P56R (p.Pro56Arg) variant of NTRK2 (Q16620)
P56R (p.Pro56Arg) in NTRK2 (Q16620) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.83 / 1. The record also includes population frequency data and structural context.
P56R (p.Pro56Arg) variant details
- p.Pro56Arg
- Ensembl rs2058659300
- Missense
- Variant Prioritization Score for Impact Estimate 0.829
- REVEL 0.85
- CADD 26.70
- PolyPhen-2 1.00
- SIFT 0.04
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available