| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.67436795G>T | CA396282986 | HSD11B2 | c.1010G>T (p.Arg337Leu) | ClinVar dbSNP |
| 16 | g.67436795G>A | CA282323483 | HSD11B2 | c.1010G>A (p.Arg337His) | dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.67436795G= | CA2229310656 | HSD11B2 | c.1010G= (p.Arg337=) | dbSNP |