P17H (p.Pro17His) variant of XPA (P23025)
P17H (p.Pro17His) in XPA (P23025) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
P17H (p.Pro17His) variant details
- p.Pro17His
- NCI-TCGA Cosmic COSV6430
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.203
- REVEL 0.14
- CADD 20.80
- PolyPhen-2 0.34
- SIFT 0.03
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available