Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.13865843G>C | CA288904 | GRIN2B | c.366C>G (p.Pro122=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.13865843G>T | CA6461422 | GRIN2B | c.366C>A (p.Pro122=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.13865843G= | CA1630855528 | GRIN2B | c.366C= (p.Pro122=) | dbSNP |