| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| Y | g.12786229G>A | CA10573232 | USP9Y | c.3178G>A (p.Ala1060Thr) n.3190G>A c.2944G>A (p.Ala982Thr) c.3193G>A (p.Ala1065Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| Y | g.12786229G= | CA2470557890 | USP9Y | c.3178G= (p.Ala1060=) n.3190G= c.2944G= (p.Ala982=) c.3193G= (p.Ala1065=) | dbSNP |