N1461S (p.Asn1461Ser) variant of GRIN2B (Q13224)
N1461S (p.Asn1461Ser) in GRIN2B (Q13224) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data, published literature, and structural context.
N1461S (p.Asn1461Ser) variant details
- p.Asn1461Ser
- rs1336696438
- gnomAD 12-13562856-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.389
- MetaLR 0.02
- MetaSVM -1.03
- CADD 18.10
- SIFT 0.10
- Population evidence available
- Structural context available
- Literature evidence available