| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.21176827G>A | CA6476680 | SLCO1B1 | c.411G>A (p.Ser137=) c.477G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.21176827G= | CA2020990607 | SLCO1B1 | c.411G= (p.Ser137=) c.477G= | dbSNP |
| 12 | g.21176827G>T | CA478866807 | SLCO1B1 | c.411G>T (p.Ser137=) c.477G>T | dbSNP gnomAD v4 |