| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.53906729T>C | CA310096151 | PRKCG | c.1928T>C (p.Phe643Ser) n.1329T>C c.1820T>C (p.Phe607Ser) c.1019T>C (p.Phe340Ser) | dbSNP |
| 19 | g.53906729T>G | CA407420356 | PRKCG | c.1928T>G (p.Phe643Cys) n.1329T>G c.1820T>G (p.Phe607Cys) c.1019T>G (p.Phe340Cys) | ClinVar dbSNP |