Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.247424912G>C | CA1495033 | NLRP3 | c.1463G>C (p.Arg488Thr) c.1328G>C (p.Arg443Thr) c.1469G>C (p.Arg490Thr) n.1644G>C | dbSNP ExAC gnomAD v2 |
1 | g.247424912G>A | CA281217 | NLRP3 | c.1463G>A (p.Arg488Lys) c.1328G>A (p.Arg443Lys) c.1469G>A (p.Arg490Lys) n.1644G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |