Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
22 | g.42132217G>A | CA14942134 | CYP2D6 | c.-1045-381C>T (n.-1045-381C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.42132217G>C | CA753333071 | CYP2D6 | c.-1045-381C>G (n.-1045-381C>G) | dbSNP |
22 | g.42132217G= | CA2406581961 | CYP2D6 | c.-1045-381C= (n.-1045-381C=) | dbSNP |