| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.99818820C>G | CA212848411 | ABCC2 | c.2302C>G (p.Arg768Gly) c.1606C>G (p.Arg536Gly) n.2491C>G n.2493C>G n.2545C>G | dbSNP |
| 10 | g.99818820C>A | CA212848412 | ABCC2 | c.2302C>A (p.Arg768=) c.1606C>A (p.Arg536=) n.2491C>A n.2493C>A n.2545C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.99818820C>T | CA119596 | ABCC2 | c.2302C>T (p.Arg768Trp) c.1606C>T (p.Arg536Trp) n.2491C>T n.2493C>T n.2545C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |