A35V (p.Ala35Val) variant of SLC2A1 (P11166)
A35V (p.Ala35Val) 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 0.77 / 1. The record also includes population frequency data and structural context.
A35V (p.Ala35Val) variant details
- p.Ala35Val
- rs773791632
- ClinGen CA803635
- ClinVar RCV001964992
- ExAC rs773791632
- Uncertain significance
- GLUT1 deficiency syndrome 1, autosomal recessive
- Missense
- Variant Prioritization Score for Impact Estimate 0.769
- REVEL 0.85
- AlphaMissense 0.53
- MetaLR 0.54
- MetaSVM 0.14
- CADD 25.90
- PolyPhen-2 0.46
- ClinVar: Uncertain significance (GLUT1 deficiency syndrome 1, autosomal recessive)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available