A22G (p.Ala22Gly) variant of AGT (Angiotensinogen)
A22G (p.Ala22Gly) in AGT (Angiotensinogen) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data and structural context.
A22G (p.Ala22Gly) variant details
- p.Ala22Gly
- rs149973083
- ClinGen CA1448389
- ClinVar RCV001947642
- ESP rs149973083
- Uncertain significance
- not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.272
- REVEL 0.20
- CADD 14.20
- PolyPhen-2 0.27
- SIFT 0.10
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the African/African-American population (allele frequency 0.0006)
- Structural context available