N38H (p.Asn38His) variant of AGT (Angiotensinogen)
N38H (p.Asn38His) in AGT (Angiotensinogen) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
N38H (p.Asn38His) variant details
- p.Asn38His
- ExAC rs753145717
- Missense
- Variant Prioritization Score for Impact Estimate 0.312
- REVEL 0.23
- CADD 22.70
- PolyPhen-2 0.81
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available