V106A (p.Val106Ala) variant of SLC2A2 (P11168)
V106A (p.Val106Ala) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.53 / 1. The record also includes population frequency data and structural context.
V106A (p.Val106Ala) variant details
- p.Val106Ala
- Ensembl rs1716035986
- Missense
- Variant Prioritization Score for Impact Estimate 0.533
- REVEL 0.48
- CADD 23.90
- PolyPhen-2 0.17
- SIFT 0.01
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available