F22L (p.Phe22Leu) variant of CDKN1A (P38936)
F22L (p.Phe22Leu) in CDKN1A (P38936) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes population frequency data and structural context.
F22L (p.Phe22Leu) variant details
- p.Phe22Leu
- ExAC rs746664004
- TOPMed rs746664004
- gnomAD rs746664004
- NCI-TCGA Cosmic COSV5518
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Population evidence available
- Structural context available