A47S (p.Ala47Ser) variant of NRXN2 (Neurexin-2)
A47S (p.Ala47Ser) in NRXN2 (Neurexin-2) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
A47S (p.Ala47Ser) variant details
- p.Ala47Ser
- gnomAD rs1252751874
- Missense
- Variant Prioritization Score for Impact Estimate 0.354
- CADD 15.40
- SIFT 0.05
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available