H1435N (p.His1435Asn) variant of GRIN2B (Q13224)
H1435N (p.His1435Asn) in GRIN2B (Q13224) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data and published literature.
H1435N (p.His1435Asn) variant details
- p.His1435Asn
- rs1200161647
- gnomAD 12-13562935-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.556
- MetaLR 0.02
- MetaSVM -1.06
- CADD 20.00
- SIFT 0.07
- Population evidence available
- Literature evidence available