F10V (p.Phe10Val) variant of ABCC2 (Q92887)
F10V (p.Phe10Val) in ABCC2 (Q92887) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.62 / 1. The record also includes population frequency data and structural context.
F10V (p.Phe10Val) variant details
- p.Phe10Val
- ExAC rs748623159
- TOPMed rs748623159
- gnomAD rs748623159
- Missense
- Variant Prioritization Score for Impact Estimate 0.62
- CADD 24.80
- PolyPhen-2 0.44
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 4.4e-05)
- Structural context available