A107T (p.Ala107Thr) variant of SLC2A1 (P11166)
A107T (p.Ala107Thr) in SLC2A1 (P11166) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of GLUT1 deficiency syndrome 1, autosomal recessive. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data, published literature, and structural context.
A107T (p.Ala107Thr) variant details
- p.Ala107Thr
- rs775307302
- ClinGen CA803557
- ClinVar RCV002858368
- ClinVar RCV005863751
- Uncertain significance
- GLUT1 deficiency syndrome 1, autosomal recessive
- Missense
- Variant Prioritization Score for Impact Estimate 0.413
- REVEL 0.49
- CADD 22.40
- PolyPhen-2 0.14
- SIFT 0.05
- ClinVar: Uncertain significance (GLUT1 deficiency syndrome 1, autosomal recessive)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Middle Eastern population (allele frequency 0.00017)
- Structural context available
- Cited in: Glucose Transporter Type 1 Deficiency Syndrome. (PMID 20301603)