G9G (p.Gly9Gly) variant of GRIN2D (O15399)
G9G (p.Gly9Gly) in GRIN2D (O15399) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.61 / 1. The record also includes population frequency data, published literature, and structural context.
G9G (p.Gly9Gly) variant details
- p.Gly9Gly
- gnomAD 19-48398419-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.605
- CADD 15.60
- Most common in the Non-Finnish European population (allele frequency 1.2e-06)
- Structural context available
- Literature evidence available