T26S (p.Thr26Ser) variant of FGFR1 (P11362)
T26S (p.Thr26Ser) in FGFR1 (P11362) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes variant effect predictions and structural context.
T26S (p.Thr26Ser) variant details
- p.Thr26Ser
- Ensembl rs2151341737
- Uncertain significance
- Missense
- MetaLR 0.40
- MetaSVM -0.42
- SIFT 0.31
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available