S35F (p.Ser35Phe) variant of SLC2A4 (P14672)
S35F (p.Ser35Phe) in SLC2A4 (P14672) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.78 / 1. The record also includes population frequency data and structural context.
S35F (p.Ser35Phe) variant details
- p.Ser35Phe
- rs376636615
- ESP rs376636615
- ExAC rs376636615
- TOPMed rs376636615
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.782
- REVEL 0.79
- CADD 25.30
- PolyPhen-2 0.75
- SIFT 0.02
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available