| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.68357802C>T | CA118099 | LRP5 | c.641C>T (p.Ala214Val) c.-1125C>T (n.-1125C>T) c.668C>T (p.Ala223Val) n.683C>T | ClinVar dbSNP |
| 11 | g.68357802C= | CA1980639860 | LRP5 | c.641C= (p.Ala214=) c.-1125C= (n.-1125C=) c.668C= (p.Ala223=) n.683C= | dbSNP |