| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.161674008T>C | CA117549 | FCGR2B | c.695T>C (p.Ile232Thr) c.674T>C (p.Ile225Thr) n.745T>C n.2063T>C c.692T>C (p.Ile231Thr) c.671T>C (p.Ile224Thr) n.924T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.161674008T>A | CA343367701 | FCGR2B | c.695T>A (p.Ile232Asn) c.674T>A (p.Ile225Asn) n.745T>A n.2063T>A c.692T>A (p.Ile231Asn) c.671T>A (p.Ile224Asn) n.924T>A | dbSNP |
| 1 | g.161674008T= | CA1139849402 | FCGR2B | c.695T= (p.Ile232=) c.674T= (p.Ile225=) n.745T= n.2063T= c.692T= (p.Ile231=) c.671T= (p.Ile224=) n.924T= | dbSNP |