S39G (p.Ser39Gly) variant of NTRK2 (Q16620)
S39G (p.Ser39Gly) in NTRK2 (Q16620) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
S39G (p.Ser39Gly) variant details
- p.Ser39Gly
- ESP rs147067960
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available