Q59H (p.Gln59His) variant of FOXP2 (Forkhead box protein P2)
Q59H (p.Gln59His) in FOXP2 (Forkhead box protein P2) 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 0.25 / 1. The record also includes population frequency data and structural context.
Q59H (p.Gln59His) variant details
- p.Gln59His
- NCI-TCGA Cosmic COSV6349
- cosmic curated COSV63494
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.247
- REVEL 0.24
- CADD 21.10
- PolyPhen-2 0.99
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available