W10C (p.Trp10Cys) variant of FGFR1 (P11362)
W10C (p.Trp10Cys) in FGFR1 (P11362) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
W10C (p.Trp10Cys) variant details
- p.Trp10Cys
- NCI-TCGA Cosmic COSV5833
- cosmic curated COSV58332
- Ensembl rs2151346019
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available