| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.45921260T>A | CA907527477 | FYCO1 | c.*505A>T (n.*505A>T) c.1308A>T n.5157A>T c.4362-2195A>T (n.4362-2195A>T) c.4252-2195A>T (n.4252-2195A>T) | dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.45921260T>C | CA10616635 | FYCO1 | c.*505A>G (n.*505A>G) c.1308A>G n.5157A>G c.4362-2195A>G (n.4362-2195A>G) c.4252-2195A>G (n.4252-2195A>G) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |