E68D (p.Glu68Asp) variant of PDGFRB (P09619)
E68D (p.Glu68Asp) in PDGFRB (P09619) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data and structural context.
E68D (p.Glu68Asp) variant details
- p.Glu68Asp
- ExAC rs766277403
- gnomAD rs766277403
- Missense
- Variant Prioritization Score for Impact Estimate 0.101
- REVEL 0.01
- CADD 7.55
- PolyPhen-2 0.00
- SIFT 0.57
- Most common in the African/African-American population (allele frequency 6e-05)
- Structural context available