| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.129562396C>T | CA266168 | OCRL | c.*1244C>T (n.*1244C>T) c.1069C>T c.952C>T (p.Arg318Cys) c.1000C>T c.63C>T c.603C>T c.481C>T (p.Arg161Cys) c.955C>T (p.Arg319Cys) c.808C>T (p.Arg270Cys) | ClinVar dbSNP COSMIC |
| X | g.129562396C>A | CA414552471 | OCRL | c.*1244C>A (n.*1244C>A) c.1069C>A c.952C>A (p.Arg318Ser) c.1000C>A c.63C>A c.603C>A c.481C>A (p.Arg161Ser) c.955C>A (p.Arg319Ser) c.808C>A (p.Arg270Ser) | ClinVar dbSNP |