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 |