P39Q (p.Pro39Gln) variant of FGFR2 (P21802)
P39Q (p.Pro39Gln) in FGFR2 (P21802) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
P39Q (p.Pro39Gln) variant details
- p.Pro39Gln
- Ensembl rs2135124832
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available