| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.124549387G>A | CA13732328 | NCOR2 | c.-164-13776C>T (n.-164-13776C>T) n.283-13776C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.124549387G= | CA2069377599 | NCOR2 | c.-164-13776C= (n.-164-13776C=) n.283-13776C= | dbSNP |