| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.53889743T>C | CA344633 | PRKCG | c.391T>C (p.Cys131Arg) n.689T>C n.693T>C c.7T>C (p.Cys3Arg) | ClinVar dbSNP |
| 19 | g.53889743T>A | CA9640271 | PRKCG | c.391T>A (p.Cys131Ser) n.689T>A n.693T>A c.7T>A (p.Cys3Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.53889743T= | CA2342579289 | PRKCG | c.391T= (p.Cys131=) n.689T= n.693T= c.7T= (p.Cys3=) | dbSNP |