| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.6999441A>T | CA397742850 | ALOX12,ALOX12-AS1 | c.782A>T (p.Gln261Leu) c.284A>T (p.Gln95Leu) n.233+10355T>A c.932A>T (p.Gln311Leu) | dbSNP |
| 17 | g.6999441A>C | CA397742849 | ALOX12,ALOX12-AS1 | c.782A>C (p.Gln261Pro) c.284A>C (p.Gln95Pro) n.233+10355T>G c.932A>C (p.Gln311Pro) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.6999441A>G | CA8333307 | ALOX12,ALOX12-AS1 | c.782A>G (p.Gln261Arg) c.284A>G (p.Gln95Arg) n.233+10355T>C c.932A>G (p.Gln311Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |