Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.21176879C>A | CA6476689 | SLCO1B1 | c.463C>A (p.Pro155Thr) c.529C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.21176879C>T | CA384104956 | SLCO1B1 | c.463C>T (p.Pro155Ser) c.529C>T | dbSNP gnomAD v2 gnomAD v4 |
12 | g.21176879C>G | CA384104957 | SLCO1B1 | c.463C>G (p.Pro155Ala) c.529C>G | dbSNP gnomAD v4 |
12 | g.21176879C= | CA2020990627 | SLCO1B1 | c.463C= (p.Pro155=) c.529C= | dbSNP |