P9S (p.Pro9Ser) variant of XPA (P23025)
P9S (p.Pro9Ser) 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.
P9S (p.Pro9Ser) variant details
- p.Pro9Ser
- ExAC rs746677235
- TOPMed rs746677235
- gnomAD rs746677235
- Missense
- Variant Prioritization Score for Impact Estimate 0.0884
- REVEL 0.07
- CADD 4.12
- PolyPhen-2 0.00
- SIFT 0.72
- Most common in the Non-Finnish European population (allele frequency 1.1e-05)
- Structural context available