F28F (p.Phe28Phe) variant of GRIN2D (O15399)
F28F (p.Phe28Phe) in GRIN2D (O15399) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data, published literature, and structural context.
F28F (p.Phe28Phe) variant details
- p.Phe28Phe
- gnomAD 19-48398476-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.583
- CADD 15.20
- Most common in the Non-Finnish European population (allele frequency 3.7e-06)
- Structural context available
- Literature evidence available