E66D (p.Glu66Asp) variant of VCP (P55072)
E66D (p.Glu66Asp) in VCP (P55072) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
E66D (p.Glu66Asp) variant details
- p.Glu66Asp
- ExAC rs773319803
- gnomAD rs773319803
- Missense
- Variant Prioritization Score for Impact Estimate 0.398
- REVEL 0.39
- CADD 17.30
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available