Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.161548543A>CCA1211499FCGR3Ac.197T>G (p.Leu66Arg)
c.194T>G (p.Leu65Arg)
c.146T>G (p.Leu49Arg)
c.305T>G (p.Leu102Arg)
c.247T>G
n.191T>G
c.302T>G (p.Leu101Arg)
c.512T>G (p.Leu171Arg)
c.509T>G (p.Leu170Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.161548543A>TCA124372FCGR3Ac.197T>A (p.Leu66His)
c.194T>A (p.Leu65His)
c.146T>A (p.Leu49His)
c.305T>A (p.Leu102His)
c.247T>A
n.191T>A
c.302T>A (p.Leu101His)
c.512T>A (p.Leu171His)
c.509T>A (p.Leu170His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.161548543A=CA1140181886FCGR3Ac.197T= (p.Leu66=)
c.194T= (p.Leu65=)
c.146T= (p.Leu49=)
c.305T= (p.Leu102=)
c.247T=
n.191T=
c.302T= (p.Leu101=)
c.512T= (p.Leu171=)
c.509T= (p.Leu170=)
dbSNP

Number of alleles fetched