V17G (p.Val17Gly) variant of PRKAA2 (P54646)
V17G (p.Val17Gly) in PRKAA2 (P54646) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
V17G (p.Val17Gly) variant details
- p.Val17Gly
- gnomAD rs1366799809
- Missense
- Variant Prioritization Score for Impact Estimate 0.304
- REVEL 0.19
- MetaLR 0.22
- MetaSVM -0.76
- CADD 23.70
- PolyPhen-2 0.27
- SIFT 0.02
- Most common in the Latino/Admixed American population (allele frequency 2.8e-05)
- Structural context available