S56G (p.Ser56Gly) variant of NOS3 (Nitric oxide synthase 3)
S56G (p.Ser56Gly) in NOS3 (Nitric oxide synthase 3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data and structural context.
S56G (p.Ser56Gly) variant details
- p.Ser56Gly
- gnomAD rs1207876196
- Missense
- Variant Prioritization Score for Impact Estimate 0.0869
- REVEL 0.02
- CADD 14.60
- PolyPhen-2 0.14
- SIFT 0.31
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available