G79A (p.Gly79Ala) variant of PDGFRB (P09619)
G79A (p.Gly79Ala) in PDGFRB (P09619) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
G79A (p.Gly79Ala) variant details
- p.Gly79Ala
- gnomAD rs1224840287
- Missense
- Variant Prioritization Score for Impact Estimate 0.333
- REVEL 0.22
- CADD 22.10
- PolyPhen-2 0.87
- SIFT 0.01
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available