| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.21006288C>T | CA022750 | APOB | c.10580G>A (p.Arg3527Gln) c.5869+4445G>A (n.5869+4445G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.21006288C>A | CA345986090 | APOB | c.10580G>T (p.Arg3527Leu) c.5869+4445G>T (n.5869+4445G>T) | ClinVar dbSNP |
| 2 | g.21006288C>G | CA345986092 | APOB | c.10580G>C (p.Arg3527Pro) c.5869+4445G>C (n.5869+4445G>C) | dbSNP |
| 2 | g.21006288C= | CA2493474703 | APOB | c.10580G= (p.Arg3527=) c.5869+4445G= (n.5869+4445G=) | dbSNP |