V10F (p.Val10Phe) variant of FGFR4 (P22455)
V10F (p.Val10Phe) in FGFR4 (P22455) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes structural context.
V10F (p.Val10Phe) variant details
- p.Val10Phe
- 1000Genomes rs1966265
- ESP rs1966265
- ExAC rs1966265
- TOPMed rs1966265
- Benign
- Missense
- EBI: Benign (in dbSNP:rs1966265)
- UniProt: Benign (in dbSNP:rs1966265)
- Structural context available