N1459del (p.Asn1459del) variant of GRIN2B (Q13224)
N1459del (p.Asn1459del) in GRIN2B (Q13224) is a missense 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.
N1459del (p.Asn1459del) variant details
- gnomAD 12-13562858-TTTG-
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.576
- CADD 18.90
- Population evidence available
- Structural context available
- Literature evidence available