| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.58077255G>A | CA343270 | FLNB | c.502G>A (p.Gly168Ser) n.645G>A n.661G>A n.647G>A | ClinVar dbSNP |
| 3 | g.58077255G>T | CA353333575 | FLNB | c.502G>T (p.Gly168Cys) n.645G>T n.661G>T n.647G>T | ClinVar dbSNP |
| 3 | g.58077255G= | CA1367486069 | FLNB | c.502G= (p.Gly168=) n.645G= n.661G= n.647G= | dbSNP |