Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.7698362G>A | CA9145232 | FCER2 | c.184C>T (p.Arg62Trp) c.181C>T (p.Arg61Trp) n.709C>T n.386C>T n.679C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.7698362G>C | CA9145233 | FCER2 | c.184C>G (p.Arg62Gly) c.181C>G (p.Arg61Gly) n.709C>G n.386C>G n.679C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |