| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.65197160T>C | CA117815 | RGS9 | c.895T>C (p.Trp299Arg) c.886T>C (p.Trp296Arg) n.823T>C n.903T>C c.307T>C (p.Trp103Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.65197160T= | CA2270722935 | RGS9 | c.895T= (p.Trp299=) c.886T= (p.Trp296=) n.823T= n.903T= c.307T= (p.Trp103=) | dbSNP |