| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.16992989C>T | CA849280177 | FGF20 | c.*83G>A (n.*83G>A) c.423G>A | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.16992989C>G | CA16328389 | FGF20 | c.*83G>C (n.*83G>C) c.423G>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.16992989C= | CA1767395887 | FGF20 | c.*83G= (n.*83G=) c.423G= | dbSNP |