| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.17000966G>C | CA12876262 | FGF20 | c.286+781C>G (n.286+781C>G) c.94+781C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.17000966G>A | CA1767406165 | FGF20 | c.286+781C>T (n.286+781C>T) c.94+781C>T | dbSNP |
| 8 | g.17000966G= | CA1767406164 | FGF20 | c.286+781C= (n.286+781C=) c.94+781C= | dbSNP |