P17S (p.Pro17Ser) variant of FGFR4 (P22455)
P17S (p.Pro17Ser) 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.
P17S (p.Pro17Ser) variant details
- p.Pro17Ser
- NCI-TCGA Cosmic COSV9944
- cosmic curated COSV99448
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available