G89V (p.Gly89Val) variant of PHF6 (PHD finger protein 6)
G89V (p.Gly89Val) in PHF6 (PHD finger protein 6) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.84 / 1. The record also includes population frequency data, published literature, and structural context.
G89V (p.Gly89Val) variant details
- p.Gly89Val
- gnomAD X-134393526-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.844
- REVEL 0.93
- CADD 28.90
- PolyPhen-2 0.95
- SIFT 0.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 2.5e-05)
- Structural context available
- Literature evidence available