Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.13561247A>G | CA15730150 | GRIN2B | c.*1536T>C (n.*1536T>C) c.69+47356T>C (n.69+47356T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.13561247A= | CA2017437044 | GRIN2B | c.*1536T= (n.*1536T=) c.69+47356T= (n.69+47356T=) | dbSNP |