Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.247424375T>C | CA116800 | NLRP3 | c.926T>C (p.Phe309Ser) c.791T>C (p.Phe264Ser) c.932T>C (p.Phe311Ser) n.1107T>C | ClinVar dbSNP |
1 | g.247424375T= | CA1141581404 | NLRP3 | c.926T= (p.Phe309=) c.791T= (p.Phe264=) c.932T= (p.Phe311=) n.1107T= | dbSNP |