Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.74749576C>A | CA14135597 | CYP1A2 | c.-9-154C>A (n.-9-154C>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.74749576C>G | CA2187824502 | CYP1A2 | c.-9-154C>G (n.-9-154C>G) | dbSNP |
15 | g.74749576C= | CA2187824501 | CYP1A2 | c.-9-154C= (n.-9-154C=) | dbSNP |