D69G (p.Asp69Gly) variant of PHF6 (PHD finger protein 6)
D69G (p.Asp69Gly) in PHF6 (PHD finger protein 6) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.64 / 1. The record also includes population frequency data and structural context.
D69G (p.Asp69Gly) variant details
- p.Asp69Gly
- gnomAD rs1319295097
- Missense
- Variant Prioritization Score for Impact Estimate 0.645
- REVEL 0.67
- CADD 29.70
- PolyPhen-2 0.95
- SIFT 0.02
- Most common in the East Asian population (allele frequency 3.3e-05)
- Structural context available