W65G (p.Trp65Gly) variant of PRNP (Major prion protein)
W65G (p.Trp65Gly) in PRNP (Major prion protein) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.63 / 1. The record also includes population frequency data and structural context.
W65G (p.Trp65Gly) variant details
- p.Trp65Gly
- TOPMed rs1382858633
- gnomAD rs1382858633
- Missense
- Variant Prioritization Score for Impact Estimate 0.628
- REVEL 0.73
- CADD 23.60
- PolyPhen-2 1.00
- SIFT 0.65
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available