| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.154586438T>C | CA126515 | FGA | c.991A>G (p.Thr331Ala) c.643+348A>G (n.643+348A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154586438T>A | CA108761553 | FGA | c.991A>T (p.Thr331Ser) c.643+348A>T (n.643+348A>T) | dbSNP |
| 4 | g.154586438T>G | CA358530710 | FGA | c.991A>C (p.Thr331Pro) c.643+348A>C (n.643+348A>C) | dbSNP |
| 4 | g.154586438T= | CA1504943495 | FGA | c.991A= (p.Thr331=) c.643+348A= (n.643+348A=) | dbSNP |