| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.21037162G>A | CA10576587 | APOB | c.477C>T (p.Gly159=) c.345C>T (p.Gly115=) c.631C>T (p.Gln211Ter) | ClinVar dbSNP gnomAD v4 |
| 2 | g.21037162G>T | CA43464856 | APOB | c.477C>A (p.Gly159=) c.345C>A (p.Gly115=) c.631C>A (p.Gln211Lys) | dbSNP |