S37F (p.Ser37Phe) variant of FOXP1 (Forkhead box protein P1)
S37F (p.Ser37Phe) in FOXP1 (Forkhead box protein P1) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The available variant effect predictions contribute to a CATVariant prioritization score of 0.76 / 1. The record also includes population frequency data and structural context.
S37F (p.Ser37Phe) variant details
- p.Ser37Phe
- TOPMed rs1383155725
- gnomAD rs1383155725
- Uncertain significance
- Missense
- Variant Prioritization Score for Impact Estimate 0.764
- CADD 28.60
- PolyPhen-2 0.09
- SIFT 0.00
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available