Q41L (p.Gln41Leu) variant of FGFR4 (P22455)
Q41L (p.Gln41Leu) in FGFR4 (P22455) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
Q41L (p.Gln41Leu) variant details
- p.Gln41Leu
- NCI-TCGA Cosmic COSV5280
- cosmic curated COSV52806
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available