Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.247425154G>T | CA345557634 | NLRP3 | c.1705G>T (p.Gly569Trp) c.1570G>T (p.Gly524Trp) c.1711G>T (p.Gly571Trp) n.1886G>T | dbSNP |
1 | g.247425154G>A | CA10577233 | NLRP3 | c.1705G>A (p.Gly569Arg) c.1570G>A (p.Gly524Arg) c.1711G>A (p.Gly571Arg) n.1886G>A | ClinVar dbSNP |
1 | g.247425154G>C | CA116788 | NLRP3 | c.1705G>C (p.Gly569Arg) c.1570G>C (p.Gly524Arg) c.1711G>C (p.Gly571Arg) n.1886G>C | ClinVar dbSNP |