V270F (p.Val270Phe) variant of FGFR2 (P21802)
V270F (p.Val270Phe) in FGFR2 (P21802) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes structural context.
V270F (p.Val270Phe) variant details
- p.Val270Phe
- Ensembl rs2134316146
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available