G9G (p.Gly9Gly) variant of NTRK2 (Q16620)
G9G (p.Gly9Gly) in NTRK2 (Q16620) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data, published literature, and structural context.
G9G (p.Gly9Gly) variant details
- p.Gly9Gly
- rs767314128
- gnomAD 9-84670775-A-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.271
- CADD 14.10
- Most common in the Finnish in Finland (FIN) population (allele frequency 7.5e-05)
- Structural context available
- Literature evidence available