| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.156115096C>T | CA017729 | LMNA | c.178C>T (p.Arg60Cys) n.553C>T c.89C>T (p.Ala30Val) n.212C>T n.356+30C>T n.329-15521C>T n.427C>T n.425C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.156115096C>G | CA017722 | LMNA | c.178C>G (p.Arg60Gly) n.553C>G c.89C>G (p.Ala30Gly) n.212C>G n.356+30C>G n.329-15521C>G n.427C>G n.425C>G | ClinVar dbSNP |