| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.44305045G>C | CA3258482 | FGF10 | c.577C>G (p.Arg193Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.44305045G>T | CA444230891 | FGF10 | c.577C>A (p.Arg193=) | dbSNP |
| 5 | g.44305045G>A | CA118866 | FGF10 | c.577C>T (p.Arg193Ter) | ClinVar dbSNP gnomAD v4 |
| 5 | g.44305045G= | CA1543079490 | FGF10 | c.577C= (p.Arg193=) | dbSNP |