S3T (p.Ser3Thr) variant of NOS1AP (O75052)
S3T (p.Ser3Thr) in NOS1AP (O75052) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
S3T (p.Ser3Thr) variant details
- p.Ser3Thr
- gnomAD rs1295249593
- Missense
- Variant Prioritization Score for Impact Estimate 0.418
- REVEL 0.21
- CADD 22.50
- PolyPhen-2 0.04
- SIFT 0.27
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available