| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.21007345del | CA10581913 | APOB | c.9523del (p.Ala3175LeufsTer?) c.5869+3388del (n.5869+3388del) | ClinVar dbSNP |
| 2 | g.21007345C= | CA2493475208 | APOB | c.9523G= (p.Ala3175=) c.5869+3388G= (n.5869+3388G=) | dbSNP dbSNP |