A13T (p.Ala13Thr) variant of XPA (P23025)
A13T (p.Ala13Thr) in XPA (P23025) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
A13T (p.Ala13Thr) variant details
- p.Ala13Thr
- ExAC rs754275652
- TOPMed rs754275652
- gnomAD rs754275652
- Missense
- Variant Prioritization Score for Impact Estimate 0.237
- REVEL 0.05
- CADD 14.90
- PolyPhen-2 0.00
- SIFT 0.32
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available