| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 20 | g.4699898C>G | CA408152886 | PRNP | c.678C>G (p.Tyr226Ter) c.*367C>G (n.*367C>G) | dbSNP gnomAD v3 gnomAD v4 |
| 20 | g.4699898C>A | CA145407 | PRNP | c.678C>A (p.Tyr226Ter) c.*367C>A (n.*367C>A) | ClinVar dbSNP |
| 20 | g.4699898C= | CA2347156660 | PRNP | c.678C= (p.Tyr226=) c.*367C= (n.*367C=) | dbSNP |