| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.99836239T>A | CA5643849 | ABCC2 | c.3563T>A (p.Val1188Glu) c.2867T>A (p.Val956Glu) n.3752T>A n.3754T>A n.3806T>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.99836239T= | CA1931496391 | ABCC2 | c.3563T= (p.Val1188=) c.2867T= (p.Val956=) n.3752T= n.3754T= n.3806T= | dbSNP |