| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.67436794C>A | CA396282974 | HSD11B2 | c.1009C>A (p.Arg337Ser) | dbSNP |
| 16 | g.67436794C>T | CA121881 | HSD11B2 | c.1009C>T (p.Arg337Cys) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.67436794C= | CA2229310644 | HSD11B2 | c.1009C= (p.Arg337=) | dbSNP |