W2C (p.Trp2Cys) variant of FGFR1 (P11362)
W2C (p.Trp2Cys) in FGFR1 (P11362) is a missense change. Clinical records from EBI and UniProt describe it as likely pathogenic. The record also includes structural context.
W2C (p.Trp2Cys) variant details
- p.Trp2Cys
- Ensembl rs1554594114
- cosmic curated COSV10881
- Likely pathogenic
- Missense
- EBI: Likely pathogenic
- UniProt: Likely pathogenic
- Structural context available