Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.161544752A>CCA1211378FCGR3Ac.523T>G (p.Phe175Val)
c.526T>G (p.Phe176Val)
c.634T>G (p.Phe212Val)
n.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
1g.161544752A>GCA1211379FCGR3Ac.523T>C (p.Phe175Leu)
c.526T>C (p.Phe176Leu)
c.634T>C (p.Phe212Leu)
n.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

Number of alleles fetched