| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.99836193A>T | CA119602 | ABCC2 | c.3517A>T (p.Ile1173Phe) c.2821A>T (p.Ile941Phe) n.3706A>T n.3708A>T n.3760A>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.99836193A>G | CA5643833 | ABCC2 | c.3517A>G (p.Ile1173Val) c.2821A>G (p.Ile941Val) n.3706A>G n.3708A>G n.3760A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |