Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.161548496C>T | CA1211474 | FCGR3A | c.244G>A (p.Asp82Asn) c.241G>A (p.Asp81Asn) c.193G>A (p.Asp65Asn) c.352G>A (p.Asp118Asn) c.294G>A n.238G>A c.349G>A (p.Asp117Asn) c.559G>A (p.Asp187Asn) c.556G>A (p.Asp186Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.161548496C= | CA1139795689 | FCGR3A | c.244G= (p.Asp82=) c.241G= (p.Asp81=) c.193G= (p.Asp65=) c.352G= (p.Asp118=) c.294G= n.238G= c.349G= (p.Asp117=) c.559G= (p.Asp187=) c.556G= (p.Asp186=) | dbSNP |