Q37P (p.Gln37Pro) variant of NRXN2 (Neurexin-2)
Q37P (p.Gln37Pro) in NRXN2 (Neurexin-2) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.54 / 1. The record also includes population frequency data and structural context.
Q37P (p.Gln37Pro) variant details
- p.Gln37Pro
- gnomAD rs1245249342
- Missense
- Variant Prioritization Score for Impact Estimate 0.535
- REVEL 0.67
- AlphaMissense 0.13
- MetaLR 0.04
- MetaSVM -1.00
- CADD 24.20
- PolyPhen-2 0.25
- Most common in the REMAINING population (allele frequency 2.1e-05)
- Structural context available