R57P (p.Arg57Pro) variant of MYLK (Q15746)
R57P (p.Arg57Pro) in MYLK (Q15746) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
R57P (p.Arg57Pro) variant details
- p.Arg57Pro
- 1000Genomes rs150006791
- ExAC rs150006791
- TOPMed rs150006791
- gnomAD rs150006791
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available