Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.40991441A>T | CA308491066 | CYP2B6 | c.136A>T (p.Met46Leu) c.38A>T n.38A>T | dbSNP |
19 | g.40991441A>G | CA9455052 | CYP2B6 | c.136A>G (p.Met46Val) c.38A>G n.38A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.40991441A= | CA2336249646 | CYP2B6 | c.136A= (p.Met46=) c.38A= n.38A= | dbSNP |
19 | g.40991441A>C | CA405967737 | CYP2B6 | c.136A>C (p.Met46Leu) c.38A>C n.38A>C | dbSNP gnomAD v4 |