| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.154585712G>C | CA3115045 | FGA | c.1717C>G (p.Arg573Gly) c.644-2C>G (n.644-2C>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.154585712G>A | CA126498 | FGA | c.1717C>T (p.Arg573Cys) c.644-2C>T (n.644-2C>T) | ClinVar dbSNP |
| 4 | g.154585712G>T | CA3115046 | FGA | c.1717C>A (p.Arg573Ser) c.644-2C>A (n.644-2C>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |