W26R (p.Trp26Arg) variant of NTRK2 (Q16620)
W26R (p.Trp26Arg) in NTRK2 (Q16620) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.62 / 1. The record also includes population frequency data and structural context.
W26R (p.Trp26Arg) variant details
- p.Trp26Arg
- 1000Genomes rs199900277
- ExAC rs199900277
- gnomAD rs199900277
- Missense
- Variant Prioritization Score for Impact Estimate 0.617
- REVEL 0.59
- CADD 26.20
- PolyPhen-2 0.98
- SIFT 0.10
- Most common in the 1KG:GBR population (allele frequency 0.0057)
- Structural context available