W73G (p.Trp73Gly) variant of PRNP (Major prion protein)
W73G (p.Trp73Gly) in PRNP (Major prion protein) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.68 / 1. The record also includes population frequency data, published literature, and structural context.
W73G (p.Trp73Gly) variant details
- p.Trp73Gly
- gnomAD 20-4699437-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.682
- REVEL 0.80
- CADD 23.40
- PolyPhen-2 1.00
- SIFT 0.50
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available
- Literature evidence available