N88S (p.Asn88Ser) variant of SLC2A1 (P11166)
N88S (p.Asn88Ser) in SLC2A1 (P11166) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
N88S (p.Asn88Ser) variant details
- p.Asn88Ser
- rs2524998983
- ClinGen CA339961597
- ClinVar RCV003441505
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available