Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.161544752A>C | CA1211378 | FCGR3A | c.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 |
1 | g.161544752A>G | CA1211379 | FCGR3A | c.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 |
1 | g.161544752A>T | CA343367436 | FCGR3A | c.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 |