V38G (p.Val38Gly) variant of FGFR1 (P11362)
V38G (p.Val38Gly) in FGFR1 (P11362) is a missense change. The record also includes variant effect predictions and structural context.
V38G (p.Val38Gly) variant details
- p.Val38Gly
- Ensembl rs2150966646
- Missense
- SIFT 0.00
- Structural context available