P74T (p.Pro74Thr) variant of FHL1 (Q13642)
P74T (p.Pro74Thr) in FHL1 (Q13642) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes population frequency data and structural context.
P74T (p.Pro74Thr) variant details
- p.Pro74Thr
- ExAC rs774990626
- gnomAD rs774990626
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available