Q1014R (p.Gln1014Arg) variant of GRIN2B (Q13224)
Q1014R (p.Gln1014Arg) in GRIN2B (Q13224) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes published literature.
Q1014R (p.Gln1014Arg) variant details
- p.Gln1014Arg
- Uncertain significance
- Missense
- EBI: uncertain significance
- UniProt: Uncertain significance
- Cited in: Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia. (PMID 22833210)