W20C (p.Trp20Cys) variant of NTRK2 (Q16620)
W20C (p.Trp20Cys) in NTRK2 (Q16620) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data and structural context.
W20C (p.Trp20Cys) variant details
- p.Trp20Cys
- TOPMed rs2058652129
- gnomAD rs2058652129
- Missense
- Variant Prioritization Score for Impact Estimate 0.392
- REVEL 0.21
- CADD 23.90
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available