Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.74720644T>G | CA272812640 | CYP1A1 | c.1384A>C (p.Ile462Leu) c.1297A>C (p.Ile433Leu) c.1300A>C (p.Ile434Leu) | dbSNP gnomAD v4 |
15 | g.74720644T>C | CA7659241 | CYP1A1 | c.1384A>G (p.Ile462Val) c.1297A>G (p.Ile433Val) c.1300A>G (p.Ile434Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.74720644T>A | CA272812639 | CYP1A1 | c.1384A>T (p.Ile462Phe) c.1297A>T (p.Ile433Phe) c.1300A>T (p.Ile434Phe) | dbSNP |