A16D (p.Ala16Asp) variant of FGFR1 (P11362)
A16D (p.Ala16Asp) in FGFR1 (P11362) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
A16D (p.Ala16Asp) variant details
- p.Ala16Asp
- ExAC rs200596591
- gnomAD rs200596591
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available