Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
20 | g.47604780C>T | CA2367203910 | NCOA3 | c.-19-17449C>T (n.-19-17449C>T) | dbSNP |
20 | g.47604780C>A | CA2367203909 | NCOA3 | c.-19-17449C>A (n.-19-17449C>A) | dbSNP |
20 | g.47604780C>G | CA315599097 | NCOA3 | c.-19-17449C>G (n.-19-17449C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |