Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.9764715G>TCA394709266GRIN2Ac.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
16g.9764715G>CCA145314GRIN2Ac.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
16g.9764715G>ACA493693294GRIN2Ac.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

Number of alleles fetched