| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.128844045C>A | CA457847816 | FLNC | c.2971C>A (p.Arg991=) | ClinVar dbSNP gnomAD v4 |
| 7 | g.128844045C>T | CA166177514 | FLNC | c.2971C>T (p.Arg991Ter) | ClinVar dbSNP gnomAD v4 |
| 7 | g.128844045C= | CA1742582084 | FLNC | c.2971C= (p.Arg991=) | dbSNP |