R37P (p.Arg37Pro) variant of PRNP (Major prion protein)
R37P (p.Arg37Pro) in PRNP (Major prion protein) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.67 / 1. The record also includes population frequency data, published literature, and structural context.
R37P (p.Arg37Pro) variant details
- p.Arg37Pro
- gnomAD 20-4699330-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.667
- REVEL 0.69
- CADD 28.40
- PolyPhen-2 1.00
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available