Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.9764715G>T | CA394709266 | GRIN2A | c.2829C>A (p.Tyr943Ter) c.2358C>A (p.Tyr786Ter) n.2422C>A c.*199C>A (n.*199C>A) c.2418C>A (p.Tyr806Ter) n.2468C>A c.2670C>A (p.Tyr890Ter) c.2571C>A (p.Tyr857Ter) c.2985C>A (p.Tyr995Ter) | dbSNP |
16 | g.9764715G>C | CA145314 | GRIN2A | c.2829C>G (p.Tyr943Ter) c.2358C>G (p.Tyr786Ter) n.2422C>G c.*199C>G (n.*199C>G) c.2418C>G (p.Tyr806Ter) n.2468C>G c.2670C>G (p.Tyr890Ter) c.2571C>G (p.Tyr857Ter) c.2985C>G (p.Tyr995Ter) | ClinVar dbSNP |
16 | g.9764715G>A | CA493693294 | GRIN2A | c.2829C>T (p.Tyr943=) c.2358C>T (p.Tyr786=) n.2422C>T c.*199C>T (n.*199C>T) c.2418C>T (p.Tyr806=) n.2468C>T c.2670C>T (p.Tyr890=) c.2571C>T (p.Tyr857=) c.2985C>T (p.Tyr995=) | dbSNP |