| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.67436156C>G | CA8110686 | HSD11B2 | c.664+14C>G (n.664+14C>G) n.527+14C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.67436156C>T | CA213041 | HSD11B2 | c.664+14C>T (n.664+14C>T) n.527+14C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.67436156C>A | CA8110687 | HSD11B2 | c.664+14C>A (n.664+14C>A) n.527+14C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |