>TCA2648790071FCGR3Ac.577+10G>A (n.577+10G>A)
c.574+10G>A (n.574+10G>A)
c.587G>A (p.Cys196Tyr)
c.526+10G>A (n.526+10G>A)
c.685+10G>A (n.685+10G>A)
c.627+10G>A
c.682+10G>A (n.682+10G>A)
c.428-1492G>A (n.428-1492G>A)
c.892+10G>A (n.892+10G>A)
c.889+10G>A (n.889+10G>A)
c.635-1492G>A (n.635-1492G>A)
 gnomAD v4
1g.161544692A=CA1202785202FCGR3Ac.577+9T= (n.577+9T=)
c.574+9T= (n.574+9T=)
c.586T= (p.Cys196=)
c.526+9T= (n.526+9T=)
c.685+9T= (n.685+9T=)
c.627+9T=
c.682+9T= (n.682+9T=)
c.428-1493T= (n.428-1493T=)
c.892+9T= (n.892+9T=)
c.889+9T= (n.889+9T=)
c.635-1493T= (n.635-1493T=)
1g.161544692A>GCA890213978FCGR3Ac.577+9T>C (n.577+9T>C)
c.574+9T>C (n.574+9T>C)
c.586T>C (p.Cys196Arg)
c.526+9T>C (n.526+9T>C)
c.685+9T>C (n.685+9T>C)
c.627+9T>C
c.682+9T>C (n.682+9T>C)
c.428-1493T>C (n.428-1493T>C)
c.892+9T>C (n.892+9T>C)
c.889+9T>C (n.889+9T>C)
c.635-1493T>C (n.635-1493T>C)
 dbSNP gnomAD v4
1g.161544692A>TCA890213983FCGR3Ac.577+9T>A (n.577+9T>A)
c.574+9T>A (n.574+9T>A)
c.586T>A (p.Cys196Ser)
c.526+9T>A (n.526+9T>A)
c.685+9T>A (n.685+9T>A)
c.627+9T>A
c.682+9T>A (n.682+9T>A)
c.428-1493T>A (n.428-1493T>A)
c.892+9T>A (n.892+9T>A)
c.889+9T>A (n.889+9T>A)
c.635-1493T>A (n.635-1493T>A)
 dbSNP
1g.161544693T>CCA1202785204FCGR3Ac.577+8A>G (n.577+8A>G)
c.574+8A>G (n.574+8A>G)
c.585A>G (p.Thr195=)
c.526+8A>G (n.526+8A>G)
c.685+8A>G (n.685+8A>G)
c.627+8A>G
c.682+8A>G (n.682+8A>G)
c.428-1494A>G (n.428-1494A>G)
c.892+8A>G (n.892+8A>G)
c.889+8A>G (n.889+8A>G)
c.635-1494A>G (n.635-1494A>G)
 dbSNP
1g.161544693T>GCA1008427424FCGR3Ac.577+8A>C (n.577+8A>C)
c.574+8A>C (n.574+8A>C)
c.585A>C (p.Thr195=)
c.526+8A>C (n.526+8A>C)
c.685+8A>C (n.685+8A>C)
c.627+8A>C
c.682+8A>C (n.682+8A>C)
c.428-1494A>C (n.428-1494A>C)
c.892+8A>C (n.892+8A>C)
c.889+8A>C (n.889+8A>C)
c.635-1494A>C (n.635-1494A>C)
 dbSNP gnomAD v3 gnomAD v4
1g.161544693T=CA1202785203FCGR3Ac.577+8A= (n.577+8A=)
c.574+8A= (n.574+8A=)
c.585A= (p.Thr195=)
c.526+8A= (n.526+8A=)
c.685+8A= (n.685+8A=)
c.627+8A=
c.682+8A= (n.682+8A=)
c.428-1494A= (n.428-1494A=)
c.892+8A= (n.892+8A=)
c.889+8A= (n.889+8A=)
c.635-1494A= (n.635-1494A=)
1g.161544694G>ACA890213984FCGR3Ac.577+7C>T (n.577+7C>T)
c.574+7C>T (n.574+7C>T)
c.584C>T (p.Thr195Ile)
c.526+7C>T (n.526+7C>T)
c.685+7C>T (n.685+7C>T)
c.627+7C>T
c.682+7C>T (n.682+7C>T)
c.428-1495C>T (n.428-1495C>T)
c.892+7C>T (n.892+7C>T)
c.889+7C>T (n.889+7C>T)
c.635-1495C>T (n.635-1495C>T)
 dbSNP gnomAD v3 gnomAD v4
1g.161544694G=CA1202785205FCGR3Ac.577+7C= (n.577+7C=)
c.574+7C= (n.574+7C=)
c.584C= (p.Thr195=)
c.526+7C= (n.526+7C=)
c.685+7C= (n.685+7C=)
c.627+7C=
c.682+7C= (n.682+7C=)
c.428-1495C= (n.428-1495C=)
c.892+7C= (n.892+7C=)
c.889+7C= (n.889+7C=)
c.635-1495C= (n.635-1495C=)
1g.161544699A>CCA343367306FCGR3Ac.577+2T>G (n.577+2T>G)
c.574+2T>G (n.574+2T>G)
c.579T>G (p.Gly193=)
c.526+2T>G (n.526+2T>G)
c.685+2T>G (n.685+2T>G)
c.627+2T>G
c.682+2T>G (n.682+2T>G)
c.428-1500T>G (n.428-1500T>G)
c.892+2T>G (n.892+2T>G)
c.889+2T>G (n.889+2T>G)
c.635-1500T>G (n.635-1500T>G)
1g.161544699A>GCA343367307FCGR3Ac.577+2T>C (n.577+2T>C)
c.574+2T>C (n.574+2T>C)
c.579T>C (p.Gly193=)
c.526+2T>C (n.526+2T>C)
c.685+2T>C (n.685+2T>C)
c.627+2T>C
c.682+2T>C (n.682+2T>C)
c.428-1500T>C (n.428-1500T>C)
c.892+2T>C (n.892+2T>C)
c.889+2T>C (n.889+2T>C)
c.635-1500T>C (n.635-1500T>C)
1g.161544699A>TCA343367308FCGR3Ac.577+2T>A (n.577+2T>A)
c.574+2T>A (n.574+2T>A)
c.579T>A (p.Gly193=)
c.526+2T>A (n.526+2T>A)
c.685+2T>A (n.685+2T>A)
c.627+2T>A
c.682+2T>A (n.682+2T>A)
c.428-1500T>A (n.428-1500T>A)
c.892+2T>A (n.892+2T>A)
c.889+2T>A (n.889+2T>A)
c.635-1500T>A (n.635-1500T>A)
1g.161544700C>ACA343367309FCGR3Ac.577+1G>T (n.577+1G>T)
c.574+1G>T (n.574+1G>T)
c.578G>T (p.Gly193Val)
c.526+1G>T (n.526+1G>T)
c.685+1G>T (n.685+1G>T)
c.627+1G>T
c.682+1G>T (n.682+1G>T)
c.428-1501G>T (n.428-1501G>T)
c.892+1G>T (n.892+1G>T)
c.889+1G>T (n.889+1G>T)
c.635-1501G>T (n.635-1501G>T)
1g.161544700C>GCA343367310FCGR3Ac.577+1G>C (n.577+1G>C)
c.574+1G>C (n.574+1G>C)
c.578G>C (p.Gly193Ala)
c.526+1G>C (n.526+1G>C)
c.685+1G>C (n.685+1G>C)
c.627+1G>C
c.682+1G>C (n.682+1G>C)
c.428-1501G>C (n.428-1501G>C)
c.892+1G>C (n.892+1G>C)
c.889+1G>C (n.889+1G>C)
c.635-1501G>C (n.635-1501G>C)
1g.161544700C>TCA343367311FCGR3Ac.577+1G>A (n.577+1G>A)
c.574+1G>A (n.574+1G>A)
c.578G>A (p.Gly193Asp)
c.526+1G>A (n.526+1G>A)
c.685+1G>A (n.685+1G>A)
c.627+1G>A
c.682+1G>A (n.682+1G>A)
c.428-1501G>A (n.428-1501G>A)
c.892+1G>A (n.892+1G>A)
c.889+1G>A (n.889+1G>A)
c.635-1501G>A (n.635-1501G>A)
 gnomAD v4
1g.161544701C>ACA343367312FCGR3Ac.577G>T (p.Gly193Cys)
c.574G>T (p.Gly192Cys)
c.526G>T (p.Gly176Cys)
c.685G>T (p.Gly229Cys)
c.627G>T
c.682G>T (p.Gly228Cys)
c.428-1502G>T (n.428-1502G>T)
c.892G>T (p.Gly298Cys)
c.889G>T (p.Gly297Cys)
c.635-1502G>T (n.635-1502G>T)
1g.161544701C>GCA343367313FCGR3Ac.577G>C (p.Gly193Arg)
c.574G>C (p.Gly192Arg)
c.526G>C (p.Gly176Arg)
c.685G>C (p.Gly229Arg)
c.627G>C
c.682G>C (p.Gly228Arg)
c.428-1502G>C (n.428-1502G>C)
c.892G>C (p.Gly298Arg)
c.889G>C (p.Gly297Arg)
c.635-1502G>C (n.635-1502G>C)
1g.161544701C>TCA343367314FCGR3Ac.577G>A (p.Gly193Ser)
c.574G>A (p.Gly192Ser)
c.526G>A (p.Gly176Ser)
c.685G>A (p.Gly229Ser)
c.627G>A
c.682G>A (p.Gly228Ser)
c.428-1502G>A (n.428-1502G>A)
c.892G>A (p.Gly298Ser)
c.889G>A (p.Gly297Ser)
c.635-1502G>A (n.635-1502G>A)
 COSMIC
1g.161544702T>ACA343367315FCGR3Ac.576A>T (p.Gln192His)
c.573A>T (p.Gln191His)
c.525A>T (p.Gln175His)
c.684A>T (p.Gln228His)
c.626A>T
c.681A>T (p.Gln227His)
c.428-1503A>T (n.428-1503A>T)
c.891A>T (p.Gln297His)
c.888A>T (p.Gln296His)
c.635-1503A>T (n.635-1503A>T)
1g.161544702T>CCA1211371FCGR3Ac.576A>G (p.Gln192=)
c.573A>G (p.Gln191=)
c.525A>G (p.Gln175=)
c.684A>G (p.Gln228=)
c.626A>G
c.681A>G (p.Gln227=)
c.428-1503A>G (n.428-1503A>G)
c.891A>G (p.Gln297=)
c.888A>G (p.Gln296=)
c.635-1503A>G (n.635-1503A>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.161544702T>GCA343367316FCGR3Ac.576A>C (p.Gln192His)
c.573A>C (p.Gln191His)
c.525A>C (p.Gln175His)
c.684A>C (p.Gln228His)
c.626A>C
c.681A>C (p.Gln227His)
c.428-1503A>C (n.428-1503A>C)
c.891A>C (p.Gln297His)
c.888A>C (p.Gln296His)
c.635-1503A>C (n.635-1503A>C)
1g.161544702T=CA1143939801FCGR3Ac.576A= (p.Gln192=)
c.573A= (p.Gln191=)
c.525A= (p.Gln175=)
c.684A= (p.Gln228=)
c.626A=
c.681A= (p.Gln227=)
c.428-1503A= (n.428-1503A=)
c.891A= (p.Gln297=)
c.888A= (p.Gln296=)
c.635-1503A= (n.635-1503A=)
1g.161544703T>ACA343367317FCGR3Ac.575A>T (p.Gln192Leu)
c.572A>T (p.Gln191Leu)
c.524A>T (p.Gln175Leu)
c.683A>T (p.Gln228Leu)
c.625A>T
c.680A>T (p.Gln227Leu)
c.428-1504A>T (n.428-1504A>T)
c.890A>T (p.Gln297Leu)
c.887A>T (p.Gln296Leu)
c.635-1504A>T (n.635-1504A>T)
1g.161544703T>CCA343367319FCGR3Ac.575A>G (p.Gln192Arg)
c.572A>G (p.Gln191Arg)
c.524A>G (p.Gln175Arg)
c.683A>G (p.Gln228Arg)
c.625A>G
c.680A>G (p.Gln227Arg)
c.428-1504A>G (n.428-1504A>G)
c.890A>G (p.Gln297Arg)
c.887A>G (p.Gln296Arg)
c.635-1504A>G (n.635-1504A>G)
 dbSNP gnomAD v2 gnomAD v4
1g.161544703T>GCA343367318FCGR3Ac.575A>C (p.Gln192Pro)
c.572A>C (p.Gln191Pro)
c.524A>C (p.Gln175Pro)
c.683A>C (p.Gln228Pro)
c.625A>C
c.680A>C (p.Gln227Pro)
c.428-1504A>C (n.428-1504A>C)
c.890A>C (p.Gln297Pro)
c.887A>C (p.Gln296Pro)
c.635-1504A>C (n.635-1504A>C)
1g.161544703T=CA1202785206FCGR3Ac.575A= (p.Gln192=)
c.572A= (p.Gln191=)
c.524A= (p.Gln175=)
c.683A= (p.Gln228=)
c.625A=
c.680A= (p.Gln227=)
c.428-1504A= (n.428-1504A=)
c.890A= (p.Gln297=)
c.887A= (p.Gln296=)
c.635-1504A= (n.635-1504A=)
1g.161544704G>ACA343367320FCGR3Ac.574C>T (p.Gln192Ter)
c.571C>T (p.Gln191Ter)
c.523C>T (p.Gln175Ter)
c.682C>T (p.Gln228Ter)
c.624C>T
c.679C>T (p.Gln227Ter)
c.428-1505C>T (n.428-1505C>T)
c.889C>T (p.Gln297Ter)
c.886C>T (p.Gln296Ter)
c.635-1505C>T (n.635-1505C>T)
1g.161544704G>CCA343367322FCGR3Ac.574C>G (p.Gln192Glu)
c.571C>G (p.Gln191Glu)
c.523C>G (p.Gln175Glu)
c.682C>G (p.Gln228Glu)
c.624C>G
c.679C>G (p.Gln227Glu)
c.428-1505C>G (n.428-1505C>G)
c.889C>G (p.Gln297Glu)
c.886C>G (p.Gln296Glu)
c.635-1505C>G (n.635-1505C>G)
1g.161544704G>TCA343367321FCGR3Ac.574C>A (p.Gln192Lys)
c.571C>A (p.Gln191Lys)
c.523C>A (p.Gln175Lys)
c.682C>A (p.Gln228Lys)
c.624C>A
c.679C>A (p.Gln227Lys)
c.428-1505C>A (n.428-1505C>A)
c.889C>A (p.Gln297Lys)
c.886C>A (p.Gln296Lys)
c.635-1505C>A (n.635-1505C>A)
 gnomAD v4
1g.161544705A>CCA421612318FCGR3Ac.573T>G (p.Thr191=)
c.570T>G (p.Thr190=)
c.522T>G (p.Thr174=)
c.681T>G (p.Thr227=)
c.623T>G
c.678T>G (p.Thr226=)
c.428-1506T>G (n.428-1506T>G)
c.888T>G (p.Thr296=)
c.885T>G (p.Thr295=)
c.635-1506T>G (n.635-1506T>G)
1g.161544705A>GCA421612320FCGR3Ac.573T>C (p.Thr191=)
c.570T>C (p.Thr190=)
c.522T>C (p.Thr174=)
c.681T>C (p.Thr227=)
c.623T>C
c.678T>C (p.Thr226=)
c.428-1506T>C (n.428-1506T>C)
c.888T>C (p.Thr296=)
c.885T>C (p.Thr295=)
c.635-1506T>C (n.635-1506T>C)
1g.161544705A>TCA421612321FCGR3Ac.573T>A (p.Thr191=)
c.570T>A (p.Thr190=)
c.522T>A (p.Thr174=)
c.681T>A (p.Thr227=)
c.623T>A
c.678T>A (p.Thr226=)
c.428-1506T>A (n.428-1506T>A)
c.888T>A (p.Thr296=)
c.885T>A (p.Thr295=)
c.635-1506T>A (n.635-1506T>A)
1g.161544706G>ACA1211372FCGR3Ac.572C>T (p.Thr191Ile)
c.569C>T (p.Thr190Ile)
c.521C>T (p.Thr174Ile)
c.680C>T (p.Thr227Ile)
c.622C>T
c.677C>T (p.Thr226Ile)
c.428-1507C>T (n.428-1507C>T)
c.887C>T (p.Thr296Ile)
c.884C>T (p.Thr295Ile)
c.635-1507C>T (n.635-1507C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.161544706G>CCA343367323FCGR3Ac.572C>G (p.Thr191Ser)
c.569C>G (p.Thr190Ser)
c.521C>G (p.Thr174Ser)
c.680C>G (p.Thr227Ser)
c.622C>G
c.677C>G (p.Thr226Ser)
c.428-1507C>G (n.428-1507C>G)
c.887C>G (p.Thr296Ser)
c.884C>G (p.Thr295Ser)
c.635-1507C>G (n.635-1507C>G)
1g.161544706G=CA1202785207FCGR3Ac.572C= (p.Thr191=)
c.569C= (p.Thr190=)
c.521C= (p.Thr174=)
c.680C= (p.Thr227=)
c.622C=
c.677C= (p.Thr226=)
c.428-1507C= (n.428-1507C=)
c.887C= (p.Thr296=)
c.884C= (p.Thr295=)
c.635-1507C= (n.635-1507C=)
1g.161544706G>TCA1211373FCGR3Ac.572C>A (p.Thr191Asn)
c.569C>A (p.Thr190Asn)
c.521C>A (p.Thr174Asn)
c.680C>A (p.Thr227Asn)
c.622C>A
c.677C>A (p.Thr226Asn)
c.428-1507C>A (n.428-1507C>A)
c.887C>A (p.Thr296Asn)
c.884C>A (p.Thr295Asn)
c.635-1507C>A (n.635-1507C>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.161544707T>ACA343367324FCGR3Ac.571A>T (p.Thr191Ser)
c.568A>T (p.Thr190Ser)
c.520A>T (p.Thr174Ser)
c.679A>T (p.Thr227Ser)
c.621A>T
c.676A>T (p.Thr226Ser)
c.428-1508A>T (n.428-1508A>T)
c.886A>T (p.Thr296Ser)
c.883A>T (p.Thr295Ser)
c.635-1508A>T (n.635-1508A>T)
1g.161544707T>CCA343367325FCGR3Ac.571A>G (p.Thr191Ala)
c.568A>G (p.Thr190Ala)
c.520A>G (p.Thr174Ala)
c.679A>G (p.Thr227Ala)
c.621A>G
c.676A>G (p.Thr226Ala)
c.428-1508A>G (n.428-1508A>G)
c.886A>G (p.Thr296Ala)
c.883A>G (p.Thr295Ala)
c.635-1508A>G (n.635-1508A>G)
1g.161544707T>GCA343367326FCGR3Ac.571A>C (p.Thr191Pro)
c.568A>C (p.Thr190Pro)
c.520A>C (p.Thr174Pro)
c.679A>C (p.Thr227Pro)
c.621A>C
c.676A>C (p.Thr226Pro)
c.428-1508A>C (n.428-1508A>C)
c.886A>C (p.Thr296Pro)
c.883A>C (p.Thr295Pro)
c.635-1508A>C (n.635-1508A>C)
 dbSNP
1g.161544707T=CA1202785208FCGR3Ac.571A= (p.Thr191=)
c.568A= (p.Thr190=)
c.520A= (p.Thr174=)
c.679A= (p.Thr227=)
c.621A=
c.676A= (p.Thr226=)
c.428-1508A= (n.428-1508A=)
c.886A= (p.Thr296=)
c.883A= (p.Thr295=)
c.635-1508A= (n.635-1508A=)
1g.161544708G>ACA421612329FCGR3Ac.570C>T (p.Ile190=)
c.567C>T (p.Ile189=)
c.519C>T (p.Ile173=)
c.678C>T (p.Ile226=)
c.620C>T
c.675C>T (p.Ile225=)
c.428-1509C>T (n.428-1509C>T)
c.885C>T (p.Ile295=)
c.882C>T (p.Ile294=)
c.635-1509C>T (n.635-1509C>T)
 dbSNP gnomAD v3 gnomAD v4
1g.161544708G>CCA343367327FCGR3Ac.570C>G (p.Ile190Met)
c.567C>G (p.Ile189Met)
c.519C>G (p.Ile173Met)
c.678C>G (p.Ile226Met)
c.620C>G
c.675C>G (p.Ile225Met)
c.428-1509C>G (n.428-1509C>G)
c.885C>G (p.Ile295Met)
c.882C>G (p.Ile294Met)
c.635-1509C>G (n.635-1509C>G)
1g.161544708G=CA1202785209FCGR3Ac.570C= (p.Ile190=)
c.567C= (p.Ile189=)
c.519C= (p.Ile173=)
c.678C= (p.Ile226=)
c.620C=
c.675C= (p.Ile225=)
c.428-1509C= (n.428-1509C=)
c.885C= (p.Ile295=)
c.882C= (p.Ile294=)
c.635-1509C= (n.635-1509C=)
1g.161544708G>TCA421612332FCGR3Ac.570C>A (p.Ile190=)
c.567C>A (p.Ile189=)
c.519C>A (p.Ile173=)
c.678C>A (p.Ile226=)
c.620C>A
c.675C>A (p.Ile225=)
c.428-1509C>A (n.428-1509C>A)
c.885C>A (p.Ile295=)
c.882C>A (p.Ile294=)
c.635-1509C>A (n.635-1509C>A)
 dbSNP
1g.161544709A>CCA343367328FCGR3Ac.569T>G (p.Ile190Ser)
c.566T>G (p.Ile189Ser)
c.518T>G (p.Ile173Ser)
c.677T>G (p.Ile226Ser)
c.619T>G
c.674T>G (p.Ile225Ser)
c.428-1510T>G (n.428-1510T>G)
c.884T>G (p.Ile295Ser)
c.881T>G (p.Ile294Ser)
c.635-1510T>G (n.635-1510T>G)
1g.161544709A>GCA343367329FCGR3Ac.569T>C (p.Ile190Thr)
c.566T>C (p.Ile189Thr)
c.518T>C (p.Ile173Thr)
c.677T>C (p.Ile226Thr)
c.619T>C
c.674T>C (p.Ile225Thr)
c.428-1510T>C (n.428-1510T>C)
c.884T>C (p.Ile295Thr)
c.881T>C (p.Ile294Thr)
c.635-1510T>C (n.635-1510T>C)
 gnomAD v4
1g.161544709A>TCA343367330FCGR3Ac.569T>A (p.Ile190Asn)
c.566T>A (p.Ile189Asn)
c.518T>A (p.Ile173Asn)
c.677T>A (p.Ile226Asn)
c.619T>A
c.674T>A (p.Ile225Asn)
c.428-1510T>A (n.428-1510T>A)
c.884T>A (p.Ile295Asn)
c.881T>A (p.Ile294Asn)
c.635-1510T>A (n.635-1510T>A)
1g.161544710T>ACA343367331FCGR3Ac.568A>T (p.Ile190Phe)
c.565A>T (p.Ile189Phe)
c.517A>T (p.Ile173Phe)
c.676A>T (p.Ile226Phe)
c.618A>T
c.673A>T (p.Ile225Phe)
c.428-1511A>T (n.428-1511A>T)
c.883A>T (p.Ile295Phe)
c.880A>T (p.Ile294Phe)
c.635-1511A>T (n.635-1511A>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.161544710T>CCA343367332FCGR3Ac.568A>G (p.Ile190Val)
c.565A>G (p.Ile189Val)
c.517A>G (p.Ile173Val)
c.676A>G (p.Ile226Val)
c.618A>G
c.673A>G (p.Ile225Val)
c.428-1511A>G (n.428-1511A>G)
c.883A>G (p.Ile295Val)
c.880A>G (p.Ile294Val)
c.635-1511A>G (n.635-1511A>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.161544710T>GCA343367333FCGR3Ac.568A>C (p.Ile190Leu)
c.565A>C (p.Ile189Leu)
c.517A>C (p.Ile173Leu)
c.676A>C (p.Ile226Leu)
c.618A>C
c.673A>C (p.Ile225Leu)
c.428-1511A>C (n.428-1511A>C)
c.883A>C (p.Ile295Leu)
c.880A>C (p.Ile294Leu)
c.635-1511A>C (n.635-1511A>C)
1g.161544710T=CA1202785210FCGR3Ac.568A= (p.Ile190=)
c.565A= (p.Ile189=)
c.517A= (p.Ile173=)
c.676A= (p.Ile226=)
c.618A=
c.673A= (p.Ile225=)
c.428-1511A= (n.428-1511A=)
c.883A= (p.Ile295=)
c.880A= (p.Ile294=)
c.635-1511A= (n.635-1511A=)
1g.161544711G>ACA1211374FCGR3Ac.567C>T (p.Thr189=)
c.564C>T (p.Thr188=)
c.516C>T (p.Thr172=)
c.675C>T (p.Thr225=)
c.617C>T
c.672C>T (p.Thr224=)
c.428-1512C>T (n.428-1512C>T)
c.882C>T (p.Thr294=)
c.879C>T (p.Thr293=)
c.635-1512C>T (n.635-1512C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.161544711G>CCA421612336FCGR3Ac.567C>G (p.Thr189=)
c.564C>G (p.Thr188=)
c.516C>G (p.Thr172=)
c.675C>G (p.Thr225=)
c.617C>G
c.672C>G (p.Thr224=)
c.428-1512C>G (n.428-1512C>G)
c.882C>G (p.Thr294=)
c.879C>G (p.Thr293=)
c.635-1512C>G (n.635-1512C>G)
1g.161544711G=CA1202785211FCGR3Ac.567C= (p.Thr189=)
c.564C= (p.Thr188=)
c.516C= (p.Thr172=)
c.675C= (p.Thr225=)
c.617C=
c.672C= (p.Thr224=)
c.428-1512C= (n.428-1512C=)
c.882C= (p.Thr294=)
c.879C= (p.Thr293=)
c.635-1512C= (n.635-1512C=)
1g.161544711G>TCA421612338FCGR3Ac.567C>A (p.Thr189=)
c.564C>A (p.Thr188=)
c.516C>A (p.Thr172=)
c.675C>A (p.Thr225=)
c.617C>A
c.672C>A (p.Thr224=)
c.428-1512C>A (n.428-1512C>A)
c.882C>A (p.Thr294=)
c.879C>A (p.Thr293=)
c.635-1512C>A (n.635-1512C>A)
1g.161544712G>ACA343367336FCGR3Ac.566C>T (p.Thr189Ile)
c.563C>T (p.Thr188Ile)
c.515C>T (p.Thr172Ile)
c.674C>T (p.Thr225Ile)
c.616C>T
c.671C>T (p.Thr224Ile)
c.428-1513C>T (n.428-1513C>T)
c.881C>T (p.Thr294Ile)
c.878C>T (p.Thr293Ile)
c.635-1513C>T (n.635-1513C>T)
 gnomAD v4
1g.161544712G>CCA343367334FCGR3Ac.566C>G (p.Thr189Ser)
c.563C>G (p.Thr188Ser)
c.515C>G (p.Thr172Ser)
c.674C>G (p.Thr225Ser)
c.616C>G
c.671C>G (p.Thr224Ser)
c.428-1513C>G (n.428-1513C>G)
c.881C>G (p.Thr294Ser)
c.878C>G (p.Thr293Ser)
c.635-1513C>G (n.635-1513C>G)
1g.161544712G>TCA343367335FCGR3Ac.566C>A (p.Thr189Asn)
c.563C>A (p.Thr188Asn)
c.515C>A (p.Thr172Asn)
c.674C>A (p.Thr225Asn)
c.616C>A
c.671C>A (p.Thr224Asn)
c.428-1513C>A (n.428-1513C>A)
c.881C>A (p.Thr294Asn)
c.878C>A (p.Thr293Asn)
c.635-1513C>A (n.635-1513C>A)
1g.161544713T>ACA343367337FCGR3Ac.565A>T (p.Thr189Ser)
c.562A>T (p.Thr188Ser)
c.514A>T (p.Thr172Ser)
c.673A>T (p.Thr225Ser)
c.615A>T
c.670A>T (p.Thr224Ser)
c.428-1514A>T (n.428-1514A>T)
c.880A>T (p.Thr294Ser)
c.877A>T (p.Thr293Ser)
c.635-1514A>T (n.635-1514A>T)
1g.161544713T>CCA343367338FCGR3Ac.565A>G (p.Thr189Ala)
c.562A>G (p.Thr188Ala)
c.514A>G (p.Thr172Ala)
c.673A>G (p.Thr225Ala)
c.615A>G
c.670A>G (p.Thr224Ala)
c.428-1514A>G (n.428-1514A>G)
c.880A>G (p.Thr294Ala)
c.877A>G (p.Thr293Ala)
c.635-1514A>G (n.635-1514A>G)
1g.161544713T>GCA343367339FCGR3Ac.565A>C (p.Thr189Pro)
c.562A>C (p.Thr188Pro)
c.514A>C (p.Thr172Pro)
c.673A>C (p.Thr225Pro)
c.615A>C
c.670A>C (p.Thr224Pro)
c.428-1514A>C (n.428-1514A>C)
c.880A>C (p.Thr294Pro)
c.877A>C (p.Thr293Pro)
c.635-1514A>C (n.635-1514A>C)
1g.161544714G>ACA421612342FCGR3Ac.564C>T (p.Ile188=)
c.561C>T (p.Ile187=)
c.513C>T (p.Ile171=)
c.672C>T (p.Ile224=)
c.614C>T
c.669C>T (p.Ile223=)
c.428-1515C>T (n.428-1515C>T)
c.879C>T (p.Ile293=)
c.876C>T (p.Ile292=)
c.635-1515C>T (n.635-1515C>T)
 COSMIC
1g.161544714G>CCA343367340FCGR3Ac.564C>G (p.Ile188Met)
c.561C>G (p.Ile187Met)
c.513C>G (p.Ile171Met)
c.672C>G (p.Ile224Met)
c.614C>G
c.669C>G (p.Ile223Met)
c.428-1515C>G (n.428-1515C>G)
c.879C>G (p.Ile293Met)
c.876C>G (p.Ile292Met)
c.635-1515C>G (n.635-1515C>G)
1g.161544714G>TCA421612340FCGR3Ac.564C>A (p.Ile188=)
c.561C>A (p.Ile187=)
c.513C>A (p.Ile171=)
c.672C>A (p.Ile224=)
c.614C>A
c.669C>A (p.Ile223=)
c.428-1515C>A (n.428-1515C>A)
c.879C>A (p.Ile293=)
c.876C>A (p.Ile292=)
c.635-1515C>A (n.635-1515C>A)
1g.161544715A>CCA343367341FCGR3Ac.563T>G (p.Ile188Ser)
c.560T>G (p.Ile187Ser)
c.512T>G (p.Ile171Ser)
c.671T>G (p.Ile224Ser)
c.613T>G
c.668T>G (p.Ile223Ser)
c.428-1516T>G (n.428-1516T>G)
c.878T>G (p.Ile293Ser)
c.875T>G (p.Ile292Ser)
c.635-1516T>G (n.635-1516T>G)
1g.161544715A>GCA343367342FCGR3Ac.563T>C (p.Ile188Thr)
c.560T>C (p.Ile187Thr)
c.512T>C (p.Ile171Thr)
c.671T>C (p.Ile224Thr)
c.613T>C
c.668T>C (p.Ile223Thr)
c.428-1516T>C (n.428-1516T>C)
c.878T>C (p.Ile293Thr)
c.875T>C (p.Ile292Thr)
c.635-1516T>C (n.635-1516T>C)
1g.161544715A>TCA343367343FCGR3Ac.563T>A (p.Ile188Asn)
c.560T>A (p.Ile187Asn)
c.512T>A (p.Ile171Asn)
c.671T>A (p.Ile224Asn)
c.613T>A
c.668T>A (p.Ile223Asn)
c.428-1516T>A (n.428-1516T>A)
c.878T>A (p.Ile293Asn)
c.875T>A (p.Ile292Asn)
c.635-1516T>A (n.635-1516T>A)
1g.161544716T>ACA343367344FCGR3Ac.562A>T (p.Ile188Phe)
c.559A>T (p.Ile187Phe)
c.511A>T (p.Ile171Phe)
c.670A>T (p.Ile224Phe)
c.612A>T
c.667A>T (p.Ile223Phe)
c.428-1517A>T (n.428-1517A>T)
c.877A>T (p.Ile293Phe)
c.874A>T (p.Ile292Phe)
c.635-1517A>T (n.635-1517A>T)
1g.161544716T>CCA343367345FCGR3Ac.562A>G (p.Ile188Val)
c.559A>G (p.Ile187Val)
c.511A>G (p.Ile171Val)
c.670A>G (p.Ile224Val)
c.612A>G
c.667A>G (p.Ile223Val)
c.428-1517A>G (n.428-1517A>G)
c.877A>G (p.Ile293Val)
c.874A>G (p.Ile292Val)
c.635-1517A>G (n.635-1517A>G)
1g.161544716T>GCA343367346FCGR3Ac.562A>C (p.Ile188Leu)
c.559A>C (p.Ile187Leu)
c.511A>C (p.Ile171Leu)
c.670A>C (p.Ile224Leu)
c.612A>C
c.667A>C (p.Ile223Leu)
c.428-1517A>C (n.428-1517A>C)
c.877A>C (p.Ile293Leu)
c.874A>C (p.Ile292Leu)
c.635-1517A>C (n.635-1517A>C)
1g.161544717G>ACA421612349FCGR3Ac.561C>T (p.Asn187=)
c.558C>T (p.Asn186=)
c.510C>T (p.Asn170=)
c.669C>T (p.Asn223=)
c.611C>T
c.666C>T (p.Asn222=)
c.428-1518C>T (n.428-1518C>T)
c.876C>T (p.Asn292=)
c.873C>T (p.Asn291=)
c.635-1518C>T (n.635-1518C>T)
1g.161544717G>CCA343367348FCGR3Ac.561C>G (p.Asn187Lys)
c.558C>G (p.Asn186Lys)
c.510C>G (p.Asn170Lys)
c.669C>G (p.Asn223Lys)
c.611C>G
c.666C>G (p.Asn222Lys)
c.428-1518C>G (n.428-1518C>G)
c.876C>G (p.Asn292Lys)
c.873C>G (p.Asn291Lys)
c.635-1518C>G (n.635-1518C>G)
1g.161544717G>TCA343367347FCGR3Ac.561C>A (p.Asn187Lys)
c.558C>A (p.Asn186Lys)
c.510C>A (p.Asn170Lys)
c.669C>A (p.Asn223Lys)
c.611C>A
c.666C>A (p.Asn222Lys)
c.428-1518C>A (n.428-1518C>A)
c.876C>A (p.Asn292Lys)
c.873C>A (p.Asn291Lys)
c.635-1518C>A (n.635-1518C>A)
1g.161544718T>ACA343367349FCGR3Ac.560A>T (p.Asn187Ile)
c.557A>T (p.Asn186Ile)
c.509A>T (p.Asn170Ile)
c.668A>T (p.Asn223Ile)
c.610A>T
c.665A>T (p.Asn222Ile)
c.428-1519A>T (n.428-1519A>T)
c.875A>T (p.Asn292Ile)
c.872A>T (p.Asn291Ile)
c.635-1519A>T (n.635-1519A>T)
1g.161544718T>CCA343367350FCGR3Ac.560A>G (p.Asn187Ser)
c.557A>G (p.Asn186Ser)
c.509A>G (p.Asn170Ser)
c.668A>G (p.Asn223Ser)
c.610A>G
c.665A>G (p.Asn222Ser)
c.428-1519A>G (n.428-1519A>G)
c.875A>G (p.Asn292Ser)
c.872A>G (p.Asn291Ser)
c.635-1519A>G (n.635-1519A>G)
 dbSNP gnomAD v3 gnomAD v4 COSMIC
1g.161544718T>GCA343367351FCGR3Ac.560A>C (p.Asn187Thr)
c.557A>C (p.Asn186Thr)
c.509A>C (p.Asn170Thr)
c.668A>C (p.Asn223Thr)
c.610A>C
c.665A>C (p.Asn222Thr)
c.428-1519A>C (n.428-1519A>C)
c.875A>C (p.Asn292Thr)
c.872A>C (p.Asn291Thr)
c.635-1519A>C (n.635-1519A>C)
1g.161544718T=CA1202785212FCGR3Ac.560A= (p.Asn187=)
c.557A= (p.Asn186=)
c.509A= (p.Asn170=)
c.668A= (p.Asn223=)
c.610A=
c.665A= (p.Asn222=)
c.428-1519A= (n.428-1519A=)
c.875A= (p.Asn292=)
c.872A= (p.Asn291=)
c.635-1519A= (n.635-1519A=)
1g.161544718_161544723delCA2648790072FCGR3Ac.555_560del (p.Val186_Asn187del)
c.552_557del (p.Val185_Asn186del)
c.504_509del (p.Val169_Asn170del)
c.663_668del (p.Val222_Asn223del)
c.605_610del
c.660_665del (p.Val221_Asn222del)
c.428-1524_428-1519del (n.428-1524_428-1519del)
c.870_875del (p.Val291_Asn292del)
c.867_872del (p.Val290_Asn291del)
c.635-1524_635-1519del (n.635-1524_635-1519del)
 gnomAD v4
1g.161544719T>ACA343367352FCGR3Ac.559A>T (p.Asn187Tyr)
c.556A>T (p.Asn186Tyr)
c.508A>T (p.Asn170Tyr)
c.667A>T (p.Asn223Tyr)
c.609A>T
c.664A>T (p.Asn222Tyr)
c.428-1520A>T (n.428-1520A>T)
c.874A>T (p.Asn292Tyr)
c.871A>T (p.Asn291Tyr)
c.635-1520A>T (n.635-1520A>T)
1g.161544719T>CCA343367353FCGR3Ac.559A>G (p.Asn187Asp)
c.556A>G (p.Asn186Asp)
c.508A>G (p.Asn170Asp)
c.667A>G (p.Asn223Asp)
c.609A>G
c.664A>G (p.Asn222Asp)
c.428-1520A>G (n.428-1520A>G)
c.874A>G (p.Asn292Asp)
c.871A>G (p.Asn291Asp)
c.635-1520A>G (n.635-1520A>G)
 gnomAD v4
1g.161544719T>GCA343367354FCGR3Ac.559A>C (p.Asn187His)
c.556A>C (p.Asn186His)
c.508A>C (p.Asn170His)
c.667A>C (p.Asn223His)
c.609A>C
c.664A>C (p.Asn222His)
c.428-1520A>C (n.428-1520A>C)
c.874A>C (p.Asn292His)
c.871A>C (p.Asn291His)
c.635-1520A>C (n.635-1520A>C)
1g.161544719_161544721delinsTCACA1202785213FCGR3Ac.557_559delinsTGA (p.Val186=)
c.554_556delinsTGA (p.Val185=)
c.506_508delinsTGA (p.Val169=)
c.665_667delinsTGA (p.Val222=)
c.607_609delinsTGA
c.662_664delinsTGA (p.Val221=)
c.428-1522_428-1520delinsTGA (n.428-1522_428-1520delinsTGA)
c.872_874delinsTGA (p.Val291=)
c.869_871delinsTGA (p.Val290=)
c.635-1522_635-1520delinsTGA (n.635-1522_635-1520delinsTGA)
1g.161544720C>ACA421612364FCGR3Ac.558G>T (p.Val186=)
c.555G>T (p.Val185=)
c.507G>T (p.Val169=)
c.666G>T (p.Val222=)
c.608G>T
c.663G>T (p.Val221=)
c.428-1521G>T (n.428-1521G>T)
c.873G>T (p.Val291=)
c.870G>T (p.Val290=)
c.635-1521G>T (n.635-1521G>T)
 gnomAD v4
1g.161544720C>GCA421612369FCGR3Ac.558G>C (p.Val186=)
c.555G>C (p.Val185=)
c.507G>C (p.Val169=)
c.666G>C (p.Val222=)
c.608G>C
c.663G>C (p.Val221=)
c.428-1521G>C (n.428-1521G>C)
c.873G>C (p.Val291=)
c.870G>C (p.Val290=)
c.635-1521G>C (n.635-1521G>C)
1g.161544720C>TCA421612361FCGR3Ac.558G>A (p.Val186=)
c.555G>A (p.Val185=)
c.507G>A (p.Val169=)
c.666G>A (p.Val222=)
c.608G>A
c.663G>A (p.Val221=)
c.428-1521G>A (n.428-1521G>A)
c.873G>A (p.Val291=)
c.870G>A (p.Val290=)
c.635-1521G>A (n.635-1521G>A)
1g.161544722_161544723delCA527135441FCGR3Ac.557_558del (p.Val186GlufsTer?)
c.554_555del (p.Val185GlufsTer?)
c.557_558del (p.Val186GlufsTer8)
c.506_507del (p.Val169GlufsTer?)
c.665_666del (p.Val222GlufsTer?)
c.607_608del
c.662_663del (p.Val221GlufsTer?)
c.428-1522_428-1521del (n.428-1522_428-1521del)
c.872_873del (p.Val291GlufsTer?)
c.869_870del (p.Val290GlufsTer?)
c.635-1522_635-1521del (n.635-1522_635-1521del)
 dbSNP gnomAD v2 gnomAD v4
1g.161544721A>CCA343367355FCGR3Ac.557T>G (p.Val186Gly)
c.554T>G (p.Val185Gly)
c.506T>G (p.Val169Gly)
c.665T>G (p.Val222Gly)
c.607T>G
c.662T>G (p.Val221Gly)
c.428-1522T>G (n.428-1522T>G)
c.872T>G (p.Val291Gly)
c.869T>G (p.Val290Gly)
c.635-1522T>G (n.635-1522T>G)
1g.161544721A>GCA343367356FCGR3Ac.557T>C (p.Val186Ala)
c.554T>C (p.Val185Ala)
c.506T>C (p.Val169Ala)
c.665T>C (p.Val222Ala)
c.607T>C
c.662T>C (p.Val221Ala)
c.428-1522T>C (n.428-1522T>C)
c.872T>C (p.Val291Ala)
c.869T>C (p.Val290Ala)
c.635-1522T>C (n.635-1522T>C)
1g.161544721A>TCA343367357FCGR3Ac.557T>A (p.Val186Glu)
c.554T>A (p.Val185Glu)
c.506T>A (p.Val169Glu)
c.665T>A (p.Val222Glu)
c.607T>A
c.662T>A (p.Val221Glu)
c.428-1522T>A (n.428-1522T>A)
c.872T>A (p.Val291Glu)
c.869T>A (p.Val290Glu)
c.635-1522T>A (n.635-1522T>A)
1g.161544722C>ACA343367358FCGR3Ac.556G>T (p.Val186Leu)
c.553G>T (p.Val185Leu)
c.505G>T (p.Val169Leu)
c.664G>T (p.Val222Leu)
c.606G>T
c.661G>T (p.Val221Leu)
c.428-1523G>T (n.428-1523G>T)
c.871G>T (p.Val291Leu)
c.868G>T (p.Val290Leu)
c.635-1523G>T (n.635-1523G>T)
1g.161544722C=CA1202785214FCGR3Ac.556G= (p.Val186=)
c.553G= (p.Val185=)
c.505G= (p.Val169=)
c.664G= (p.Val222=)
c.606G=
c.661G= (p.Val221=)
c.428-1523G= (n.428-1523G=)
c.871G= (p.Val291=)
c.868G= (p.Val290=)
c.635-1523G= (n.635-1523G=)
1g.161544722C>GCA343367359FCGR3Ac.556G>C (p.Val186Leu)
c.553G>C (p.Val185Leu)
c.505G>C (p.Val169Leu)
c.664G>C (p.Val222Leu)
c.606G>C
c.661G>C (p.Val221Leu)
c.428-1523G>C (n.428-1523G>C)
c.871G>C (p.Val291Leu)
c.868G>C (p.Val290Leu)
c.635-1523G>C (n.635-1523G>C)
 gnomAD v4
1g.161544722C>TCA343367360FCGR3Ac.556G>A (p.Val186Met)
c.553G>A (p.Val185Met)
c.505G>A (p.Val169Met)
c.664G>A (p.Val222Met)
c.606G>A
c.661G>A (p.Val221Met)
c.428-1523G>A (n.428-1523G>A)
c.871G>A (p.Val291Met)
c.868G>A (p.Val290Met)
c.635-1523G>A (n.635-1523G>A)
 dbSNP gnomAD v2 gnomAD v4
1g.161544723A=CA1202785215FCGR3Ac.555T= (p.Thr185=)
c.552T= (p.Thr184=)
c.504T= (p.Thr168=)
c.663T= (p.Thr221=)
c.605T=
c.660T= (p.Thr220=)
c.428-1524T= (n.428-1524T=)
c.870T= (p.Thr290=)
c.867T= (p.Thr289=)
c.635-1524T= (n.635-1524T=)
1g.161544723A>CCA421612375FCGR3Ac.555T>G (p.Thr185=)
c.552T>G (p.Thr184=)
c.504T>G (p.Thr168=)
c.663T>G (p.Thr221=)
c.605T>G
c.660T>G (p.Thr220=)
c.428-1524T>G (n.428-1524T>G)
c.870T>G (p.Thr290=)
c.867T>G (p.Thr289=)
c.635-1524T>G (n.635-1524T>G)
 gnomAD v4
1g.161544723A>GCA1211375FCGR3Ac.555T>C (p.Thr185=)
c.552T>C (p.Thr184=)
c.504T>C (p.Thr168=)
c.663T>C (p.Thr221=)
c.605T>C
c.660T>C (p.Thr220=)
c.428-1524T>C (n.428-1524T>C)
c.870T>C (p.Thr290=)
c.867T>C (p.Thr289=)
c.635-1524T>C (n.635-1524T>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.161544723A>TCA421612373FCGR3Ac.555T>A (p.Thr185=)
c.552T>A (p.Thr184=)
c.504T>A (p.Thr168=)
c.663T>A (p.Thr221=)
c.605T>A
c.660T>A (p.Thr220=)
c.428-1524T>A (n.428-1524T>A)
c.870T>A (p.Thr290=)
c.867T>A (p.Thr289=)
c.635-1524T>A (n.635-1524T>A)
1g.161544724G>ACA343367361FCGR3Ac.554C>T (p.Thr185Ile)
c.551C>T (p.Thr184Ile)
c.503C>T (p.Thr168Ile)
c.662C>T (p.Thr221Ile)
c.604C>T
c.659C>T (p.Thr220Ile)
c.428-1525C>T (n.428-1525C>T)
c.869C>T (p.Thr290Ile)
c.866C>T (p.Thr289Ile)
c.635-1525C>T (n.635-1525C>T)
1g.161544724G>CCA343367363FCGR3Ac.554C>G (p.Thr185Ser)
c.551C>G (p.Thr184Ser)
c.503C>G (p.Thr168Ser)
c.662C>G (p.Thr221Ser)
c.604C>G
c.659C>G (p.Thr220Ser)
c.428-1525C>G (n.428-1525C>G)
c.869C>G (p.Thr290Ser)
c.866C>G (p.Thr289Ser)
c.635-1525C>G (n.635-1525C>G)
1g.161544724G>TCA343367362FCGR3Ac.554C>A (p.Thr185Asn)
c.551C>A (p.Thr184Asn)
c.503C>A (p.Thr168Asn)
c.662C>A (p.Thr221Asn)
c.604C>A
c.659C>A (p.Thr220Asn)
c.428-1525C>A (n.428-1525C>A)
c.869C>A (p.Thr290Asn)
c.866C>A (p.Thr289Asn)
c.635-1525C>A (n.635-1525C>A)
1g.161544725T>ACA343367364FCGR3Ac.553A>T (p.Thr185Ser)
c.550A>T (p.Thr184Ser)
c.502A>T (p.Thr168Ser)
c.661A>T (p.Thr221Ser)
c.603A>T
c.658A>T (p.Thr220Ser)
c.428-1526A>T (n.428-1526A>T)
c.868A>T (p.Thr290Ser)
c.865A>T (p.Thr289Ser)
c.635-1526A>T (n.635-1526A>T)
1g.161544725T>CCA343367365FCGR3Ac.553A>G (p.Thr185Ala)
c.550A>G (p.Thr184Ala)
c.502A>G (p.Thr168Ala)
c.661A>G (p.Thr221Ala)
c.603A>G
c.658A>G (p.Thr220Ala)
c.428-1526A>G (n.428-1526A>G)
c.868A>G (p.Thr290Ala)
c.865A>G (p.Thr289Ala)
c.635-1526A>G (n.635-1526A>G)
1g.161544725T>GCA343367366FCGR3Ac.553A>C (p.Thr185Pro)
c.550A>C (p.Thr184Pro)
c.502A>C (p.Thr168Pro)
c.661A>C (p.Thr221Pro)
c.603A>C
c.658A>C (p.Thr220Pro)
c.428-1526A>C (n.428-1526A>C)
c.868A>C (p.Thr290Pro)
c.865A>C (p.Thr289Pro)
c.635-1526A>C (n.635-1526A>C)
1g.161544726C>ACA343367367FCGR3Ac.552G>T (p.Glu184Asp)
c.549G>T (p.Glu183Asp)
c.501G>T (p.Glu167Asp)
c.660G>T (p.Glu220Asp)
c.602G>T
c.657G>T (p.Glu219Asp)
c.428-1527G>T (n.428-1527G>T)
c.867G>T (p.Glu289Asp)
c.864G>T (p.Glu288Asp)
c.635-1527G>T (n.635-1527G>T)
1g.161544726C>GCA343367368FCGR3Ac.552G>C (p.Glu184Asp)
c.549G>C (p.Glu183Asp)
c.501G>C (p.Glu167Asp)
c.660G>C (p.Glu220Asp)
c.602G>C
c.657G>C (p.Glu219Asp)
c.428-1527G>C (n.428-1527G>C)
c.867G>C (p.Glu289Asp)
c.864G>C (p.Glu288Asp)
c.635-1527G>C (n.635-1527G>C)
1g.161544726C>TCA421612382FCGR3Ac.552G>A (p.Glu184=)
c.549G>A (p.Glu183=)
c.501G>A (p.Glu167=)
c.660G>A (p.Glu220=)
c.602G>A
c.657G>A (p.Glu219=)
c.428-1527G>A (n.428-1527G>A)
c.867G>A (p.Glu289=)
c.864G>A (p.Glu288=)
c.635-1527G>A (n.635-1527G>A)
1g.161544727T>ACA343367369FCGR3Ac.551A>T (p.Glu184Val)
c.548A>T (p.Glu183Val)
c.500A>T (p.Glu167Val)
c.659A>T (p.Glu220Val)
c.601A>T
c.656A>T (p.Glu219Val)
c.428-1528A>T (n.428-1528A>T)
c.866A>T (p.Glu289Val)
c.863A>T (p.Glu288Val)
c.635-1528A>T (n.635-1528A>T)
1g.161544727T>CCA343367370FCGR3Ac.551A>G (p.Glu184Gly)
c.548A>G (p.Glu183Gly)
c.500A>G (p.Glu167Gly)
c.659A>G (p.Glu220Gly)
c.601A>G
c.656A>G (p.Glu219Gly)
c.428-1528A>G (n.428-1528A>G)
c.866A>G (p.Glu289Gly)
c.863A>G (p.Glu288Gly)
c.635-1528A>G (n.635-1528A>G)
1g.161544727T>GCA343367371FCGR3Ac.551A>C (p.Glu184Ala)
c.548A>C (p.Glu183Ala)
c.500A>C (p.Glu167Ala)
c.659A>C (p.Glu220Ala)
c.601A>C
c.656A>C (p.Glu219Ala)
c.428-1528A>C (n.428-1528A>C)
c.866A>C (p.Glu289Ala)
c.863A>C (p.Glu288Ala)
c.635-1528A>C (n.635-1528A>C)
1g.161544728C>ACA343367372FCGR3Ac.550G>T (p.Glu184Ter)
c.547G>T (p.Glu183Ter)
c.499G>T (p.Glu167Ter)
c.658G>T (p.Glu220Ter)
c.600G>T
c.655G>T (p.Glu219Ter)
c.428-1529G>T (n.428-1529G>T)
c.865G>T (p.Glu289Ter)
c.862G>T (p.Glu288Ter)
c.635-1529G>T (n.635-1529G>T)
1g.161544728C>GCA343367373FCGR3Ac.550G>C (p.Glu184Gln)
c.547G>C (p.Glu183Gln)
c.499G>C (p.Glu167Gln)
c.658G>C (p.Glu220Gln)
c.600G>C
c.655G>C (p.Glu219Gln)
c.428-1529G>C (n.428-1529G>C)
c.865G>C (p.Glu289Gln)
c.862G>C (p.Glu288Gln)
c.635-1529G>C (n.635-1529G>C)
 COSMIC
1g.161544728C>TCA343367374FCGR3Ac.550G>A (p.Glu184Lys)
c.547G>A (p.Glu183Lys)
c.499G>A (p.Glu167Lys)
c.658G>A (p.Glu220Lys)
c.600G>A
c.655G>A (p.Glu219Lys)
c.428-1529G>A (n.428-1529G>A)
c.865G>A (p.Glu289Lys)
c.862G>A (p.Glu288Lys)
c.635-1529G>A (n.635-1529G>A)
1g.161544729T>ACA421612393FCGR3Ac.549A>T (p.Ser183=)
c.546A>T (p.Ser182=)
c.498A>T (p.Ser166=)
c.657A>T (p.Ser219=)
c.599A>T
c.654A>T (p.Ser218=)
c.428-1530A>T (n.428-1530A>T)
c.864A>T (p.Ser288=)
c.861A>T (p.Ser287=)
c.635-1530A>T (n.635-1530A>T)
1g.161544729T>CCA421612394FCGR3Ac.549A>G (p.Ser183=)
c.546A>G (p.Ser182=)
c.498A>G (p.Ser166=)
c.657A>G (p.Ser219=)
c.599A>G
c.654A>G (p.Ser218=)
c.428-1530A>G (n.428-1530A>G)
c.864A>G (p.Ser288=)
c.861A>G (p.Ser287=)
c.635-1530A>G (n.635-1530A>G)
 gnomAD v4
1g.161544729T>GCA421612395FCGR3Ac.549A>C (p.Ser183=)
c.546A>C (p.Ser182=)
c.498A>C (p.Ser166=)
c.657A>C (p.Ser219=)
c.599A>C
c.654A>C (p.Ser218=)
c.428-1530A>C (n.428-1530A>C)
c.864A>C (p.Ser288=)
c.861A>C (p.Ser287=)
c.635-1530A>C (n.635-1530A>C)
1g.161544730G>ACA343367376FCGR3Ac.548C>T (p.Ser183Leu)
c.545C>T (p.Ser182Leu)
c.497C>T (p.Ser166Leu)
c.656C>T (p.Ser219Leu)
c.598C>T
c.653C>T (p.Ser218Leu)
c.428-1531C>T (n.428-1531C>T)
c.863C>T (p.Ser288Leu)
c.860C>T (p.Ser287Leu)
c.635-1531C>T (n.635-1531C>T)
1g.161544730G>CCA343367377FCGR3Ac.548C>G (p.Ser183Ter)
c.545C>G (p.Ser182Ter)
c.497C>G (p.Ser166Ter)
c.656C>G (p.Ser219Ter)
c.598C>G
c.653C>G (p.Ser218Ter)
c.428-1531C>G (n.428-1531C>G)
c.863C>G (p.Ser288Ter)
c.860C>G (p.Ser287Ter)
c.635-1531C>G (n.635-1531C>G)
1g.161544730G>TCA343367375FCGR3Ac.548C>A (p.Ser183Ter)
c.545C>A (p.Ser182Ter)
c.497C>A (p.Ser166Ter)
c.656C>A (p.Ser219Ter)
c.598C>A
c.653C>A (p.Ser218Ter)
c.428-1531C>A (n.428-1531C>A)
c.863C>A (p.Ser288Ter)
c.860C>A (p.Ser287Ter)
c.635-1531C>A (n.635-1531C>A)
1g.161544731A>CCA343367380FCGR3Ac.547T>G (p.Ser183Ala)
c.544T>G (p.Ser182Ala)
c.496T>G (p.Ser166Ala)
c.655T>G (p.Ser219Ala)
c.597T>G
c.652T>G (p.Ser218Ala)
c.428-1532T>G (n.428-1532T>G)
c.862T>G (p.Ser288Ala)
c.859T>G (p.Ser287Ala)
c.635-1532T>G (n.635-1532T>G)
1g.161544731A>GCA343367378FCGR3Ac.547T>C (p.Ser183Pro)
c.544T>C (p.Ser182Pro)
c.496T>C (p.Ser166Pro)
c.655T>C (p.Ser219Pro)
c.597T>C
c.652T>C (p.Ser218Pro)
c.428-1532T>C (n.428-1532T>C)
c.862T>C (p.Ser288Pro)
c.859T>C (p.Ser287Pro)
c.635-1532T>C (n.635-1532T>C)
1g.161544731A>TCA343367379FCGR3Ac.547T>A (p.Ser183Thr)
c.544T>A (p.Ser182Thr)
c.496T>A (p.Ser166Thr)
c.655T>A (p.Ser219Thr)
c.597T>A
c.652T>A (p.Ser218Thr)
c.428-1532T>A (n.428-1532T>A)
c.862T>A (p.Ser288Thr)
c.859T>A (p.Ser287Thr)
c.635-1532T>A (n.635-1532T>A)
1g.161544732A=CA1202785216FCGR3Ac.546T= (p.Ser182=)
c.543T= (p.Ser181=)
c.495T= (p.Ser165=)
c.654T= (p.Ser218=)
c.596T=
c.651T= (p.Ser217=)
c.428-1533T= (n.428-1533T=)
c.861T= (p.Ser287=)
c.858T= (p.Ser286=)
c.635-1533T= (n.635-1533T=)
1g.161544732A>CCA421612402FCGR3Ac.546T>G (p.Ser182=)
c.543T>G (p.Ser181=)
c.495T>G (p.Ser165=)
c.654T>G (p.Ser218=)
c.596T>G
c.651T>G (p.Ser217=)
c.428-1533T>G (n.428-1533T>G)
c.861T>G (p.Ser287=)
c.858T>G (p.Ser286=)
c.635-1533T>G (n.635-1533T>G)
1g.161544732A>GCA421612403FCGR3Ac.546T>C (p.Ser182=)
c.543T>C (p.Ser181=)
c.495T>C (p.Ser165=)
c.654T>C (p.Ser218=)
c.596T>C
c.651T>C (p.Ser217=)
c.428-1533T>C (n.428-1533T>C)
c.861T>C (p.Ser287=)
c.858T>C (p.Ser286=)
c.635-1533T>C (n.635-1533T>C)
 dbSNP
1g.161544732A>TCA421612404FCGR3Ac.546T>A (p.Ser182=)
c.543T>A (p.Ser181=)
c.495T>A (p.Ser165=)
c.654T>A (p.Ser218=)
c.596T>A
c.651T>A (p.Ser217=)
c.428-1533T>A (n.428-1533T>A)
c.861T>A (p.Ser287=)
c.858T>A (p.Ser286=)
c.635-1533T>A (n.635-1533T>A)
1g.161544733G>ACA343367381FCGR3Ac.545C>T (p.Ser182Phe)
c.542C>T (p.Ser181Phe)
c.494C>T (p.Ser165Phe)
c.653C>T (p.Ser218Phe)
c.595C>T
c.650C>T (p.Ser217Phe)
c.428-1534C>T (n.428-1534C>T)
c.860C>T (p.Ser287Phe)
c.857C>T (p.Ser286Phe)
c.635-1534C>T (n.635-1534C>T)
1g.161544733G>CCA343367382FCGR3Ac.545C>G (p.Ser182Cys)
c.542C>G (p.Ser181Cys)
c.494C>G (p.Ser165Cys)
c.653C>G (p.Ser218Cys)
c.595C>G
c.650C>G (p.Ser217Cys)
c.428-1534C>G (n.428-1534C>G)
c.860C>G (p.Ser287Cys)
c.857C>G (p.Ser286Cys)
c.635-1534C>G (n.635-1534C>G)
1g.161544733G>TCA343367383FCGR3Ac.545C>A (p.Ser182Tyr)
c.542C>A (p.Ser181Tyr)
c.494C>A (p.Ser165Tyr)
c.653C>A (p.Ser218Tyr)
c.595C>A
c.650C>A (p.Ser217Tyr)
c.428-1534C>A (n.428-1534C>A)
c.860C>A (p.Ser287Tyr)
c.857C>A (p.Ser286Tyr)
c.635-1534C>A (n.635-1534C>A)
1g.161544734A>CCA343367384FCGR3Ac.544T>G (p.Ser182Ala)
c.541T>G (p.Ser181Ala)
c.493T>G (p.Ser165Ala)
c.652T>G (p.Ser218Ala)
c.594T>G
c.649T>G (p.Ser217Ala)
c.428-1535T>G (n.428-1535T>G)
c.859T>G (p.Ser287Ala)
c.856T>G (p.Ser286Ala)
c.635-1535T>G (n.635-1535T>G)
1g.161544734A>GCA343367385FCGR3Ac.544T>C (p.Ser182Pro)
c.541T>C (p.Ser181Pro)
c.493T>C (p.Ser165Pro)
c.652T>C (p.Ser218Pro)
c.594T>C
c.649T>C (p.Ser217Pro)
c.428-1535T>C (n.428-1535T>C)
c.859T>C (p.Ser287Pro)
c.856T>C (p.Ser286Pro)
c.635-1535T>C (n.635-1535T>C)
 gnomAD v4
1g.161544734A>TCA343367386FCGR3Ac.544T>A (p.Ser182Thr)
c.541T>A (p.Ser181Thr)
c.493T>A (p.Ser165Thr)
c.652T>A (p.Ser218Thr)
c.594T>A
c.649T>A (p.Ser217Thr)
c.428-1535T>A (n.428-1535T>A)
c.859T>A (p.Ser287Thr)
c.856T>A (p.Ser286Thr)
c.635-1535T>A (n.635-1535T>A)
 gnomAD v4
1g.161544735C>ACA421612406FCGR3Ac.543G>T (p.Val181=)
c.540G>T (p.Val180=)
c.492G>T (p.Val164=)
c.651G>T (p.Val217=)
c.593G>T
c.648G>T (p.Val216=)
c.428-1536G>T (n.428-1536G>T)
c.858G>T (p.Val286=)
c.855G>T (p.Val285=)
c.635-1536G>T (n.635-1536G>T)
1g.161544735C=CA1141851418FCGR3Ac.543G= (p.Val181=)
c.540G= (p.Val180=)
c.492G= (p.Val164=)
c.651G= (p.Val217=)
c.593G=
c.648G= (p.Val216=)
c.428-1536G= (n.428-1536G=)
c.858G= (p.Val286=)
c.855G= (p.Val285=)
c.635-1536G= (n.635-1536G=)
1g.161544735C>GCA421612407FCGR3Ac.543G>C (p.Val181=)
c.540G>C (p.Val180=)
c.492G>C (p.Val164=)
c.651G>C (p.Val217=)
c.593G>C
c.648G>C (p.Val216=)
c.428-1536G>C (n.428-1536G>C)
c.858G>C (p.Val286=)
c.855G>C (p.Val285=)
c.635-1536G>C (n.635-1536G>C)
1g.161544735C>TCA1211376FCGR3Ac.543G>A (p.Val181=)
c.540G>A (p.Val180=)
c.492G>A (p.Val164=)
c.651G>A (p.Val217=)
c.593G>A
c.648G>A (p.Val216=)
c.428-1536G>A (n.428-1536G>A)
c.858G>A (p.Val286=)
c.855G>A (p.Val285=)
c.635-1536G>A (n.635-1536G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.161544736A=CA1202785217FCGR3Ac.542T= (p.Val181=)
c.539T= (p.Val180=)
c.491T= (p.Val164=)
c.650T= (p.Val217=)
c.592T=
c.647T= (p.Val216=)
c.428-1537T= (n.428-1537T=)
c.857T= (p.Val286=)
c.854T= (p.Val285=)
c.635-1537T= (n.635-1537T=)
1g.161544736A>CCA343367387FCGR3Ac.542T>G (p.Val181Gly)
c.539T>G (p.Val180Gly)
c.491T>G (p.Val164Gly)
c.650T>G (p.Val217Gly)
c.592T>G
c.647T>G (p.Val216Gly)
c.428-1537T>G (n.428-1537T>G)
c.857T>G (p.Val286Gly)
c.854T>G (p.Val285Gly)
c.635-1537T>G (n.635-1537T>G)
1g.161544736A>GCA343367388FCGR3Ac.542T>C (p.Val181Ala)
c.539T>C (p.Val180Ala)
c.491T>C (p.Val164Ala)
c.650T>C (p.Val217Ala)
c.592T>C
c.647T>C (p.Val216Ala)
c.428-1537T>C (n.428-1537T>C)
c.857T>C (p.Val286Ala)
c.854T>C (p.Val285Ala)
c.635-1537T>C (n.635-1537T>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.161544736A>TCA343367389FCGR3Ac.542T>A (p.Val181Glu)
c.539T>A (p.Val180Glu)
c.491T>A (p.Val164Glu)
c.650T>A (p.Val217Glu)
c.592T>A
c.647T>A (p.Val216Glu)
c.428-1537T>A (n.428-1537T>A)
c.857T>A (p.Val286Glu)
c.854T>A (p.Val285Glu)
c.635-1537T>A (n.635-1537T>A)
1g.161544737C>ACA343367391FCGR3Ac.541G>T (p.Val181Leu)
c.538G>T (p.Val180Leu)
c.490G>T (p.Val164Leu)
c.649G>T (p.Val217Leu)
c.591G>T
c.646G>T (p.Val216Leu)
c.428-1538G>T (n.428-1538G>T)
c.856G>T (p.Val286Leu)
c.853G>T (p.Val285Leu)
c.635-1538G>T (n.635-1538G>T)
1g.161544737C=CA1202785218FCGR3Ac.541G= (p.Val181=)
c.538G= (p.Val180=)
c.490G= (p.Val164=)
c.649G= (p.Val217=)
c.591G=
c.646G= (p.Val216=)
c.428-1538G= (n.428-1538G=)
c.856G= (p.Val286=)
c.853G= (p.Val285=)
c.635-1538G= (n.635-1538G=)
1g.161544737C>GCA343367392FCGR3Ac.541G>C (p.Val181Leu)
c.538G>C (p.Val180Leu)
c.490G>C (p.Val164Leu)
c.649G>C (p.Val217Leu)
c.591G>C
c.646G>C (p.Val216Leu)
c.428-1538G>C (n.428-1538G>C)
c.856G>C (p.Val286Leu)
c.853G>C (p.Val285Leu)
c.635-1538G>C (n.635-1538G>C)
1g.161544737C>TCA343367390FCGR3Ac.541G>A (p.Val181Met)
c.538G>A (p.Val180Met)
c.490G>A (p.Val164Met)
c.649G>A (p.Val217Met)
c.591G>A
c.646G>A (p.Val216Met)
c.428-1538G>A (n.428-1538G>A)
c.856G>A (p.Val286Met)
c.853G>A (p.Val285Met)
c.635-1538G>A (n.635-1538G>A)
 dbSNP
1g.161544738A=CA1202785219FCGR3Ac.540T= (p.Asn180=)
c.537T= (p.Asn179=)
c.489T= (p.Asn163=)
c.648T= (p.Asn216=)
c.590T=
c.645T= (p.Asn215=)
c.428-1539T= (n.428-1539T=)
c.855T= (p.Asn285=)
c.852T= (p.Asn284=)
c.635-1539T= (n.635-1539T=)
1g.161544738A>CCA1211377FCGR3Ac.540T>G (p.Asn180Lys)
c.537T>G (p.Asn179Lys)
c.489T>G (p.Asn163Lys)
c.648T>G (p.Asn216Lys)
c.590T>G
c.645T>G (p.Asn215Lys)
c.428-1539T>G (n.428-1539T>G)
c.855T>G (p.Asn285Lys)
c.852T>G (p.Asn284Lys)
c.635-1539T>G (n.635-1539T>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.161544738A>GCA421612413FCGR3Ac.540T>C (p.Asn180=)
c.537T>C (p.Asn179=)
c.489T>C (p.Asn163=)
c.648T>C (p.Asn216=)
c.590T>C
c.645T>C (p.Asn215=)
c.428-1539T>C (n.428-1539T>C)
c.855T>C (p.Asn285=)
c.852T>C (p.Asn284=)
c.635-1539T>C (n.635-1539T>C)
1g.161544738A>TCA343367393FCGR3Ac.540T>A (p.Asn180Lys)
c.537T>A (p.Asn179Lys)
c.489T>A (p.Asn163Lys)
c.648T>A (p.Asn216Lys)
c.590T>A
c.645T>A (p.Asn215Lys)
c.428-1539T>A (n.428-1539T>A)
c.855T>A (p.Asn285Lys)
c.852T>A (p.Asn284Lys)
c.635-1539T>A (n.635-1539T>A)
1g.161544739T>ACA343367394FCGR3Ac.539A>T (p.Asn180Ile)
c.536A>T (p.Asn179Ile)
c.488A>T (p.Asn163Ile)
c.647A>T (p.Asn216Ile)
c.589A>T
c.644A>T (p.Asn215Ile)
c.428-1540A>T (n.428-1540A>T)
c.854A>T (p.Asn285Ile)
c.851A>T (p.Asn284Ile)
c.635-1540A>T (n.635-1540A>T)
1g.161544739T>CCA343367395FCGR3Ac.539A>G (p.Asn180Ser)
c.536A>G (p.Asn179Ser)
c.488A>G (p.Asn163Ser)
c.647A>G (p.Asn216Ser)
c.589A>G
c.644A>G (p.Asn215Ser)
c.428-1540A>G (n.428-1540A>G)
c.854A>G (p.Asn285Ser)
c.851A>G (p.Asn284Ser)
c.635-1540A>G (n.635-1540A>G)
1g.161544739T>GCA343367396FCGR3Ac.539A>C (p.Asn180Thr)
c.536A>C (p.Asn179Thr)
c.488A>C (p.Asn163Thr)
c.647A>C (p.Asn216Thr)
c.589A>C
c.644A>C (p.Asn215Thr)
c.428-1540A>C (n.428-1540A>C)
c.854A>C (p.Asn285Thr)
c.851A>C (p.Asn284Thr)
c.635-1540A>C (n.635-1540A>C)
1g.161544743dupCA2573939368FCGR3Ac.539dup (p.Asn180LysfsTer?)
c.536dup (p.Asn179LysfsTer?)
c.539dup (p.Asn180LysfsTer15)
c.488dup (p.Asn163LysfsTer?)
c.647dup (p.Asn216LysfsTer?)
c.589dup
c.644dup (p.Asn215LysfsTer?)
c.428-1540dup (n.428-1540dup)
c.854dup (p.Asn285LysfsTer?)
c.851dup (p.Asn284LysfsTer?)
c.635-1540dup (n.635-1540dup)
 gnomAD v4
1g.161544739_161544747dupCA2648790073FCGR3Ac.531_539dup (p.Lys179_Asn180insLysSerLys)
c.528_536dup (p.Lys178_Asn179insLysSerLys)
c.480_488dup (p.Lys162_Asn163insLysSerLys)
c.639_647dup (p.Lys215_Asn216insLysSerLys)
c.581_589dup
c.636_644dup (p.Lys214_Asn215insLysSerLys)
c.428-1548_428-1540dup (n.428-1548_428-1540dup)
c.846_854dup (p.Lys284_Asn285insLysSerLys)
c.843_851dup (p.Lys283_Asn284insLysSerLys)
c.635-1548_635-1540dup (n.635-1548_635-1540dup)
 gnomAD v4
1g.161544740T>ACA343367399FCGR3Ac.538A>T (p.Asn180Tyr)
c.535A>T (p.Asn179Tyr)
c.487A>T (p.Asn163Tyr)
c.646A>T (p.Asn216Tyr)
c.588A>T
c.643A>T (p.Asn215Tyr)
c.428-1541A>T (n.428-1541A>T)
c.853A>T (p.Asn285Tyr)
c.850A>T (p.Asn284Tyr)
c.635-1541A>T (n.635-1541A>T)
 dbSNP gnomAD v3 gnomAD v4
1g.161544740T>CCA343367397FCGR3Ac.538A>G (p.Asn180Asp)
c.535A>G (p.Asn179Asp)
c.487A>G (p.Asn163Asp)
c.646A>G (p.Asn216Asp)
c.588A>G
c.643A>G (p.Asn215Asp)
c.428-1541A>G (n.428-1541A>G)
c.853A>G (p.Asn285Asp)
c.850A>G (p.Asn284Asp)
c.635-1541A>G (n.635-1541A>G)
1g.161544740T>GCA343367398FCGR3Ac.538A>C (p.Asn180His)
c.535A>C (p.Asn179His)
c.487A>C (p.Asn163His)
c.646A>C (p.Asn216His)
c.588A>C
c.643A>C (p.Asn215His)
c.428-1541A>C (n.428-1541A>C)
c.853A>C (p.Asn285His)
c.850A>C (p.Asn284His)
c.635-1541A>C (n.635-1541A>C)
1g.161544740T=CA1202785220FCGR3Ac.538A= (p.Asn180=)
c.535A= (p.Asn179=)
c.487A= (p.Asn163=)
c.646A= (p.Asn216=)
c.588A=
c.643A= (p.Asn215=)
c.428-1541A= (n.428-1541A=)
c.853A= (p.Asn285=)
c.850A= (p.Asn284=)
c.635-1541A= (n.635-1541A=)
1g.161544741T>ACA343367400FCGR3Ac.537A>T (p.Lys179Asn)
c.534A>T (p.Lys178Asn)
c.486A>T (p.Lys162Asn)
c.645A>T (p.Lys215Asn)
c.587A>T
c.642A>T (p.Lys214Asn)
c.428-1542A>T (n.428-1542A>T)
c.852A>T (p.Lys284Asn)
c.849A>T (p.Lys283Asn)
c.635-1542A>T (n.635-1542A>T)
1g.161544741T>CCA421612421FCGR3Ac.537A>G (p.Lys179=)
c.534A>G (p.Lys178=)
c.486A>G (p.Lys162=)
c.645A>G (p.Lys215=)
c.587A>G
c.642A>G (p.Lys214=)
c.428-1542A>G (n.428-1542A>G)
c.852A>G (p.Lys284=)
c.849A>G (p.Lys283=)
c.635-1542A>G (n.635-1542A>G)
1g.161544741T>GCA343367401FCGR3Ac.537A>C (p.Lys179Asn)
c.534A>C (p.Lys178Asn)
c.486A>C (p.Lys162Asn)
c.645A>C (p.Lys215Asn)
c.587A>C
c.642A>C (p.Lys214Asn)
c.428-1542A>C (n.428-1542A>C)
c.852A>C (p.Lys284Asn)
c.849A>C (p.Lys283Asn)
c.635-1542A>C (n.635-1542A>C)
1g.161544742T>ACA343367402FCGR3Ac.536A>T (p.Lys179Ile)
c.533A>T (p.Lys178Ile)
c.485A>T (p.Lys162Ile)
c.644A>T (p.Lys215Ile)
c.586A>T
c.641A>T (p.Lys214Ile)
c.428-1543A>T (n.428-1543A>T)
c.851A>T (p.Lys284Ile)
c.848A>T (p.Lys283Ile)
c.635-1543A>T (n.635-1543A>T)
1g.161544742T>CCA343367403FCGR3Ac.536A>G (p.Lys179Arg)
c.533A>G (p.Lys178Arg)
c.485A>G (p.Lys162Arg)
c.644A>G (p.Lys215Arg)
c.586A>G
c.641A>G (p.Lys214Arg)
c.428-1543A>G (n.428-1543A>G)
c.851A>G (p.Lys284Arg)
c.848A>G (p.Lys283Arg)
c.635-1543A>G (n.635-1543A>G)
1g.161544742T>GCA343367404FCGR3Ac.536A>C (p.Lys179Thr)
c.533A>C (p.Lys178Thr)
c.485A>C (p.Lys162Thr)
c.644A>C (p.Lys215Thr)
c.586A>C
c.641A>C (p.Lys214Thr)
c.428-1543A>C (n.428-1543A>C)
c.851A>C (p.Lys284Thr)
c.848A>C (p.Lys283Thr)
c.635-1543A>C (n.635-1543A>C)
1g.161544743T>ACA343367407FCGR3Ac.535A>T (p.Lys179Ter)
c.532A>T (p.Lys178Ter)
c.484A>T (p.Lys162Ter)
c.643A>T (p.Lys215Ter)
c.585A>T
c.640A>T (p.Lys214Ter)
c.428-1544A>T (n.428-1544A>T)
c.850A>T (p.Lys284Ter)
c.847A>T (p.Lys283Ter)
c.635-1544A>T (n.635-1544A>T)
1g.161544743T>CCA343367406FCGR3Ac.535A>G (p.Lys179Glu)
c.532A>G (p.Lys178Glu)
c.484A>G (p.Lys162Glu)
c.643A>G (p.Lys215Glu)
c.585A>G
c.640A>G (p.Lys214Glu)
c.428-1544A>G (n.428-1544A>G)
c.850A>G (p.Lys284Glu)
c.847A>G (p.Lys283Glu)
c.635-1544A>G (n.635-1544A>G)
1g.161544743T>GCA343367405FCGR3Ac.535A>C (p.Lys179Gln)
c.532A>C (p.Lys178Gln)
c.484A>C (p.Lys162Gln)
c.643A>C (p.Lys215Gln)
c.585A>C
c.640A>C (p.Lys214Gln)
c.428-1544A>C (n.428-1544A>C)
c.850A>C (p.Lys284Gln)
c.847A>C (p.Lys283Gln)
c.635-1544A>C (n.635-1544A>C)
1g.161544744A=CA1202785221FCGR3Ac.534T= (p.Ser178=)
c.531T= (p.Ser177=)
c.483T= (p.Ser161=)
c.642T= (p.Ser214=)
c.584T=
c.639T= (p.Ser213=)
c.428-1545T= (n.428-1545T=)
c.849T= (p.Ser283=)
c.846T= (p.Ser282=)
c.635-1545T= (n.635-1545T=)
1g.161544744A>CCA343367408FCGR3Ac.534T>G (p.Ser178Arg)
c.531T>G (p.Ser177Arg)
c.483T>G (p.Ser161Arg)
c.642T>G (p.Ser214Arg)
c.584T>G
c.639T>G (p.Ser213Arg)
c.428-1545T>G (n.428-1545T>G)
c.849T>G (p.Ser283Arg)
c.846T>G (p.Ser282Arg)
c.635-1545T>G (n.635-1545T>G)
1g.161544744A>GCA31715250FCGR3Ac.534T>C (p.Ser178=)
c.531T>C (p.Ser177=)
c.483T>C (p.Ser161=)
c.642T>C (p.Ser214=)
c.584T>C
c.639T>C (p.Ser213=)
c.428-1545T>C (n.428-1545T>C)
c.849T>C (p.Ser283=)
c.846T>C (p.Ser282=)
c.635-1545T>C (n.635-1545T>C)
 dbSNP gnomAD v4
1g.161544744A>TCA343367410FCGR3Ac.534T>A (p.Ser178Arg)
c.531T>A (p.Ser177Arg)
c.483T>A (p.Ser161Arg)
c.642T>A (p.Ser214Arg)
c.584T>A
c.639T>A (p.Ser213Arg)
c.428-1545T>A (n.428-1545T>A)
c.849T>A (p.Ser283Arg)
c.846T>A (p.Ser282Arg)
c.635-1545T>A (n.635-1545T>A)
1g.161544745C>ACA343367411FCGR3Ac.533G>T (p.Ser178Ile)
c.530G>T (p.Ser177Ile)
c.482G>T (p.Ser161Ile)
c.641G>T (p.Ser214Ile)
c.583G>T
c.638G>T (p.Ser213Ile)
c.428-1546G>T (n.428-1546G>T)
c.848G>T (p.Ser283Ile)
c.845G>T (p.Ser282Ile)
c.635-1546G>T (n.635-1546G>T)
1g.161544745C>GCA343367412FCGR3Ac.533G>C (p.Ser178Thr)
c.530G>C (p.Ser177Thr)
c.482G>C (p.Ser161Thr)
c.641G>C (p.Ser214Thr)
c.583G>C
c.638G>C (p.Ser213Thr)
c.428-1546G>C (n.428-1546G>C)
c.848G>C (p.Ser283Thr)
c.845G>C (p.Ser282Thr)
c.635-1546G>C (n.635-1546G>C)
1g.161544745C>TCA343367414FCGR3Ac.533G>A (p.Ser178Asn)
c.530G>A (p.Ser177Asn)
c.482G>A (p.Ser161Asn)
c.641G>A (p.Ser214Asn)
c.583G>A
c.638G>A (p.Ser213Asn)
c.428-1546G>A (n.428-1546G>A)
c.848G>A (p.Ser283Asn)
c.845G>A (p.Ser282Asn)
c.635-1546G>A (n.635-1546G>A)
1g.161544746T>ACA343367416FCGR3Ac.532A>T (p.Ser178Cys)
c.529A>T (p.Ser177Cys)
c.481A>T (p.Ser161Cys)
c.640A>T (p.Ser214Cys)
c.582A>T
c.637A>T (p.Ser213Cys)
c.428-1547A>T (n.428-1547A>T)
c.847A>T (p.Ser283Cys)
c.844A>T (p.Ser282Cys)
c.635-1547A>T (n.635-1547A>T)
1g.161544746T>CCA343367417FCGR3Ac.532A>G (p.Ser178Gly)
c.529A>G (p.Ser177Gly)
c.481A>G (p.Ser161Gly)
c.640A>G (p.Ser214Gly)
c.582A>G
c.637A>G (p.Ser213Gly)
c.428-1547A>G (n.428-1547A>G)
c.847A>G (p.Ser283Gly)
c.844A>G (p.Ser282Gly)
c.635-1547A>G (n.635-1547A>G)
1g.161544746T>GCA343367418FCGR3Ac.532A>C (p.Ser178Arg)
c.529A>C (p.Ser177Arg)
c.481A>C (p.Ser161Arg)
c.640A>C (p.Ser214Arg)
c.582A>C
c.637A>C (p.Ser213Arg)
c.428-1547A>C (n.428-1547A>C)
c.847A>C (p.Ser283Arg)
c.844A>C (p.Ser282Arg)
c.635-1547A>C (n.635-1547A>C)
 gnomAD v4
1g.161544747C>ACA421612425FCGR3Ac.531G>T (p.Gly177=)
c.528G>T (p.Gly176=)
c.480G>T (p.Gly160=)
c.639G>T (p.Gly213=)
c.581G>T
c.636G>T (p.Gly212=)
c.428-1548G>T (n.428-1548G>T)
c.846G>T (p.Gly282=)
c.843G>T (p.Gly281=)
c.635-1548G>T (n.635-1548G>T)
1g.161544747C=CA1202785222FCGR3Ac.531G= (p.Gly177=)
c.528G= (p.Gly176=)
c.480G= (p.Gly160=)
c.639G= (p.Gly213=)
c.581G=
c.636G= (p.Gly212=)
c.428-1548G= (n.428-1548G=)
c.846G= (p.Gly282=)
c.843G= (p.Gly281=)
c.635-1548G= (n.635-1548G=)
1g.161544747C>GCA421612428FCGR3Ac.531G>C (p.Gly177=)
c.528G>C (p.Gly176=)
c.480G>C (p.Gly160=)
c.639G>C (p.Gly213=)
c.581G>C
c.636G>C (p.Gly212=)
c.428-1548G>C (n.428-1548G>C)
c.846G>C (p.Gly282=)
c.843G>C (p.Gly281=)
c.635-1548G>C (n.635-1548G>C)
 dbSNP gnomAD v4
1g.161544747C>TCA421612426FCGR3Ac.531G>A (p.Gly177=)
c.528G>A (p.Gly176=)
c.480G>A (p.Gly160=)
c.639G>A (p.Gly213=)
c.581G>A
c.636G>A (p.Gly212=)
c.428-1548G>A (n.428-1548G>A)
c.846G>A (p.Gly282=)
c.843G>A (p.Gly281=)
c.635-1548G>A (n.635-1548G>A)
1g.161544748C>ACA343367420FCGR3Ac.530G>T (p.Gly177Val)
c.527G>T (p.Gly176Val)
c.479G>T (p.Gly160Val)
c.638G>T (p.Gly213Val)
c.580G>T
c.635G>T (p.Gly212Val)
c.428-1549G>T (n.428-1549G>T)
c.845G>T (p.Gly282Val)
c.842G>T (p.Gly281Val)
c.635-1549G>T (n.635-1549G>T)
 dbSNP
1g.161544748C>GCA343367422FCGR3Ac.530G>C (p.Gly177Ala)
c.527G>C (p.Gly176Ala)
c.479G>C (p.Gly160Ala)
c.638G>C (p.Gly213Ala)
c.580G>C
c.635G>C (p.Gly212Ala)
c.428-1549G>C (n.428-1549G>C)
c.845G>C (p.Gly282Ala)
c.842G>C (p.Gly281Ala)
c.635-1549G>C (n.635-1549G>C)
1g.161544748C>TCA343367423FCGR3Ac.530G>A (p.Gly177Glu)
c.527G>A (p.Gly176Glu)
c.479G>A (p.Gly160Glu)
c.638G>A (p.Gly213Glu)
c.580G>A
c.635G>A (p.Gly212Glu)
c.428-1549G>A (n.428-1549G>A)
c.845G>A (p.Gly282Glu)
c.842G>A (p.Gly281Glu)
c.635-1549G>A (n.635-1549G>A)
 gnomAD v4
1g.161544749C>ACA343367424FCGR3Ac.529G>T (p.Gly177Trp)
c.526G>T (p.Gly176Trp)
c.478G>T (p.Gly160Trp)
c.637G>T (p.Gly213Trp)
c.579G>T
c.634G>T (p.Gly212Trp)
c.428-1550G>T (n.428-1550G>T)
c.844G>T (p.Gly282Trp)
c.841G>T (p.Gly281Trp)
c.635-1550G>T (n.635-1550G>T)
1g.161544749C>GCA343367425FCGR3Ac.529G>C (p.Gly177Arg)
c.526G>C (p.Gly176Arg)
c.478G>C (p.Gly160Arg)
c.637G>C (p.Gly213Arg)
c.579G>C
c.634G>C (p.Gly212Arg)
c.428-1550G>C (n.428-1550G>C)
c.844G>C (p.Gly282Arg)
c.841G>C (p.Gly281Arg)
c.635-1550G>C (n.635-1550G>C)
 gnomAD v4
1g.161544749C>TCA343367426FCGR3Ac.529G>A (p.Gly177Arg)
c.526G>A (p.Gly176Arg)
c.478G>A (p.Gly160Arg)
c.637G>A (p.Gly213Arg)
c.579G>A
c.634G>A (p.Gly212Arg)
c.428-1550G>A (n.428-1550G>A)
c.844G>A (p.Gly282Arg)
c.841G>A (p.Gly281Arg)
c.635-1550G>A (n.635-1550G>A)
1g.161544750A>CCA343367427FCGR3Ac.528T>G (p.Phe176Leu)
c.525T>G (p.Phe175Leu)
c.477T>G (p.Phe159Leu)
c.636T>G (p.Phe212Leu)
c.578T>G
c.633T>G (p.Phe211Leu)
c.428-1551T>G (n.428-1551T>G)
c.843T>G (p.Phe281Leu)
c.840T>G (p.Phe280Leu)
c.635-1551T>G (n.635-1551T>G)
1g.161544750A>GCA421612435FCGR3Ac.528T>C (p.Phe176=)
c.525T>C (p.Phe175=)
c.477T>C (p.Phe159=)
c.636T>C (p.Phe212=)
c.578T>C
c.633T>C (p.Phe211=)
c.428-1551T>C (n.428-1551T>C)
c.843T>C (p.Phe281=)
c.840T>C (p.Phe280=)
c.635-1551T>C (n.635-1551T>C)
1g.161544750A>TCA343367429FCGR3Ac.528T>A (p.Phe176Leu)
c.525T>A (p.Phe175Leu)
c.477T>A (p.Phe159Leu)
c.636T>A (p.Phe212Leu)
c.578T>A
c.633T>A (p.Phe211Leu)
c.428-1551T>A (n.428-1551T>A)
c.843T>A (p.Phe281Leu)
c.840T>A (p.Phe280Leu)
c.635-1551T>A (n.635-1551T>A)
1g.161544754delCA2648790074FCGR3Ac.528del (p.Phe176LeufsTer11)
c.525del (p.Phe175LeufsTer11)
c.477del (p.Phe159LeufsTer11)
c.636del (p.Phe212LeufsTer11)
c.578del
c.633del (p.Phe211LeufsTer11)
c.428-1551del (n.428-1551del)
c.843del (p.Phe281LeufsTer11)
c.840del (p.Phe280LeufsTer11)
c.635-1551del (n.635-1551del)
 gnomAD v4
1g.161544751A>CCA343367430FCGR3Ac.527T>G (p.Phe176Cys)
c.524T>G (p.Phe175Cys)
c.476T>G (p.Phe159Cys)
c.635T>G (p.Phe212Cys)
c.577T>G
c.632T>G (p.Phe211Cys)
c.428-1552T>G (n.428-1552T>G)
c.842T>G (p.Phe281Cys)
c.839T>G (p.Phe280Cys)
c.635-1552T>G (n.635-1552T>G)
1g.161544751A>GCA343367431FCGR3Ac.527T>C (p.Phe176Ser)
c.524T>C (p.Phe175Ser)
c.476T>C (p.Phe159Ser)
c.635T>C (p.Phe212Ser)
c.577T>C
c.632T>C (p.Phe211Ser)
c.428-1552T>C (n.428-1552T>C)
c.842T>C (p.Phe281Ser)
c.839T>C (p.Phe280Ser)
c.635-1552T>C (n.635-1552T>C)
 gnomAD v4
1g.161544751A>TCA343367433FCGR3Ac.527T>A (p.Phe176Tyr)
c.524T>A (p.Phe175Tyr)
c.476T>A (p.Phe159Tyr)
c.635T>A (p.Phe212Tyr)
c.577T>A
c.632T>A (p.Phe211Tyr)
c.428-1552T>A (n.428-1552T>A)
c.842T>A (p.Phe281Tyr)
c.839T>A (p.Phe280Tyr)
c.635-1552T>A (n.635-1552T>A)
1g.161544752A=CA1139793706FCGR3Ac.526T= (p.Phe176=)
c.523T= (p.Phe175=)
c.475T= (p.Phe159=)
c.634T= (p.Phe212=)
c.576T=
c.631T= (p.Phe211=)
c.428-1553T= (n.428-1553T=)
c.841T= (p.Phe281=)
c.838T= (p.Phe280=)
c.635-1553T= (n.635-1553T=)
1g.161544752A>CCA1211378FCGR3Ac.526T>G (p.Phe176Val)
c.523T>G (p.Phe175Val)
c.475T>G (p.Phe159Val)
c.634T>G (p.Phe212Val)
c.576T>G
c.631T>G (p.Phe211Val)
c.428-1553T>G (n.428-1553T>G)
c.841T>G (p.Phe281Val)
c.838T>G (p.Phe280Val)
c.635-1553T>G (n.635-1553T>G)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.161544752A>GCA1211379FCGR3Ac.526T>C (p.Phe176Leu)
c.523T>C (p.Phe175Leu)
c.475T>C (p.Phe159Leu)
c.634T>C (p.Phe212Leu)
c.576T>C
c.631T>C (p.Phe211Leu)
c.428-1553T>C (n.428-1553T>C)
c.841T>C (p.Phe281Leu)
c.838T>C (p.Phe280Leu)
c.635-1553T>C (n.635-1553T>C)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.161544752A>TCA343367436FCGR3Ac.526T>A (p.Phe176Ile)
c.523T>A (p.Phe175Ile)
c.475T>A (p.Phe159Ile)
c.634T>A (p.Phe212Ile)
c.576T>A
c.631T>A (p.Phe211Ile)
c.428-1553T>A (n.428-1553T>A)
c.841T>A (p.Phe281Ile)
c.838T>A (p.Phe280Ile)
c.635-1553T>A (n.635-1553T>A)
 dbSNP gnomAD v4
1g.161544753A>CCA421612439FCGR3Ac.525T>G (p.Leu175=)
c.522T>G (p.Leu174=)
c.474T>G (p.Leu158=)
c.633T>G (p.Leu211=)
c.575T>G
c.630T>G (p.Leu210=)
c.428-1554T>G (n.428-1554T>G)
c.840T>G (p.Leu280=)
c.837T>G (p.Leu279=)
c.635-1554T>G (n.635-1554T>G)
1g.161544753A>GCA421612440FCGR3Ac.525T>C (p.Leu175=)
c.522T>C (p.Leu174=)
c.474T>C (p.Leu158=)
c.633T>C (p.Leu211=)
c.575T>C
c.630T>C (p.Leu210=)
c.428-1554T>C (n.428-1554T>C)
c.840T>C (p.Leu280=)
c.837T>C (p.Leu279=)
c.635-1554T>C (n.635-1554T>C)
1g.161544753A>TCA421612441FCGR3Ac.525T>A (p.Leu175=)
c.522T>A (p.Leu174=)
c.474T>A (p.Leu158=)
c.633T>A (p.Leu211=)
c.575T>A
c.630T>A (p.Leu210=)
c.428-1554T>A (n.428-1554T>A)
c.840T>A (p.Leu280=)
c.837T>A (p.Leu279=)
c.635-1554T>A (n.635-1554T>A)
1g.161544754A>CCA343367438FCGR3Ac.524T>G (p.Leu175Arg)
c.521T>G (p.Leu174Arg)
c.473T>G (p.Leu158Arg)
c.632T>G (p.Leu211Arg)
c.574T>G
c.629T>G (p.Leu210Arg)
c.428-1555T>G (n.428-1555T>G)
c.839T>G (p.Leu280Arg)
c.836T>G (p.Leu279Arg)
c.635-1555T>G (n.635-1555T>G)
 gnomAD v4
1g.161544754A>GCA343367440FCGR3Ac.524T>C (p.Leu175Pro)
c.521T>C (p.Leu174Pro)
c.473T>C (p.Leu158Pro)
c.632T>C (p.Leu211Pro)
c.574T>C
c.629T>C (p.Leu210Pro)
c.428-1555T>C (n.428-1555T>C)
c.839T>C (p.Leu280Pro)
c.836T>C (p.Leu279Pro)
c.635-1555T>C (n.635-1555T>C)
1g.161544754A>TCA343367442FCGR3Ac.524T>A (p.Leu175His)
c.521T>A (p.Leu174His)
c.473T>A (p.Leu158His)
c.632T>A (p.Leu211His)
c.574T>A
c.629T>A (p.Leu210His)
c.428-1555T>A (n.428-1555T>A)
c.839T>A (p.Leu280His)
c.836T>A (p.Leu279His)
c.635-1555T>A (n.635-1555T>A)
1g.161544755G>ACA343367443FCGR3Ac.523C>T (p.Leu175Phe)
c.520C>T (p.Leu174Phe)
c.472C>T (p.Leu158Phe)
c.631C>T (p.Leu211Phe)
c.573C>T
c.628C>T (p.Leu210Phe)
c.428-1556C>T (n.428-1556C>T)
c.838C>T (p.Leu280Phe)
c.835C>T (p.Leu279Phe)
c.635-1556C>T (n.635-1556C>T)
 gnomAD v4
1g.161544755G>CCA343367444FCGR3Ac.523C>G (p.Leu175Val)
c.520C>G (p.Leu174Val)
c.472C>G (p.Leu158Val)
c.631C>G (p.Leu211Val)
c.573C>G
c.628C>G (p.Leu210Val)
c.428-1556C>G (n.428-1556C>G)
c.838C>G (p.Leu280Val)
c.835C>G (p.Leu279Val)
c.635-1556C>G (n.635-1556C>G)
1g.161544755G=CA1202785223FCGR3Ac.523C= (p.Leu175=)
c.520C= (p.Leu174=)
c.472C= (p.Leu158=)
c.631C= (p.Leu211=)
c.573C=
c.628C= (p.Leu210=)
c.428-1556C= (n.428-1556C=)
c.838C= (p.Leu280=)
c.835C= (p.Leu279=)
c.635-1556C= (n.635-1556C=)
1g.161544755G>TCA343367445FCGR3Ac.523C>A (p.Leu175Ile)
c.520C>A (p.Leu174Ile)
c.472C>A (p.Leu158Ile)
c.631C>A (p.Leu211Ile)
c.573C>A
c.628C>A (p.Leu210Ile)
c.428-1556C>A (n.428-1556C>A)
c.838C>A (p.Leu280Ile)
c.835C>A (p.Leu279Ile)
c.635-1556C>A (n.635-1556C>A)
1g.161544756C>ACA421612442FCGR3Ac.522G>T (p.Gly174=)
c.519G>T (p.Gly173=)
c.471G>T (p.Gly157=)
c.630G>T (p.Gly210=)
c.572G>T
c.627G>T (p.Gly209=)
c.428-1557G>T (n.428-1557G>T)
c.837G>T (p.Gly279=)
c.834G>T (p.Gly278=)
c.635-1557G>T (n.635-1557G>T)
 gnomAD v4
1g.161544756C>GCA421612443FCGR3Ac.522G>C (p.Gly174=)
c.519G>C (p.Gly173=)
c.471G>C (p.Gly157=)
c.630G>C (p.Gly210=)
c.572G>C
c.627G>C (p.Gly209=)
c.428-1557G>C (n.428-1557G>C)
c.837G>C (p.Gly279=)
c.834G>C (p.Gly278=)
c.635-1557G>C (n.635-1557G>C)
1g.161544756C>TCA421612445FCGR3Ac.522G>A (p.Gly174=)
c.519G>A (p.Gly173=)
c.471G>A (p.Gly157=)
c.630G>A (p.Gly210=)
c.572G>A
c.627G>A (p.Gly209=)
c.428-1557G>A (n.428-1557G>A)
c.837G>A (p.Gly279=)
c.834G>A (p.Gly278=)
c.635-1557G>A (n.635-1557G>A)
 gnomAD v4 COSMIC
1g.161544760dupCA527135442FCGR3Ac.522dup (p.Leu175AlafsTer5)
c.519dup (p.Leu174AlafsTer5)
c.471dup (p.Leu158AlafsTer5)
c.630dup (p.Leu211AlafsTer5)
c.572dup
c.627dup (p.Leu210AlafsTer5)
c.428-1557dup (n.428-1557dup)
c.837dup (p.Leu280AlafsTer5)
c.834dup (p.Leu279AlafsTer5)
c.635-1557dup (n.635-1557dup)
 dbSNP gnomAD v2 gnomAD v4
1g.161544760delCA2648790075FCGR3Ac.522del (p.Leu175PhefsTer12)
c.519del (p.Leu174PhefsTer12)
c.471del (p.Leu158PhefsTer12)
c.630del (p.Leu211PhefsTer12)
c.572del
c.627del (p.Leu210PhefsTer12)
c.428-1557del (n.428-1557del)
c.837del (p.Leu280PhefsTer12)
c.834del (p.Leu279PhefsTer12)
c.635-1557del (n.635-1557del)
 gnomAD v4
1g.161544757C>ACA343367450FCGR3Ac.521G>T (p.Gly174Val)
c.518G>T (p.Gly173Val)
c.470G>T (p.Gly157Val)
c.629G>T (p.Gly210Val)
c.571G>T
c.626G>T (p.Gly209Val)
c.428-1558G>T (n.428-1558G>T)
c.836G>T (p.Gly279Val)
c.833G>T (p.Gly278Val)
c.635-1558G>T (n.635-1558G>T)
1g.161544757C=CA1202785224FCGR3Ac.521G= (p.Gly174=)
c.518G= (p.Gly173=)
c.470G= (p.Gly157=)
c.629G= (p.Gly210=)
c.571G=
c.626G= (p.Gly209=)
c.428-1558G= (n.428-1558G=)
c.836G= (p.Gly279=)
c.833G= (p.Gly278=)
c.635-1558G= (n.635-1558G=)
1g.161544757C>GCA343367448FCGR3Ac.521G>C (p.Gly174Ala)
c.518G>C (p.Gly173Ala)
c.470G>C (p.Gly157Ala)
c.629G>C (p.Gly210Ala)
c.571G>C
c.626G>C (p.Gly209Ala)
c.428-1558G>C (n.428-1558G>C)
c.836G>C (p.Gly279Ala)
c.833G>C (p.Gly278Ala)
c.635-1558G>C (n.635-1558G>C)
1g.161544757C>TCA1211380FCGR3Ac.521G>A (p.Gly174Glu)
c.518G>A (p.Gly173Glu)
c.470G>A (p.Gly157Glu)
c.629G>A (p.Gly210Glu)
c.571G>A
c.626G>A (p.Gly209Glu)
c.428-1558G>A (n.428-1558G>A)
c.836G>A (p.Gly279Glu)
c.833G>A (p.Gly278Glu)
c.635-1558G>A (n.635-1558G>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.161544757_161544758insACA2648790076FCGR3Ac.520_521insT (p.Gly174ValfsTer6)
c.517_518insT (p.Gly173ValfsTer6)
c.469_470insT (p.Gly157ValfsTer6)
c.628_629insT (p.Gly210ValfsTer6)
c.570_571insT
c.625_626insT (p.Gly209ValfsTer6)
c.428-1559_428-1558insT (n.428-1559_428-1558insT)
c.835_836insT (p.Gly279ValfsTer6)
c.832_833insT (p.Gly278ValfsTer6)
c.635-1559_635-1558insT (n.635-1559_635-1558insT)
 gnomAD v4
1g.161544758C>ACA343367452FCGR3Ac.520G>T (p.Gly174Trp)
c.517G>T (p.Gly173Trp)
c.469G>T (p.Gly157Trp)
c.628G>T (p.Gly210Trp)
c.570G>T
c.625G>T (p.Gly209Trp)
c.428-1559G>T (n.428-1559G>T)
c.835G>T (p.Gly279Trp)
c.832G>T (p.Gly278Trp)
c.635-1559G>T (n.635-1559G>T)
1g.161544758C>GCA343367455FCGR3Ac.520G>C (p.Gly174Arg)
c.517G>C (p.Gly173Arg)
c.469G>C (p.Gly157Arg)
c.628G>C (p.Gly210Arg)
c.570G>C
c.625G>C (p.Gly209Arg)
c.428-1559G>C (n.428-1559G>C)
c.835G>C (p.Gly279Arg)
c.832G>C (p.Gly278Arg)
c.635-1559G>C (n.635-1559G>C)
1g.161544758C>TCA343367453FCGR3Ac.520G>A (p.Gly174Arg)
c.517G>A (p.Gly173Arg)
c.469G>A (p.Gly157Arg)
c.628G>A (p.Gly210Arg)
c.570G>A
c.625G>A (p.Gly209Arg)
c.428-1559G>A (n.428-1559G>A)
c.835G>A (p.Gly279Arg)
c.832G>A (p.Gly278Arg)
c.635-1559G>A (n.635-1559G>A)
 gnomAD v4
1g.161544759C>ACA343367456FCGR3Ac.519G>T (p.Arg173Ser)
c.516G>T (p.Arg172Ser)
c.468G>T (p.Arg156Ser)
c.627G>T (p.Arg209Ser)
c.569G>T
c.624G>T (p.Arg208Ser)
c.428-1560G>T (n.428-1560G>T)
c.834G>T (p.Arg278Ser)
c.831G>T (p.Arg277Ser)
c.635-1560G>T (n.635-1560G>T)
 gnomAD v4
1g.161544759C=CA1202785225FCGR3Ac.519G= (p.Arg173=)
c.516G= (p.Arg172=)
c.468G= (p.Arg156=)
c.627G= (p.Arg209=)
c.569G=
c.624G= (p.Arg208=)
c.428-1560G= (n.428-1560G=)
c.834G= (p.Arg278=)
c.831G= (p.Arg277=)
c.635-1560G= (n.635-1560G=)
1g.161544759C>GCA1211382FCGR3Ac.519G>C (p.Arg173Ser)
c.516G>C (p.Arg172Ser)
c.468G>C (p.Arg156Ser)
c.627G>C (p.Arg209Ser)
c.569G>C
c.624G>C (p.Arg208Ser)
c.428-1560G>C (n.428-1560G>C)
c.834G>C (p.Arg278Ser)
c.831G>C (p.Arg277Ser)
c.635-1560G>C (n.635-1560G>C)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.161544759C>TCA1211381FCGR3Ac.519G>A (p.Arg173=)
c.516G>A (p.Arg172=)
c.468G>A (p.Arg156=)
c.627G>A (p.Arg209=)
c.569G>A
c.624G>A (p.Arg208=)
c.428-1560G>A (n.428-1560G>A)
c.834G>A (p.Arg278=)
c.831G>A (p.Arg277=)
c.635-1560G>A (n.635-1560G>A)
 dbSNP ExAC gnomAD v2
1g.161544760C>ACA343367458FCGR3Ac.518G>T (p.Arg173Met)
c.515G>T (p.Arg172Met)
c.467G>T (p.Arg156Met)
c.626G>T (p.Arg209Met)
c.568G>T
c.623G>T (p.Arg208Met)
c.428-1561G>T (n.428-1561G>T)
c.833G>T (p.Arg278Met)
c.830G>T (p.Arg277Met)
c.635-1561G>T (n.635-1561G>T)
1g.161544760C>GCA343367459FCGR3Ac.518G>C (p.Arg173Thr)
c.515G>C (p.Arg172Thr)
c.467G>C (p.Arg156Thr)
c.626G>C (p.Arg209Thr)
c.568G>C
c.623G>C (p.Arg208Thr)
c.428-1561G>C (n.428-1561G>C)
c.833G>C (p.Arg278Thr)
c.830G>C (p.Arg277Thr)
c.635-1561G>C (n.635-1561G>C)
1g.161544760C>TCA343367460FCGR3Ac.518G>A (p.Arg173Lys)
c.515G>A (p.Arg172Lys)
c.467G>A (p.Arg156Lys)
c.626G>A (p.Arg209Lys)
c.568G>A
c.623G>A (p.Arg208Lys)
c.428-1561G>A (n.428-1561G>A)
c.833G>A (p.Arg278Lys)
c.830G>A (p.Arg277Lys)
c.635-1561G>A (n.635-1561G>A)
 gnomAD v4
1g.161544760_161544761delinsCTCA1202785226FCGR3Ac.517_518delinsAG (p.Arg173=)
c.514_515delinsAG (p.Arg172=)
c.466_467delinsAG (p.Arg156=)
c.625_626delinsAG (p.Arg209=)
c.567_568delinsAG
c.622_623delinsAG (p.Arg208=)
c.428-1562_428-1561delinsAG (n.428-1562_428-1561delinsAG)
c.832_833delinsAG (p.Arg278=)
c.829_830delinsAG (p.Arg277=)
c.635-1562_635-1561delinsAG (n.635-1562_635-1561delinsAG)
1g.161544761delCA1211383FCGR3Ac.517del (p.Arg173GlyfsTer14)
c.514del (p.Arg172GlyfsTer14)
c.466del (p.Arg156GlyfsTer14)
c.625del (p.Arg209GlyfsTer14)
c.567del
c.622del (p.Arg208GlyfsTer14)
c.428-1562del (n.428-1562del)
c.832del (p.Arg278GlyfsTer14)
c.829del (p.Arg277GlyfsTer14)
c.635-1562del (n.635-1562del)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.161544761T>ACA343367462FCGR3Ac.517A>T (p.Arg173Trp)
c.514A>T (p.Arg172Trp)
c.466A>T (p.Arg156Trp)
c.625A>T (p.Arg209Trp)
c.567A>T
c.622A>T (p.Arg208Trp)
c.428-1562A>T (n.428-1562A>T)
c.832A>T (p.Arg278Trp)
c.829A>T (p.Arg277Trp)
c.635-1562A>T (n.635-1562A>T)
 dbSNP gnomAD v3 gnomAD v4
1g.161544761T>CCA343367464FCGR3Ac.517A>G (p.Arg173Gly)
c.514A>G (p.Arg172Gly)
c.466A>G (p.Arg156Gly)
c.625A>G (p.Arg209Gly)
c.567A>G
c.622A>G (p.Arg208Gly)
c.428-1562A>G (n.428-1562A>G)
c.832A>G (p.Arg278Gly)
c.829A>G (p.Arg277Gly)
c.635-1562A>G (n.635-1562A>G)
1g.161544761T>GCA421612448FCGR3Ac.517A>C (p.Arg173=)
c.514A>C (p.Arg172=)
c.466A>C (p.Arg156=)
c.625A>C (p.Arg209=)
c.567A>C
c.622A>C (p.Arg208=)
c.428-1562A>C (n.428-1562A>C)
c.832A>C (p.Arg278=)
c.829A>C (p.Arg277=)
c.635-1562A>C (n.635-1562A>C)
1g.161544761T=CA1202785227FCGR3Ac.517A= (p.Arg173=)
c.514A= (p.Arg172=)
c.466A= (p.Arg156=)
c.625A= (p.Arg209=)
c.567A=
c.622A= (p.Arg208=)
c.428-1562A= (n.428-1562A=)
c.832A= (p.Arg278=)
c.829A= (p.Arg277=)
c.635-1562A= (n.635-1562A=)
1g.161544762G>ACA1211384FCGR3Ac.516C>T (p.Cys172=)
c.513C>T (p.Cys171=)
c.465C>T (p.Cys155=)
c.624C>T (p.Cys208=)
c.566C>T
c.621C>T (p.Cys207=)
c.428-1563C>T (n.428-1563C>T)
c.831C>T (p.Cys277=)
c.828C>T (p.Cys276=)
c.635-1563C>T (n.635-1563C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
1g.161544762G>CCA343367468FCGR3Ac.516C>G (p.Cys172Trp)
c.513C>G (p.Cys171Trp)
c.465C>G (p.Cys155Trp)
c.624C>G (p.Cys208Trp)
c.566C>G
c.621C>G (p.Cys207Trp)
c.428-1563C>G (n.428-1563C>G)
c.831C>G (p.Cys277Trp)
c.828C>G (p.Cys276Trp)
c.635-1563C>G (n.635-1563C>G)
1g.161544762G=CA1202785228FCGR3Ac.516C= (p.Cys172=)
c.513C= (p.Cys171=)
c.465C= (p.Cys155=)
c.624C= (p.Cys208=)
c.566C=
c.621C= (p.Cys207=)
c.428-1563C= (n.428-1563C=)
c.831C= (p.Cys277=)
c.828C= (p.Cys276=)
c.635-1563C= (n.635-1563C=)
1g.161544762G>TCA343367470FCGR3Ac.516C>A (p.Cys172Ter)
c.513C>A (p.Cys171Ter)
c.465C>A (p.Cys155Ter)
c.624C>A (p.Cys208Ter)
c.566C>A
c.621C>A (p.Cys207Ter)
c.428-1563C>A (n.428-1563C>A)
c.831C>A (p.Cys277Ter)
c.828C>A (p.Cys276Ter)
c.635-1563C>A (n.635-1563C>A)
 gnomAD v4
1g.161544763C>ACA1211385FCGR3Ac.515G>T (p.Cys172Phe)
c.512G>T (p.Cys171Phe)
c.464G>T (p.Cys155Phe)
c.623G>T (p.Cys208Phe)
c.565G>T
c.620G>T (p.Cys207Phe)
c.428-1564G>T (n.428-1564G>T)
c.830G>T (p.Cys277Phe)
c.827G>T (p.Cys276Phe)
c.635-1564G>T (n.635-1564G>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.161544763C=CA1149151868FCGR3Ac.515G= (p.Cys172=)
c.512G= (p.Cys171=)
c.464G= (p.Cys155=)
c.623G= (p.Cys208=)
c.565G=
c.620G= (p.Cys207=)
c.428-1564G= (n.428-1564G=)
c.830G= (p.Cys277=)
c.827G= (p.Cys276=)
c.635-1564G= (n.635-1564G=)
1g.161544763C>GCA343367473FCGR3Ac.515G>C (p.Cys172Ser)
c.512G>C (p.Cys171Ser)
c.464G>C (p.Cys155Ser)
c.623G>C (p.Cys208Ser)
c.565G>C
c.620G>C (p.Cys207Ser)
c.428-1564G>C (n.428-1564G>C)
c.830G>C (p.Cys277Ser)
c.827G>C (p.Cys276Ser)
c.635-1564G>C (n.635-1564G>C)
1g.161544763C>TCA343367474FCGR3Ac.515G>A (p.Cys172Tyr)
c.512G>A (p.Cys171Tyr)
c.464G>A (p.Cys155Tyr)
c.623G>A (p.Cys208Tyr)
c.565G>A
c.620G>A (p.Cys207Tyr)
c.428-1564G>A (n.428-1564G>A)
c.830G>A (p.Cys277Tyr)
c.827G>A (p.Cys276Tyr)
c.635-1564G>A (n.635-1564G>A)
 dbSNP gnomAD v2 gnomAD v4
1g.161544764A=CA1202785229FCGR3Ac.514T= (p.Cys172=)
c.511T= (p.Cys171=)
c.463T= (p.Cys155=)
c.622T= (p.Cys208=)
c.564T=
c.619T= (p.Cys207=)
c.428-1565T= (n.428-1565T=)
c.829T= (p.Cys277=)
c.826T= (p.Cys276=)
c.635-1565T= (n.635-1565T=)
1g.161544764A>CCA343367479FCGR3Ac.514T>G (p.Cys172Gly)
c.511T>G (p.Cys171Gly)
c.463T>G (p.Cys155Gly)
c.622T>G (p.Cys208Gly)
c.564T>G
c.619T>G (p.Cys207Gly)
c.428-1565T>G (n.428-1565T>G)
c.829T>G (p.Cys277Gly)
c.826T>G (p.Cys276Gly)
c.635-1565T>G (n.635-1565T>G)
1g.161544764A>GCA343367477FCGR3Ac.514T>C (p.Cys172Arg)
c.511T>C (p.Cys171Arg)
c.463T>C (p.Cys155Arg)
c.622T>C (p.Cys208Arg)
c.564T>C
c.619T>C (p.Cys207Arg)
c.428-1565T>C (n.428-1565T>C)
c.829T>C (p.Cys277Arg)
c.826T>C (p.Cys276Arg)
c.635-1565T>C (n.635-1565T>C)
 dbSNP COSMIC
1g.161544764A>TCA343367478FCGR3Ac.514T>A (p.Cys172Ser)
c.511T>A (p.Cys171Ser)
c.463T>A (p.Cys155Ser)
c.622T>A (p.Cys208Ser)
c.564T>A
c.619T>A (p.Cys207Ser)
c.428-1565T>A (n.428-1565T>A)
c.829T>A (p.Cys277Ser)
c.826T>A (p.Cys276Ser)
c.635-1565T>A (n.635-1565T>A)
1g.161544765G>ACA421612452FCGR3Ac.513C>T (p.Phe171=)
c.510C>T (p.Phe170=)
c.462C>T (p.Phe154=)
c.621C>T (p.Phe207=)
c.563C>T
c.618C>T (p.Phe206=)
c.428-1566C>T (n.428-1566C>T)
c.828C>T (p.Phe276=)
c.825C>T (p.Phe275=)
c.635-1566C>T (n.635-1566C>T)
1g.161544765G>CCA343367480FCGR3Ac.513C>G (p.Phe171Leu)
c.510C>G (p.Phe170Leu)
c.462C>G (p.Phe154Leu)
c.621C>G (p.Phe207Leu)
c.563C>G
c.618C>G (p.Phe206Leu)
c.428-1566C>G (n.428-1566C>G)
c.828C>G (p.Phe276Leu)
c.825C>G (p.Phe275Leu)
c.635-1566C>G (n.635-1566C>G)
1g.161544765G>TCA343367481FCGR3Ac.513C>A (p.Phe171Leu)
c.510C>A (p.Phe170Leu)
c.462C>A (p.Phe154Leu)
c.621C>A (p.Phe207Leu)
c.563C>A
c.618C>A (p.Phe206Leu)
c.428-1566C>A (n.428-1566C>A)
c.828C>A (p.Phe276Leu)
c.825C>A (p.Phe275Leu)
c.635-1566C>A (n.635-1566C>A)
1g.161544766A>CCA343367483FCGR3Ac.512T>G (p.Phe171Cys)
c.509T>G (p.Phe170Cys)
c.461T>G (p.Phe154Cys)
c.620T>G (p.Phe207Cys)
c.562T>G
c.617T>G (p.Phe206Cys)
c.428-1567T>G (n.428-1567T>G)
c.827T>G (p.Phe276Cys)
c.824T>G (p.Phe275Cys)
c.635-1567T>G (n.635-1567T>G)
1g.161544766A>GCA343367485FCGR3Ac.512T>C (p.Phe171Ser)
c.509T>C (p.Phe170Ser)
c.461T>C (p.Phe154Ser)
c.620T>C (p.Phe207Ser)
c.562T>C
c.617T>C (p.Phe206Ser)
c.428-1567T>C (n.428-1567T>C)
c.827T>C (p.Phe276Ser)
c.824T>C (p.Phe275Ser)
c.635-1567T>C (n.635-1567T>C)
1g.161544766A>TCA343367486FCGR3Ac.512T>A (p.Phe171Tyr)
c.509T>A (p.Phe170Tyr)
c.461T>A (p.Phe154Tyr)
c.620T>A (p.Phe207Tyr)
c.562T>A
c.617T>A (p.Phe206Tyr)
c.428-1567T>A (n.428-1567T>A)
c.827T>A (p.Phe276Tyr)
c.824T>A (p.Phe275Tyr)
c.635-1567T>A (n.635-1567T>A)
1g.161544767A=CA1202785230FCGR3Ac.511T= (p.Phe171=)
c.508T= (p.Phe170=)
c.460T= (p.Phe154=)
c.619T= (p.Phe207=)
c.561T=
c.616T= (p.Phe206=)
c.428-1568T= (n.428-1568T=)
c.826T= (p.Phe276=)
c.823T= (p.Phe275=)
c.635-1568T= (n.635-1568T=)
1g.161544767A>CCA343367488FCGR3Ac.511T>G (p.Phe171Val)
c.508T>G (p.Phe170Val)
c.460T>G (p.Phe154Val)
c.619T>G (p.Phe207Val)
c.561T>G
c.616T>G (p.Phe206Val)
c.428-1568T>G (n.428-1568T>G)
c.826T>G (p.Phe276Val)
c.823T>G (p.Phe275Val)
c.635-1568T>G (n.635-1568T>G)
 dbSNP gnomAD v2 gnomAD v4
1g.161544767A>GCA343367489FCGR3Ac.511T>C (p.Phe171Leu)
c.508T>C (p.Phe170Leu)
c.460T>C (p.Phe154Leu)
c.619T>C (p.Phe207Leu)
c.561T>C
c.616T>C (p.Phe206Leu)
c.428-1568T>C (n.428-1568T>C)
c.826T>C (p.Phe276Leu)
c.823T>C (p.Phe275Leu)
c.635-1568T>C (n.635-1568T>C)
1g.161544767A>TCA1211386FCGR3Ac.511T>A (p.Phe171Ile)
c.508T>A (p.Phe170Ile)
c.460T>A (p.Phe154Ile)
c.619T>A (p.Phe207Ile)
c.561T>A
c.616T>A (p.Phe206Ile)
c.428-1568T>A (n.428-1568T>A)
c.826T>A (p.Phe276Ile)
c.823T>A (p.Phe275Ile)
c.635-1568T>A (n.635-1568T>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.161544768G>ACA421612454FCGR3Ac.510C>T (p.Tyr170=)
c.507C>T (p.Tyr169=)
c.459C>T (p.Tyr153=)
c.618C>T (p.Tyr206=)
c.560C>T
c.615C>T (p.Tyr205=)
c.428-1569C>T (n.428-1569C>T)
c.825C>T (p.Tyr275=)
c.822C>T (p.Tyr274=)
c.635-1569C>T (n.635-1569C>T)
1g.161544768G>CCA343367491FCGR3Ac.510C>G (p.Tyr170Ter)
c.507C>G (p.Tyr169Ter)
c.459C>G (p.Tyr153Ter)
c.618C>G (p.Tyr206Ter)
c.560C>G
c.615C>G (p.Tyr205Ter)
c.428-1569C>G (n.428-1569C>G)
c.825C>G (p.Tyr275Ter)
c.822C>G (p.Tyr274Ter)
c.635-1569C>G (n.635-1569C>G)
1g.161544768G>TCA343367493FCGR3Ac.510C>A (p.Tyr170Ter)
c.507C>A (p.Tyr169Ter)
c.459C>A (p.Tyr153Ter)
c.618C>A (p.Tyr206Ter)
c.560C>A
c.615C>A (p.Tyr205Ter)
c.428-1569C>A (n.428-1569C>A)
c.825C>A (p.Tyr275Ter)
c.822C>A (p.Tyr274Ter)
c.635-1569C>A (n.635-1569C>A)
1g.161544770_161544781delCA2573939412FCGR3Ac.499_510del (p.Ser167_Tyr170del)
c.496_507del (p.Ser166_Tyr169del)
c.448_459del (p.Ser150_Tyr153del)
c.607_618del (p.Ser203_Tyr206del)
c.549_560del
c.604_615del (p.Ser202_Tyr205del)
c.428-1580_428-1569del (n.428-1580_428-1569del)
c.814_825del (p.Ser272_Tyr275del)
c.811_822del (p.Ser271_Tyr274del)
c.635-1580_635-1569del (n.635-1580_635-1569del)
1g.161544769T>ACA343367496FCGR3Ac.509A>T (p.Tyr170Phe)
c.506A>T (p.Tyr169Phe)
c.458A>T (p.Tyr153Phe)
c.617A>T (p.Tyr206Phe)
c.559A>T
c.614A>T (p.Tyr205Phe)
c.428-1570A>T (n.428-1570A>T)
c.824A>T (p.Tyr275Phe)
c.821A>T (p.Tyr274Phe)
c.635-1570A>T (n.635-1570A>T)
1g.161544769T>CCA1211387FCGR3Ac.509A>G (p.Tyr170Cys)
c.506A>G (p.Tyr169Cys)
c.458A>G (p.Tyr153Cys)
c.617A>G (p.Tyr206Cys)
c.559A>G
c.614A>G (p.Tyr205Cys)
c.428-1570A>G (n.428-1570A>G)
c.824A>G (p.Tyr275Cys)
c.821A>G (p.Tyr274Cys)
c.635-1570A>G (n.635-1570A>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.161544769T>GCA343367494FCGR3Ac.509A>C (p.Tyr170Ser)
c.506A>C (p.Tyr169Ser)
c.458A>C (p.Tyr153Ser)
c.617A>C (p.Tyr206Ser)
c.559A>C
c.614A>C (p.Tyr205Ser)
c.428-1570A>C (n.428-1570A>C)
c.824A>C (p.Tyr275Ser)
c.821A>C (p.Tyr274Ser)
c.635-1570A>C (n.635-1570A>C)
 dbSNP gnomAD v2 gnomAD v4
1g.161544769T=CA1147915952FCGR3Ac.509A= (p.Tyr170=)
c.506A= (p.Tyr169=)
c.458A= (p.Tyr153=)
c.617A= (p.Tyr206=)
c.559A=
c.614A= (p.Tyr205=)
c.428-1570A= (n.428-1570A=)
c.824A= (p.Tyr275=)
c.821A= (p.Tyr274=)
c.635-1570A= (n.635-1570A=)
1g.161544770A=CA1202785231FCGR3Ac.508T= (p.Tyr170=)
c.505T= (p.Tyr169=)
c.457T= (p.Tyr153=)
c.616T= (p.Tyr206=)
c.558T=
c.613T= (p.Tyr205=)
c.428-1571T= (n.428-1571T=)
c.823T= (p.Tyr275=)
c.820T= (p.Tyr274=)
c.635-1571T= (n.635-1571T=)
1g.161544770A>CCA31715354FCGR3Ac.508T>G (p.Tyr170Asp)
c.505T>G (p.Tyr169Asp)
c.457T>G (p.Tyr153Asp)
c.616T>G (p.Tyr206Asp)
c.558T>G
c.613T>G (p.Tyr205Asp)
c.428-1571T>G (n.428-1571T>G)
c.823T>G (p.Tyr275Asp)
c.820T>G (p.Tyr274Asp)
c.635-1571T>G (n.635-1571T>G)
 dbSNP
1g.161544770A>GCA343367498FCGR3Ac.508T>C (p.Tyr170His)
c.505T>C (p.Tyr169His)
c.457T>C (p.Tyr153His)
c.616T>C (p.Tyr206His)
c.558T>C
c.613T>C (p.Tyr205His)
c.428-1571T>C (n.428-1571T>C)
c.823T>C (p.Tyr275His)
c.820T>C (p.Tyr274His)
c.635-1571T>C (n.635-1571T>C)
1g.161544770A>TCA343367500FCGR3Ac.508T>A (p.Tyr170Asn)
c.505T>A (p.Tyr169Asn)
c.457T>A (p.Tyr153Asn)
c.616T>A (p.Tyr206Asn)
c.558T>A
c.613T>A (p.Tyr205Asn)
c.428-1571T>A (n.428-1571T>A)
c.823T>A (p.Tyr275Asn)
c.820T>A (p.Tyr274Asn)
c.635-1571T>A (n.635-1571T>A)
1g.161544771G>ACA421612455FCGR3Ac.507C>T (p.Ser169=)
c.504C>T (p.Ser168=)
c.456C>T (p.Ser152=)
c.615C>T (p.Ser205=)
c.557C>T
c.612C>T (p.Ser204=)
c.428-1572C>T (n.428-1572C>T)
c.822C>T (p.Ser274=)
c.819C>T (p.Ser273=)
c.635-1572C>T (n.635-1572C>T)
 gnomAD v4
1g.161544771G>CCA421612456FCGR3Ac.507C>G (p.Ser169=)
c.504C>G (p.Ser168=)
c.456C>G (p.Ser152=)
c.615C>G (p.Ser205=)
c.557C>G
c.612C>G (p.Ser204=)
c.428-1572C>G (n.428-1572C>G)
c.822C>G (p.Ser274=)
c.819C>G (p.Ser273=)
c.635-1572C>G (n.635-1572C>G)
1g.161544771G>TCA421612457FCGR3Ac.507C>A (p.Ser169=)
c.504C>A (p.Ser168=)
c.456C>A (p.Ser152=)
c.615C>A (p.Ser205=)
c.557C>A
c.612C>A (p.Ser204=)
c.428-1572C>A (n.428-1572C>A)
c.822C>A (p.Ser274=)
c.819C>A (p.Ser273=)
c.635-1572C>A (n.635-1572C>A)

Number of alleles fetched