F18V (p.Phe18Val) variant of NTRK2 (Q16620)
F18V (p.Phe18Val) in NTRK2 (Q16620) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data and structural context.
F18V (p.Phe18Val) variant details
- p.Phe18Val
- TOPMed rs1172673440
- gnomAD rs1172673440
- Missense
- Variant Prioritization Score for Impact Estimate 0.377
- REVEL 0.32
- CADD 22.90
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available