| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.58077195T>G | CA353333429 | FLNB | c.442T>G (p.Trp148Gly) n.585T>G n.601T>G n.587T>G | dbSNP COSMIC |
| 3 | g.58077195T>A | CA341841 | FLNB | c.442T>A (p.Trp148Arg) n.585T>A n.601T>A n.587T>A | ClinVar dbSNP |
| 3 | g.58077195T= | CA1367486045 | FLNB | c.442T= (p.Trp148=) n.585T= n.601T= n.587T= | dbSNP |