| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.74720646G>T | CA7659242 | CYP1A1 | c.1382C>A (p.Thr461Asn) c.1295C>A (p.Thr432Asn) c.1298C>A (p.Thr433Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.74720646G>A | CA7659243 | CYP1A1 | c.1382C>T (p.Thr461Ile) c.1295C>T (p.Thr432Ile) c.1298C>T (p.Thr433Ile) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.74720646G= | CA2187814938 | CYP1A1 | c.1382C= (p.Thr461=) c.1295C= (p.Thr432=) c.1298C= (p.Thr433=) | dbSNP |
| 15 | g.74720646G>C | CA393164185 | CYP1A1 | c.1382C>G (p.Thr461Ser) c.1295C>G (p.Thr432Ser) c.1298C>G (p.Thr433Ser) | dbSNP |