| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.15529699C>G | CA16043077 | CYP4F22 | c.223-10C>G (n.223-10C>G) | ClinVar dbSNP |
| 19 | g.15529699C>T | CA2642410989 | CYP4F22 | c.223-10C>T (n.223-10C>T) | dbSNP gnomAD v4 |
| 19 | g.15529699C= | CA2324923156 | CYP4F22 | c.223-10C= (n.223-10C=) | dbSNP |