| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.134425256C>T | CA121315 | PHF6 | c.*943C>T (n.*943C>T) c.922C>T (p.Arg308Ter) c.1024C>T (p.Arg342Ter) c.*636C>T (n.*636C>T) c.1027C>T (p.Arg343Ter) | ClinVar dbSNP COSMIC |
| X | g.134425256C>A | CA518649367 | PHF6 | c.*943C>A (n.*943C>A) c.922C>A (p.Arg308=) c.1024C>A (p.Arg342=) c.*636C>A (n.*636C>A) c.1027C>A (p.Arg343=) | dbSNP |