| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 18 | g.62354492C>T | CA118116 | TNFRSF11A | c.385C>T (p.Arg129Cys) c.267C>T (p.Ala89=) n.400C>T c.220C>T (p.Arg74Cys) c.165C>T (p.Ala55=) | ClinVar dbSNP gnomAD v4 |
| 18 | g.62354492C>G | CA402612354 | TNFRSF11A | c.385C>G (p.Arg129Gly) c.267C>G (p.Ala89=) n.400C>G c.220C>G (p.Arg74Gly) c.165C>G (p.Ala55=) | dbSNP |