P23H (p.Pro23His) variant of CYP17A1 (P05093)
P23H (p.Pro23His) in CYP17A1 (P05093) 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 0.18 / 1. The record also includes population frequency data and structural context.
P23H (p.Pro23His) variant details
- p.Pro23His
- rs368405367
- NCI-TCGA Cosmic COSV1008
- cosmic curated COSV10088
- ESP rs368405367
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.18
- REVEL 0.15
- CADD 10.90
- PolyPhen-2 0.53
- SIFT 0.29
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available