V22G (p.Val22Gly) variant of NTRK2 (Q16620)
V22G (p.Val22Gly) in NTRK2 (Q16620) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
V22G (p.Val22Gly) variant details
- p.Val22Gly
- ExAC rs772667595
- gnomAD rs772667595
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available