G9D (p.Gly9Asp) variant of GRIN2D (O15399)
G9D (p.Gly9Asp) in GRIN2D (O15399) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data and structural context.
G9D (p.Gly9Asp) variant details
- p.Gly9Asp
- TOPMed rs972423258
- Missense
- Variant Prioritization Score for Impact Estimate 0.339
- REVEL 0.10
- ESM-1b 0.68
- AlphaMissense 0.25
- CADD 24.20
- PolyPhen-2 0.35
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 2.4e-06)
- Structural context available