G14W (p.Gly14Trp) variant of WWTR1 (Q9GZV5)
G14W (p.Gly14Trp) in WWTR1 (Q9GZV5) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data, experimental measurements, and structural context.
G14W (p.Gly14Trp) variant details
- p.Gly14Trp
- gnomAD rs1320220699
- Missense
- Variant Prioritization Score for Impact Estimate 0.558
- REVEL 0.39
- CADD 31.00
- PolyPhen-2 0.99
- SIFT 0.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 5.6e-05)
- Structural context available
- WWTR1 WW domain domainome 1.0: score -0.421