Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.13774962C>G | CA2017535728 | GRIN2B | c.412-21047G>C (n.412-21047G>C) | dbSNP |
12 | g.13774962C>A | CA603463540 | GRIN2B | c.412-21047G>T (n.412-21047G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.13774962C>T | CA13759300 | GRIN2B | c.412-21047G>A (n.412-21047G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |