P9A (p.Pro9Ala) variant of XPA (P23025)
P9A (p.Pro9Ala) in XPA (P23025) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data and structural context.
P9A (p.Pro9Ala) variant details
- p.Pro9Ala
- ExAC rs746677235
- TOPMed rs746677235
- gnomAD rs746677235
- Missense
- Variant Prioritization Score for Impact Estimate 0.0929
- REVEL 0.09
- CADD 2.36
- PolyPhen-2 0.00
- SIFT 0.72
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.0001)
- Structural context available