S98F (p.Ser98Phe) variant of SLC2A2 (P11168)
S98F (p.Ser98Phe) in SLC2A2 (P11168) 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 0.86 / 1. The record also includes population frequency data and structural context.
S98F (p.Ser98Phe) variant details
- p.Ser98Phe
- NCI-TCGA TCGA novel
- Ensembl rs1716037949
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.857
- REVEL 0.90
- CADD 28.30
- PolyPhen-2 1.00
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available