Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.18400860G>C | CA370636771 | NAT2 | c.857G>C (p.Gly286Ala) c.467G>C (p.Gly156Ala) | dbSNP |
8 | g.18400860G>A | CA114453 | NAT2 | c.857G>A (p.Gly286Glu) c.467G>A (p.Gly156Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.18400860G= | CA1768219186 | NAT2 | c.857G= (p.Gly286=) c.467G= (p.Gly156=) | dbSNP |