S56G (p.Ser56Gly) variant of NRXN2 (Neurexin-2)
S56G (p.Ser56Gly) in NRXN2 (Neurexin-2) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.53 / 1. The record also includes population frequency data and structural context.
S56G (p.Ser56Gly) variant details
- p.Ser56Gly
- gnomAD rs1157043042
- Missense
- Variant Prioritization Score for Impact Estimate 0.527
- CADD 20.50
- SIFT 0.00
- Most common in the 1KG:ITU population (allele frequency 0.0049)
- Structural context available