Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.161548543A>C | CA1211499 | FCGR3A | c.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 |
1 | g.161548543A>T | CA124372 | FCGR3A | c.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 |