N38S (p.Asn38Ser) variant of AGT (Angiotensinogen)
N38S (p.Asn38Ser) in AGT (Angiotensinogen) 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.
N38S (p.Asn38Ser) variant details
- p.Asn38Ser
- TOPMed rs987415444
- gnomAD rs987415444
- Missense
- Variant Prioritization Score for Impact Estimate 0.354
- REVEL 0.20
- CADD 3.30
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available