| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.99760836G>C | CA368367575 | CYP3A4 | c.1492C>G (p.Pro498Ala) n.834C>G c.1399C>G (p.Pro467Ala) c.940C>G (p.Pro314Ala) c.1252C>G (p.Pro418Ala) c.949C>G (p.Pro317Ala) c.1396C>G (p.Pro466Ala) c.1489C>G (p.Pro497Ala) | dbSNP gnomAD v2 |
| 7 | g.99760836G>A | CA4369481 | CYP3A4 | c.1492C>T (p.Pro498Ser) n.834C>T c.1399C>T (p.Pro467Ser) c.940C>T (p.Pro314Ser) c.1252C>T (p.Pro418Ser) c.949C>T (p.Pro317Ser) c.1396C>T (p.Pro466Ser) c.1489C>T (p.Pro497Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |