Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.247425248A>G | CA16043366 | NLRP3 | c.1799A>G (p.Gln600Arg) c.1664A>G (p.Gln555Arg) c.1805A>G (p.Gln602Arg) n.1980A>G | ClinVar dbSNP |
1 | g.247425248A= | CA1232098959 | NLRP3 | c.1799A= (p.Gln600=) c.1664A= (p.Gln555=) c.1805A= (p.Gln602=) n.1980A= | dbSNP |