G9E (p.Gly9Glu) variant of NTRK2 (Q16620)
G9E (p.Gly9Glu) in NTRK2 (Q16620) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.48 / 1. The record also includes population frequency data and structural context.
G9E (p.Gly9Glu) variant details
- p.Gly9Glu
- TOPMed rs1421322179
- gnomAD rs1421322179
- Missense
- Variant Prioritization Score for Impact Estimate 0.48
- REVEL 0.49
- CADD 25.40
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available