| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.124500686G>A | CA10588831 | NR5A1 | c.274C>T (p.Arg92Trp) c.39+262C>T (n.39+262C>T) c.13C>T (p.Arg5Trp) | ClinVar dbSNP |
| 9 | g.124500686G= | CA1878469626 | NR5A1 | c.274C= (p.Arg92=) c.39+262C= (n.39+262C=) c.13C= (p.Arg5=) | dbSNP |