F21L (p.Phe21Leu) variant of MYCN (N-myc proto-oncogene protein)
F21L (p.Phe21Leu) in MYCN (N-myc proto-oncogene protein) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
F21L (p.Phe21Leu) variant details
- p.Phe21Leu
- TOPMed rs1477455904
- gnomAD rs1477455904
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- UniProt: Uncertain significance
- Structural context available