A88S (p.Ala88Ser) variant of SLC2A2 (P11168)
A88S (p.Ala88Ser) 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 0.14 / 1. The record also includes population frequency data and structural context.
A88S (p.Ala88Ser) variant details
- p.Ala88Ser
- rs763255363
- ExAC rs763255363
- gnomAD rs763255363
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.136
- REVEL 0.18
- CADD 0.88
- PolyPhen-2 0.01
- SIFT 0.87
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the East Asian population (allele frequency 5e-05)
- Structural context available