Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.44388443T>G | CA118872 | FGF10 | c.240A>C (p.Arg80Ser) | ClinVar dbSNP |
5 | g.44388443T>C | CA444400475 | FGF10 | c.240A>G (p.Arg80=) | dbSNP gnomAD v4 |
5 | g.44388443T= | CA1543090831 | FGF10 | c.240A= (p.Arg80=) | dbSNP |