Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.13561795T>A | CA685660979 | GRIN2B | c.*988A>T (n.*988A>T) c.69+46808A>T (n.69+46808A>T) | dbSNP |
12 | g.13561795T>G | CA233131473 | GRIN2B | c.*988A>C (n.*988A>C) c.69+46808A>C (n.69+46808A>C) | dbSNP gnomAD v3 gnomAD v4 |
12 | g.13561795T>C | CA10636844 | GRIN2B | c.*988A>G (n.*988A>G) c.69+46808A>G (n.69+46808A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |