| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.26905645G>C | CA373125157 | PLAA | c.2254C>G (p.Leu752Val) c.2185C>G (p.Leu729Val) n.2559C>G | dbSNP |
| 9 | g.26905645G>A | CA373125155 | PLAA | c.2254C>T (p.Leu752Phe) c.2185C>T (p.Leu729Phe) n.2559C>T | ClinVar dbSNP |