| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.41170234C>T | CA412758928 | USP9X | c.2891C>T (p.Ser964Leu) c.2876C>T (p.Ser959Leu) c.2723C>T (p.Ser908Leu) c.2106C>T | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
| X | g.41170234C>A | CA16043272 | USP9X | c.2891C>A (p.Ser964Ter) c.2876C>A (p.Ser959Ter) c.2723C>A (p.Ser908Ter) c.2106C>A | ClinVar dbSNP |