Chr Mutation (hg38) CAid Gene Transcript Linkouts
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

Number of alleles fetched