Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.3010156C>G | CA362574637 | NQO2 | c.139C>G (p.Leu47Val) c.*151C>G (n.*151C>G) | dbSNP |
6 | g.3010156C>A | CA362574614 | NQO2 | c.139C>A (p.Leu47Ile) c.*151C>A (n.*151C>A) | dbSNP gnomAD v4 |
6 | g.3010156C>T | CA3617788 | NQO2 | c.139C>T (p.Leu47Phe) c.*151C>T (n.*151C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |