p.Arg11 Pro13del variant of GRIN2D (O15399)
p.Arg11 Pro13del in GRIN2D (O15399) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.65 / 1. The record also includes population frequency data, published literature, and structural context.
p.Arg11 Pro13del variant details
- rs1360207254
- gnomAD 19-48398416-CGGCC
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.653
- CADD 21.10
- Most common in the REMAINING population (allele frequency 2.8e-05)
- Structural context available
- Literature evidence available