| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.128848926C>T | CA10586205 | FLNC | c.4871C>T (p.Ser1624Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.128848926C>A | CA369203436 | FLNC | c.4871C>A (p.Ser1624Ter) | dbSNP |
| 7 | g.128848926C= | CA1742562914 | FLNC | c.4871C= (p.Ser1624=) | dbSNP |