A19G (p.Ala19Gly) variant of AGT (Angiotensinogen)
A19G (p.Ala19Gly) in AGT (Angiotensinogen) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
A19G (p.Ala19Gly) variant details
- p.Ala19Gly
- TOPMed rs1244732417
- gnomAD rs1244732417
- Missense
- Variant Prioritization Score for Impact Estimate 0.283
- REVEL 0.21
- CADD 16.40
- PolyPhen-2 0.32
- SIFT 0.00
- Most common in the Latino/Admixed American population (allele frequency 4.5e-05)
- Structural context available