S55T (p.Ser55Thr) variant of SLC2A1 (P11166)
S55T (p.Ser55Thr) 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 available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes structural context.
S55T (p.Ser55Thr) variant details
- p.Ser55Thr
- rs794727508
- ClinGen CA019088
- ClinVar RCV000177260
- Ensembl rs794727508
- Uncertain significance
- not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.353
- AlphaMissense 0.07
- MetaLR 0.24
- MetaSVM -0.92
- PolyPhen-2 0.00
- SIFT 0.19
- MutPred 0.38
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available