F99L (p.Phe99Leu) variant of STAT6 (P42226)
F99L (p.Phe99Leu) in STAT6 (P42226) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F99L (p.Phe99Leu) variant details
- p.Phe99Leu
- NCI-TCGA Cosmic COSV5567
- cosmic curated COSV55671
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available